Efficiency and power in genetic association studies.
paper
Cited
Public
Unavailable
- Authors
- de Bakker, Paul I W; Yelensky, Roman; Pe'er, Itsik; Gabriel, Stacey B; Daly, Mark J; Altshuler, David
- Year
- 2005
- Journal
- Nature genetics
- PMID
- 16244653
- DOI
- 10.1038/ng1669
We investigated selection and analysis of tag SNPs for genome-wide association studies by specifically examining the relationship between investment in genotyping and statistical power. Do pairwise or multimarker methods maximize efficiency and power? To what extent is power compromised when tags are selected from an incomplete resource such as HapMap? We addressed these questions using genotype data from the HapMap ENCODE project, association studies simulated under a realistic disease model, and empirical correction for multiple hypothesis testing. We demonstrate a haplotype-based tagging method that uniformly outperforms single-marker tests and methods for prioritization that markedly increase tagging efficiency. Examining all observed haplotypes for association, rather than just those that are proxies for known SNPs, increases power to detect rare causal alleles, at the cost of reduced power to detect common causal alleles. Power is robust to the completeness of the reference panel from which tags are selected. These findings have implications for prioritizing tag SNPs and interpreting association studies.
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|---|---|---|---|---|
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| Runx1 transcription factor modulates opioid analgesia and withdrawal in humans and rodents. | Leduc-Pessah H et al. | — | 2026 | → |
| A Large Multicenter Brazilian Case-Control Study Exploring Genetic Variations in Interferon Regulatory Factor 6 and the Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate. | Machado RA et al. | — | 2025 | → |
| DLG2 rs11607886 polymorphism associated with schizophrenia and precuneus functional changes. | Zhu H et al. | — | 2025 | → |
| Disparities in ABO blood type determination across diverse ancestries: a systematic review and validation in the All of Us Research Program. | Martinez KL et al. | — | 2024 | → |
| HASCH - A high-throughput amplicon-based SNP-platform for medicinal cannabis and industrial hemp genotyping applications. | Mansueto L et al. | — | 2024 | → |
| <i>TMEM132C</i> rs7296262 Single-Nucleotide Polymorphism Is Significantly Associated with Nausea Induced by Opioids Administered for Cancer Pain and Postoperative Pain. | Kang Y et al. | — | 2024 | → |
| rs12411980 single-nucleotide polymorphism related to <i>PRTFDC1</i> expression is significantly associated with phantom tooth pain. | Araida J et al. | — | 2024 | → |
| A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population. | Mauleekoonphairoj J et al. | — | 2023 | → |
| Circadian Gene Variants in Diseases. | Gršković P et al. | — | 2023 | → |
| Haplotype blocks for genomic prediction: a comparative evaluation in multiple crop datasets. | Weber SE et al. | — | 2023 | → |
| Haplotype-tagged SNPs improve genomic prediction accuracy for Fusarium head blight resistance and yield-related traits in wheat. | Alemu A et al. | — | 2023 | → |
| Identification of <i>PROK2</i> gene polymorphisms as predictors of methamphetamine use disorder risk and indicators of craving scale in the Chinese Han population. | Jiang Z et al. | — | 2023 | → |
| <i>P2X3</i>-<i>P2X7</i> SNPs and gene-gene and gene-environment interactions on pediatric asthma. | Li L et al. | — | 2023 | → |
| Single-Nucleotide Polymorphisms of the <i>PAR2</i> and <i>IL-17A</i> Genes Are Significantly Associated with Chronic Pain. | Soeda M et al. | — | 2023 | → |
| The peroxisome proliferator-activated receptor γ coactivator-1 alpha rs8192678 (Gly482Ser) variant and hepatitis B virus clearance. | Abounouh K et al. | — | 2023 | → |
| The rs216009 single-nucleotide polymorphism of the <i>CACNA1C</i> gene is associated with phantom tooth pain. | Morii M et al. | — | 2023 | → |
| [Association study between haplotypes of WNT signaling pathway genes and nonsyndromic oral clefts among Chinese Han populations]. | Wang MY et al. | — | 2022 | → |
| Cohort Profile: The Alliance for Maternal and Newborn Health Improvement (AMANHI) biobanking study. | Aftab F et al. | — | 2022 | → |
| Dissecting Complex Traits Using Omics Data: A Review on the Linear Mixed Models and Their Application in GWAS. | Alamin M et al. | — | 2022 | → |
| Gene-environment interactions between CREB1 and childhood maltreatment on aggression among male Chinese adolescents. | Zhang Y et al. | — | 2022 | → |
| Genetic Analysis Reveals the Prognostic Significance of the DNA Mismatch Repair Gene <i>MSH2</i> in Advanced Prostate Cancer. | Chang HH et al. | — | 2022 | → |
| Interactions between exposure to polycyclic aromatic hydrocarbons and xenobiotic metabolism genes, and risk of breast cancer. | Lee DG et al. | — | 2022 | → |
| Interpretation of Manhattan Plots and Other Outputs of Genome-Wide Association Studies. | Wang J et al. | — | 2022 | → |
| Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci. | Laaksonen J et al. | — | 2022 | → |
| Polymorphic variants of <i>IGF2BP3</i> and <i>SENCR</i> have an impact on predisposition and/or progression of Ewing sarcoma. | Martinelli M et al. | — | 2022 | → |
| Polymorphisms in the mTOR-PI3K-Akt pathway, energy balance-related exposures and colorectal cancer risk in the Netherlands Cohort Study. | Simons CCJM et al. | — | 2022 | → |
| Recombination and mutation shape variations in the major histocompatibility complex. | Sun Y et al. | — | 2022 | → |
| Single-nucleotide polymorphisms of the SLC17A9 and P2RY12 genes are significantly associated with phantom tooth pain. | Soeda M et al. | — | 2022 | → |
| Tag Variants of LGALS-3 Containing Haplotype Block in Advanced Carotid Atherosclerosis. | Djordjevic A et al. | — | 2022 | → |
| The Roles of <i>MTRR</i> and <i>MTHFR</i> Gene Polymorphisms in Colorectal Cancer Survival. | Wang Y et al. | — | 2022 | → |
| Using population-specific add-on polymorphisms to improve genotype imputation in underrepresented populations. | Xu ZM et al. | — | 2022 | → |
| Variants Tagging <i>LGALS-3</i> Haplotype Block in Association with First Myocardial Infarction and Plasma Galectin-3 Six Months after the Acute Event. | Djordjevic A et al. | — | 2022 | → |
| Association between MIF gene promoter rs755622 and susceptibility to coronary artery disease and inflammatory cytokines in the Chinese Han population. | Luo JY et al. | — | 2021 | → |
| A Workflow for Selection of Single Nucleotide Polymorphic Markers for Studying of Genetics of Ischemic Stroke Outcomes. | Khvorykh G et al. | — | 2021 | → |
| Diet Modulates the Effects of Genetic Variants on the Vitamin D Metabolic Pathway and Bone Mineral Density in Mexican Postmenopausal Women. | Rivera-Paredez B et al. | — | 2021 | → |
| Genetic susceptibility to multiple sclerosis in African Americans. | Goodin DS et al. | — | 2021 | → |
| Genetic susceptibility to multiple sclerosis: interactions between conserved extended haplotypes of the MHC and other susceptibility regions. | Goodin DS et al. | — | 2021 | → |
| Genetic Variants in Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug-Induced Acute Urticaria/Angioedema. | Jurado-Escobar R et al. | — | 2021 | → |
| Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations. | Xie C et al. | — | 2021 | → |
| How Genetics Might Explain the Unusual Link Between Malaria and COVID-19. | Rusmini M et al. | — | 2021 | → |
| Polymorphisms in eicosanoid-related biosynthesis enzymes associated with acute urticaria/angioedema induced by nonsteroidal anti-inflammatory drug hypersensitivity. | Jurado-Escobar R et al. | — | 2021 | → |
| Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine. | Juang JJ et al. | — | 2021 | → |
| SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population. | Chen JH et al. | — | 2021 | → |
| The nature of genetic and environmental susceptibility to multiple sclerosis. | Goodin DS et al. | — | 2021 | → |
| A New Risk Variant for Multiple Sclerosis at 11q23.3 <i>Locus</i> Is Associated with Expansion of <i>CXCR5+</i> Circulating Regulatory T Cells. | Gil-Varea E et al. | — | 2020 | → |
| Association Analysis Between Common Variants of the <i>TRPM1</i> Gene and Three Mental Disorders in the Han Chinese Population. | Ma C et al. | — | 2020 | → |
| Association of <i>DEAR1</i> Tagging Single Nucleotide Polymorphisms With Breast Cancer in a Sample of Colombian Population: A Case Control Study. | Beltrán AP et al. | — | 2020 | → |
| A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients. | Wu T et al. | — | 2020 | → |
| Characterizing the impact of an exotic soybean line on elite cultivar development. | Stewart-Brown BB et al. | — | 2020 | → |
| Common variants in FAN1, located in 15q13.3, confer risk for schizophrenia and bipolar disorder in Han Chinese. | Jian X et al. | — | 2020 | → |
| Eagle: multi-locus association mapping on a genome-wide scale made routine. | George AW et al. | — | 2020 | → |
| Muscle-Liver Trafficking of BCAA-Derived Nitrogen Underlies Obesity-Related Glycine Depletion. | White PJ et al. | — | 2020 | → |
| Single‐marker and haplotype‐based association analysis of anthracnose (Colletotrichum dematium) resistance in spinach (Spinacia oleracea) | Awika HO et al. | — | 2020 | — |
| The Genetic Polymorphism of <i>CYP3A4</i> rs<i>2242480</i> is Associated with Sirolimus Trough Concentrations Among Adult Renal Transplant Recipients. | Lolita L et al. | — | 2020 | → |
| The Impact of the Circadian Genes <i>CLOCK</i> and <i>ARNTL</i> on Myocardial Infarction. | Škrlec I et al. | — | 2020 | → |
| ACTN3 is associated with children's physical fitness in Han Chinese. | Zhang Q et al. | — | 2019 | → |
| A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers. | Biasoli D et al. | — | 2019 | → |
| Effects of X-chromosome Tenomodulin Genetic Variants on Obesity in a Children's Cohort and Implications of the Gene in Adipocyte Metabolism. | Ruiz-Ojeda FJ et al. | — | 2019 | → |
| Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk. | Schuetz JM et al. | — | 2019 | → |
| Genetic variants in the circadian rhythm pathway as indicators of prostate cancer progression. | Yu CC et al. | — | 2019 | → |
| Genomic Selection for Yield and Seed Composition Traits Within an Applied Soybean Breeding Program. | Stewart-Brown BB et al. | — | 2019 | → |
| Investigating Gene-Gene and Gene-Environment Interactions in the Association Between Overnutrition and Obesity-Related Phenotypes. | Tessier F et al. | — | 2019 | → |
| Mathematical Properties of Linkage Disequilibrium Statistics Defined by Normalization of the Coefficient D = pAB - pApB. | Kang JTL et al. | — | 2019 | → |
| Minor alleles are associated with white rust (<i>Albugo occidentalis</i>) susceptibility in spinach (<i>Spinacia oleracea</i>). | Awika HO et al. | — | 2019 | → |
| Multi-allelic QTL analysis of protein content in a bi-parental population of cultivated tetraploid potato. | Klaassen MT et al. | — | 2019 | → |
| Postmortem brain tissue as an underutilized resource to study the molecular pathology of neuropsychiatric disorders across different ethnic populations. | Vornholt E et al. | — | 2019 | → |
| Primary closed angle glaucoma in the Basset Hound: Genetic investigations using genome-wide association and RNA sequencing strategies. | Oliver JAC et al. | — | 2019 | → |
| Toll-like receptor 3 acts as a suppressor gene in breast cancer initiation and progression: a two-stage association study and functional investigation. | Fan L et al. | — | 2019 | → |
| Variations in circadian genes and individual nocturnal symptoms of insomnia. The HUNT study. | Bragantini D et al. | — | 2019 | → |
| A Genetic Polymorphism in <i>CTLA-4</i> Is Associated with Overall Survival in Sunitinib-Treated Patients with Clear Cell Metastatic Renal Cell Carcinoma. | Liu X et al. | — | 2018 | → |
| Alcohol intake, ADH1B and ADH1C genotypes, and the risk of colorectal cancer by sex and subsite in the Netherlands Cohort Study. | Offermans NSM et al. | — | 2018 | → |
| Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism. | Wu T et al. | — | 2018 | → |
| A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN. | Devasenapathy S et al. | — | 2018 | → |
| A Pilot Study Investigating the Influence of Glucagon-Like Peptide-1 Receptor Single Nucleotide Polymorphisms on Gastric Emptying Rate in Caucasian Men. | Yau AMW et al. | — | 2018 | → |
| Association between GOLGB1 tag-polymorphisms and nonsyndromic cleft palate only in the Brazilian population. | Machado RA et al. | — | 2018 | → |
| Association of fat mass and obesity-associated and retinitis pigmentosa guanosine triphosphatase (GTPase) regulator-interacting protein-1 like polymorphisms with body mass index in Chinese women. | Chen B et al. | — | 2018 | → |
| Association of hyperhomocysteinemia with genetic variants in key enzymes of homocysteine metabolism and methotrexate toxicity in rheumatoid arthritis patients. | Chaabane S et al. | — | 2018 | → |
| Associations of NADPH oxidase-related genes with blood pressure changes and incident hypertension: The GenSalt Study. | Li H et al. | — | 2018 | → |
| Association study of FGF18 with developmental dyslexia in Chinese population. | Chen H et al. | — | 2018 | → |
| Effective Genomic Selection in a Narrow-Genepool Crop with Low-Density Markers: Asian Rapeseed as an Example. | Werner CR et al. | — | 2018 | → |
| Effects of genetic variants of ST8SIA2 and NCAM1 genes on seasonal mood changes and circadian preference in the general population. | Yang SY et al. | — | 2018 | → |
| Genetic polymorphisms of NOS2 and predisposition to fracture non-union: A case control study based on Han Chinese population. | Huang W et al. | — | 2018 | → |
| Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion. | Hodžić A et al. | — | 2018 | → |
| Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients. | Jacobs DI et al. | — | 2018 | → |
| Highly conserved extended haplotypes of the major histocompatibility complex and their relationship to multiple sclerosis susceptibility. | Goodin DS et al. | — | 2018 | → |
| <i>ADAM33</i> gene polymorphisms in Southwestern Iranian patients with asthma. | Farjadian S et al. | — | 2018 | → |
| Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. | Wojcik GL et al. | — | 2018 | → |
| Molecular Basis for Dysregulated Activation of NKX2-5 in the Vascular Remodeling of Systemic Sclerosis. | Dritsoula A et al. | — | 2018 | → |
| Multiple genomic regions influence root morphology and seedling growth in cultivated sunflower (Helianthus annuus L.) under well-watered and water-limited conditions. | Masalia RR et al. | — | 2018 | → |
| Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence. | Kelaï S et al. | — | 2018 | → |
| NF-kB2 Genetic Variations are Significantly Associated with Non-Small Cell Lung Cancer Risk and Overall Survival. | Dimitrakopoulos FD et al. | — | 2018 | → |
| Pharmacogenetics of oral antidiabetes drugs: evidence for diverse signals at the IRS1 locus. | Prudente S et al. | — | 2018 | → |
| Possible effect of SNAIL family transcriptional repressor 1 polymorphisms in non-syndromic cleft lip with or without cleft palate. | Cura F et al. | — | 2018 | → |
| The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites. | O'Reilly J et al. | — | 2018 | → |
| Tools for Genetic Studies in Experimental Populations of Polyploids. | Bourke PM et al. | — | 2018 | → |
| An adaptive threshold determination method of feature screening for genomic selection. | Fu G et al. | — | 2017 | → |
| Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis. | Achour Y et al. | — | 2017 | → |
| Association between taste receptor (TAS) genes and the perception of wine characteristics. | Carrai M et al. | — | 2017 | → |
| Association between the zinc finger protein 804A (ZNF804A) gene and the risk of schizophrenia and bipolar I disorder across diagnostic boundaries. | Baek JH et al. | — | 2017 | → |
| Association of ACVRL1 Genetic Polymorphisms with Arteriovenous Malformations: A Case-Control Study and Meta-Analysis. | Ge M et al. | — | 2017 | → |
| Association of Topoisomerase II (TOP2A) and Dual-Specificity Phosphatase 6 (DUSP6) Single Nucleotide Polymorphisms with Radiation Treatment Response and Prognosis of Lung Cancer in Han Chinese. | Wang TL et al. | — | 2017 | → |
| Associations between arsenic (+3 oxidation state) methyltransferase (AS3MT) and N-6 adenine-specific DNA methyltransferase 1 (N6AMT1) polymorphisms, arsenic metabolism, and cancer risk in a chilean population. | de la Rosa R et al. | — | 2017 | → |
| Associations Between Genetic Variants of NADPH Oxidase-Related Genes and Blood Pressure Responses to Dietary Sodium Intervention: The GenSalt Study. | Han X et al. | — | 2017 | → |
| Detecting genetic association through shortest paths in a bidirected graph. | Ueki M et al. | — | 2017 | → |
| Evaluation of the interaction between genetic variants of GAD1 and miRNA in bipolar disorders. | Chung YE et al. | — | 2017 | → |
| Frequency of common polymorphisms in <b><i>Caveolin 1</i></b> ( <b><i>CAV1</i></b> ) gene in adults with high serum triglycerides from Colombian Caribbean Coast. | Mora-Garcia GJ et al. | — | 2017 | → |
| Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility. | Hodžić A et al. | — | 2017 | → |
| Genetic Variation in S100B Modulates Neural Processing of Visual Scenes in Han Chinese. | Kong XZ et al. | — | 2017 | → |
| Genome-Enabled Prediction of Breeding Values for Feedlot Average Daily Weight Gain in Nelore Cattle. | Somavilla AL et al. | — | 2017 | → |
| Increased expression of IL12B mRNA transcribed from the risk haplotype for Crohn's disease is a risk factor for disease relapse in Japanese patients. | Kakuta Y et al. | — | 2017 | → |
| Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer. | Carter H et al. | — | 2017 | → |
| Interactive Influence of N6AMT1 and As3MT Genetic Variations on Arsenic Metabolism in the Population of Inner Mongolia, China. | Chen X et al. | — | 2017 | → |
| NOTCH4 gene polymorphisms as potential risk factors for brain arteriovenous malformation development and hemorrhagic presentation. | Delev D et al. | — | 2017 | → |
| Polymorphisms in CYP2C9 are associated with response to indomethacin among neonates with patent ductus arteriosus. | Smith CJ et al. | — | 2017 | → |
| Stress-related psychological symptoms contribute to axial pain persistence after motor vehicle collision: path analysis results from a prospective longitudinal study. | Feinberg RK et al. | — | 2017 | → |
| The association study of nonsyndromic cleft lip with or without cleft palate identified risk variants of the GLI3 gene in a Chinese population. | Wang Y et al. | — | 2017 | → |
| THE PPARGC1A - GLY482SER POLYMORPHISM (RS8192678) AND THE METABOLIC SYNDROME IN A CENTRAL ROMANIAN POPULATION. | Csép K et al. | — | 2017 | → |
| The YWHAE gene confers risk to major depressive disorder in the male group of Chinese Han population. | Liu J et al. | — | 2017 | → |
| Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention. | Billings LK et al. | — | 2017 | → |
| Vitamin D receptor and calcium-sensing receptor polymorphisms and colorectal cancer survival in the Newfoundland population. | Zhu Y et al. | — | 2017 | → |
| A common polymorphism in the ABCB1 gene is associated with side effects of PGP-dependent antidepressants in a large naturalistic Dutch cohort. | Bet PM et al. | — | 2016 | → |
| An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation. | Brundin L et al. | — | 2016 | → |
| A powerful score-based test statistic for detecting gene-gene co-association. | Xu J et al. | — | 2016 | → |
| Association between AUTS2 haplotypes and alcohol dependence in a Japanese population. | Narita S et al. | — | 2016 | → |
| Association between UGT2B7 gene polymorphisms and fentanyl sensitivity in patients undergoing painful orthognathic surgery. | Muraoka W et al. | — | 2016 | → |
| Association of functional genetic variants of transcription factor Forkhead Box P3 and Nuclear Factor-κB with end-stage renal disease and renal allograft outcome. | Misra MK et al. | — | 2016 | → |
| Association of genetic variations of selenoprotein genes, plasma selenium levels, and prostate cancer aggressiveness at diagnosis. | Xie W et al. | — | 2016 | → |
| Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. | Wang Y et al. | — | 2016 | → |
| Association study of MMP8 gene in osteoarthritis. | Näkki A et al. | — | 2016 | → |
| Association study of PNPLA2 gene with histological parameters of NAFLD in an obese population. | Zegers D et al. | — | 2016 | → |
| CD99 polymorphisms significantly influence the probability to develop Ewing sarcoma in earlier age and patient disease progression. | Martinelli M et al. | — | 2016 | → |
| Common Genetic Variation in CYP17A1 and Response to Abiraterone Acetate in Patients with Metastatic Castration-Resistant Prostate Cancer. | Binder M et al. | — | 2016 | → |
| Controversial opinion: evaluation of EGR1 and LAMA2 loci for high myopia in Chinese populations. | Lin FY et al. | — | 2016 | → |
| Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriages. | Misra MK et al. | — | 2016 | → |
| Determinants of acquired activated protein C resistance and D-dimer in breast cancer. | Tinholt M et al. | — | 2016 | → |
| Discovering Genome-Wide Tag SNPs Based on the Mutual Information of the Variants. | Elmas A et al. | — | 2016 | → |
| DNA repair variants and breast cancer risk. | Grundy A et al. | — | 2016 | → |
| Effects of the MAOA gene and levels of exposure to violence on antisocial outcomes. | Ouellet-Morin I et al. | — | 2016 | → |
| Enabling Privacy-Preserving GWASs in Heterogeneous Human Populations. | Simmons S et al. | — | 2016 | → |
| Evaluating the Role of Genetic Variants on first-line antiepileptic drug response in North India: Significance of SCN1A and GABRA1 Gene Variants in Phenytoin Monotherapy and its Serum Drug Levels. | Baghel R et al. | — | 2016 | → |
| Evaluation of association of common variants in HTR1A and HTR5A with schizophrenia and executive function. | Guan F et al. | — | 2016 | → |
| Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 9q22.33 and 14q13.3 detects novel candidate functional SNPs in Europeans from metropolitan France and Melanesians from New Caledonia. | Tcheandjieu C et al. | — | 2016 | → |
| Functional variants of 17q12-21 are associated with allergic asthma but not allergic rhinitis. | Andiappan AK et al. | — | 2016 | → |
| Genetic association between NRG1 and schizophrenia, major depressive disorder, bipolar disorder in Han Chinese population. | Wen Z et al. | — | 2016 | → |
| Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions. | Mirkovic B et al. | — | 2016 | → |
| Genetic Determinants of Methotrexate Toxicity in Tunisian Patients with Rheumatoid Arthritis: A Study of Polymorphisms Involved in the MTX Metabolic Pathway. | Chaabane S et al. | — | 2016 | → |
| Genetics of Diabetic Kidney Disease. | Florez JC | — | 2016 | → |
| Genetic variants determining survival and fertility in an adverse African environment: a population-based large-scale candidate gene association study. | Koopman JJ et al. | — | 2016 | → |
| Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion. | Müller A et al. | — | 2016 | → |
| Genetic variation in vitamin D-related genes and risk of breast cancer among women of European and East Asian descent. | Shi J et al. | — | 2016 | → |
| Germline Genetic Variants in the Wnt/β-Catenin Pathway as Predictors of Colorectal Cancer Risk. | Hildebrandt MA et al. | — | 2016 | → |
| High plasma chemerin is associated with renal dysfunction and predictive for cardiovascular events - Insights from phenotype and genotype characterization. | Leiherer A et al. | — | 2016 | → |
| Impact of host genetic polymorphisms on vaccine induced antibody response. | Linnik JE et al. | — | 2016 | → |
| Inherited Variants in Wnt Pathway Genes Influence Outcomes of Prostate Cancer Patients Receiving Androgen Deprivation Therapy. | Geng JH et al. | — | 2016 | → |
| Integrating haplotype-specific linkage maps in tetraploid species using SNP markers. | Bourke PM et al. | — | 2016 | → |
| Interleukin 6 SNP rs1800797 associates with the risk of adult-onset asthma. | Lajunen TK et al. | — | 2016 | → |
| Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity. | Van Camp JK et al. | — | 2016 | → |
| Methylation quantitative trait loci within the TOMM20 gene are associated with metabolic syndrome-related lipid alterations in severely obese subjects. | de Toro-Martín J et al. | — | 2016 | → |
| Modification of the association between early adversity and obsessive-compulsive disorder by polymorphisms in the MAOA, MAOB and COMT genes. | McGregor NW et al. | — | 2016 | → |
| Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study. | Qu LS et al. | — | 2016 | → |
| Polymorphisms in NRGN are associated with schizophrenia, major depressive disorder and bipolar disorder in the Han Chinese population. | Wen Z et al. | — | 2016 | → |
| Polymorphisms of Insulin-Like Growth Factor 1 Pathway Genes and Breast Cancer Risk. | Shi J et al. | — | 2016 | → |
| Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes. | Kaartokallio T et al. | — | 2016 | → |
| Quantitative trait loci mapping for Gibberella ear rot resistance and associated agronomic traits using genotyping-by-sequencing in maize. | Kebede AZ et al. | — | 2016 | → |
| Quercetin intake, MATE1 polymorphism, and metabolic syndrome in Korean population: Hallym aging study. | Lee JE et al. | — | 2016 | → |
| Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity. | Raj P et al. | — | 2016 | → |
| Role played by the SP4 gene in schizophrenia and major depressive disorder in the Han Chinese population. | Chen J et al. | — | 2016 | → |
| Sex-specific association between the albumin D-element binding protein gene and metabolic syndrome in patients with bipolar disorder and schizophrenia. | Kim EY et al. | — | 2016 | → |
| Systematic assessment of the influence of complement gene polymorphisms on kidney transplant outcome. | Ermini L et al. | — | 2016 | → |
| The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility. | Wang Y et al. | — | 2016 | → |
| Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes. | Francis SM et al. | — | 2016 | → |
| A haplotype of the norepinephrine transporter gene (SLC6A2) is associated with visual memory in attention-deficit/hyperactivity disorder. | Shang CY et al. | — | 2015 | → |
| A multiancestry study identifies novel genetic associations with CHRNA5 methylation in human brain and risk of nicotine dependence. | Hancock DB et al. | — | 2015 | → |
| Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular Hypertension. | Hogewind BF et al. | — | 2015 | → |
| Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2. | Kolder ICRM et al. | — | 2015 | → |
| A penalized likelihood approach for investigating gene-drug interactions in pharmacogenetic studies. | Neely ML et al. | — | 2015 | → |
| A spatial haplotype copying model with applications to genotype imputation. | Yang WY et al. | — | 2015 | → |
| Association between AKT1 Gene Polymorphism rs2498794 and Smoking-Related Traits with reference to Cancer Susceptibility. | Nishizawa D et al. | — | 2015 | → |
| Association between ST8SIA2 and the Risk of Schizophrenia and Bipolar I Disorder across Diagnostic Boundaries. | Yang SY et al. | — | 2015 | → |
| Association of CRP genetic variants with blood concentrations of C-reactive protein and colorectal cancer risk. | Nimptsch K et al. | — | 2015 | → |
| Association of interleukin 22 polymorphisms with gastric cancer risk. | Qin SY et al. | — | 2015 | → |
| Associations of PER3 and RORA Circadian Gene Polymorphisms and Depressive Symptoms in Older Adults. | Maglione JE et al. | — | 2015 | → |
| Associations of Renin-Angiotensin-Aldosterone System Genes With Blood Pressure Changes and Hypertension Incidence. | He WJ et al. | — | 2015 | → |
| Association study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population. | Chen H et al. | — | 2015 | → |
| Calcium intake, polymorphisms of the calcium-sensing receptor, and recurrent/aggressive prostate cancer. | Binder M et al. | — | 2015 | → |
| Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. | Carvajal-Carmona LG et al. | — | 2015 | → |
| Cohort Profile: The Nicotine Dependence in Teens (NDIT) Study. | O'Loughlin J et al. | — | 2015 | → |
| Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer. | O'Mara TA et al. | — | 2015 | → |
| Cytotoxic T-lymphocyte antigen 4 gene polymorphism influences the incidence of symptomatic human cytomegalovirus infection after renal transplantation. | Misra MK et al. | — | 2015 | → |
| Evaluation of genetic susceptibility of common variants in CACNA1D with schizophrenia in Han Chinese. | Guan F et al. | — | 2015 | → |
| Evidence for schizophrenia susceptibility alleles in the Indian population: An association of neurodevelopmental genes in case-control and familial samples. | Jajodia A et al. | — | 2015 | → |
| Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency. | Choi JH et al. | — | 2015 | → |
| Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit. | Baeza-Richer C et al. | — | 2015 | → |
| Genetic interaction analysis of TCF7L2 for biochemical recurrence after radical prostatectomy in localized prostate cancer. | Chen CS et al. | — | 2015 | → |
| Genetic modifiers of folate, vitamin B-12, and homocysteine status in a cross-sectional study of the Canadian population. | Zinck JW et al. | — | 2015 | → |
| Genetic variants in the Hippo pathway predict biochemical recurrence after radical prostatectomy for localized prostate cancer. | Huang CY et al. | — | 2015 | → |
| Genetic variants of inducible costimulator are associated with allergic asthma susceptibility. | Andiappan AK et al. | — | 2015 | → |
| Genetic Variation and Insulin Resistance in Middle-Aged Chinese Men. | Villegas R et al. | — | 2015 | → |
| Genetic variation in cell cycle regulatory gene AURKA and association with intrinsic breast cancer subtype. | Taylor NJ et al. | — | 2015 | → |
| Genetic variation in estrogen and progesterone pathway genes and breast cancer risk: an exploration of tumor subtype-specific effects. | Nyante SJ et al. | — | 2015 | → |
| Genetic variation in the TNF/TRAF2/ASK1/p38 kinase signaling pathway as markers for postoperative pulmonary complications in lung cancer patients. | Hildebrandt MA et al. | — | 2015 | → |
| Genetic variations in the annexin A5 gene and the risk of pregnancy-related venous thrombosis. | Dahm AE et al. | — | 2015 | → |
| Genome-Wide Association Mapping for Leaf Tip Necrosis and Pseudo-black Chaff in Relation to Durable Rust Resistance in Wheat. | Juliana P et al. | — | 2015 | → |
| GIMAP GTPase family genes: potential modifiers in autoimmune diabetes, asthma, and allergy. | Heinonen MT et al. | — | 2015 | → |
| Haplotype-based approach to known MS-associated regions increases the amount of explained risk. | Khankhanian P et al. | — | 2015 | → |
| HLA-allelotype associations with nevirapine-induced hypersensitivity reactions and hepatotoxicity: a systematic review of the literature and meta-analysis. | Cornejo Castro EM et al. | — | 2015 | → |
| Identification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas. | Luzón-Toro B et al. | — | 2015 | → |
| IRF6 Is a Marker of Severity in Nonsyndromic Cleft Lip/Palate. | Kerameddin S et al. | — | 2015 | → |
| Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis. | Zhang B et al. | — | 2015 | → |
| Leveraging global gene expression patterns to predict expression of unmeasured genes. | Rudd J et al. | — | 2015 | → |
| Natural Variation in the Flag Leaf Morphology of Rice Due to a Mutation of the NARROW LEAF 1 Gene in Oryza sativa L. | Taguchi-Shiobara F et al. | — | 2015 | → |
| Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults. | Hochner H et al. | — | 2015 | → |
| Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. | Shim U et al. | — | 2015 | → |
| Polymorphisms of IKBKE gene are associated with major depressive disorder and panic disorder. | Traks T et al. | — | 2015 | → |
| Population-specific association of genes for telomere-associated proteins with longevity in an Italian population. | Crocco P et al. | — | 2015 | → |
| Possible Gender-Related Modulation by the ROCK1 Gene in Colorectal Cancer Susceptibility. | Zucchini C et al. | — | 2015 | → |
| Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions. | Wang Y et al. | — | 2015 | → |
| Premenopausal plasma carotenoids, fluorescent oxidation products, and subsequent breast cancer risk in the nurses' health studies. | Sisti JS et al. | — | 2015 | → |
| Proper Use of Allele-Specific Expression Improves Statistical Power for <i>cis</i>-eQTL Mapping with RNA-Seq Data. | Hu YJ et al. | — | 2015 | → |
| Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies. | Wojcik GL et al. | — | 2015 | → |
| Statistical analysis for genome-wide association study. | Zeng P et al. | — | 2015 | → |
| TACR1 gene polymorphism and sex differences in postoperative nausea and vomiting. | Hayase T et al. | — | 2015 | → |
| The association of elastin gene variants with two angiographic subtypes of polypoidal choroidal vasculopathy. | Yanagisawa S et al. | — | 2015 | → |
| The genetic basis of population fecundity prediction across multiple field populations of Nilaparvata lugens. | Sun ZX et al. | — | 2015 | → |
| The genetics of POAG in black South Africans: a candidate gene association study. | Williams SE et al. | — | 2015 | → |
| The NVL gene confers risk for both major depressive disorder and schizophrenia in the Han Chinese population. | Wang M et al. | — | 2015 | → |
| The possible role of EZH2 and DNMT1 polymorphisms in sporadic triple-negative breast carcinoma in southern Chinese females. | Tao R et al. | — | 2015 | → |
| Tumor expression, plasma levels and genetic polymorphisms of the coagulation inhibitor TFPI are associated with clinicopathological parameters and survival in breast cancer, in contrast to the coagulation initiator TF. | Tinholt M et al. | — | 2015 | → |
| Using Network Methodology to Infer Population Substructure. | Prokopenko D et al. | — | 2015 | → |
| Variant of BCL3 gene is strongly associated with five-year survival of non-small-cell lung cancer patients. | Dimitrakopoulos FI et al. | — | 2015 | → |
| A 3'UTR polymorphism of IL-6R is associated with Chinese pediatric tuberculosis. | Shen C et al. | — | 2014 | → |
| A genetic variant of PPARA modulates cardiovascular risk biomarkers after milk consumption. | Loria-Kohen V et al. | — | 2014 | → |
| AKAP9 is a genetic modifier of congenital long-QT syndrome type 1. | de Villiers CP et al. | — | 2014 | → |
| Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS). | Studer J et al. | — | 2014 | → |
| Association between KCNJ6 (GIRK2) gene polymorphism rs2835859 and post-operative analgesia, pain sensitivity, and nicotine dependence. | Nishizawa D et al. | — | 2014 | → |
| Association between the DAT1 gene and spatial working memory in attention deficit hyperactivity disorder. | Shang CY et al. | — | 2014 | → |
| Association of a single nucleotide polymorphism in HOXB9 with developmental dysplasia of the hip: a case-control study. | Hao Z et al. | — | 2014 | → |
| Association of <i>XRCC1</i> and <i>XRCC3</i> gene haplotypes with the development of radiation-induced fibrosis in patients with nasopharyngeal carcinoma. | Cheuk IW et al. | — | 2014 | → |
| Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. | Nelson EC et al. | — | 2014 | → |
| Association of the KCNJ5 gene with Tourette Syndrome and Attention-Deficit/Hyperactivity Disorder. | Gomez L et al. | — | 2014 | → |
| Association study identifying a new susceptibility gene (AUTS2) for schizophrenia. | Zhang B et al. | — | 2014 | → |
| Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population. | Sun Y et al. | — | 2014 | → |
| Breast cancer risk, nightwork, and circadian clock gene polymorphisms. | Truong T et al. | — | 2014 | → |
| CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population. | He K et al. | — | 2014 | → |
| CD11a polymorphisms regulate TH2 cell homing and TH2-related disease. | Knight JM et al. | — | 2014 | → |
| Common genetic variation in sFRP5 is associated with fat distribution in men. | Van Camp JK et al. | — | 2014 | → |
| Common variation at PPARGC1A/B and change in body composition and metabolic traits following preventive interventions: the Diabetes Prevention Program. | Franks PW et al. | — | 2014 | → |
| Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. | Lemaitre RN et al. | — | 2014 | → |
| CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in Vietnam. | Grant AV et al. | — | 2014 | → |
| Development of a broad-based ADME panel for use in pharmacogenomic studies. | Brown AM et al. | — | 2014 | → |
| Differences in meiotic recombination rates in childhood acute lymphoblastic leukemia at an MHC class II hotspot close to disease associated haplotypes. | Thompson P et al. | — | 2014 | → |
| Estimation of linkage disequilibrium and interspecific gene flow in Ficedula flycatchers by a newly developed 50k single-nucleotide polymorphism array. | Kawakami T et al. | — | 2014 | → |
| Evidence of the involvement of the DHFR gene in nonsyndromic cleft lip with or without cleft palate. | Martinelli M et al. | — | 2014 | → |
| Examining the polymorphisms in the hypoxia pathway genes in relation to outcome in colorectal cancer. | Haja Mohideen AM et al. | — | 2014 | → |
| Fast pairwise IBD association testing in genome-wide association studies. | Han B et al. | — | 2014 | → |
| FCGR2C polymorphisms associate with HIV-1 vaccine protection in RV144 trial. | Li SS et al. | — | 2014 | → |
| FTO polymorphisms moderate the association of food reinforcement with energy intake. | Scheid JL et al. | — | 2014 | → |
| FVB/NJ mice demonstrate a youthful sensitivity to noise-induced hearing loss and provide a useful genetic model for the study of neural hearing loss. | Ho MK et al. | — | 2014 | → |
| Genetic association study of adiposity and melanocortin-4 receptor (MC4R) common variants: replication and functional characterization of non-coding regions. | Evans DS et al. | — | 2014 | → |
| Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe. | Carreras-Torres R et al. | — | 2014 | → |
| Genetic variants and early cigarette smoking and nicotine dependence phenotypes in adolescents. | O'Loughlin J et al. | — | 2014 | → |
| Genetic variations in UDP-glucuronosyltransferase 2B15 in a Korean population. | Hwang MS et al. | — | 2014 | → |
| Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients. | Kaur H et al. | — | 2014 | → |
| G-protein β3 subunit genetic variation moderates five-year depressive symptom trajectories of primary care attendees. | Bousman CA et al. | — | 2014 | → |
| Haplotypes of P2RX7 gene polymorphisms are associated with both cold pain sensitivity and analgesic effect of fentanyl. | Ide S et al. | — | 2014 | → |
| Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study. | Kuo PH et al. | — | 2014 | → |
| Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. | Deelen P et al. | — | 2014 | → |
| Imputation without doing imputation: a new method for the detection of non-genotyped causal variants. | Howey R et al. | — | 2014 | → |
| Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: a case-control study. | Tinholt M et al. | — | 2014 | → |
| Inflammation-related genetic variants predict toxicity following definitive radiotherapy for lung cancer. | Pu X et al. | — | 2014 | → |
| Inflammation-related genetic variations and survival in patients with advanced non-small cell lung cancer receiving first-line chemotherapy. | Pu X et al. | — | 2014 | → |
| Influence of MILR1 promoter polymorphism on expression levels and the phenotype of atopy. | Nanatsue K et al. | — | 2014 | → |
| ITIH family genes confer risk to schizophrenia and major depressive disorder in the Han Chinese population. | He K et al. | — | 2014 | → |
| LRRC4 haplotypes are associated with pituitary adenoma in a Chinese population. | Xiao L et al. | — | 2014 | → |
| Maternal but not fetal FADS gene variants modify the association between maternal long-chain PUFA intake in pregnancy and birth weight. | Moltó-Puigmartí C et al. | — | 2014 | → |
| Methylenetetrahydrofolate reductase (MTHFR) genetic variation and major depressive disorder prognosis: A five-year prospective cohort study of primary care attendees. | Bousman CA et al. | — | 2014 | → |
| No man is an island: living in a disadvantaged neighborhood influences chronic pain development after motor vehicle collision. | Ulirsch JC et al. | — | 2014 | → |
| Novel single nucleotide polymorphisms of the insulin-like growth factor-I gene and their associations with growth traits in common carp (Cyprinus carpio L.). | Feng X et al. | — | 2014 | → |
| Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. | Shim U et al. | — | 2014 | → |
| Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. | Denis M et al. | — | 2014 | → |
| Platelet-specific collagen receptor glycoprotein VI gene variants affect recurrent pregnancy loss. | Siddesh A et al. | — | 2014 | → |
| Polymorphisms in vascular endothelial growth factor receptor 2 are associated with better response rates to ranibizumab treatment in age-related macular degeneration. | Hermann MM et al. | — | 2014 | → |
| Polymorphisms of SP110 are associated with both pulmonary and extra-pulmonary tuberculosis among the Vietnamese. | Fox GJ et al. | — | 2014 | → |
| Premenopausal plasma ferritin levels, HFE polymorphisms, and risk of breast cancer in the nurses' health study II. | Graff RE et al. | — | 2014 | → |
| Prognostic impact of telomere maintenance gene polymorphisms on hepatocellular carcinoma patients with chronic hepatitis B. | Jung SW et al. | — | 2014 | → |
| PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals. | Nelson EC et al. | — | 2014 | → |
| Sequence variants of the HTR3A gene contribute to the genetic prediction of postoperative nausea in Taiwan. | Joy Lin YM et al. | — | 2014 | → |
| SIBLING family genes and bone mineral density: association and allele-specific expression in humans. | Alam I et al. | — | 2014 | → |
| Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations. | Goodin DS et al. | — | 2014 | → |
| Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population. | Chen H et al. | — | 2014 | → |
| SULF2 strongly prediposes to fasting and postprandial triglycerides in patients with obesity and type 2 diabetes mellitus. | Hassing HC et al. | — | 2014 | → |
| TGFBI (βIG-H3) is a diabetes-risk gene based on mouse and human genetic studies. | Han B et al. | — | 2014 | → |
| The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke. | Pedneault M et al. | — | 2014 | → |
| The association of host and genetic melanoma risk factors with Breslow thickness in the Western Australian Melanoma Health Study. | Cadby G et al. | — | 2014 | → |
| The evidence for the contribution of the autism susceptibility candidate 2 (AUTS2) gene in heroin dependence susceptibility. | Dang W et al. | — | 2014 | → |
| The utility of low-density genotyping for imputation in the Thoroughbred horse. | Corbin LJ et al. | — | 2014 | → |
| Two single-nucleotide polymorphisms in the DKK1 gene are associated with developmental dysplasia of the hip in the Chinese Han female population. | Liu S et al. | — | 2014 | → |
| Variation in genes related to hepatic lipid metabolism and changes in waist circumference and body weight. | Meidtner K et al. | — | 2014 | → |
| Variation in oxytocin receptor gene (OXTR) polymorphisms is associated with emotional and behavioral reactions to betrayal. | Tabak BA et al. | — | 2014 | → |
| VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis. | Avidan N et al. | — | 2014 | → |
| WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening. | Velázquez-Cruz R et al. | — | 2014 | → |
| 17q12-21 and asthma: interactions with early-life environmental exposures. | Blekic M et al. | — | 2013 | → |
| ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas. | Johnatty SE et al. | — | 2013 | → |
| ABCC11/MRP8 polymorphisms affect 5-fluorouracil-induced severe toxicity and hepatic expression. | Magdy T et al. | — | 2013 | → |
| Ablation of LGR4 promotes energy expenditure by driving white-to-brown fat switch. | Wang J et al. | — | 2013 | → |
| A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. | Lubieniecka JM et al. | — | 2013 | → |
| A genetic variant in granzyme B is associated with progression of joint destruction in rheumatoid arthritis. | Knevel R et al. | — | 2013 | → |
| A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication. | Hein R et al. | — | 2013 | → |
| ALOX5 is associated with tuberculosis in a subset of the pediatric population of North China. | Shen C et al. | — | 2013 | → |
| ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. | Nelson EC et al. | — | 2013 | → |
| Applications of multifactor dimensionality reduction to genome-wide data using the R package 'MDR'. | Winham S | — | 2013 | → |
| A Single Nucleotide Polymorphism within the Interferon Gamma Receptor 2 Gene Perfectly Coincides with Polledness in Holstein Cattle. | Glatzer S et al. | — | 2013 | → |
| Association between genetic polymorphisms in Ca(v)2.3 (R-type) Ca2+ channels and fentanyl sensitivity in patients undergoing painful cosmetic surgery. | Ide S et al. | — | 2013 | → |
| Association of AMP-activated protein kinase with risk and progression of non-Hodgkin lymphoma. | Hoffman AE et al. | — | 2013 | → |
| Association of a NOD2 gene polymorphism and T-helper 17 cells with presumed ocular toxoplasmosis. | Dutra MS et al. | — | 2013 | → |
| Association of rs1344706 in the ZNF804A gene with schizophrenia in a case/control sample from Indonesia. | Schwab SG et al. | — | 2013 | → |
| Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study. | Tang W et al. | — | 2013 | → |
| Association of the brain-derived neurotrophic factor gene G196A rs6265 polymorphisms and the cognitive function and clinical symptoms of schizophrenia. | Zhai J et al. | — | 2013 | → |
| Association of the PDYN gene with alcohol dependence and the propensity to drink in negative emotional states. | Karpyak VM et al. | — | 2013 | → |
| Association of XRCC3 and XRCC4 gene polymorphisms, family history of cancer and tobacco smoking with non-small-cell lung cancer in a Chinese population: a case-control study. | He F et al. | — | 2013 | → |
| Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA). | Shah SA et al. | — | 2013 | → |
| Associations between single-nucleotide polymorphisms in the PI3K-PTEN-AKT-mTOR pathway and increased risk of brain metastasis in patients with non-small cell lung cancer. | Li Q et al. | — | 2013 | → |
| Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. | Zhao Z et al. | — | 2013 | → |
| Association study of germline variants in CCNB1 and CDK1 with breast cancer susceptibility, progression, and survival among Chinese Han women. | Li Y et al. | — | 2013 | → |
| CD2AP is associated with end-stage renal disease in patients with type 1 diabetes. | Hyvönen ME et al. | — | 2013 | → |
| CDKN2B expression in adipose tissue of familial combined hyperlipidemia patients. | Horswell SD et al. | — | 2013 | → |
| CNTNAP2 polymorphisms and structural brain connectivity: a diffusion-tensor imaging study. | Clemm von Hohenberg C et al. | — | 2013 | → |
| Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly. | Evans DS et al. | — | 2013 | → |
| Common genetic variants in Wnt signaling pathway genes as potential prognostic biomarkers for colorectal cancer. | Ting WC et al. | — | 2013 | → |
| Common genetic variation of the calcium-sensing receptor and lethal prostate cancer risk. | Shui IM et al. | — | 2013 | → |
| Corticotropin-releasing hormone system polymorphisms are associated with children's cortisol reactivity. | Sheikh HI et al. | — | 2013 | → |
| Defining the contribution of CNTNAP2 to autism susceptibility. | Sampath S et al. | — | 2013 | → |
| Development of a genotyping microarray for studying the role of gene-environment interactions in risk for lung cancer. | Baldwin DA et al. | — | 2013 | → |
| DNA repair gene variants in relation to overall cancer risk: a population-based study. | Alberg AJ et al. | — | 2013 | → |
| Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort. | Kukshal P et al. | — | 2013 | → |
| DUSP1 Gene Polymorphisms Are Associated with Obesity-Related Metabolic Complications among Severely Obese Patients and Impact on Gene Methylation and Expression. | Guénard F et al. | — | 2013 | → |
| Effects of NRG1 and DAOA genetic variation on transition to psychosis in individuals at ultra-high risk for psychosis. | Bousman CA et al. | — | 2013 | → |
| Efficiently identifying significant associations in genome-wide association studies. | Kostem E et al. | — | 2013 | → |
| Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis. | Connelly JJ et al. | — | 2013 | → |
| Evaluation of PAX3 genetic variants and nevus number. | Ogbah Z et al. | — | 2013 | → |
| Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls. | Panagopoulos VN et al. | — | 2013 | → |
| Family-based study of HTR2A in suicide attempts: observed gene, gene × environment and parent-of-origin associations. | Ben-Efraim YJ et al. | — | 2013 | → |
| Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. | Li X et al. | — | 2013 | → |
| Genetic association study of WNT10B polymorphisms with BMD and adiposity parameters in Danish and Belgian males. | Van Camp JK et al. | — | 2013 | → |
| Genetic factors influencing bone mineral content in a black South African population. | May A et al. | — | 2013 | → |
| Genetic variants in IL1A and IL1B contribute to the susceptibility to 2009 pandemic H1N1 influenza A virus. | Liu Y et al. | — | 2013 | → |
| Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis. | Trouw LA et al. | — | 2013 | → |
| Genetic variation in AKT1, PTEN and the 8q24 locus, and the risk of testicular germ cell tumor. | Andreassen KE et al. | — | 2013 | → |
| Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility. | Hodžić A et al. | — | 2013 | → |
| Genetic variation in ESR2 and estrogen receptor-beta expression in lung tumors. | Song JY et al. | — | 2013 | → |
| Genetic variation in FADS genes and plasma cholesterol levels in 2-year-old infants: KOALA Birth Cohort Study. | Moltó-Puigmartí C et al. | — | 2013 | → |
| Genetic variation in the vaspin gene affects circulating serum vaspin concentrations. | Breitfeld J et al. | — | 2013 | → |
| Germline variants of base excision repair genes and breast cancer: A polymorphism in DNA polymerase gamma modifies gene expression and breast cancer risk. | Popanda O et al. | — | 2013 | → |
| Host genetic risk factors for community-acquired pneumonia. | Salnikova LE et al. | — | 2013 | → |
| Identification of single nucleotide polymorphisms in genes involved in digestive and metabolic processes associated with feed efficiency and performance traits in beef cattle. | Abo-Ismail MK et al. | — | 2013 | → |
| Insulin receptor substrate 1 (IRS1) variants confer risk of diabetes in the Boston Puerto Rican Health Study. | Feng X et al. | — | 2013 | → |
| Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma. | Acevedo N et al. | — | 2013 | → |
| Interleukin-13 genetic variants, household carpet use and childhood asthma. | Tsai CH et al. | — | 2013 | → |
| Investigation of six testicular germ cell tumor susceptibility genes suggests a parent-of-origin effect in SPRY4. | Karlsson R et al. | — | 2013 | → |
| Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. | Zou F et al. | — | 2013 | → |
| MAP2K3 is associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation. | Bian L et al. | — | 2013 | → |
| MAP3K7 and GSTZ1 are associated with human longevity: a two-stage case-control study using a multilocus genotyping. | Di Cianni F et al. | — | 2013 | → |
| Mapping of immune-mediated disease genes. | Ricaño-Ponce I et al. | — | 2013 | → |
| Moderation of antipsychotic-induced weight gain by energy balance gene variants in the RUPP autism network risperidone studies. | Nurmi EL et al. | — | 2013 | → |
| No conclusive evidence for association of polymorphisms in the adiponectin receptor 1 gene, AdipoR1, with common obesity. | Beckers S et al. | — | 2013 | → |
| No important role for genetic variation in the Chibby gene in monogenic and complex obesity. | Van Camp JK et al. | — | 2013 | → |
| Nucleotide variation in IL-10 and IL-12 and their receptors and cervical and vulvar cancer risk: a hybrid case-parent triad and case-control study. | Hussain SK et al. | — | 2013 | → |
| Pharmacogenetics-based population pharmacokinetic analysis of etravirine in HIV-1 infected individuals. | Lubomirov R et al. | — | 2013 | → |
| Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposure. | Bortsov AV et al. | — | 2013 | → |
| Polyunsaturated Fatty Acids Modulate the Association between PIK3CA-KCNMB3 Genetic Variants and Insulin Resistance. | Zheng JS et al. | — | 2013 | → |
| Population parameters incorporated into genome-wide tagSNP selection. | Silesian AP et al. | — | 2013 | → |
| Prognostic significance of cyclin D1 polymorphisms on prostate-specific antigen recurrence after radical prostatectomy. | Yu CC et al. | — | 2013 | → |
| Resequencing three candidate genes for major depressive disorder in a Dutch cohort. | Verbeek EC et al. | — | 2013 | → |
| Retracted article: Common variation in PPARGC1A/B and progression to diabetes or change in metabolic traits following preventive interventions: the Diabetes Prevention Program. | — | — | 2013 | → |
| Serum 25-hydroxyvitamin D3 levels and vitamin D receptor variants in melanoma patients from the Mediterranean area of Barcelona. | Ogbah Z et al. | — | 2013 | → |
| Sex- and subtype-specific analysis of H2AFX polymorphisms in non-Hodgkin lymphoma. | Bretherick KL et al. | — | 2013 | → |
| Shift work, circadian gene variants and risk of breast cancer. | Grundy A et al. | — | 2013 | → |
| Single-nucleotide polymorphisms in GALNT8 are associated with the response to interferon therapy for chronic hepatitis C. | Nakano R et al. | — | 2013 | → |
| SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS. | Merelli I et al. | — | 2013 | → |
| SNP-SNP interaction network in angiogenesis genes associated with prostate cancer aggressiveness. | Lin HY et al. | — | 2013 | → |
| Survival prediction based on inherited gene variation analysis. | Cicek MS et al. | — | 2013 | → |
| The association between the Angiotensin-Converting Enzyme-2 gene and blood pressure in a cohort study of adolescents. | Malard L et al. | — | 2013 | → |
| The SNPs in the human genetic blueprint era. | Giampaoli S et al. | — | 2013 | → |
| Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population. | Zhao L et al. | — | 2013 | → |
| Vitamin D status: multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient. | Lucas RM et al. | — | 2013 | → |
| A Collective Ranking Method for Genome-wide Association Studies. | Liu J et al. | — | 2012 | → |
| A common variant of the MACC1 gene is significantly associated with overall survival in colorectal cancer patients. | Lang AH et al. | — | 2012 | → |
| A comparison of gene region simulation methods. | Hendricks AE et al. | — | 2012 | → |
| A comprehensive investigation on common polymorphisms in the MDR1/ABCB1 transporter gene and susceptibility to colorectal cancer. | Campa D et al. | — | 2012 | → |
| A comprehensive study of polymorphisms in ABCB1, ABCC2 and ABCG2 and lung cancer chemotherapy response and prognosis. | Campa D et al. | — | 2012 | → |
| A comprehensive study of polymorphisms in the ABCB1, ABCC2, ABCG2, NR1I2 genes and lymphoma risk. | Campa D et al. | — | 2012 | → |
| A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. | Verbeek EC et al. | — | 2012 | → |
| A genetic instrument for Mendelian randomization of fibrinogen. | Ken-Dror G et al. | — | 2012 | → |
| A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. | Kääb S et al. | — | 2012 | → |
| Analysis of inner ear potassium recycling genes as potential factors associated with tinnitus. | Pawełczyk M et al. | — | 2012 | → |
| An ancient founder mutation in PROKR2 impairs human reproduction. | Avbelj Stefanija M et al. | — | 2012 | → |
| A novel bayesian graphical model for genome-wide multi-SNP association mapping. | Zhang Y | — | 2012 | → |
| A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype. | Ruczinski I et al. | — | 2012 | → |
| A population-based study of hedgehog pathway gene variants in relation to the dual risk of basal cell carcinoma plus another cancer. | Jorgensen TJ et al. | — | 2012 | → |
| Appetite regulation genes are associated with body mass index in black South African adolescents: a genetic association study. | Lombard Z et al. | — | 2012 | → |
| Are AHSG polymorphisms directly associated with coronary atherosclerosis? | Muendlein A et al. | — | 2012 | → |
| Association analysis between HOXD9 genes and the development of developmental dysplasia of the hip in Chinese female Han population. | Tian W et al. | — | 2012 | → |
| Association between variations in cell cycle genes and idiopathic pulmonary fibrosis. | Korthagen NM et al. | — | 2012 | → |
| Association mapping and disease: evolutionary perspectives. | Besenbacher S et al. | — | 2012 | → |
| Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth. | Saito M et al. | — | 2012 | → |
| Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population. | Mostowska A et al. | — | 2012 | → |
| Association of IREB2 and CHRNA3 polymorphisms with airflow obstruction in severe alpha-1 antitrypsin deficiency. | Kim WJ et al. | — | 2012 | → |
| Association of LIPA gene polymorphisms with obesity-related metabolic complications among severely obese patients. | Guénard F et al. | — | 2012 | → |
| Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese. | Guan F et al. | — | 2012 | → |
| Association of sirolimus adverse effects with m-TOR, p70S6K or Raptor polymorphisms in kidney transplant recipients. | Woillard JB et al. | — | 2012 | → |
| Association of TGFβ1 and clinical factors with scar outcome following melanoma excision. | Ward SV et al. | — | 2012 | → |
| Association of the 15q25 and 5p15 lung cancer susceptibility regions with gene expression in lung tumor tissue. | Fehringer G et al. | — | 2012 | → |
| Association of the innate immunity and inflammation pathway with advanced prostate cancer risk. | Kazma R et al. | — | 2012 | → |
| Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population. | Liu X et al. | — | 2012 | → |
| Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations. | Ben Hamad M et al. | — | 2012 | → |
| Association study of human leukocyte antigen-DRB1 alleles with rheumatoid arthritis in south Tunisian patients. | Ben Hamad M et al. | — | 2012 | → |
| Association study of serotonin pathway genes in attempted suicide. | Judy JT et al. | — | 2012 | → |
| AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. | Morley AP et al. | — | 2012 | → |
| Bitter taste receptor polymorphisms and human aging. | Campa D et al. | — | 2012 | → |
| Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis. | Dahm AE et al. | — | 2012 | → |
| Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed. | Hsu YH et al. | — | 2012 | → |
| COL1A1 association and otosclerosis: a meta-analysis. | Schrauwen I et al. | — | 2012 | → |
| Common genetic risk variants of TLR2 are not associated with periodontitis in large European case-control populations. | Richter GM et al. | — | 2012 | → |
| Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. | Ermini L et al. | — | 2012 | → |
| Common variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/2), adiponectin concentrations, and diabetes incidence in the Diabetes Prevention Program. | Mather KJ et al. | — | 2012 | → |
| Common variation in fatty acid genes and resuscitation from sudden cardiac arrest. | Johnson CO et al. | — | 2012 | → |
| Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse. | Wu JM et al. | — | 2012 | → |
| Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world. | Vrieze SI et al. | — | 2012 | → |
| Conformational Differences between Active Angiotensins and Their Inactive Precursors. | Solopova ON et al. | — | 2012 | → |
| Contribution of the TGFB1 Gene to Myocardial Infarction Susceptibility. | Barsova RM et al. | — | 2012 | → |
| Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility. | Castro FA et al. | — | 2012 | → |
| CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients. | Pelucchi S et al. | — | 2012 | → |
| Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. | Igo RP et al. | — | 2012 | → |
| Efficiency and power as a function of sequence coverage, SNP array density, and imputation. | Flannick J et al. | — | 2012 | → |
| Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts. | Lopez LM et al. | — | 2012 | → |
| Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. | Cozier YC et al. | — | 2012 | → |
| Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study. | Rice TK et al. | — | 2012 | → |
| Functional characterisation of the bovine neuropeptide Y gene promoter and evaluation of the transcriptional activities of promoter haplotypes. | Alam T et al. | — | 2012 | → |
| Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma. | Martin LJ et al. | — | 2012 | → |
| Gemcitabine metabolic pathway genetic polymorphisms and response in patients with non-small cell lung cancer. | Li L et al. | — | 2012 | → |
| Generation of synthetic data and experimental designs in evaluating interactions for association studies. | Chen Y et al. | — | 2012 | → |
| Genetic association between WNT10B polymorphisms and obesity in a Belgian case-control population is restricted to males. | Van Camp JK et al. | — | 2012 | → |
| Genetic association of the EGR2 gene with bipolar disorder in Korea. | Kim SH et al. | — | 2012 | → |
| Genetic contribution to C-reactive protein levels in severe obesity. | Faucher G et al. | — | 2012 | → |
| Genetic polymorphisms in obesity-related genes and endometrial cancer risk. | Chen X et al. | — | 2012 | → |
| Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women. | Schuh-Huerta SM et al. | — | 2012 | → |
| Genetic variants in platelet factor 4 modulate inflammatory and platelet activation biomarkers. | Bhatnagar P et al. | — | 2012 | → |
| Genetic variation in cell death genes and risk of non-Hodgkin lymphoma. | Schuetz JM et al. | — | 2012 | → |
| Genetic variation in complement regulators and susceptibility to age-related macular degeneration. | Cipriani V et al. | — | 2012 | → |
| Gene variations in sex hormone pathways and the risk of testicular germ cell tumour: a case-parent triad study in a Norwegian-Swedish population. | Kristiansen W et al. | — | 2012 | → |
| Genome-wide association mapping with longitudinal data. | Furlotte NA et al. | — | 2012 | → |
| Genome-wide association studies with metabolomics. | Adamski J | — | 2012 | → |
| G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation. | Weinsheimer S et al. | — | 2012 | → |
| Harnessing genomics and genome biology to understand malaria biology. | Volkman SK et al. | — | 2012 | → |
| Heterogeneity of the Stearoyl-CoA desaturase-1 (SCD1) gene and metabolic risk factors in the EPIC-Potsdam study. | Arregui M et al. | — | 2012 | → |
| Higher FKBP5, COMT, CHRNA5, and CRHR1 allele burdens are associated with PTSD and interact with trauma exposure: implications for neuropsychiatric research and treatment. | Boscarino JA et al. | — | 2012 | → |
| HLA and SNP haplotype mapping in the Japanese population. | Kitajima H et al. | — | 2012 | → |
| Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia. | Verbrugghe P et al. | — | 2012 | → |
| Incorporating prior information into association studies. | Darnell G et al. | — | 2012 | → |
| Insulin resistance and the polycystic ovary syndrome revisited: an update on mechanisms and implications. | Diamanti-Kandarakis E et al. | — | 2012 | → |
| Integrative approach to pain genetics identifies pain sensitivity loci across diseases. | Ruau D et al. | — | 2012 | → |
| Introduction to genetic association studies. | Lewis CM et al. | — | 2012 | → |
| Leptin and leptin receptor genes in relation to premenopausal breast cancer incidence and grade in Caucasian women. | Gu F et al. | — | 2012 | → |
| Longevity candidate genes and their association with personality traits in the elderly. | Luciano M et al. | — | 2012 | → |
| MAT1A variants modulate the effect of dietary fatty acids on plasma homocysteine concentrations. | Huang T et al. | — | 2012 | → |
| Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse. | Wu JM et al. | — | 2012 | → |
| Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis. | Knüppel S et al. | — | 2012 | → |
| NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2. | Muise AM et al. | — | 2012 | → |
| Network biology methods integrating biological data for translational science. | Bebek G et al. | — | 2012 | → |
| Optimal use of regression models in genome-wide association studies. | Powell JE et al. | — | 2012 | → |
| PLXNC1 and RDH13 associated with bilateral convergent strabismus with exophthalmus in German Brown cattle. | Fink S et al. | — | 2012 | → |
| Population model-based inter-diplotype similarity measure for accurate diplotype clustering. | Onuki R et al. | — | 2012 | → |
| Population pharmacokinetic analysis and pharmacogenetics of raltegravir in HIV-positive and healthy individuals. | Arab-Alameddine M et al. | — | 2012 | → |
| Positive association of CC2D1A and CC2D2A gene haplotypes with mental retardation in a Han Chinese population. | Shi ZY et al. | — | 2012 | → |
| Positive association of CD36 gene variants with the visual outcome of photodynamic therapy in polypoidal choroidal vasculopathy. | Honda S et al. | — | 2012 | → |
| Prediction of genetic values of quantitative traits with epistatic effects in plant breeding populations. | Wang D et al. | — | 2012 | → |
| Predictors of survival in never-smokers with non-small cell lung cancer: a large-scale, two-phase genetic study. | Pu X et al. | — | 2012 | → |
| Role of the 12q24.12 locus in the onset of preeclampsia: an Italian case-control study. | Di Gaetano C et al. | — | 2012 | → |
| Sequence-based association and selection scans identify drug resistance loci in the Plasmodium falciparum malaria parasite. | Park DJ et al. | — | 2012 | → |
| Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases. | Huhn S et al. | — | 2012 | → |
| Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares. | Le Floch E et al. | — | 2012 | → |
| Similarity-based multimarker association tests for continuous traits. | Lin WY et al. | — | 2012 | → |
| Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. | Kim W et al. | — | 2012 | → |
| SLC22A1-ABCB1 haplotype profiles predict imatinib pharmacokinetics in Asian patients with chronic myeloid leukemia. | Singh O et al. | — | 2012 | → |
| SNP selection and classification of genome-wide SNP data using stratified sampling random forests. | Wu Q et al. | — | 2012 | → |
| The Association between genetic variations of CHI3L1, levels of the encoded glycoprotein YKL-40 and the lipid profile in a Danish population. | Thomsen SB et al. | — | 2012 | → |
| The association of V249I and T280M fractalkine receptor haplotypes with disease course of multiple sclerosis. | Stojković L et al. | — | 2012 | → |
| The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity. | Kim SH et al. | — | 2012 | → |
| The Genetic Diversity and Structure of Linkage Disequilibrium of the MTHFR Gene in Populations of Northern Eurasia. | Trifonova EA et al. | — | 2012 | → |
| The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease. | Watson CT et al. | — | 2012 | → |
| Toll-like receptor gene polymorphisms confer susceptibility to graft-versus-host disease in allogenic hematopoietic stem cell transplantation. | Sivula J et al. | — | 2012 | → |
| TRM: a powerful two-stage machine learning approach for identifying SNP-SNP interactions. | Lin HY et al. | — | 2012 | → |
| Unraveling the autoimmune translational research process layer by layer. | Blumberg RS et al. | — | 2012 | → |
| Variations of CHI3L1, levels of the encoded glycoprotein YKL-40 and prediction of fatal and non-fatal ischemic stroke. | Rathcke CN et al. | — | 2012 | → |
| VEGF pathway genetic variants as biomarkers of treatment outcome with bevacizumab: an analysis of data from the AViTA and AVOREN randomised trials. | Lambrechts D et al. | — | 2012 | → |
| Vitamin D-related genetic variation, plasma vitamin D, and risk of lethal prostate cancer: a prospective nested case-control study. | Shui IM et al. | — | 2012 | → |
| Accessing and selecting genetic markers from available resources. | Bell CG | — | 2011 | → |
| Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease. | Grant AV et al. | — | 2011 | → |
| A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia. | Mouzat K et al. | — | 2011 | → |
| A comprehensive association analysis of homocysteine metabolic pathway genes in Singaporean Chinese with ischemic stroke. | Low HQ et al. | — | 2011 | → |
| A DNA pooling-based case-control study of myopia candidate genes COL11A1, COL18A1, FBN1, and PLOD1 in a Chinese population. | Yip SP et al. | — | 2011 | → |
| A genetic polymorphism in the CAV1 gene associates with the development of bronchiolitis obliterans syndrome after lung transplantation. | Kastelijn EA et al. | — | 2011 | → |
| A genome-wide screen of gene-gene interactions for rheumatoid arthritis susceptibility. | Liu C et al. | — | 2011 | → |
| A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. | Krüger R et al. | — | 2011 | → |
| A multistage association study identifies a breast cancer genetic locus at NCOA7. | Higginbotham KS et al. | — | 2011 | → |
| Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. | Greenwood TA et al. | — | 2011 | → |
| Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations. | Mikhak B et al. | — | 2011 | → |
| An interaction between Nrf2 polymorphisms and smoking status affects annual decline in FEV1: a longitudinal retrospective cohort study. | Masuko H et al. | — | 2011 | → |
| An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese. | Zhang G et al. | — | 2011 | → |
| A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals. | Brugts JJ et al. | — | 2011 | → |
| A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia. | Kelly M et al. | — | 2011 | → |
| Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. | Tore S et al. | — | 2011 | → |
| A principal components-based clustering method to identify variants associated with complex traits. | Black MH et al. | — | 2011 | → |
| Association between polymorphisms in GRIK2 gene and obsessive-compulsive disorder: a family-based study. | Sampaio AS et al. | — | 2011 | → |
| Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin. | Carrai M et al. | — | 2011 | → |
| Association between the dopamine transporter gene and the inattentive subtype of attention deficit hyperactivity disorder in Taiwan. | Shang CY et al. | — | 2011 | → |
| Association between variants of the leptin receptor gene (LEPR) and overweight: a systematic review and an analysis of the CoLaus study. | Bender N et al. | — | 2011 | → |
| Association of ADIPOQ gene variants with body weight, type 2 diabetes and serum adiponectin concentrations: the Finnish Diabetes Prevention Study. | Siitonen N et al. | — | 2011 | → |
| Association of ADIPOR2 gene variants with cardiovascular disease and type 2 diabetes risk in individuals with impaired glucose tolerance: the Finnish Diabetes Prevention Study. | Siitonen N et al. | — | 2011 | → |
| Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYS. | Isackson PJ et al. | — | 2011 | → |
| Association of COPD candidate genes with computed tomography emphysema and airway phenotypes in severe COPD. | Kim WJ et al. | — | 2011 | → |
| Association of genetic polymorphisms in cell-cycle control genes and susceptibility to endometrial cancer among Chinese women. | Cai H et al. | — | 2011 | → |
| Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk. | Demontis D et al. | — | 2011 | → |
| Association of GWAS-based candidate genes with HDL-cholesterol levels before and after bariatric surgery in the Swedish obese subjects study. | Sarzynski MA et al. | — | 2011 | → |
| Association of HTR2A polymorphisms with chronic widespread pain and the extent of musculoskeletal pain: results from two population-based cohorts. | Nicholl BI et al. | — | 2011 | → |
| Association of JAK-STAT pathway related genes with lymphoma risk: results of a European case-control study (EpiLymph). | Butterbach K et al. | — | 2011 | → |
| Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy. | Kuzmanić Samija R et al. | — | 2011 | → |
| Association of polymorphisms of interleukin-8, CXCR1, CXCR2, and selectin with allograft outcomes in kidney transplantation. | Ro H et al. | — | 2011 | → |
| Association of specific genotypes in metastatic suppressor HTPAP with tumor metastasis and clinical prognosis in hepatocellular carcinoma. | Ren N et al. | — | 2011 | → |
| Association of variants in the carnosine peptidase 1 gene (CNDP1) with diabetic nephropathy in American Indians. | Chakkera HA et al. | — | 2011 | → |
| Associations of markers in 11 obesity candidate genes with maximal weight loss and weight regain in the SOS bariatric surgery cases. | Sarzynski MA et al. | — | 2011 | → |
| Association study in eating disorders: TPH2 associates with anorexia nervosa and self-induced vomiting. | Slof-Op 't Landt MC et al. | — | 2011 | → |
| Association study of MC4R with complex obesity and replication of the rs17782313 association signal. | Beckers S et al. | — | 2011 | → |
| Association study of POMC variants with body composition measures and nutrient choice. | Ternouth A et al. | — | 2011 | → |
| BLOCK-BASED BAYESIAN EPISTASIS ASSOCIATION MAPPING WITH APPLICATION TO WTCCC TYPE 1 DIABETES DATA. | Zhang BY et al. | — | 2011 | → |
| Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area. | Kähler AK et al. | — | 2011 | → |
| CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection. | Schaefer AS et al. | — | 2011 | → |
| Combinations of SNPs related to signal transduction in bipolar disorder. | Koefoed P et al. | — | 2011 | → |
| Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer. | Notaridou M et al. | — | 2011 | → |
| Common genetic variants are associated with accelerated bone mineral density loss after hematopoietic cell transplantation. | Yao S et al. | — | 2011 | → |
| Common genetic variation in adiponectin, leptin, and leptin receptor and association with breast cancer subtypes. | Nyante SJ et al. | — | 2011 | → |
| Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype. | McGregor TL et al. | — | 2011 | → |
| Common polymorphisms in the adiponectin and its receptor genes, adiponectin levels and the risk of prostate cancer. | Dhillon PK et al. | — | 2011 | → |
| Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease. | Westaway SK et al. | — | 2011 | → |
| Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. | Cox DG et al. | — | 2011 | → |
| Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. | Signorello LB et al. | — | 2011 | → |
| Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness. | Bigdeli TB et al. | — | 2011 | → |
| Corticotrophin-releasing hormone type 1 receptor gene (CRHR1) variants predict posttraumatic stress disorder onset and course in pediatric injury patients. | Amstadter AB et al. | — | 2011 | → |
| Corticotropin-releasing hormone receptor type 1 (CRHR1) genetic variation and stress interact to influence reward learning. | Bogdan R et al. | — | 2011 | → |
| DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. | Gusev A et al. | — | 2011 | → |
| Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. | Hoffmann TJ et al. | — | 2011 | → |
| Developing biobanks in developing countries. | Rudan I et al. | — | 2011 | → |
| Effect of obesity on the association between ATF3 gene haplotypes and C-reactive protein level in Taiwanese. | Wu S et al. | — | 2011 | → |
| Efficient genomewide selection of PCA-correlated tSNPs for genotype imputation. | Javed A et al. | — | 2011 | → |
| Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM). | Sale MM et al. | — | 2011 | → |
| Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility. | Juko-Pecirep I et al. | — | 2011 | → |
| Evidence of an involvement of TFAP2A gene in non-syndromic cleft lip with or without cleft palate: an Italian study. | Martinelli M et al. | — | 2011 | → |
| Evidence of associations between bipolar disorder and the brain-derived neurotrophic factor (BDNF) gene. | Sears C et al. | — | 2011 | → |
| Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus. | Mero IL et al. | — | 2011 | → |
| Family-based genetic association study of DLGAP3 in Tourette Syndrome. | Crane J et al. | — | 2011 | → |
| Ficolin-2 levels and FCN2 haplotypes influence hepatitis B infection outcome in Vietnamese patients. | Hoang TV et al. | — | 2011 | → |
| Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels. | Parikh H et al. | — | 2011 | → |
| Genes of the unfolded protein response pathway harbor risk alleles for primary open angle glaucoma. | Carbone MA et al. | — | 2011 | → |
| Genetic association of bipolar disorder with the β(3) nicotinic receptor subunit gene. | Hartz SM et al. | — | 2011 | → |
| Genetic contribution of the leukotriene pathway to coronary artery disease. | Hartiala J et al. | — | 2011 | → |
| Genetic determinants of coronary heart disease: new discoveries and insights from genome-wide association studies. | Patel RS et al. | — | 2011 | → |
| Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study. | Lehtinen AB et al. | — | 2011 | → |
| Genetic variability in the IL1RN gene and the balance between interleukin (IL)-1 receptor agonist and IL-1β in idiopathic pulmonary fibrosis. | Barlo NP et al. | — | 2011 | → |
| Genetic variability of the fatty acid synthase pathway is not associated with prostate cancer risk in the European Prospective Investigation on Cancer (EPIC). | Campa D et al. | — | 2011 | → |
| Genetic variability of the mTOR pathway and prostate cancer risk in the European Prospective Investigation on Cancer (EPIC). | Campa D et al. | — | 2011 | → |
| Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. | Bates TC et al. | — | 2011 | → |
| Genetic variants in COX-2, non-steroidal anti-inflammatory drugs, and breast cancer risk: the Western New York Exposures and Breast Cancer (WEB) Study. | Brasky TM et al. | — | 2011 | → |
| Genetic variants in the KIF6 region and coronary event reduction from statin therapy. | Li Y et al. | — | 2011 | → |
| Genetic variants in the renin-angiotensin-aldosterone system and blood pressure responses to potassium intake. | He J et al. | — | 2011 | → |
| Genetic variants of TSLP and asthma in an admixed urban population. | Liu M et al. | — | 2011 | → |
| Genetic variation in BDNF is associated with allergic asthma and allergic rhinitis in an ethnic Chinese population in Singapore. | Andiappan AK et al. | — | 2011 | → |
| Genetic variation in DNA repair pathway genes and melanoma risk. | Zhang M et al. | — | 2011 | → |
| Genetic variation in GREM1 is a risk factor for fibrosis in pulmonary sarcoidosis. | Heron M et al. | — | 2011 | → |
| Genome-wide association study of epirubicin-induced leukopenia in Japanese patients. | Srinivasan Y et al. | — | 2011 | → |
| Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. | Zlojutro M et al. | — | 2011 | → |
| Glutathione pathway gene variation and risk of autism spectrum disorders. | Bowers K et al. | — | 2011 | → |
| Haplotype analysis improved evidence for candidate genes for intramuscular fat percentage from a genome wide association study of cattle. | Barendse W | — | 2011 | → |
| HLA-DRB1 reduces the risk of type 2 diabetes mellitus by increased insulin secretion. | Williams RC et al. | — | 2011 | → |
| Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes. | Windelinckx A et al. | — | 2011 | → |
| Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. | Small KS et al. | — | 2011 | → |
| Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. | Vinkhuyzen AA et al. | — | 2011 | → |
| Identity-by-descent-based phasing and imputation in founder populations using graphical models. | Palin K et al. | — | 2011 | → |
| IL17A genetic variation is associated with altered susceptibility to Gram-positive infection and mortality of severe sepsis. | Nakada TA et al. | — | 2011 | → |
| Implication of next-generation sequencing on association studies. | Siu H et al. | — | 2011 | → |
| Improved risk prediction for Crohn's disease with a multi-locus approach. | Kang J et al. | — | 2011 | → |
| Increased expression of NKX2.3 mRNA transcribed from the risk haplotype for ulcerative colitis in the involved colonic mucosa. | Arai T et al. | — | 2011 | → |
| Increasing power of genome-wide association studies by collecting additional single-nucleotide polymorphisms. | Kostem E et al. | — | 2011 | → |
| Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms. | Chung PY et al. | — | 2011 | → |
| Influence of candidate genes on attention problems in children: a longitudinal study. | van Beijsterveldt CE et al. | — | 2011 | → |
| Interaction between genetic variants of DLGAP3 and SLC1A1 affecting the risk of atypical antipsychotics-induced obsessive-compulsive symptoms. | Ryu S et al. | — | 2011 | → |
| Lack of association of indoleamine 2,3-dioxygenase polymorphisms with interferon-alpha-related depression in hepatitis C. | Galvão-de Almeida A et al. | — | 2011 | → |
| Limited associations of dopamine system genes with alcohol dependence and related traits in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD). | Hack LM et al. | — | 2011 | → |
| Local genealogies in a linear mixed model for genome-wide association mapping in complex pedigreed populations. | Sahana G et al. | — | 2011 | → |
| Medium-throughput SNP genotyping using mass spectrometry: multiplex SNP genotyping using the iPLEX® Gold assay. | Millis MP | — | 2011 | → |
| Meta-analyses of genes modulating intracellular T3 bio-availability reveal a possible role for the DIO3 gene in osteoarthritis susceptibility. | Meulenbelt I et al. | — | 2011 | → |
| Microcephaly genes and risk of late-onset Alzheimer disease. | Erten-Lyons D et al. | — | 2011 | → |
| Mind the dbGAP: the application of data mining to identify biological mechanisms. | Wooten EC et al. | — | 2011 | → |
| Multilocus association testing of quantitative traits based on partial least-squares analysis. | Zhang F et al. | — | 2011 | → |
| Novel genetic variants in the chromosome 5p15.33 region associate with lung cancer risk. | Pande M et al. | — | 2011 | → |
| Novel variants in the PRDX6 Gene and the risk of Acute Lung Injury following major trauma. | Rushefski M et al. | — | 2011 | → |
| PAX6 haplotypes are associated with high myopia in Han chinese. | Jiang B et al. | — | 2011 | → |
| Plasma glutathione peroxidase in pediatric stroke families. | Nowak-Göttl U et al. | — | 2011 | → |
| Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. | Minear MA et al. | — | 2011 | → |
| Polymorphisms in IL10 are associated with total Immunoglobulin E levels and Schistosoma mansoni infection intensity in a Brazilian population. | Grant AV et al. | — | 2011 | → |
| Polymorphisms in oxidative stress-related genes and postmenopausal breast cancer risk. | Seibold P et al. | — | 2011 | → |
| POMC and TP53 genetic variability and risk of basal cell carcinoma of skin: Interaction between host and genetic factors. | Rizzato C et al. | — | 2011 | → |
| PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies. | Huang J et al. | — | 2011 | → |
| Progress and promise of genome-wide association studies for human complex trait genetics. | Stranger BE et al. | — | 2011 | → |
| Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery disease. | Ricketts SL et al. | — | 2011 | → |
| Protein expressions and genetic variations of SLC5A8 in prostate cancer risk and aggressiveness. | Lin HY et al. | — | 2011 | → |
| Recent human evolution has shaped geographical differences in susceptibility to disease. | Marigorta UM et al. | — | 2011 | → |
| Relationship between genetic variation in the glutaminase gene GLS1 and brain glutamine/glutamate ratio measured in vivo. | Öngür D et al. | — | 2011 | → |
| Replication and extension of association between common genetic variants in SIM1 and human adiposity. | Swarbrick MM et al. | — | 2011 | → |
| Replication of the SH2B1 rs7498665 association with obesity in a Belgian study population. | Beckers S et al. | — | 2011 | → |
| Risk variants in the S100B gene, associated with elevated S100B levels, are also associated with visuospatial disability of schizophrenia. | Zhai J et al. | — | 2011 | → |
| Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1. | Pasmant E et al. | — | 2011 | → |
| Sexual dysfunction during treatment with serotonergic and noradrenergic antidepressants: clinical description and the role of the 5-HTTLPR. | Strohmaier J et al. | — | 2011 | → |
| Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans. | Deo RC et al. | — | 2011 | → |
| Single nucleotide polymorphisms that increase expression of the guanosine triphosphatase RAC1 are associated with ulcerative colitis. | Muise AM et al. | — | 2011 | → |
| SNP-by-fitness and SNP-by-BMI interactions from seven candidate genes and incident hypertension after 20 years of follow-up: the CARDIA Fitness Study. | Sarzynski MA et al. | — | 2011 | → |
| SNPPicker: high quality tag SNP selection across multiple populations. | Sicotte H et al. | — | 2011 | → |
| Strategies for genotyping. | Crawford DC et al. | — | 2011 | → |
| Technological issues and experimental design of gene association studies. | Distefano JK et al. | — | 2011 | → |
| The association of genetic variants in interleukin-1 genes with cognition: findings from the cardiovascular health study. | Benke KS et al. | — | 2011 | → |
| The expression of myosin heavy chain (MHC) genes in human skeletal muscle is related to metabolic characteristics involved in the pathogenesis of type 2 diabetes. | Olsson AH et al. | — | 2011 | → |
| The MDGA1 gene confers risk to schizophrenia and bipolar disorder. | Li J et al. | — | 2011 | → |
| The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene. | Snowden JS et al. | — | 2011 | → |
| Variation in genes coding for AMP-activated protein kinase (AMPK) and breast cancer risk in the European Prospective Investigation on Cancer (EPIC). | Campa D et al. | — | 2011 | → |
| Variation in the von Willebrand factor gene is associated with von Willebrand factor levels and with the risk for cardiovascular disease. | van Schie MC et al. | — | 2011 | → |
| Vitamin D receptor gene polymorphisms are associated with adiposity phenotypes. | Ochs-Balcom HM et al. | — | 2011 | → |
| ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat. | Phillips CM et al. | — | 2010 | → |
| A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. | Feng Q et al. | — | 2010 | → |
| ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir. | Lubomirov R et al. | — | 2010 | → |
| A functional polymorphism (-603A --> G) in the tissue factor gene promoter is associated with adult-onset asthma. | Isada A et al. | — | 2010 | → |
| A gene-wide investigation on polymorphisms in the taste receptor 2R14 (TAS2R14) and susceptibility to colorectal cancer. | Campa D et al. | — | 2010 | → |
| A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. | Nakashima M et al. | — | 2010 | → |
| A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. | Uno S et al. | — | 2010 | → |
| A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. | Schaefer AS et al. | — | 2010 | → |
| Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies. | Zhang L et al. | — | 2010 | → |
| A haplotype of CYP2C9 associated with warfarin sensitivity in mechanical heart valve replacement patients. | Lee SJ et al. | — | 2010 | → |
| A high-resolution association mapping panel for the dissection of complex traits in mice. | Bennett BJ et al. | — | 2010 | → |
| A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. | El Kares R et al. | — | 2010 | → |
| Allele and haplotype frequency distribution in PTPN22 gene across variable ethnic groups: Implications for genetic association studies for autoimmune diseases. | Lins TC et al. | — | 2010 | → |
| A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01. | Cree BA et al. | — | 2010 | → |
| Analyses and comparison of imputation-based association methods. | Pei YF et al. | — | 2010 | → |
| Analysis of untyped SNPs: maximum likelihood and imputation methods. | Hu YJ et al. | — | 2010 | → |
| Anxiety and depression in children and adults: influence of serotonergic and neurotrophic genes? | Middeldorp CM et al. | — | 2010 | → |
| APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men. | Ken-Dror G et al. | — | 2010 | → |
| A population-based study of IGF axis polymorphisms and the esophageal inflammation, metaplasia, adenocarcinoma sequence. | McElholm AR et al. | — | 2010 | → |
| Application of gene network analysis techniques identifies AXIN1/PDIA2 and endoglin haplotypes associated with bicuspid aortic valve. | Wooten EC et al. | — | 2010 | → |
| A promoter polymorphism -2122C>T of CHI3L1 is associated with serum low density lipoprotein cholesterol level in Korean subjects. | Lee H et al. | — | 2010 | → |
| Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample. | Tesli M et al. | — | 2010 | → |
| Association analysis of Wnt pathway genes on prostate-specific antigen recurrence after radical prostatectomy. | Huang SP et al. | — | 2010 | → |
| Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients. | Kohli MA et al. | — | 2010 | → |
| Association of polyaminergic loci with anxiety, mood disorders, and attempted suicide. | Fiori LM et al. | — | 2010 | → |
| Association of single-nucleotide polymorphisms from 17 candidate genes with baseline symptom-limited exercise test duration and decrease in duration over 20 years: the Coronary Artery Risk Development in Young Adults (CARDIA) fitness study. | Sarzynski MA et al. | — | 2010 | → |
| Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension. | Sallinen R et al. | — | 2010 | → |
| Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle length. | Taylor KC et al. | — | 2010 | → |
| Association study of PDE4B gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples. | Kähler AK et al. | — | 2010 | → |
| Association with replication between estrogen-related receptor gamma (ESRRgamma) polymorphisms and bone phenotypes in women of European ancestry. | Elfassihi L et al. | — | 2010 | → |
| A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts. | Kalsi G et al. | — | 2010 | → |
| Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. | Dimasi DP et al. | — | 2010 | → |
| Case-control association study of TGOLN2 in attempted suicide. | Mahon PB et al. | — | 2010 | → |
| Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy. | Leak TS et al. | — | 2010 | → |
| Clinical significance of genetic variations in the PI3K/PTEN/AKT/mTOR pathway in Korean patients with colorectal cancer. | Kim JG et al. | — | 2010 | → |
| CLOCK gene is implicated in weight reduction in obese patients participating in a dietary programme based on the Mediterranean diet. | Garaulet M et al. | — | 2010 | → |
| CLOCK in breast tumorigenesis: genetic, epigenetic, and transcriptional profiling analyses. | Hoffman AE et al. | — | 2010 | → |
| Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation. | Cho MH et al. | — | 2010 | → |
| Common genetic variants in fatty acid-binding protein-4 (FABP4) and clinical diabetes risk in the Women's Health Initiative Observational Study. | Chan KH et al. | — | 2010 | → |
| Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease. | Peloso GM et al. | — | 2010 | → |
| Common INSIG2 polymorphisms are associated with age-related changes in body size and high-density lipoprotein cholesterol from young adulthood to middle age. | Fornage M et al. | — | 2010 | → |
| Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population. | Wang T et al. | — | 2010 | → |
| Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program. | Jablonski KA et al. | — | 2010 | → |
| Common variants in cardiac ion channel genes are associated with sudden cardiac death. | Albert CM et al. | — | 2010 | → |
| Common variants in the gene for the serotonin receptor 6 (HTR6) do not contribute to obesity. | Peeters AV et al. | — | 2010 | → |
| Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations. | Johansson S et al. | — | 2010 | → |
| Comparison of association mapping methods in a complex pedigreed population. | Sahana G et al. | — | 2010 | → |
| Comparisons of multi-marker association methods to detect association between a candidate region and disease. | Ballard DH et al. | — | 2010 | → |
| Confirmation of association between multiple sclerosis and CYP27B1. | Sundqvist E et al. | — | 2010 | → |
| COX-2 is associated with periodontitis in Europeans. | Schaefer AS et al. | — | 2010 | → |
| CREB1 is a strong genetic predictor of the variation in exercise heart rate response to regular exercise: the HERITAGE Family Study. | Rankinen T et al. | — | 2010 | → |
| CYP2D6 gene variants: association with breast cancer specific survival in a cohort of breast cancer patients from the United Kingdom treated with adjuvant tamoxifen. | Abraham JE et al. | — | 2010 | → |
| Differences and similarities in the serotonergic diathesis for suicide attempts and mood disorders: a 22-year longitudinal gene-environment study. | Brezo J et al. | — | 2010 | → |
| Discovering genetic associations with high-dimensional neuroimaging phenotypes: A sparse reduced-rank regression approach. | Vounou M et al. | — | 2010 | → |
| Does genetic regulation of IgE begin in utero? Evidence from T(H)1/T(H)2 gene polymorphisms and cord blood total IgE. | Hong X et al. | — | 2010 | → |
| Effect of genetic variation in the human fatty acid synthase gene (FASN) on obesity and fat depot-specific mRNA expression. | Schleinitz D et al. | — | 2010 | → |
| Eighteen insulin-like growth factor pathway genes, circulating levels of IGF-I and its binding protein, and risk of prostate and breast cancer. | Gu F et al. | — | 2010 | → |
| EMINIM: an adaptive and memory-efficient algorithm for genotype imputation. | Kang HM et al. | — | 2010 | → |
| Entropy-supported marker selection and Mantel statistics for haplotype sharing analysis. | Schulz A et al. | — | 2010 | → |
| Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis? | Koehler ML et al. | — | 2010 | → |
| Evaluation of candidate genes for cholinesterase activity in farmworkers exposed to organophosphorus pesticides: association of single nucleotide polymorphisms in BCHE. | Howard TD et al. | — | 2010 | → |
| Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot". | Johnatty SE et al. | — | 2010 | → |
| Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study. | Palmer ND et al. | — | 2010 | → |
| Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians. | Briant JA et al. | — | 2010 | → |
| Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian population. | Rouault K et al. | — | 2010 | → |
| Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging. | Nicodemus KK et al. | — | 2010 | → |
| Evolutionary genomics of animal personality. | van Oers K et al. | — | 2010 | → |
| FastTagger: an efficient algorithm for genome-wide tag SNP selection using multi-marker linkage disequilibrium. | Liu G et al. | — | 2010 | → |
| Fine-mapping in African Americans of 8 recently discovered genetic loci for plasma lipids: the Jackson Heart Study. | Keebler ME et al. | — | 2010 | → |
| Fine mapping of a quantitative trait locus for osteochondrosis on horse chromosome 2. | Dierks C et al. | — | 2010 | → |
| Fine mapping of the association with obesity at the FTO locus in African-derived populations. | Hassanein MT et al. | — | 2010 | → |
| Fine-mapping reveals novel alternative splicing of the dopamine transporter. | Talkowski ME et al. | — | 2010 | → |
| Five common single nucleotide polymorphisms in the PALB2 gene and susceptibility to breast cancer in eastern Chinese population. | Cao AY et al. | — | 2010 | → |
| GABRR1 and GABRR2, encoding the GABA-A receptor subunits rho1 and rho2, are associated with alcohol dependence. | Xuei X et al. | — | 2010 | → |
| Gene-gene interaction between serotonin transporter (SLC6A4) and CLOCK modulates the risk of metabolic syndrome in rotating shiftworkers. | Sookoian S et al. | — | 2010 | → |
| Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome. | Phillips CM et al. | — | 2010 | → |
| Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9. | Ellis JA et al. | — | 2010 | → |
| Genetic association analysis of LARS2 with type 2 diabetes. | Reiling E et al. | — | 2010 | → |
| Genetic associations of variants in genes encoding HIV-dependency factors required for HIV-1 infection. | Chinn LW et al. | — | 2010 | → |
| Genetic determinants of treatment benefit of the angiotensin-converting enzyme-inhibitor perindopril in patients with stable coronary artery disease. | Brugts JJ et al. | — | 2010 | → |
| Genetic diversity at endoplasmic reticulum aminopeptidases is maintained by balancing selection and is associated with natural resistance to HIV-1 infection. | Cagliani R et al. | — | 2010 | → |
| Genetic polymorphisms and human sensitivity to opioid analgesics. | Nishizawa D et al. | — | 2010 | → |
| Genetic polymorphisms in MMP7 and reduced serum levels associate with the development of bronchiolitis obliterans syndrome after lung transplantation. | Kastelijn EA et al. | — | 2010 | → |
| Genetic polymorphisms in vitamin D receptor VDR/RXRA influence the likelihood of colon adenoma recurrence. | Egan JB et al. | — | 2010 | → |
| Genetic risk factors for post-infectious irritable bowel syndrome following a waterborne outbreak of gastroenteritis. | Villani AC et al. | — | 2010 | → |
| Genetics of Vascular Dementia. | Murray ME et al. | — | 2010 | → |
| Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk. | Pierce BL et al. | — | 2010 | → |
| Genetic variability and linkage disequilibrium patterns in the bovine DNAJA1 gene. | Marty A et al. | — | 2010 | → |
| Genetic variants in human CLOCK associate with total energy intake and cytokine sleep factors in overweight subjects (GOLDN population). | Garaulet M et al. | — | 2010 | → |
| Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. | Hendrickson SL et al. | — | 2010 | → |
| Genetic variants in the renin-angiotensin-aldosterone system and salt sensitivity of blood pressure. | Gu D et al. | — | 2010 | → |
| Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study. | Ruiz-Narvaez EA et al. | — | 2010 | → |
| Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer. | Wang X et al. | — | 2010 | → |
| Genetic variation at the phospholipid transfer protein locus affects its activity and high-density lipoprotein size and is a novel marker of cardiovascular disease susceptibility. | Vergeer M et al. | — | 2010 | → |
| Genetic variation in neuroendocrine genes associates with somatic symptoms in the general population: results from the EPIFUND study. | Holliday KL et al. | — | 2010 | → |
| Genetic variation in pentraxin (PTX) 3 gene associates with PTX3 production and fertility in women. | May L et al. | — | 2010 | → |
| Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study. | Holliday KL et al. | — | 2010 | → |
| Genetic variation in the retinoid X receptor and calcium-sensing receptor and risk of colorectal cancer in the Colon Cancer Family Registry. | Jacobs ET et al. | — | 2010 | → |
| Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone. | Chung PY et al. | — | 2010 | → |
| Genetic variations in UDP-glucuronosyltransferase 2B7 gene (UGT2B7) in a Korean population. | Hwang MS et al. | — | 2010 | → |
| Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data. | Yoshimi A et al. | — | 2010 | → |
| Genome-wide association studies and beyond. | Witte JS | — | 2010 | → |
| Genome-wide association studies: a powerful tool for neurogenomics. | Cowperthwaite MC et al. | — | 2010 | → |
| Genome wide linkage study, using a 250K SNP map, of Plasmodium falciparum infection and mild malaria attack in a Senegalese population. | Milet J et al. | — | 2010 | → |
| Genotype imputation for genome-wide association studies. | Marchini J et al. | — | 2010 | → |
| Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men. | Ken-Dror G et al. | — | 2010 | → |
| High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. | Maestrini E et al. | — | 2010 | → |
| High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. | Strom SP et al. | — | 2010 | → |
| IL-22RA2 associates with multiple sclerosis and macrophage effector mechanisms in experimental neuroinflammation. | Beyeen AD et al. | — | 2010 | → |
| Impact of group IVA cytosolic phospholipase A2 gene polymorphisms on phenotypic features of patients with familial adenomatous polyposis. | Umeno J et al. | — | 2010 | → |
| Inherited determinants of ovarian cancer survival. | Goode EL et al. | — | 2010 | → |
| Inherited variations in AR, ESR1, and ESR2 genes are not associated with prostate cancer aggressiveness or with efficacy of androgen deprivation therapy. | Sun T et al. | — | 2010 | → |
| INSIG1 influences obesity-related hypertriglyceridemia in humans. | Smith EM et al. | — | 2010 | → |
| Interethnic comparisons of important pharmacology genes using SNP databases: potential application to drug regulatory assessments. | Chen J et al. | — | 2010 | → |
| Interleukin 18 receptor 1 expression distinguishes patients with multiple sclerosis. | Gillett A et al. | — | 2010 | → |
| Interleukin-22 genetic polymorphisms and risk of colon cancer. | Thompson CL et al. | — | 2010 | → |
| Introduction to linkage disequilibrium, the HapMap, and imputation. | Neale BM | — | 2010 | → |
| Investigation of the association of BMP gene variants with nephropathy in Type 1 diabetes mellitus. | McKnight AJ et al. | — | 2010 | → |
| Lack of association between common genetic variation in endothelial lipase (LIPG) and the risk for CAD and DVT. | Vergeer M et al. | — | 2010 | → |
| Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes. | Boraska V et al. | — | 2010 | → |
| Leptin receptor polymorphisms interact with polyunsaturated fatty acids to augment risk of insulin resistance and metabolic syndrome in adults. | Phillips CM et al. | — | 2010 | → |
| Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus. | Fan J et al. | — | 2010 | → |
| MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. | Li Y et al. | — | 2010 | → |
| MAT1A variants are associated with hypertension, stroke, and markers of DNA damage and are modulated by plasma vitamin B-6 and folate. | Lai CQ et al. | — | 2010 | → |
| Methodological and statistical issues in pharmacogenomics. | Peters BJ et al. | — | 2010 | → |
| Methodological challenges of genome-wide association analysis in Africa. | Teo YY et al. | — | 2010 | → |
| Methods: genetic epidemiology. | Benke KS et al. | — | 2010 | → |
| Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms. | Santana R et al. | — | 2010 | → |
| Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway. | Manolescu DC et al. | — | 2010 | → |
| Nicotinic acetylcholine receptor genes on chromosome 15q25.1 are associated with nicotine and opioid dependence severity. | Erlich PM et al. | — | 2010 | → |
| NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study. | Chu AY et al. | — | 2010 | → |
| Nucleotide polymorphism of the TNF gene cluster in six Chinese populations. | Zhang Y et al. | — | 2010 | → |
| Patterns of linkage disequilibrium in different populations: implications and opportunities for lipid-associated loci identified from genome-wide association studies. | Teo YY et al. | — | 2010 | → |
| PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis. | Ishizaki Y et al. | — | 2010 | → |
| PER2 variantion is associated with depression vulnerability. | Lavebratt C et al. | — | 2010 | → |
| PERIOD2 variants are associated with abdominal obesity, psycho-behavioral factors, and attrition in the dietary treatment of obesity. | Garaulet M et al. | — | 2010 | → |
| Peroxisome proliferator-activated receptor-delta genotype influences metabolic phenotype and may influence lipid response to statin therapy in humans: a genetics of diabetes audit and research Tayside study. | Burch LR et al. | — | 2010 | → |
| Polymorphisms in fatty-acid-metabolism-related genes are associated with colorectal cancer risk. | Hoeft B et al. | — | 2010 | → |
| Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment. | Horstmann S et al. | — | 2010 | → |
| Polymorphisms in innate immunity genes associated with development of bronchiolitis obliterans after lung transplantation. | Kastelijn EA et al. | — | 2010 | → |
| Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C-reactive protein. | Halder I et al. | — | 2010 | → |
| Polymorphisms in the TOX3/LOC643714 locus and risk of breast cancer in African-American women. | Ruiz-Narváez EA et al. | — | 2010 | → |
| Polymorphisms in TLR4 and TLR2 genes, cytokine production and survival in rural Ghana. | May L et al. | — | 2010 | → |
| Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study. | Campa D et al. | — | 2010 | → |
| Population- and genome-specific patterns of linkage disequilibrium and SNP variation in spring and winter wheat (Triticum aestivum L.). | Chao S et al. | — | 2010 | → |
| Protein phosphatase 2A subunit gene haplotypes and proliferative breast disease modify breast cancer risk. | Dupont WD et al. | — | 2010 | → |
| PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3). | Dossus L et al. | — | 2010 | → |
| PTPN1 polymorphisms are associated with total and low-density lipoprotein cholesterol. | Bauer F et al. | — | 2010 | → |
| Recent advances in the genetics of rheumatoid arthritis. | Raychaudhuri S | — | 2010 | → |
| Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis. | Su H et al. | — | 2010 | → |
| Replicated genetic evidence supports a role for HOMER2 in schizophrenia. | Gilks WP et al. | — | 2010 | → |
| Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. | Riley B et al. | — | 2010 | → |
| Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia. | Wedenoja J et al. | — | 2010 | → |
| Role of genetic variation in insulin-like growth factor 1 receptor on insulin resistance and arterial hypertension. | Sookoian S et al. | — | 2010 | → |
| Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis. | Muhle H et al. | — | 2010 | → |
| Screen and clean: a tool for identifying interactions in genome-wide association studies. | Wu J et al. | — | 2010 | → |
| Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies. | Musumeci L et al. | — | 2010 | → |
| SNPTransformer: a lightweight toolkit for genome-wide association studies. | Dong C | — | 2010 | → |
| Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome. | Sharma N et al. | — | 2010 | → |
| [Systemic lupus erythematosus. «What do we know and where are we heading?»]. | Alarcón Riquelme ME | — | 2010 | → |
| The complex genetic architecture of the metabolome. | Chan EK et al. | — | 2010 | → |
| The core circadian gene Cryptochrome 2 influences breast cancer risk, possibly by mediating hormone signaling. | Hoffman AE et al. | — | 2010 | → |
| The dopamine D3 receptor (DRD3) gene and risk of schizophrenia: case-control studies and an updated meta-analysis. | Nunokawa A et al. | — | 2010 | → |
| The genetics of NOD-like receptors in Crohn's disease. | Cummings JR et al. | — | 2010 | → |
| The identification of colon cancer susceptibility genes by using genome-wide scans. | Daley D | — | 2010 | → |
| The influence of common gene variants of the xenobiotic receptor (PXR) in genetic susceptibility to intrahepatic cholestasis of pregnancy. | Castaño G et al. | — | 2010 | → |
| The missing linkage: what pharmacogenetic associations are left to find in CYP3A? | Perera MA | — | 2010 | → |
| The nuclear receptor PXR gene variants are associated with liver injury in nonalcoholic fatty liver disease. | Sookoian S et al. | — | 2010 | → |
| TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26. | Kurata R et al. | — | 2010 | → |
| TSLP polymorphisms are associated with asthma in a sex-specific fashion. | Hunninghake GM et al. | — | 2010 | → |
| Understanding the evolution of defense metabolites in Arabidopsis thaliana using genome-wide association mapping. | Chan EK et al. | — | 2010 | → |
| Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID. | Offer SM et al. | — | 2010 | → |
| Useful genetic variation databases for oncologists investigating the genetic basis of variable treatment response and survival in cancer. | Savas S | — | 2010 | → |
| USING LINEAR PREDICTORS TO IMPUTE ALLELE FREQUENCIES FROM SUMMARY OR POOLED GENOTYPE DATA. | Wen X et al. | — | 2010 | → |
| Variants in ASK1 are associated with skeletal muscle ASK1 expression, in vivo insulin resistance, and type 2 diabetes in Pima Indians. | Bian L et al. | — | 2010 | → |
| Variation in TREK1 gene linked to depression-resistant phenotype is associated with potentiated neural responses to rewards in humans. | Dillon DG et al. | — | 2010 | → |
| A breast cancer risk haplotype in the caspase-8 gene. | Shephard ND et al. | — | 2009 | → |
| Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures. | Wray NR et al. | — | 2009 | → |
| A common haplotype of the LBP gene predisposes to severe sepsis. | Flores C et al. | — | 2009 | → |
| A common variant in low-density lipoprotein receptor-related protein 6 gene (LRP6) is associated with LDL-cholesterol. | Tomaszewski M et al. | — | 2009 | → |
| Adipose tissue expression and genetic variants of the bone morphogenetic protein receptor 1A gene (BMPR1A) are associated with human obesity. | Böttcher Y et al. | — | 2009 | → |
| A fast algorithm for genome-wide haplotype pattern mining. | Besenbacher S et al. | — | 2009 | → |
| A genetic variant of G6PC2 is associated with type 2 diabetes and fasting plasma glucose level in the Chinese population. | Hu C et al. | — | 2009 | → |
| A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. | Schrauwen I et al. | — | 2009 | → |
| Alcohol sensitivity in Drosophila: translational potential of systems genetics. | Morozova TV et al. | — | 2009 | → |
| Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. | Kim SH et al. | — | 2009 | → |
| Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss. | Pawelczyk M et al. | — | 2009 | → |
| An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders. | Oudot T et al. | — | 2009 | → |
| A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). | Djurovic S et al. | — | 2009 | → |
| Approaches to the identification of susceptibility genes. | Collins A | — | 2009 | → |
| A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity. | Blakemore AI et al. | — | 2009 | → |
| A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity. | Liu Y et al. | — | 2009 | → |
| A single nucleotide polymorphism on exon-4 of the gene encoding PPARdelta is associated with reduced height in adults and children. | Burch LR et al. | — | 2009 | → |
| Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs. | Santos PS et al. | — | 2009 | → |
| Association between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgery. | Nishizawa D et al. | — | 2009 | → |
| Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults. | Ichikawa S et al. | — | 2009 | → |
| Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study. | Fisher E et al. | — | 2009 | → |
| Association of ATP1B1 single-nucleotide polymorphisms with blood pressure and hypertension in a Chinese population. | Xiao B et al. | — | 2009 | → |
| Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity. | Pawlikowska L et al. | — | 2009 | → |
| Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus. | He B et al. | — | 2009 | → |
| Association of markers in the 3' region of the GluR5 kainate receptor subunit gene to alcohol dependence. | Kranzler HR et al. | — | 2009 | → |
| Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE). | Djurovic S et al. | — | 2009 | → |
| Association of OSBPL11 gene polymorphisms with cardiovascular disease risk factors in obesity. | Bouchard L et al. | — | 2009 | → |
| Association of regions on chromosomes 6 and 7 with blood pressure in Nigerian families. | Tayo BO et al. | — | 2009 | → |
| Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study. | Sutton BS et al. | — | 2009 | → |
| Association of the calcium-sensing receptor gene with blood pressure and urinary calcium in African-Americans. | Jung J et al. | — | 2009 | → |
| Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS). | Gaysina D et al. | — | 2009 | → |
| Association of the progesterone receptor gene with endometrial cancer risk in a Chinese population. | Xu WH et al. | — | 2009 | → |
| Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease. | Brand OJ et al. | — | 2009 | → |
| Association of thymidylate synthase gene with endometrial cancer risk in a Chinese population. | Xu WH et al. | — | 2009 | → |
| Association of thymidylate synthase variants with 5-fluorouracil cytotoxicity. | Peters EJ et al. | — | 2009 | → |
| Association of variation in the interleukin-1 gene family with diabetes and glucose homeostasis. | Luotola K et al. | — | 2009 | → |
| Associations between decay-accelerating factor polymorphisms and allergic respiratory diseases. | Kawai T et al. | — | 2009 | → |
| Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer. | Sehl ME et al. | — | 2009 | → |
| Associations of glutamate decarboxylase genes with initial sensitivity and age-at-onset of alcohol dependence in the Irish Affected Sib Pair Study of Alcohol Dependence. | Kuo PH et al. | — | 2009 | → |
| Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects. | Saito A et al. | — | 2009 | → |
| ATOM: a powerful gene-based association test by combining optimally weighted markers. | Li M et al. | — | 2009 | → |
| ATRIUM: testing untyped SNPs in case-control association studies with related individuals. | Wang Z et al. | — | 2009 | → |
| A variant in long palate, lung and nasal epithelium clone 1 is associated with cholera in a Bangladeshi population. | Larocque RC et al. | — | 2009 | → |
| BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis. | Kawashima K et al. | — | 2009 | → |
| Bone morphogenetic protein 7 (BMP7) gene polymorphisms are associated with inverse relationships between vascular calcification and BMD: the Diabetes Heart Study. | Freedman BI et al. | — | 2009 | → |
| Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk. | Goode EL et al. | — | 2009 | → |
| Clock-cancer connection in non-Hodgkin's lymphoma: a genetic association study and pathway analysis of the circadian gene cryptochrome 2. | Hoffman AE et al. | — | 2009 | → |
| CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids. | Garaulet M et al. | — | 2009 | → |
| Coding variant I62V in the complement factor H gene is strongly associated with polypoidal choroidal vasculopathy. | Kondo N et al. | — | 2009 | → |
| Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study. | Reiner AP et al. | — | 2009 | → |
| Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer. | Mavaddat N et al. | — | 2009 | → |
| Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer. | Udler MS et al. | — | 2009 | → |
| Common polymorphisms in the prostaglandin pathway genes and their association with breast cancer susceptibility and survival. | Abraham JE et al. | — | 2009 | → |
| Common variants in the NLRP3 region contribute to Crohn's disease susceptibility. | Villani AC et al. | — | 2009 | → |
| Comparison of identical single nucleotide polymorphisms genotyped by the GeneChip Targeted Genotyping 25K, Affymetrix 500K and Illumina 550K platforms. | Kim KK et al. | — | 2009 | → |
| C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery. | Perry TE et al. | — | 2009 | → |
| C-reactive protein haplotype is associated with high PSA as a marker of metastatic prostate cancer but not with overall cancer risk. | Eklund CM et al. | — | 2009 | → |
| Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip. | Spencer CC et al. | — | 2009 | → |
| Development of predictive models for airflow obstruction in alpha-1-antitrypsin deficiency. | Castaldi PJ et al. | — | 2009 | → |
| Dietary saturated fat modulates the association between STAT3 polymorphisms and abdominal obesity in adults. | Phillips CM et al. | — | 2009 | → |
| Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian population. | Rouault K et al. | — | 2009 | → |
| Drug-induced liver injury: insights from genetic studies. | Andrade RJ et al. | — | 2009 | → |
| Effect of variation in ITGAE on risk of sarcoidosis, CD103 expression, and chest radiography. | Heron M et al. | — | 2009 | → |
| EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. | Weinsheimer S et al. | — | 2009 | → |
| Estimating population haplotype frequencies from pooled SNP data using incomplete database information. | Pirinen M | — | 2009 | → |
| Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence. | Agrawal A et al. | — | 2009 | → |
| Evidence of association of interleukin-1 receptor-like 1 gene polymorphisms with chronic rhinosinusitis. | Castano R et al. | — | 2009 | → |
| Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height. | Johansson A et al. | — | 2009 | → |
| Family-based analysis of tumor necrosis factor and lymphotoxin-alpha tag polymorphisms with type 1 diabetes in the population of South Croatia. | Boraska V et al. | — | 2009 | → |
| Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36. | Wojciechowski R et al. | — | 2009 | → |
| Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus. | Perera D et al. | — | 2009 | → |
| Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations. | Koskinen LL et al. | — | 2009 | → |
| Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis. | McCauley JL et al. | — | 2009 | → |
| G72/G30 (DAOA) and juvenile-onset mood disorders. | Gomez L et al. | — | 2009 | → |
| Gains in power for exhaustive analyses of haplotypes using variable-sized sliding window strategy: a comparison of association-mapping strategies. | Guo Y et al. | — | 2009 | → |
| Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study. | Reiling E et al. | — | 2009 | → |
| Genetic association analysis of COPD candidate genes with bronchodilator responsiveness. | Kim WJ et al. | — | 2009 | → |
| Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. | Jugessur A et al. | — | 2009 | → |
| Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study. | Deo RC et al. | — | 2009 | → |
| Genetic epidemiology in aging research. | Fallin MD et al. | — | 2009 | → |
| Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease. | McGovern DP et al. | — | 2009 | → |
| Genetic polymorphism, linkage disequilibrium, haplotype structure and novel allele analysis of CYP2C19 and CYP2D6 in Han Chinese. | Zhou Q et al. | — | 2009 | → |
| Genetic polymorphisms of peptidase inhibitor 3 (elafin) are associated with acute respiratory distress syndrome. | Tejera P et al. | — | 2009 | → |
| Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project. | Perroud N et al. | — | 2009 | → |
| Genetic predictors of response to antidepressants in the GENDEP project. | Uher R et al. | — | 2009 | → |
| Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations. | Lee HS et al. | — | 2009 | → |
| Genetics of anxiety disorders: the complex road from DSM to DNA. | Smoller JW et al. | — | 2009 | → |
| Genetic variants associated with deep vein thrombosis: the F11 locus. | Li Y et al. | — | 2009 | → |
| Genetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twins. | Rönn T et al. | — | 2009 | → |
| Genetic variation in genes of the fatty acid synthesis pathway and breast cancer risk. | Campa D et al. | — | 2009 | → |
| Genetic variation in healthy oldest-old. | Halaschek-Wiener J et al. | — | 2009 | → |
| Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis. | Villani AC et al. | — | 2009 | → |
| Genetic variation in the progesterone receptor and metabolism pathways and hormone therapy in relation to breast cancer risk. | Reding KW et al. | — | 2009 | → |
| Genetic variation in the serotonin 2A receptor and suicidal ideation in a sample of 270 Irish high-density schizophrenia families. | Fanous AH et al. | — | 2009 | → |
| Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations. | Kao WH et al. | — | 2009 | → |
| Genetic variations in the PI3K/PTEN/AKT/mTOR pathway are associated with clinical outcomes in esophageal cancer patients treated with chemoradiotherapy. | Hildebrandt MA et al. | — | 2009 | → |
| Gene-trait similarity regression for multimarker-based association analysis. | Tzeng JY et al. | — | 2009 | → |
| Genome-wide and fine-resolution association analysis of malaria in West Africa. | Jallow M et al. | — | 2009 | → |
| Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. | Sullivan PF et al. | — | 2009 | → |
| Genome-wide association studies using single-nucleotide polymorphisms versus haplotypes: an empirical comparison with data from the North American Rheumatoid Arthritis Consortium. | Shim H et al. | — | 2009 | → |
| Genome-wide association study in humans. | Smith JG et al. | — | 2009 | → |
| Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. | Chioza BA et al. | — | 2009 | → |
| Genome-wide strategies for discovering genetic influences on cognition and cognitive disorders: methodological considerations. | Potkin SG et al. | — | 2009 | → |
| Genotype imputation. | Li Y et al. | — | 2009 | → |
| Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap-CEU populations. | Pardo L et al. | — | 2009 | → |
| Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation. | Boraska V et al. | — | 2009 | → |
| Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease. | Sutherland GT et al. | — | 2009 | → |
| Haplotype-based association of regulator of G-protein signaling 5 gene polymorphisms with essential hypertension and metabolic parameters in Chinese. | Xiao B et al. | — | 2009 | → |
| Haploview: Visualization and analysis of SNP genotype data. | Barrett JC | — | 2009 | → |
| High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. | Barcellos LF et al. | — | 2009 | → |
| High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females. | Saruta M et al. | — | 2009 | → |
| Hypothesis-driven candidate gene association studies: practical design and analytical considerations. | Jorgensen TJ et al. | — | 2009 | → |
| Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods. | Liang X et al. | — | 2009 | → |
| IGF-I and IGFBP-3 polymorphisms in relation to circulating levels among African American and Caucasian women. | D'Aloisio AA et al. | — | 2009 | → |
| IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. | Suppiah V et al. | — | 2009 | → |
| Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing. | Everett KV et al. | — | 2009 | → |
| Insulin-like growth factor-1- and interleukin-6-related gene variation and risk of multiple myeloma. | Birmann BM et al. | — | 2009 | → |
| Integration of genomic and genetic approaches implicates IREB2 as a COPD susceptibility gene. | DeMeo DL et al. | — | 2009 | → |
| Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations. | Moreno-Estrada A et al. | — | 2009 | → |
| Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. | Heck A et al. | — | 2009 | → |
| Investigation of DNA polymorphisms in SMAD genes for genetic predisposition to diabetic nephropathy in patients with type 1 diabetes mellitus. | McKnight AJ et al. | — | 2009 | → |
| Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer. | Möckelmann N et al. | — | 2009 | → |
| Isolated populations as treasure troves in genetic epidemiology: the case of the Basques. | Garagnani P et al. | — | 2009 | → |
| Is there still a need for candidate gene approaches in the era of genome-wide association studies? | Wilkening S et al. | — | 2009 | → |
| Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power. | Becker T et al. | — | 2009 | → |
| Laboratory methods for high-throughput genotyping. | Edenberg HJ et al. | — | 2009 | → |
| Lack of association of TIM3 polymorphisms and allergic phenotypes. | Zhang J et al. | — | 2009 | → |
| Linkage effects and analysis of finite sample errors in the HapMap. | Zaitlen N et al. | — | 2009 | → |
| Maximizing power in association studies. | Halperin E et al. | — | 2009 | → |
| Methodological Issues in Multistage Genome-wide Association Studies. | Thomas DC et al. | — | 2009 | → |
| Moderation of antidepressant response by the serotonin transporter gene. | Huezo-Diaz P et al. | — | 2009 | → |
| Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. | Laramie JM et al. | — | 2009 | → |
| Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample. | Hardin J et al. | — | 2009 | → |
| No association between DGKH and bipolar disorder in a Scandinavian case-control sample. | Tesli M et al. | — | 2009 | → |
| Novel genetic variants in the alpha-adducin and guanine nucleotide binding protein beta-polypeptide 3 genes and salt sensitivity of blood pressure. | Kelly TN et al. | — | 2009 | → |
| On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism data. | Lemire M | — | 2009 | → |
| OPRM1 Asn40Asp predicts response to naltrexone treatment: a haplotype-based approach. | Oroszi G et al. | — | 2009 | → |
| Overview of the Rapid Response data. | Brown WM et al. | — | 2009 | → |
| Polymorphisms in E-cadherin (CDH1) result in a mis-localised cytoplasmic protein that is associated with Crohn's disease. | Muise AM et al. | — | 2009 | → |
| Polymorphisms in the FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium. | Johnatty SE et al. | — | 2009 | → |
| Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population. | Chu X et al. | — | 2009 | → |
| Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion. | Newhouse S et al. | — | 2009 | → |
| Polymorphisms in uracil-processing genes, but not one-carbon nutrients, are associated with altered DNA uracil concentrations in an urban Puerto Rican population. | Chanson A et al. | — | 2009 | → |
| Positive association of common variants in CD36 with neovascular age-related macular degeneration. | Kondo N et al. | — | 2009 | → |
| Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes. | Fry AE et al. | — | 2009 | → |
| PRKCA: a positional candidate gene for body mass index and asthma. | Murphy A et al. | — | 2009 | → |
| Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II. | Koenen KC et al. | — | 2009 | → |
| Rapid and accurate multiple testing correction and power estimation for millions of correlated markers. | Han B et al. | — | 2009 | → |
| ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population. | Peterson H et al. | — | 2009 | → |
| Role of in silico tools in gene discovery. | Yu B | — | 2009 | → |
| Screening for replication of genome-wide SNP associations in sporadic ALS. | Cronin S et al. | — | 2009 | → |
| Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future. | Alaerts M et al. | — | 2009 | → |
| Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic Old Order Amish. | Naj AC et al. | — | 2009 | → |
| Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations. | Teo YY et al. | — | 2009 | → |
| Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration. | Tolppanen AM et al. | — | 2009 | → |
| SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. | Xu Z et al. | — | 2009 | → |
| SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. | Kondo N et al. | — | 2009 | → |
| Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae. | Kenny EE et al. | — | 2009 | → |
| Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer. | Quaye L et al. | — | 2009 | → |
| Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders. | Misener VL et al. | — | 2009 | → |
| Targeted genome-wide investigation identifies novel SNPs associated with diabetic nephropathy. | McKnight AJ et al. | — | 2009 | → |
| Testing the circadian gene hypothesis in prostate cancer: a population-based case-control study. | Zhu Y et al. | — | 2009 | → |
| The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series. | Korman BD et al. | — | 2009 | → |
| The major histocompatibility complex conserved extended haplotype 8.1 in AIDS-related non-Hodgkin lymphoma. | Aissani B et al. | — | 2009 | → |
| Two-stage case-control association study of polymorphisms in rheumatoid arthritis susceptibility genes with schizophrenia. | Watanabe Y et al. | — | 2009 | → |
| Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration. | Rollinson S et al. | — | 2009 | → |
| Understanding cardiovascular disease through the lens of genome-wide association studies. | Arking DE et al. | — | 2009 | → |
| Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1. | Sabbagh A et al. | — | 2009 | → |
| Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation. | Egyud MR et al. | — | 2009 | → |
| Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans. | Leak TS et al. | — | 2009 | → |
| Variants in neuropeptide Y receptor 1 and 5 are associated with nutrient-specific food intake and are under recent selection in Europeans. | Elbers CC et al. | — | 2009 | → |
| Variation in CHI3LI in relation to type 2 diabetes and related quantitative traits. | Rathcke CN et al. | — | 2009 | → |
| Variation in IL7R predisposes to sarcoid inflammation. | Heron M et al. | — | 2009 | → |
| Variation in the ATP-binding cassette transporter 2 gene is a separate risk factor for systemic lupus erythematosus within the MHC. | Ramos PS et al. | — | 2009 | → |
| Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: the Finnish Diabetes Prevention Study. | Salopuro T et al. | — | 2009 | → |
| Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. | Brookes KJ et al. | — | 2008 | → |
| Common single-nucleotide polymorphisms in DNA double-strand break repair genes and breast cancer risk. | Pooley KA et al. | — | 2008 | → |
| Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk. | Webb E et al. | — | 2008 | → |
| Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder. | Liu L et al. | — | 2008 | → |
| Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function. | Kempf L et al. | — | 2008 | → |
| Genetic susceptibility to infection-mediated preterm birth. | Himes KP et al. | — | 2008 | → |
| Identification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal women. | Thompson DJ et al. | — | 2008 | → |
| Increasing the number of SNP loci does not necessarily improve prediction power at least in the comparison of MTHFR SNP and haplotypes. | Miyaki K et al. | — | 2008 | → |