Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits.
paper
Cited
Public
Unavailable
- Authors
- Purcell, S; Cherny, S S; Sham, P C
- Year
- 2003
- Journal
- Bioinformatics (Oxford, England)
- PMID
- 12499305
- DOI
- 10.1093/bioinformatics/19.1.149
SUMMARY: A website for performing power calculations for the design of linkage and association genetic mapping studies of complex traits. AVAILABILITY: The package is made available athttp://statgen.iop.kcl.ac.uk/gpc/.
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| Evaluation of previous substance dependence genome-wide significant findings in a Spanish sample. | Pineda-Cirera L et al. | — | 2018 | → |
| Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. | Mowat AJ et al. | — | 2018 | → |
| Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer. | Traylor M et al. | — | 2018 | → |
| Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population. | O'Beirne SL et al. | — | 2018 | → |
| Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior. | Kopp ND et al. | — | 2018 | → |
| Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. | Fan BJ et al. | — | 2018 | → |
| Fetal Microsatellite in the Heme Oxygenase 1 Promoter Is Associated With Severe and Early-Onset Preeclampsia. | Kaartokallio T et al. | — | 2018 | → |
| Functional variants in intercellular adhesion molecule-1 and toll-like receptor-4 genes are more frequent in children with febrile urinary tract infection with renal parenchymal involvement. | Hussein A et al. | — | 2018 | → |
| Genetic analysis of deep phenotyping projects in common disorders. | Gershon ES et al. | — | 2018 | → |
| Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit. | Gilbert JR et al. | — | 2018 | → |
| Genetic association study of CSNK1E gene in bipolar disorder and circadian characteristics. | Lee KY et al. | — | 2018 | → |
| Genetic determinants of hepatic steatosis and serum cytokeratin-18 fragment levels in Taiwanese children. | Lin YC et al. | — | 2018 | → |
| Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis. | Loft ND et al. | — | 2018 | → |
| Genetics of Amyotrophic Lateral Sclerosis. | Ghasemi M et al. | — | 2018 | → |
| Genetic variation in gonadal impairment in female survivors of childhood cancer: a PanCareLIFE study protocol. | van der Kooi ALF et al. | — | 2018 | → |
| Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos. | Cid-Soto MA et al. | — | 2018 | → |
| Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. | Savage JE et al. | — | 2018 | → |
| Genome-wide associations identify novel candidate loci associated with genetic susceptibility to tuberculosis in wild boar. | Queirós J et al. | — | 2018 | → |
| Genome-wide association study identifies loci associated with milk leukocyte phenotypes following experimental challenge with Streptococcus uberis. | Siebert L et al. | — | 2018 | → |
| Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. | Visconti A et al. | — | 2018 | → |
| Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration. | Lorés-Motta L et al. | — | 2018 | → |
| Genomic analysis of morphometric traits in bighorn sheep using the Ovine Infinium<sup>®</sup> HD SNP BeadChip. | Miller JM et al. | — | 2018 | → |
| GREB1 genetic variants are associated with bone mineral density in Caucasians. | Hegarty KG et al. | — | 2018 | → |
| Heterozygous TYROBP deletion (PLOSL<sub>FIN</sub>) is not a strong risk factor for cognitive impairment. | Kaivola K et al. | — | 2018 | → |
| Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. | Chen JA et al. | — | 2018 | → |
| Lack of association of mirSNP rs11174811 in AVPR1A gene with arterial blood pressure and hypertension in South Indian population. | Koshy L et al. | — | 2018 | → |
| No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children. | Bozdogan ST et al. | — | 2018 | → |
| Nonsynonymous Variants in <i>PAX4</i> and <i>GLP1R</i> Are Associated With Type 2 Diabetes in an East Asian Population. | Kwak SH et al. | — | 2018 | → |
| Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders. | Ishizuka K et al. | — | 2018 | → |
| Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility. | Yu Y et al. | — | 2018 | → |
| Redefining the Phenotype of Dental Caries. | Weber M et al. | — | 2018 | → |
| Rigor and reproducibility in genetic research on eating disorders. | Hübel C et al. | — | 2018 | → |
| Study of Deiodinase Type 2 Polymorphisms in Graves' Disease and Ophthalmopathy in a Swedish Population. | Shahida B et al. | — | 2018 | → |
| Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. | Wadelius M et al. | — | 2018 | → |
| Targeted capture sequencing identifies novel genetic variations in Chinese patients with idiopathic inflammatory myopathies. | Peng QL et al. | — | 2018 | → |
| The Association between SNPs and a Quantitative Trait: Power Calculation. | Delongchamp R et al. | — | 2018 | → |
| The Impact of FSHR Gene Polymorphisms Ala307Thr and Asn680Ser in the Endometriosis Development. | André GM et al. | — | 2018 | → |
| Transcription factor 7-like 2 gene links increased in vivo insulin synthesis to type 2 diabetes. | Jainandunsing S et al. | — | 2018 | → |
| Transcription factor 7-like 2 single nucleotide polymorphisms are associated with lipid profile in the Balinese. | Oktavianthi S et al. | — | 2018 | → |
| Utility of pooled sequencing for association mapping in nonmodel organisms. | Micheletti SJ et al. | — | 2018 | → |
| Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients. | Sohn M et al. | — | 2018 | → |
| ADAM23 is a common risk gene for canine idiopathic epilepsy. | Koskinen LL et al. | — | 2017 | → |
| A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11. | Bhutta MF et al. | — | 2017 | → |
| Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. | Sapkota Y et al. | — | 2017 | → |
| An unbiased index to quantify participant's phenotypic contribution to an open-access cohort. | Chan Y et al. | — | 2017 | → |
| A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus. | Gilles A et al. | — | 2017 | → |
| Arterial stiffness and blood pressure improvement in aldosterone-producing adenoma harboring KCNJ5 mutations after adrenalectomy. | Chang CH et al. | — | 2017 | → |
| Association between HTR1B alleles and suicidal ideation in individuals with major depressive disorder. | Kao WT et al. | — | 2017 | → |
| Association between NAT2 polymorphisms and the risk of schizophrenia in a Northern Chinese Han population. | Luan Z et al. | — | 2017 | → |
| Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. | Treutlein J et al. | — | 2017 | → |
| Association of ARHGAP18 polymorphisms with schizophrenia in the Chinese-Han population. | Guo W et al. | — | 2017 | → |
| Association of frequent genetic variants in platelet activation pathway genes with large-vessel ischemic stroke in Polish population. | Postula M et al. | — | 2017 | → |
| Association of GWAS Top Genes With Late-Onset Alzheimer's Disease in Colombian Population. | Moreno DJ et al. | — | 2017 | → |
| Association of MiR-149 (RS2292832) Variant with the Risk of Coronary Artery Disease. | Ghaffarzadeh M et al. | — | 2017 | → |
| Association of oligodendrocytes differentiation regulator gene DUSP15 with autism. | Tian Y et al. | — | 2017 | → |
| Association of vitamin D receptor gene polymorphisms and periodontitis in a Taiwanese Han population. | Ho YP et al. | — | 2017 | → |
| Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. | Guo MH et al. | — | 2017 | → |
| Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. | Leo PJ et al. | — | 2017 | → |
| Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility. | Takeuchi M et al. | — | 2017 | → |
| Design Considerations for Genetic Linkage and Association Studies. | Nsengimana J et al. | — | 2017 | → |
| Discovery of novel heart rate-associated loci using the Exome Chip. | van den Berg ME et al. | — | 2017 | → |
| Down syndrome and the complexity of genome dosage imbalance. | Antonarakis SE | — | 2017 | → |
| Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study. | Sardahaee FS et al. | — | 2017 | → |
| Elucidating the genetic basis of an oligogenic birth defect using whole genome sequence data in a non-model organism, Bubalus bubalis. | Whitacre LK et al. | — | 2017 | → |
| Evaluating the Impact of Functional Genetic Variation on HIV-1 Control. | McLaren PJ et al. | — | 2017 | → |
| Evidence for a Link Between Fkbp5/FKBP5, Early Life Social Relations and Alcohol Drinking in Young Adult Rats and Humans. | Nylander I et al. | — | 2017 | → |
| Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist. | Martin J et al. | — | 2017 | → |
| Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans. | Folsom AR et al. | — | 2017 | → |
| Fine mapping genetic associations between the HLA region and extremely high intelligence. | Zabaneh D et al. | — | 2017 | → |
| Gene Polymorphisms for Both Auto-antigen and Immune-Modulating Proteins Are Associated with the Susceptibility of Autoimmune Myasthenia Gravis. | Li HF et al. | — | 2017 | → |
| Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study. | Traylor M et al. | — | 2017 | → |
| Genetic effects on life-history traits in the Glanville fritillary butterfly. | Duplouy A et al. | — | 2017 | → |
| Genetic factors are stressed variably by onset age-based sample selection in psoriasis: A hint from major histocompatibility complex region-based analysis. | Ye L et al. | — | 2017 | → |
| Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians. | Melroy-Greif WE et al. | — | 2017 | → |
| Genetic loci associated with an earlier age at onset in multiplex schizophrenia. | Woolston AL et al. | — | 2017 | → |
| Genetic polymorphisms underlying the skeletal Class III phenotype. | Cruz CV et al. | — | 2017 | → |
| Genetic predisposition to bevacizumab-induced hypertension. | Frey MK et al. | — | 2017 | → |
| Genetics of Depression: Progress at Last. | Mullins N et al. | — | 2017 | → |
| Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population. | Hallberg P et al. | — | 2017 | → |
| Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock. | Vilander LM et al. | — | 2017 | → |
| Genome-wide analyses identify common variants associated with macular telangiectasia type 2. | Scerri TS et al. | — | 2017 | → |
| Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. | Marenholz I et al. | — | 2017 | → |
| Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. | Coleman JRI et al. | — | 2017 | → |
| Genome-wide association study of Parkinson's disease in East Asians. | Foo JN et al. | — | 2017 | → |
| Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations. | Melroy-Greif WE et al. | — | 2017 | → |
| Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. | Ortega-Alonso A et al. | — | 2017 | → |
| Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank. | Howard DM et al. | — | 2017 | → |
| HLA-DPB1 variant rs3117242 is associated with anti-neutrophil cytoplasmic antibody-associated vasculitides in a Han Chinese population. | Wu Z et al. | — | 2017 | → |
| <i>AdmixPower</i>: Statistical Power and Sample Size Estimation for Mapping Genetic Loci in Admixed Populations. | Gautam Y et al. | — | 2017 | → |
| Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer. | Carter H et al. | — | 2017 | → |
| Interleukin-6-174G > C (rs1800795) polymorphism distribution and its association with rheumatoid arthritis: A case-control study and meta-analysis. | Dar SA et al. | — | 2017 | → |
| Investigating the relationship between iron and depression. | Mills NT et al. | — | 2017 | → |
| Juvenile-onset myasthenia gravis: autoantibody status, clinical characteristics and genetic polymorphisms. | Hong Y et al. | — | 2017 | → |
| Lack of replication of previous autism spectrum disorder GWAS hits in European populations. | Torrico B et al. | — | 2017 | → |
| <i>UNC5C</i> variants are associated with cerebral amyloid angiopathy. | Yang HS et al. | — | 2017 | → |
| Mitochondrial genome variation and prostate cancer: a review of the mutational landscape and application to clinical management. | Kalsbeek AMF et al. | — | 2017 | → |
| MMP20 rs1784418 Protects Certain Populations against Caries. | Filho AV et al. | — | 2017 | → |
| Polymorphism of the SNAP25 gene is associated with symptom improvement in schizophrenic patients treated with amisulpride. | Kang SG et al. | — | 2017 | → |
| Polymorphisms of RAD51B are associated with rheumatoid arthritis and erosion in rheumatoid arthritis patients. | Zhi L et al. | — | 2017 | → |
| Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort. | Abdullah N et al. | — | 2017 | → |
| Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders. | Ishizuka K et al. | — | 2017 | → |
| Rare PDCD11 variations are not associated with risk of schizophrenia in Japan. | Hoya S et al. | — | 2017 | → |
| The DCDC2 deletion is not a risk factor for dyslexia. | Scerri TS et al. | — | 2017 | → |
| The Genetic Landscape of Renal Complications in Type 1 Diabetes. | Sandholm N et al. | — | 2017 | → |
| The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interaction. | Bomfim IL et al. | — | 2017 | → |
| TOX and ADIPOQ Gene Polymorphisms Are Associated with Antipsychotic-Induced Weight Gain in Han Chinese. | Li S et al. | — | 2017 | → |
| Transethnic Replication Study to Assess the Association Between Clozapine-Induced Agranulocytosis/Granulocytopenia and Genes at 12p12.2 in a Japanese Population. | Saito T et al. | — | 2017 | → |
| Transplant genetics and genomics. | Yang JY et al. | — | 2017 | → |
| Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants. | Kantojärvi K et al. | — | 2017 | → |
| Variations in ADIPOR1 But Not ADIPOR2 are Associated With Hypertriglyceridemia and Diabetes in an Admixed Latin American Population. | Mora-García G et al. | — | 2017 | → |
| Vascular endothelial growth factor gene variations as a risk predictor in disc degeneration. | Amaro A et al. | — | 2017 | → |
| Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. | Peng Q et al. | — | 2017 | → |
| A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy. | Huang L et al. | — | 2016 | → |
| Analysis of association between common variants in the SLCO6A1 gene with schizophrenia, bipolar disorder and major depressive disorder in the Han Chinese population. | Khan RA et al. | — | 2016 | → |
| Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia. | Rees E et al. | — | 2016 | → |
| An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance. | Gordon D et al. | — | 2016 | → |
| An RGS2 3'UTR polymorphism is associated with preeclampsia in overweight women. | Karppanen T et al. | — | 2016 | → |
| A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans. | Clapham KR et al. | — | 2016 | → |
| A single-nucleotide polymorphism in the MicroRNA-146a gene is associated with diabetic nephropathy and sight-threatening diabetic retinopathy in Caucasian patients. | Kaidonis G et al. | — | 2016 | → |
| Association Between Genes Involved in Craniofacial Development and Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population. | Machado RA et al. | — | 2016 | → |
| Association between polymorphisms in transforming growth factor-β1 and sporadic Alzheimer's disease in a Chinese population. | Yang Q et al. | — | 2016 | → |
| Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study. | Ting WH et al. | — | 2016 | → |
| Association of DISC1, BDNF, and COMT polymorphisms with exploratory eye movement of schizophrenia in a Chinese Han population. | Dong Z et al. | — | 2016 | → |
| Association of Matrix Metalloproteinase-9 (MMP9) Variants with Primary Angle Closure and Primary Angle Closure Glaucoma. | Chen X et al. | — | 2016 | → |
| Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population. | Xu Q et al. | — | 2016 | → |
| Association study of androgen signaling pathway genes in polycystic ovary syndrome. | Ketefian A et al. | — | 2016 | → |
| A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder. | Mahmuda NA et al. | — | 2016 | → |
| A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells. | Cigliola V et al. | — | 2016 | → |
| Case-Control Studies Are Not Familial Studies. | Wang Z et al. | — | 2016 | → |
| Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment. | Turner S et al. | — | 2016 | → |
| Clinical and Genetic Determinants of Cardiomyopathy Risk among Hematopoietic Cell Transplantation Survivors. | Leger KJ et al. | — | 2016 | → |
| CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches. | Werling AM et al. | — | 2016 | → |
| Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development. | Mueller KL et al. | — | 2016 | → |
| Common variants in QPCT gene confer risk of schizophrenia in the Han Chinese population. | Khan RA et al. | — | 2016 | → |
| Copy number variation in bipolar disorder. | Green EK et al. | — | 2016 | → |
| Determination of NLRP3 (rs4612666) and IL-1B (rs1143634) genetic polymorphisms in periodontally diseased and healthy subjects. | Isaza-Guzmán DM et al. | — | 2016 | → |
| Differential burden of rare protein truncating variants in Alzheimer's disease patients compared to centenarians. | Freudenberg-Hua Y et al. | — | 2016 | → |
| Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease. | Peyrot WJ et al. | — | 2016 | → |
| Effect of common polymorphisms of the farnesoid X receptor and bile acid transporters on the pharmacokinetics of ursodeoxycholic acid. | Hu M et al. | — | 2016 | → |
| Effect of G(-174)C polymorphism in interleukin-6 gene on cardiovascular disease in type 2 diabetes patients. | Buraczynska M et al. | — | 2016 | → |
| Epidermal growth factor gene is a newly identified candidate gene for gout. | Han L et al. | — | 2016 | → |
| Evaluation of results from genome-wide studies of language and reading in a novel independent dataset. | Carrion-Castillo A et al. | — | 2016 | → |
| Evaluation of the association of single nucleotide polymorphisms in the PRPH2 gene with adult-onset foveomacular vitelliform dystrophy. | Grunin M et al. | — | 2016 | → |
| Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia. | Guan F et al. | — | 2016 | → |
| Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes. | Prasad RB et al. | — | 2016 | → |
| Exome arrays capture polygenic rare variant contributions to schizophrenia. | Richards AL et al. | — | 2016 | → |
| Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants. | Kaartokallio T et al. | — | 2016 | → |
| Gender-Specific Association of ATP2B1 Variants with Susceptibility to Essential Hypertension in the Han Chinese Population. | Xu J et al. | — | 2016 | → |
| Genetic and clinical variables identify predictors for chronic kidney disease in type 2 diabetes. | Jiang G 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 characteristics of inflammatory bowel disease in a Japanese population. | Fuyuno Y et al. | — | 2016 | → |
| Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study. | Li Z et al. | — | 2016 | → |
| Genetics: Implications for Prevention and Management of Coronary Artery Disease. | Assimes TL et al. | — | 2016 | → |
| Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population. | Hallberg P et al. | — | 2016 | → |
| Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. | Bailey JN et al. | — | 2016 | → |
| Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. | Hou L et al. | — | 2016 | → |
| Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway. | Cocchi E et al. | — | 2016 | → |
| Genome-wide association study of antisocial personality disorder. | Rautiainen MR et al. | — | 2016 | → |
| Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders. | Coleman JR et al. | — | 2016 | → |
| Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density. | Mullin BH et al. | — | 2016 | → |
| Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project. | Auer PL et al. | — | 2016 | → |
| Heritability and confirmation of genetic association studies for childhood asthma in twins. | Ullemar V et al. | — | 2016 | → |
| Human leukocyte antigen class II (DRB1 and DQB1) alleles and haplotypes frequencies in patients with pemphigus vulgaris among the Serbian population. | Zivanovic D et al. | — | 2016 | → |
| Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. | Hyde CL et al. | — | 2016 | → |
| Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome-Wide Association Study. | Julià A et al. | — | 2016 | → |
| Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia. | Genovese G et al. | — | 2016 | → |
| Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders. | Ishizuka K et al. | — | 2016 | → |
| Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans. | Yoon SC et al. | — | 2016 | → |
| Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. | Kerns SL et al. | — | 2016 | → |
| Meta-analysis of the DRD5 VNTR in persistent ADHD. | Klein M et al. | — | 2016 | → |
| Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. | Natarajan P et al. | — | 2016 | → |
| Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population. | Takasaki Y et al. | — | 2016 | → |
| Next-generation re-sequencing of genes involved in increased platelet reactivity in diabetic patients on acetylsalicylic acid. | Postula M et al. | — | 2016 | → |
| Non-replication of the association between 5HTTLPR and response to psychological therapy for child anxiety disorders. | Lester KJ et al. | — | 2016 | → |
| On Sample Size and Power Calculation for Variant Set-Based Association Tests. | Wu B et al. | — | 2016 | → |
| Phenotypic extremes in rare variant study designs. | Peloso GM et al. | — | 2016 | → |
| Plasma endothelin-1 and single nucleotide polymorphisms of <i>endothelin-1 and endothelin type A receptor genes</i> as risk factors for normal tension glaucoma. | Kosior-Jarecka E et al. | — | 2016 | → |
| Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients. | Žavbi M et al. | — | 2016 | → |
| Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin system. | Biswas N et al. | — | 2016 | → |
| Positive association of genetic variations in the phospholipase C-like 1 gene with dermatomyositis in Chinese Han. | Wang Q 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 | → |
| Protective Role of Maternal P.VAL158MET Catechol-O-Methyltransferase Polymorphism against Early-Onset Preeclampsia and its Complications. | Krnjeta T et al. | — | 2016 | → |
| Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease. | Kohli MA et al. | — | 2016 | → |
| Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. | van 't Hof FN et al. | — | 2016 | → |
| SurvivalGWAS_Power: a user friendly tool for power calculations in pharmacogenetic studies with "time to event" outcomes. | Syed H et al. | — | 2016 | → |
| Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set. | de Vries B et al. | — | 2016 | → |
| Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution. | Patel AP et al. | — | 2016 | → |
| Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits. | Pinto R et al. | — | 2016 | → |
| The Association between NOS3 Gene Polymorphisms and Hypoxic-Ischemic Encephalopathy Susceptibility and Symptoms in Chinese Han Population. | Wu Y et al. | — | 2016 | → |
| The HLA-C*06 allele as a possible genetic predisposing factor to psoriasis in South Indian Tamils. | Indhumathi S et al. | — | 2016 | → |
| The Human MSI2 Gene is Associated with Schizophrenia in the Chinese Han Population. | Luan Z et al. | — | 2016 | → |
| The phenotypic legacy of admixture between modern humans and Neandertals. | Simonti CN et al. | — | 2016 | → |
| The polymorphisms of MSH6 gene are associated with AIDS progression in a northern Chinese population. | Wang C et al. | — | 2016 | → |
| The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers. | Laitman Y et al. | — | 2016 | → |
| The role of Pannexin gene variants in schizophrenia: systematic analysis of phenotypes. | Gawlik M et al. | — | 2016 | → |
| Two-stage replication of previous genome-wide association studies of AS3MT-CNNM2-NT5C2 gene cluster region in a large schizophrenia case-control sample from Han Chinese population. | Guan F et al. | — | 2016 | → |
| Type 2 Diabetes Risk Allele Loci in the Qatari Population. | O'Beirne SL et al. | — | 2016 | → |
| Uromodulin gene variants and their association with renal function and blood pressure in cats: a pilot study. | Jepson RE et al. | — | 2016 | → |
| Variant of PBX2 gene in the 6p21.3 asthma susceptibility locus is associated with allergic rhinitis in Chinese subjects. | Zhao Y et al. | — | 2016 | → |
| Variants in the autophagy-related gene IRGM confer susceptibility to non-alcoholic fatty liver disease by modulating lipophagy. | Lin YC et al. | — | 2016 | → |
| Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. | Balendra R et al. | — | 2016 | → |
| Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. | Porta M et al. | — | 2016 | → |
| What Cure Models Can Teach us About Genome-Wide Survival Analysis. | Stringer S et al. | — | 2016 | → |
| Whole-genome association analysis of treatment response in obsessive-compulsive disorder. | Qin H et al. | — | 2016 | → |
| A2BP1 gene polymorphisms association with olanzapine-induced weight gain. | Dong L et al. | — | 2015 | → |
| A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. | Aung T et al. | — | 2015 | → |
| A First Step toward Personalized Medicine in Osteosarcoma: Pharmacogenetics as Predictive Marker of Outcome after Chemotherapy-Based Treatment. | Hagleitner MM et al. | — | 2015 | → |
| A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationships. | Visscher PM et al. | — | 2015 | → |
| A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism. | Loukola A et al. | — | 2015 | → |
| A genome-wide association study of periodontitis in a Japanese population. | Shimizu S et al. | — | 2015 | → |
| A guide on gene prioritization in studies of psychiatric disorders. | Stringer S et al. | — | 2015 | → |
| Amino Acid Variation in HLA Class II Proteins Is a Major Determinant of Humoral Response to Common Viruses. | Hammer C et al. | — | 2015 | → |
| Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing. | He J et al. | — | 2015 | → |
| An association study between USP34 and polycystic ovary syndrome. | Zhao S et al. | — | 2015 | → |
| Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. | Liu JZ et al. | — | 2015 | → |
| Association analysis for corticotropin releasing hormone polymorphisms with the risk of major depressive disorder and the response to antidepressants. | Chang HS et al. | — | 2015 | → |
| Association between CCR6 and rheumatoid arthritis: a meta-analysis. | Cheng P et al. | — | 2015 | → |
| Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese. | Gu Z et al. | — | 2015 | → |
| Association of ARRB1 polymorphisms with the risk of major depressive disorder and with treatment response to mirtazapine. | Chang HS et al. | — | 2015 | → |
| Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis. | Fan BJ et al. | — | 2015 | → |
| Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma. | Miao C et al. | — | 2015 | → |
| Association of LRP5, TCF7L2, and GCG variants and type 2 diabetes mellitus as well as fasting plasma glucose and lipid metabolism indexes. | Wang J et al. | — | 2015 | → |
| Association of open-angle glaucoma loci with incident glaucoma in the Blue Mountains Eye Study. | Burdon KP et al. | — | 2015 | → |
| Association of polymorphisms in interleukin (IL)-12A and -B genes with rheumatoid arthritis in a Chinese population. | Wang EY et al. | — | 2015 | → |
| Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk. | Huentelman MJ et al. | — | 2015 | → |
| Association of the Catechol O-Methyltransferase Val158-Met Polymorphism and Reduced Interference Control in Korean Children with Attention-Deficit Hyperactivity Disorder. | Park S et al. | — | 2015 | → |
| Association of TNFSF8 regulatory variants with excessive inflammatory responses but not leprosy per se. | Fava VM et al. | — | 2015 | → |
| Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families. | Fontoura C et al. | — | 2015 | → |
| Associations between ALOX, COX, and CRP polymorphisms and breast cancer among Hispanic and non-Hispanic white women: The breast cancer health disparities study. | Connor AE et al. | — | 2015 | → |
| Association Study between the CD157/BST1 Gene and Autism Spectrum Disorders in a Japanese Population. | Yokoyama S et al. | — | 2015 | → |
| Association study of H2AFZ with schizophrenia in a Japanese case-control sample. | Jitoku D et al. | — | 2015 | → |
| Association Study of N-Methyl-D-Aspartate Receptor Subunit 2B (GRIN2B) Polymorphisms and Schizophrenia Symptoms in the Han Chinese Population. | Yang Y et al. | — | 2015 | → |
| Association study of the SLITRK5 gene and Tourette syndrome. | Zhang K et al. | — | 2015 | → |
| Candidate gene-environment interaction research: reflections and recommendations. | Dick DM et al. | — | 2015 | → |
| Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia. | Huang CC et al. | — | 2015 | → |
| Cluster headache and the hypocretin receptor 2 reconsidered: a genetic association study and meta-analysis. | Weller CM et al. | — | 2015 | → |
| Common NOTCH3 Variants and Cerebral Small-Vessel Disease. | Rutten-Jacobs LC et al. | — | 2015 | → |
| Common variants of HTR1A and SLC6A4 confer the increasing risk of Schizophrenia susceptibility: A population-based association and epistasis analysis. | Lin H et al. | — | 2015 | → |
| COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study. | Sampaio AS et al. | — | 2015 | → |
| Converging evidence does not support GIT1 as an ADHD risk gene. | Klein M et al. | — | 2015 | → |
| Cytokine gene polymorphisms in obstructive sleep apnoea/hypopnoea syndrome. | Bielicki P et al. | — | 2015 | → |
| Do Genetic Susceptibility Variants Associate with Disease Severity in Early Active Rheumatoid Arthritis? | Scott IC et al. | — | 2015 | → |
| Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. | Jacobsen KK et al. | — | 2015 | → |
| Evaluation of genetic polymorphisms in clusterin and tumor necrosis factor-alpha genes in South Indian individuals with pseudoexfoliation syndrome. | Dubey SK et al. | — | 2015 | → |
| Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's disease. | Schulte EC et al. | — | 2015 | → |
| Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population. | Nouri N et al. | — | 2015 | → |
| Filaggrin loss-of-function mutations are not associated with atopic dermatitis that develops in late childhood or adulthood. | Rupnik H et al. | — | 2015 | → |
| FUT2: filling the gap between genes and environment in Behçet's disease? | Xavier JM et al. | — | 2015 | → |
| Genetic analysis of the glyoxalase system in schizophrenia. | Bangel FN et al. | — | 2015 | → |
| Genetic Case-Control Study for Eight Polymorphisms Associated with Rheumatoid Arthritis. | Saad MN et al. | — | 2015 | → |
| Genetic markers in the EET metabolic pathway are associated with outcomes in patients with aneurysmal subarachnoid hemorrhage. | Donnelly MK et al. | — | 2015 | → |
| Genetic overlap between diagnostic subtypes of ischemic stroke. | Holliday EG et al. | — | 2015 | → |
| Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry. | do Rego Borges A et al. | — | 2015 | → |
| Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans. | Saykin AJ et al. | — | 2015 | → |
| Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. | Tapper W et al. | — | 2015 | → |
| Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. | Li C et al. | — | 2015 | → |
| Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. | Stuart PE et al. | — | 2015 | → |
| Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking. | Pirastu N et al. | — | 2015 | → |
| Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes. | Miller FW et al. | — | 2015 | → |
| Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. | Jacobsen KK et al. | — | 2015 | → |
| Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. | Gelernter J et al. | — | 2015 | → |
| Genome-wide association study of schizophrenia in Ashkenazi Jews. | Goes FS et al. | — | 2015 | → |
| Genome-wide significant association with seven novel multiple sclerosis risk loci. | Lill CM et al. | — | 2015 | → |
| Genome-wide Survey of Runs of Homozygosity Identifies Recessive Loci for Bone Mineral Density in Caucasian and Chinese Populations. | Yang TL et al. | — | 2015 | → |
| Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene. | Nievergelt CM et al. | — | 2015 | → |
| High frequency of DQB1*05 and absolute absence of DRB1*13 in muscle-specific tyrosine kinase positive myasthenia gravis. | Nikolic AV et al. | — | 2015 | → |
| Homogeneous case subgroups increase power in genetic association studies. | Traylor M et al. | — | 2015 | → |
| Identification of a common risk haplotype for canine idiopathic epilepsy in the ADAM23 gene. | Koskinen LL et al. | — | 2015 | → |
| Identification of new susceptibility loci for IgA nephropathy in Han Chinese. | Li M et al. | — | 2015 | → |
| Independent Replication and Meta-Analysis for Endometriosis Risk Loci. | Sapkota Y et al. | — | 2015 | → |
| Inherited mtDNA variations are not strong risk factors in human prion disease. | Hudson G et al. | — | 2015 | → |
| Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans. | Ferguson JF et al. | — | 2015 | → |
| Interaction between common variants of FTO and MC4R is associated with risk of PCOS. | Yuan H et al. | — | 2015 | → |
| Interaction of DRD2TaqI, COMT, and ALDH2 genes associated with bipolar II disorder comorbid with anxiety disorders in Han Chinese in Taiwan. | Hu MC et al. | — | 2015 | → |
| Interactions between paraoxonase 1 genetic polymorphisms and smoking and their effects on oxidative stress and lung cancer risk in a Korean population. | Eom SY et al. | — | 2015 | → |
| Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS. | Schrewe L et al. | — | 2015 | → |
| Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. | Pettigrew KA et al. | — | 2015 | → |
| Matrix metalloproteinase-2 (MMP-2) gene polymorphism and cardiovascular comorbidity in type 2 diabetes patients. | Buraczynska M et al. | — | 2015 | → |
| Matrix Metalloproteinase-9 (MMP-9) Gene Polymorphism in Stroke Patients. | Buraczynska K et al. | — | 2015 | → |
| Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease. | Spataro N et al. | — | 2015 | → |
| Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins. | Sugimoto M et al. | — | 2015 | → |
| MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. | Nischwitz S et al. | — | 2015 | → |
| New loci and coding variants confer risk for age-related macular degeneration in East Asians. | Cheng CY et al. | — | 2015 | → |
| No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins. | Murdoch JD et al. | — | 2015 | → |
| No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. | Garcia-Etxebarria K et al. | — | 2015 | → |
| Polymorphisms in CaSR and CLDN14 Genes Associated with Increased Risk of Kidney Stone Disease in Patients from the Eastern Part of India. | Guha M et al. | — | 2015 | → |
| Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. | Matsson H et al. | — | 2015 | → |
| Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. | McLaren PJ et al. | — | 2015 | → |
| Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia. | Huusko JM et al. | — | 2015 | → |
| Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. | Hafrén L et al. | — | 2015 | → |
| Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder. | Ramos EM et al. | — | 2015 | → |
| Psychiatric symptoms in adolescents: FKBP5 genotype--early life adversity interaction effects. | Comasco E et al. | — | 2015 | → |
| Race and Melanocortin 1 Receptor Polymorphism R163Q Are Associated with Post-Burn Hypertrophic Scarring: A Prospective Cohort Study. | Sood RF et al. | — | 2015 | → |
| Rare variant association studies: considerations, challenges and opportunities. | Auer PL et al. | — | 2015 | → |
| Rare variants in MYD88, IRAK4 and IKBKG and susceptibility to invasive pneumococcal disease: a population-based case-control study. | Ellis MK et al. | — | 2015 | → |
| Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia. | Merner ND et al. | — | 2015 | → |
| Serum total bilirubin levels and coronary heart disease--Causal association or epiphenomenon? | Kunutsor SK | — | 2015 | → |
| Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population. | Chen S et al. | — | 2015 | → |
| SPS: A Simulation Tool for Calculating Power of Set-Based Genetic Association Tests. | Li J et al. | — | 2015 | → |
| Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. | Usher CL et al. | — | 2015 | → |
| The association of proopiomelanocortin polymorphisms with the risk of major depressive disorder and the response to antidepressants via interactions with stressful life events. | Chang HS et al. | — | 2015 | → |
| The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). | Helgeland Ø et al. | — | 2015 | → |
| The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease. | Moutsianas L et al. | — | 2015 | → |
| TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study. | Ortega-Cubero S et al. | — | 2015 | → |
| Two-stage comprehensive evaluation of genetic susceptibility of common variants in FBXO38, AP3B2 and WHAMM to severe chronic periodontitis. | Shang D et al. | — | 2015 | → |
| TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. | Diogo D et al. | — | 2015 | → |
| Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions: An Observational Study. | Lee IT et al. | — | 2015 | → |
| Variation in complement protein C1q is not a major contributor to cognitive impairment in Parkinson's disease. | Carbutt S et al. | — | 2015 | → |
| 8q24 risk alleles and prostate cancer in African-Barbadian men. | Cropp CD et al. | — | 2014 | → |
| ABCA1 rs1883025 polymorphism shows no association with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in a Northern Chinese population. | Li F et al. | — | 2014 | → |
| ABO histo-blood group might modulate predisposition to Crohn's disease and affect disease behavior. | Forni D et al. | — | 2014 | → |
| Adiponectin gene (ADIPOQ) polymorphisms correlate with the progression of nephropathy in Taiwanese male patients with type 2 diabetes. | Chung HF et al. | — | 2014 | → |
| Adiponectin gene variants and the risk of coronary heart disease: a 16-year longitudinal study. | Cheung CY et al. | — | 2014 | → |
| A genome-wide association meta-analysis of preschool internalizing problems. | Benke KS et al. | — | 2014 | → |
| A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis. | Julià A et al. | — | 2014 | → |
| A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. | Baron-Cohen S et al. | — | 2014 | → |
| A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. | Nelson CL et al. | — | 2014 | → |
| A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus. | Cai DC et al. | — | 2014 | → |
| A large-scale screen for coding variants predisposing to psoriasis. | Tang H et al. | — | 2014 | → |
| Analysis of FokI polymorphism of vitamin D receptor gene in intervertebral disc degeneration. | Vieira LA et al. | — | 2014 | → |
| Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations. | Foo JN et al. | — | 2014 | → |
| An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases. | Chan Y et al. | — | 2014 | → |
| An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. | Zochling J et al. | — | 2014 | → |
| Anti-TNF treatment response in rheumatoid arthritis patients is associated with genetic variation in the NLRP3-inflammasome. | Sode J et al. | — | 2014 | → |
| Apolipoprotein C3 gene polymorphisms in Southern Indian patients with nonalcoholic fatty liver disease. | Puppala J et al. | — | 2014 | → |
| A polymorphism in the DNA repair domain of APEX1 is associated with the radiation-induced pneumonitis risk among lung cancer patients after radiotherapy. | Li H et al. | — | 2014 | → |
| A possible genetic association with chronic fatigue in primary Sjögren's syndrome: a candidate gene study. | Norheim KB et al. | — | 2014 | → |
| Are IL2 promoter polymorphisms associated with MS in Iranian patients? - We do not know. | Jabalameli MR et al. | — | 2014 | → |
| Assessing accuracy of genotype imputation in American Indians. | Malhotra A et al. | — | 2014 | → |
| Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease. | Flint J et al. | — | 2014 | → |
| Association between norepinephrine transporter gene (SLC6A2) polymorphisms and suicide in patients with major depressive disorder. | Kim YK et al. | — | 2014 | → |
| Association of BTG2, CYR61, ZFP36, and SCD gene polymorphisms with Graves' disease and ophthalmopathy. | Planck T et al. | — | 2014 | → |
| Association of common genetic variants with lipid traits in the Indian population. | Walia GK et al. | — | 2014 | → |
| Association of interleukin-4 genetic polymorphisms with sporadic Alzheimer's disease in Chinese Han population. | Li W et al. | — | 2014 | → |
| Association of NCAM1 polymorphisms with autism and parental age at conception in a Chinese Han population. | Zhang J et al. | — | 2014 | → |
| Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. | Schulte EC et al. | — | 2014 | → |
| BMI-associated alleles do not constitute risk alleles for polycystic ovary syndrome independently of BMI: a case-control study. | Louwers YV et al. | — | 2014 | → |
| Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate. | Melhem NM et al. | — | 2014 | → |
| Characterizing the genetic basis of bacterial phenotypes using genome-wide association studies: a new direction for bacteriology. | Read TD et al. | — | 2014 | → |
| CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. | Rees E et al. | — | 2014 | → |
| Colorectal cancer susceptibility: apparent gender-related modulation by ABCB1 gene polymorphisms. | Martinelli M et al. | — | 2014 | → |
| Common TLR1 genetic variation is not associated with death from melioidosis, a common cause of sepsis in rural Thailand. | Chantratita N et al. | — | 2014 | → |
| Common variants associated with general and MMR vaccine-related febrile seizures. | Feenstra B et al. | — | 2014 | → |
| Comparative gene expression profiling analysis of lymphoblastoid cells reveals neuron-specific enolase gene (ENO2) as a susceptibility gene of heroin dependence. | Liao DL et al. | — | 2014 | → |
| Complement factor I polymorphism is not associated with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a chinese population. | Yang F et al. | — | 2014 | → |
| CTLA4 variants and haplotype contribute genetic susceptibility to myasthenia gravis in northern Chinese population. | Sun L et al. | — | 2014 | → |
| Deeper, longer phenotyping to accelerate the discovery of the genetic architectures of diseases. | — | — | 2014 | → |
| Ethnic background and genetic variation in the evaluation of cancer risk: a systematic review. | Jing L et al. | — | 2014 | → |
| Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. | Vishal M et al. | — | 2014 | → |
| Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex. | Guella I et al. | — | 2014 | → |
| Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. | Ma RC et al. | — | 2014 | → |
| FTO genetic variants and risk of obesity and type 2 diabetes: a meta-analysis of 28,394 Indians. | Vasan SK et al. | — | 2014 | → |
| Functional gene-set analysis does not support a major role for synaptic function in attention deficit/hyperactivity disorder (ADHD). | Hammerschlag AR et al. | — | 2014 | → |
| Functional polymorphism in the brain-derived neurotrophic factor gene interacts with stressful life events but not childhood maltreatment in the etiology of depression. | Brown GW et al. | — | 2014 | → |
| Gene-gene interaction between CETP and APOE polymorphisms confers higher risk for hypertriglyceridemia in oldest-old Chinese women. | Sun L et al. | — | 2014 | → |
| Genetic analysis of GABRB3 at 15q12 as a candidate gene of schizophrenia. | Huang CC et al. | — | 2014 | → |
| Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. | Shen L et al. | — | 2014 | → |
| Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India. | Balmiki N et al. | — | 2014 | → |
| Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. | Sommen M et al. | — | 2014 | → |
| Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. | Koh SP et al. | — | 2014 | → |
| Genetic associations to germinal centre formation in primary Sjogren's syndrome. | Reksten TR et al. | — | 2014 | → |
| Genetic association study between methyl-CpG-binding domain genes and schizophrenia among Chinese family trios. | Xie B et al. | — | 2014 | → |
| Genetic association study of TNFAIP3, IFIH1, IRF5 polymorphisms with polymyositis/dermatomyositis in Chinese Han population. | Chen S et al. | — | 2014 | → |
| Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. | Mullins N et al. | — | 2014 | → |
| Genetic studies of Crohn's disease: past, present and future. | Liu JZ et al. | — | 2014 | → |
| Genetic study of diabetic retinopathy: recruitment methodology and analysis of baseline characteristics. | Kaidonis G et al. | — | 2014 | → |
| Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis. | Patel RS et al. | — | 2014 | → |
| Genetic variants for type 2 diabetes and new-onset cancer in Chinese with type 2 diabetes. | Ma RC et al. | — | 2014 | → |
| Genetic variation in Otos is associated with cisplatin-induced ototoxicity. | Spracklen TF et al. | — | 2014 | → |
| Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia. | Wouters MM et al. | — | 2014 | → |
| Genome-wide association study of ancestry-specific TB risk in the South African Coloured population. | Chimusa ER et al. | — | 2014 | → |
| Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. | Luykx JJ et al. | — | 2014 | → |
| Genome-wide association study of proneness to anger. | Mick E et al. | — | 2014 | → |
| Genome-wide association study of receptive language ability of 12-year-olds. | Harlaar N et al. | — | 2014 | → |
| Genome-wide association study of sleep duration in the Finnish population. | Ollila HM et al. | — | 2014 | → |
| Genome wide association study: searching for genes underlying body mass index in the Chinese. | Yang F et al. | — | 2014 | → |
| Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. | Schrauwen I et al. | — | 2014 | → |
| IL10 polymorphisms associated with Behçet's disease in Chinese Han. | Wu Z et al. | — | 2014 | → |
| Impact of measurement error on testing genetic association with quantitative traits. | Liao J et al. | — | 2014 | → |
| Influence of MILR1 promoter polymorphism on expression levels and the phenotype of atopy. | Nanatsue K et al. | — | 2014 | → |
| Interleukin-23 receptor polymorphisms are associated with Alzheimer's disease in Han Chinese. | Liu Y et al. | — | 2014 | → |
| ITIH3 polymorphism may confer susceptibility to psychiatric disorders by altering the expression levels of GLT8D1. | Sasayama D et al. | — | 2014 | → |
| ITIH family genes confer risk to schizophrenia and major depressive disorder in the Han Chinese population. | He K et al. | — | 2014 | → |
| Lack of association of the caspase-12 long allele with community-acquired pneumonia in people of African descent. | Chen J et al. | — | 2014 | → |
| Lupus risk variants in the PXK locus alter B-cell receptor internalization. | Vaughn SE et al. | — | 2014 | → |
| Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. | Ng MC et al. | — | 2014 | → |
| Mutational analysis of angiogenin gene in Parkinson's disease. | Chen ML et al. | — | 2014 | → |
| Osteopontin gene SNPs (rs9138, rs11730582) mediate susceptibility to external root resorption in orthodontic patients. | Iglesias-Linares A et al. | — | 2014 | → |
| Pharmacogenetic analysis of GLCCI1 in three north European pediatric asthma populations with a reported use of inhaled corticosteroids. | Vijverberg SJ et al. | — | 2014 | → |
| Polymorphism in microRNA-196a2 contributes to the risk of cardiovascular disease in type 2 diabetes patients. | Buraczynska M et al. | — | 2014 | → |
| Power analysis and sample size estimation for sequence-based association studies. | Wang GT et al. | — | 2014 | → |
| Protein kinase cAMP-dependent regulatory type II beta (PRKAR2B) gene variants in antipsychotic-induced weight gain. | Gagliano SA et al. | — | 2014 | → |
| Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. | Hudson G et al. | — | 2014 | → |
| Recovering power in association mapping panels with variable levels of linkage disequilibrium. | Rincent R et al. | — | 2014 | → |
| Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis. | Saito T et al. | — | 2014 | → |
| Reply: Comment on 'The NQO1 polymorphism C609T (Pro187Ser) and cancer susceptibility: a comprehensive meta-analysis'. | Lajin B et al. | — | 2014 | → |
| RFC1 80G>A is a genetic determinant of methotrexate efficacy in rheumatoid arthritis: a human genome epidemiologic review and meta-analysis of observational studies. | Kung TN et al. | — | 2014 | → |
| Role of peroxisome proliferator-activated receptor gamma gene polymorphisms in type 2 diabetes mellitus patients of West Bengal, India. | Pattanayak AK et al. | — | 2014 | → |
| Single-nucleotide polymorphisms in PtoCesA7 and their association with growth and wood properties in Populus tomentosa. | Tian J et al. | — | 2014 | → |
| SORL1 genetic variants modulate risk of amnestic mild cognitive impairment in northern Han Chinese. | Gao X et al. | — | 2014 | → |
| Statistical power and significance testing in large-scale genetic studies. | Sham PC et al. | — | 2014 | → |
| The calcium-sensing receptor R990G polymorphism is associated with increased risk of hypertriglyceridemia in obese Chinese. | He YH et al. | — | 2014 | → |
| The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. | Clarke TK et al. | — | 2014 | → |
| The genetics of major depression. | Flint J et al. | — | 2014 | → |
| The impact of coronary artery disease risk loci on ischemic heart failure severity and prognosis: association analysis in the COntrolled ROsuvastatin multiNAtional trial in heart failure (CORONA). | Haver VG et al. | — | 2014 | → |
| The impact of large-scale genomic methods in orthopaedic disorders: insights from genome-wide association studies. | Paria N et al. | — | 2014 | → |
| The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. | Hooli BV et al. | — | 2014 | → |
| TIMP-1 polymorphisms in a Chinese Han population with intracerebral hemorrhage. | Wang HX et al. | — | 2014 | → |
| TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease. | Liu YL et al. | — | 2014 | → |
| Type II transmembrane serine protease gene variants associate with breast cancer. | Luostari K et al. | — | 2014 | → |
| Validation of type 2 diabetes risk variants identified by genome-wide association studies in Han Chinese population: a replication study and meta-analysis. | Chang YC et al. | — | 2014 | → |
| Variation at HLA-DRB1 is associated with resistance to enteric fever. | Dunstan SJ et al. | — | 2014 | → |
| Whole-genome analyses of whole-brain data: working within an expanded search space. | Medland SE et al. | — | 2014 | → |
| Absence of an association between lumican promoter variants and high myopia in the Korean population. | Park SH et al. | — | 2013 | → |
| A closer look at FBXO41 as a Parkinson's disease risk factor. | King CR et al. | — | 2013 | → |
| A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. | Ludwig KU et al. | — | 2013 | → |
| A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. | Tran C et al. | — | 2013 | → |
| A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. | Bartha I et al. | — | 2013 | → |
| A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. | Julià A et al. | — | 2013 | → |
| Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease. | Requena T et al. | — | 2013 | → |
| A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. | Kapoor M et al. | — | 2013 | → |
| A novel method for analyzing genetic association with longitudinal phenotypes. | Londono D et al. | — | 2013 | → |
| A population-specific uncommon variant in GRIN3A associated with schizophrenia. | Takata A et al. | — | 2013 | → |
| A prospective validation pharmacogenomic study in the adjuvant setting of colorectal cancer patients treated with the 5-fluorouracil/leucovorin/oxaliplatin (FOLFOX4) regimen. | Cecchin E et al. | — | 2013 | → |
| Association analysis of the HLA-C gene in Japanese alopecia areata. | Haida Y et al. | — | 2013 | → |
| Association between P478S polymorphism of the filaggrin gene & atopic dermatitis. | Kim SY et al. | — | 2013 | → |
| Association between polymorphisms in the renin-angiotensin-aldosterone system genes and essential hypertension in the Han Chinese population. | Ji L et al. | — | 2013 | → |
| Association of 11β-hydroxysteroid dehydrogenase type 1 gene polymorphisms with serum alanine aminotransferase activity. | Moon SS et al. | — | 2013 | → |
| Association of a tagging single nucleotide polymorphism in the androgen receptor gene region with susceptibility to severe hypospadias in a Caucasian population. | Adamovic T et al. | — | 2013 | → |
| Association of estrogen receptor alpha gene polymorphism with age at onset, general psychopathology symptoms, and therapeutic effect of schizophrenia. | Wang S et al. | — | 2013 | → |
| Association of genetic variants with primary angle closure glaucoma in two different populations. | Awadalla MS et al. | — | 2013 | → |
| Association of GWAS-linked loci with late-onset Alzheimer's disease in a northern Han Chinese population. | Tan L et al. | — | 2013 | → |
| Association of MTHFR C677T polymorphism with schizophrenia and its effect on episodic memory and gray matter density in patients. | Zhang Y et al. | — | 2013 | → |
| Association of rheumatoid arthritis risk alleles with response to anti-TNF biologics: results from the CORRONA registry and meta-analysis. | Pappas DA et al. | — | 2013 | → |
| Association of serotonin transporter gene (SLC6A4) polymorphisms with schizophrenia susceptibility and symptoms in a Chinese-Han population. | Li W et al. | — | 2013 | → |
| Association of STAT4 polymorphisms with susceptibility to type-1 autoimmune hepatitis in the Japanese population. | Migita K et al. | — | 2013 | → |
| Association of the variations in the HSD3β gene with primary aldosteronism. | Wu VC et al. | — | 2013 | → |
| Association of vaspin gene polymorphisms with coronary artery disease in Chinese population and function study. | Li HL et al. | — | 2013 | → |
| Associations between the genotypes and phenotype of CYP3A and the lipid response to simvastatin in Chinese patients with hypercholesterolemia. | Hu M et al. | — | 2013 | → |
| Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. | Gupta V et al. | — | 2013 | → |
| Association study of 71 European Crohn's disease susceptibility loci in a Japanese population. | Hirano A et al. | — | 2013 | → |
| Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population. | Hu X et al. | — | 2013 | → |
| Association study of OPRM1 polymorphisms with Schizophrenia in Han Chinese population. | Ding S et al. | — | 2013 | → |
| BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies. | Xu C et al. | — | 2013 | → |
| Calpain-10 gene polymorphisms in type 2 diabetes and its micro- and macrovascular complications. | Buraczynska M et al. | — | 2013 | → |
| Calpastatin gene (CAST) is not associated with late onset sporadic Parkinson's disease in the Han Chinese population. | Zhang L et al. | — | 2013 | → |
| Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex. | Qi L et al. | — | 2013 | → |
| CD2AP is associated with end-stage renal disease in patients with type 1 diabetes. | Hyvönen ME et al. | — | 2013 | → |
| CD53, a suppressor of inflammatory cytokine production, is associated with population asthma risk via the functional promoter polymorphism -1560 C>T. | Lee H et al. | — | 2013 | → |
| Ceruloplasmin and heart failure in the Atherosclerosis Risk in Communities study. | Dadu RT et al. | — | 2013 | → |
| Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes. | Sandholm N et al. | — | 2013 | → |
| Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese. | Yan Y et al. | — | 2013 | → |
| Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome. | Li T et al. | — | 2013 | → |
| Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage. | Anderson CD et al. | — | 2013 | → |
| Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes. | Van Cauwenberghe C et al. | — | 2013 | → |
| Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population. | Wang YL et al. | — | 2013 | → |
| Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome. | Louwers YV et al. | — | 2013 | → |
| Dietary aflatoxin B1 intake, genetic polymorphisms of CYP1A2, CYP2E1, EPHX1, GSTM1, and GSTT1, and gastric cancer risk in Korean. | Eom SY et al. | — | 2013 | → |
| DNA pooling base genome-wide association study identifies variants at NRXN3 associated with delayed encephalopathy after acute carbon monoxide poisoning. | Li W et al. | — | 2013 | → |
| Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. | McDavid A et al. | — | 2013 | → |
| Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. | Kasperaviciute D et al. | — | 2013 | → |
| Evaluating reported candidate gene associations with polycystic ovary syndrome. | Pau C et al. | — | 2013 | → |
| Evaluation of single nucleotide polymorphisms in the miR-183-96-182 cluster in adulthood attention-deficit and hyperactivity disorder (ADHD) and substance use disorders (SUDs). | Sánchez-Mora C et al. | — | 2013 | → |
| Evaluation of the relationship between the ZNF804A single nucleotide polymorphism rs1344706 A/C variant and schizophrenia subtype in Han Chinese patients. | Yang Y et al. | — | 2013 | → |
| First genome-wide association study on anxiety-related behaviours in childhood. | Trzaskowski M et al. | — | 2013 | → |
| Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. | Wooten EC et al. | — | 2013 | → |
| Four common polymorphisms in microRNAs and the risk of adult glioma in a Chinese case-control study. | Hu E et al. | — | 2013 | → |
| Gender-specific association of the interleukin 18 gene with symptomatic gallstone disease. | Shih SC et al. | — | 2013 | → |
| Genetic analysis of recently identified osteoporosis susceptibility genes in southern Chinese. | Xiao SM et al. | — | 2013 | → |
| Genetic analysis of the IL8 gene polymorphism (rs4073) in generalized aggressive periodontitis. | Andia DC et al. | — | 2013 | → |
| Genetic association of adrenergic receptor alpha 2A with obesity and type 2 diabetes. | Långberg EC et al. | — | 2013 | → |
| Genetic associations of psoriasis in a Pakistani population. | Shaiq PA et al. | — | 2013 | → |
| Genetic loci associated with Alzheimer's disease and cerebrospinal fluid biomarkers in a Finnish case-control cohort. | Elias-Sonnenschein LS et al. | — | 2013 | → |
| Genetics of callous-unemotional behavior in children. | Viding E et al. | — | 2013 | → |
| Genetics of emergent suicidality during antidepressive treatment--data from a naturalistic study on a large sample of inpatients with a major depressive episode. | Musil R et al. | — | 2013 | → |
| Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study. | Kondo K et al. | — | 2013 | → |
| Genetic variation at the IGF1 locus shows association with post-stroke outcome and to circulating IGF1. | Aberg ND et al. | — | 2013 | → |
| Genetic variation-optimized treatment benefit of angiotensin-converting enzyme inhibitors in patients with stable coronary artery disease: a 12-year follow-up study. | Lee JK et al. | — | 2013 | → |
| Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder. | Chen DT et al. | — | 2013 | → |
| Genome-wide association study of co-occurring anxiety in major depression. | Schosser A et al. | — | 2013 | → |
| GSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individuals. | Dobson-Stone C et al. | — | 2013 | → |
| Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura. | Roecklein KA et al. | — | 2013 | → |
| Identification of genetic associations of SP110/MYBBP1A/RELA with pulmonary tuberculosis in the Chinese Han population. | Cai L et al. | — | 2013 | → |
| Identification of seven loci affecting mean telomere length and their association with disease. | Codd V et al. | — | 2013 | → |
| IL12B and IL23R gene SNPs in Japanese psoriasis. | Oka A et al. | — | 2013 | → |
| IL-23A, IL-23R, IL-17A and IL-17R polymorphisms in different psoriatic arthritis clinical manifestations in the northern Italian population. | Catanoso MG et al. | — | 2013 | → |
| Impact of inherited genetic variants associated with lipid profile, hypertension, and coronary artery disease on the risk of intracranial and abdominal aortic aneurysms. | van 't Hof FN et al. | — | 2013 | → |
| Insights from genome-wide association studies of drug response. | Zhou K et al. | — | 2013 | → |
| ITGA1 polymorphisms and haplotypes are associated with gastric cancer risk in a Korean population. | Yim DH et al. | — | 2013 | → |
| Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke. | Liao YC et al. | — | 2013 | → |
| Lack of association between STK39 and hypertension in the Chinese population. | Xu J et al. | — | 2013 | → |
| MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. | International Multiple Sclerosis Genetics Consortium et al. | — | 2013 | → |
| Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1. | Stewart SE et al. | — | 2013 | → |
| Mining the human phenome using allelic scores that index biological intermediates. | Evans DM et al. | — | 2013 | → |
| Myosin Vb gene is associated with schizophrenia in Chinese Han population. | Chen Y et al. | — | 2013 | → |
| No influence of brain-derived neurotrophic factor (BDNF) polymorphisms on treatment response in a naturalistic sample of patients with major depression. | Musil R et al. | — | 2013 | → |
| Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy. | Lee SH et al. | — | 2013 | → |
| NQO1 609C>T polymorphism interaction with tobacco smoking and alcohol drinking increases colorectal cancer risk in a Chinese population. | Peng XE et al. | — | 2013 | → |
| Polymorphisms of TP53 are markers of bladder cancer vulnerability and prognosis. | Lin HY et al. | — | 2013 | → |
| P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure. | Koizumi A et al. | — | 2013 | → |
| Proinflammatory cytokine IL-1 β polymorphisms in sudden sensorineural hearing loss. | Um JY et al. | — | 2013 | → |
| Protective effect of an ERAP1 haplotype in ankylosing spondylitis: investigating non-MHC genes in HLA-B27-positive individuals. | Bettencourt BF et al. | — | 2013 | → |
| Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. | Campbell NG et al. | — | 2013 | → |
| Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. | Diogo D et al. | — | 2013 | → |
| Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population. | Lin CH et al. | — | 2013 | → |
| Relationship between polymorphisms in vitamin D metabolism-related genes and the risk of rickets in Han Chinese children. | Zhang Y et al. | — | 2013 | → |
| Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. | Kloiber S et al. | — | 2013 | → |
| RIT2 variant is not associated with Parkinson's disease in a Taiwanese population. | Lin CH et al. | — | 2013 | → |
| Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis. | Lautner-Csorba O et al. | — | 2013 | → |
| Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease. | Pihlstrøm L et al. | — | 2013 | → |
| The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome. | Sailani MR et al. | — | 2013 | → |
| The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. | Verweij KJ et al. | — | 2013 | → |
| The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation? | Hilbers FS et al. | — | 2013 | → |
| The molecular genetic architecture of self-employment. | van der Loos MJ et al. | — | 2013 | → |
| The Val66Met polymorphism of the BDNF gene in anorexia nervosa: new data and a meta-analysis. | Brandys MK et al. | — | 2013 | → |
| Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome. | Plummer JT et al. | — | 2013 | → |
| Trans-ethnical shift of the risk genotype in the CETP I405V with longevity: a Chinese case-control study and meta-analysis. | Sun L et al. | — | 2013 | → |
| Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. | Ng MC et al. | — | 2013 | → |
| TYK2 rs34536443 polymorphism is associated with a decreased susceptibility to endometriosis-related infertility. | Peluso C et al. | — | 2013 | → |
| Using phenotypic heterogeneity to increase the power of genome-wide association studies: application to age at onset of ischaemic stroke subphenotypes. | Traylor M et al. | — | 2013 | → |
| Variants in endothelial nitric oxide synthase (eNOS) gene in idiopathic infertile Brazilian men. | Bianco B et al. | — | 2013 | → |
| μ-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption. | Rouvinen-Lagerström N et al. | — | 2013 | → |
| 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium. | Warren H et al. | — | 2012 | → |
| A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucoma. | Awadalla MS et al. | — | 2012 | → |
| A genetic association study of DNA methylation levels in the DRD4 gene region finds associations with nearby SNPs. | Docherty SJ et al. | — | 2012 | → |
| A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians. | Png E et al. | — | 2012 | → |
| A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. | Kenny EE et al. | — | 2012 | → |
| A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity. | Lopez LM et al. | — | 2012 | → |
| A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: genetic risk is modulated by obesity. | Been LF et al. | — | 2012 | → |
| Analysis of vitamin D receptor gene (VDR) polymorphisms in Turner syndrome patients. | Bianco B et al. | — | 2012 | → |
| An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disorders. | Matsunaga S et al. | — | 2012 | → |
| ANKH and susceptibility to and severity of ankylosing spondylitis. | Pimentel-Santos FM et al. | — | 2012 | → |
| A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample. | Sintas C et al. | — | 2012 | → |
| A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. | Braun TR et al. | — | 2012 | → |
| A replication study of the association between rheumatoid arthritis and deletion of the late cornified envelope genes LCE3B and LCE3C. | Bergboer JG et al. | — | 2012 | → |
| Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs. | Gupta V et al. | — | 2012 | → |
| Association analysis of STX1A gene variants in common forms of migraine. | Tropeano M et al. | — | 2012 | → |
| Association between ghrelin gene (GHRL) polymorphisms and clinical response to atypical antipsychotic drugs in Han Chinese schizophrenia patients. | Yang Y et al. | — | 2012 | → |
| Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the alcohol challenge twin study. | Lind PA et al. | — | 2012 | → |
| Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population. | Liang S et al. | — | 2012 | → |
| Association genetics in Corymbia citriodora subsp. variegata identifies single nucleotide polymorphisms affecting wood growth and cellulosic pulp yield. | Dillon SK et al. | — | 2012 | → |
| Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients. | Fachal L et al. | — | 2012 | → |
| Association of CDX1 binding site of periostin gene with bone mineral density and vertebral fracture risk. | Xiao SM et al. | — | 2012 | → |
| Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients. | Parmar AS et al. | — | 2012 | → |
| Association of interleukin-18 gene polymorphism with body mass index in women. | Kim HL et al. | — | 2012 | → |
| Association of single nucleotide polymorphisms in TCF2 with type 2 diabetes susceptibility in a Han Chinese population. | Zhang X et al. | — | 2012 | → |
| Association of SNPs linked to increased expression of SLC1A1 with schizophrenia. | Horiuchi Y et al. | — | 2012 | → |
| Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process. | Kuot A et al. | — | 2012 | → |
| Association study of C1qA polymorphisms with systemic lupus erythematosus in a Han population. | Cao CW et al. | — | 2012 | → |
| Association study of early-immediate genes in childhood-onset mood disorders and suicide attempt. | Strauss J et al. | — | 2012 | → |
| Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population. | Parmar AS et al. | — | 2012 | → |
| Association study of GRIK1 gene polymorphisms in schizophrenia: case-control and family-based studies. | Hirata Y et al. | — | 2012 | → |
| Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population. | Li W et al. | — | 2012 | → |
| Association study of susceptibility genes for late-onset Alzheimer's disease in the Japanese population. | Ohara T et al. | — | 2012 | → |
| A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism. | Karjalainen MK et al. | — | 2012 | → |
| AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. | Morley AP et al. | — | 2012 | → |
| Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males. | Han Y et al. | — | 2012 | → |
| Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk. | Bettens K et al. | — | 2012 | → |
| Candidate system analysis in ADHD: evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1. | Ribasés M et al. | — | 2012 | → |
| Cardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure. | Wu CK et al. | — | 2012 | → |
| Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome. | Hill LD et al. | — | 2012 | → |
| Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1. | Pahl L et al. | — | 2012 | → |
| Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism. | Walford GA et al. | — | 2012 | → |
| C-reactive protein as a predictor of hypertension in the Hong Kong Cardiovascular Risk Factor Prevalence Study (CRISPS) cohort. | Cheung BM et al. | — | 2012 | → |
| Design considerations for genetic linkage and association studies. | Nsengimana J et al. | — | 2012 | → |
| Effects of statin treatments and polymorphisms in UGT1A1 and SLCO1B1 on serum bilirubin levels in Chinese patients with hypercholesterolaemia. | Hu M et al. | — | 2012 | → |
| Evaluation of a partial genome screening of two asthma susceptibility regions using bayesian network based bayesian multilevel analysis of relevance. | Ungvári I et al. | — | 2012 | → |
| Evaluation of seven common lipid associated loci in a large Indian sib pair study. | Rafiq S et al. | — | 2012 | → |
| Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. | Visscher PM et al. | — | 2012 | → |
| Evolutionary conserved longevity genes and human cognitive abilities in elderly cohorts. | Lopez LM et al. | — | 2012 | → |
| Exome sequencing and the genetic basis of complex traits. | Kiezun A et al. | — | 2012 | → |
| Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. | Attar H et al. | — | 2012 | → |
| Fcγ receptor polymorphisms do not predict response to intravenous immunoglobulin in myasthenia gravis. | Barnett C et al. | — | 2012 | → |
| Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans. | McLaren PJ et al. | — | 2012 | → |
| Further evidence of association of the ABCA4 gene with cleft lip/palate. | Fontoura C et al. | — | 2012 | → |
| Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. | van Eerde AM et al. | — | 2012 | → |
| Genetic adaptation of the hypoxia-inducible factor pathway to oxygen pressure among eurasian human populations. | Ji LD et al. | — | 2012 | → |
| Genetic and functional analyses of early growth response (EGR) family genes in schizophrenia. | Cheng MC et al. | — | 2012 | → |
| Genetic and functional analyses of the gene encoding synaptophysin in schizophrenia. | Shen YC et al. | — | 2012 | → |
| Genetic and functional analysis of the gene encoding GAP-43 in schizophrenia. | Shen YC et al. | — | 2012 | → |
| Genetic and functional analysis of the gene encoding neurogranin in schizophrenia. | Shen YC et al. | — | 2012 | → |
| Genetic association analyses of PDYN polymorphisms with heroin and cocaine addiction. | Clarke TK et al. | — | 2012 | → |
| Genetic mapping of quantitative trait loci for disease-related phenotypes. | Devoto M et al. | — | 2012 | → |
| Genetic polymorphisms in the DNA repair gene XRCC1 and susceptibility to glioma in a Han population in northeastern China: a case-control study. | Wang D et al. | — | 2012 | → |
| Genetic variability of interleukin4 gene in Taiwanese children with biliary atresia. | Lee HC et al. | — | 2012 | → |
| Genetic variants in fibrinolytic system-related genes in infertile women with and without endometriosis. | Brandes A et al. | — | 2012 | → |
| Genetic variants in PNPLA3 and risk of non-alcoholic fatty liver disease in a Han Chinese population. | Peng XE et al. | — | 2012 | → |
| Genetic variants near PDGFRA are associated with corneal curvature in Australians. | Mishra A et al. | — | 2012 | → |
| Genetic variation at CR1 increases risk of cerebral amyloid angiopathy. | Biffi A et al. | — | 2012 | → |
| Genetic variation in cholesterol ester transfer protein, serum CETP activity, and coronary artery disease risk in Asian Indian diabetic cohort. | Schierer A et al. | — | 2012 | → |
| Genetic variation in the carbonyl reductase 3 gene confers risk of type 2 diabetes and insulin resistance: a potential regulator of adipogenesis. | Chang YC et al. | — | 2012 | → |
| Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis. | Liedén A et al. | — | 2012 | → |
| Genetic variation in the TNF gene is associated with susceptibility to severe sepsis, but not with mortality. | Song Z et al. | — | 2012 | → |
| Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma. | Vithana EN et al. | — | 2012 | → |
| Genome-wide association of BMI in African Americans. | Ng MC et al. | — | 2012 | → |
| Genome-wide associations for investigating time-dependent genetic effects for milk production traits in dairy cattle. | Strucken EM et al. | — | 2012 | → |
| Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. | Candille SI et al. | — | 2012 | → |
| Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. | Adrianto I et al. | — | 2012 | → |
| Genome-wide association study of vascular dementia. | Schrijvers EM et al. | — | 2012 | → |
| HLA class II is a factor in cardiovascular morbidity and mortality rates in patients with type 1 diabetes. | Söderlund J et al. | — | 2012 | → |
| Hypercontrols in genotype-phenotype analysis reveal ancestral haplotypes associated with essential hypertension. | Balam-Ortiz E et al. | — | 2012 | → |
| Identification of common variants associated with human hippocampal and intracranial volumes. | Stein JL et al. | — | 2012 | → |
| Implication of European-derived adiposity loci in African Americans. | Hester JM et al. | — | 2012 | → |
| Influence of methylenetetrahydrofolate reductase C677T gene polymorphisms in Algerian infertile men with azoospermia or severe oligozoospermia. | Chellat D et al. | — | 2012 | → |
| INPPL1 is associated with the metabolic syndrome in men with Type 1 diabetes, but not with diabetic nephropathy. | Hyvönen ME et al. | — | 2012 | → |
| Interaction between smoking and functional polymorphism in the TGFB1 gene is associated with ischaemic heart disease and myocardial infarction in patients with rheumatoid arthritis: a cross-sectional study. | Chen Y et al. | — | 2012 | → |
| Introduction to genetic association studies. | Lewis CM et al. | — | 2012 | → |
| Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics. | Schuhmacher A et al. | — | 2012 | → |
| Lack of association between ABCC2 gene variants and treatment response in epilepsy. | Hilger E et al. | — | 2012 | → |
| Longevity candidate genes and their association with personality traits in the elderly. | Luciano M et al. | — | 2012 | → |
| Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk. | Marquez M et al. | — | 2012 | → |
| MDM2 SNP309T>G polymorphism increases susceptibility to hepatitis B virus-related hepatocellular carcinoma in a northeast Han Chinese population. | Wang X et al. | — | 2012 | → |
| MMP3 and TIMP1 variants contribute to chronic periodontitis and may be implicated in disease progression. | Letra A et al. | — | 2012 | → |
| Molecular genetic studies of gene identification for sarcopenia. | Tan LJ et al. | — | 2012 | → |
| Most reported genetic associations with general intelligence are probably false positives. | Chabris CF et al. | — | 2012 | → |
| NLRP1 gene polymorphism influences gene transcription and is a risk factor for rheumatoid arthritis in han chinese. | Sui J et al. | — | 2012 | → |
| No association of ALOX5AP polymorphisms with risk of MRI-defined brain infarcts. | Barral S et al. | — | 2012 | → |
| No consistent evidence for association between mtDNA variants and Alzheimer disease. | Hudson G et al. | — | 2012 | → |
| Non-replication of genome-wide-based associations of efficient food conversion in dairy cows. | Littlejohn M et al. | — | 2012 | → |
| Non-syndromic cleft palate: analysis of TBX22 exon 5 gene mutation. | Jiang RS et al. | — | 2012 | → |
| Paediatric-onset psoriasis is associated with ERAP1 and IL23R loci, LCE3C_LCE3B deletion and HLA-C*06. | Bergboer JG et al. | — | 2012 | → |
| Polymorphisms in SP110 are not associated with pulmonary tuberculosis in Indonesians. | Png E et al. | — | 2012 | → |
| Predictive role of multilocus genetic polymorphisms in cardiovascular disease and inflammation-related genes on chronic kidney disease in Type 2 diabetes--an 8-year prospective cohort analysis of 1163 patients. | Wang Y et al. | — | 2012 | → |
| Rapid multiplex high resolution melting method to analyze inflammatory related SNPs in preterm birth. | Pereyra S et al. | — | 2012 | → |
| Relationship between DDAH gene variants and serum ADMA level in individuals with type 1 diabetes. | Fogarty RD et al. | — | 2012 | → |
| Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts. | Goodarzi MO et al. | — | 2012 | → |
| Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. | Hammer C et al. | — | 2012 | → |
| Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study. | Chen CT et al. | — | 2012 | → |
| Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study. | Vávrová J et al. | — | 2012 | → |
| Risk variants for psoriasis vulgaris in a large case-control collection and association with clinical subphenotypes. | Julià A et al. | — | 2012 | → |
| Sample size and statistical power calculation in genetic association studies. | Hong EP et al. | — | 2012 | → |
| Single-nucleotide polymorphism rs2290692 in the 3'UTR of ITPKC associated with susceptibility to Kawasaki disease in a Han Chinese population. | Peng Q 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 | → |
| SNP in the genome-wide association study hotspot on chromosome 9p21 confers susceptibility to diabetic nephropathy in type 1 diabetes. | Fagerholm E et al. | — | 2012 | → |
| SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population. | Carreño O et al. | — | 2012 | → |
| TGFβ1 SNPs and radio-induced toxicity in prostate cancer patients. | Fachal L et al. | — | 2012 | → |
| The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies. | Dennis J et al. | — | 2012 | → |
| The HLA-B gene and Hashimoto disease in Han Chinese children: a case-control and family-based study. | Huang CY et al. | — | 2012 | → |
| The HLA-DRB1 gene and Graves disease in Taiwanese children: a case-control and family-based study. | Wu YL et al. | — | 2012 | → |
| The influence of the HLA-DRB1 and HLA-DQB1 allele heterogeneity on disease risk and severity in Iranian patients with multiple sclerosis. | Kollaee A et al. | — | 2012 | → |
| The melatonin receptor 1A (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis. | Esposito T et al. | — | 2012 | → |
| The nuclear factor-kB functional promoter polymorphism is associated with endometriosis and infertility. | Bianco B et al. | — | 2012 | → |
| The Promises and Pitfalls of Genoeconomics* | Benjamin DJ et al. | — | 2012 | → |
| The search for genetic modifiers of disease severity in the β-hemoglobinopathies. | Lettre G | — | 2012 | → |
| TOMM40 in Cerebral Amyloid Angiopathy Related Intracerebral Hemorrhage: Comparative Genetic Analysis with Alzheimer's Disease. | Valant V et al. | — | 2012 | → |
| Two genetic variants in FABP1 and susceptibility to non-alcohol fatty liver disease in a Chinese population. | Peng XE et al. | — | 2012 | → |
| Two variants in the fibulin2 gene are associated with lower systolic blood pressure and decreased risk of hypertension. | Vallvé JC et al. | — | 2012 | → |
| Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. | Tielbeek JJ et al. | — | 2012 | → |
| Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population. | Andiappan AK et al. | — | 2012 | → |
| Variants in follicle-stimulating hormone receptor gene in infertile Brazilian men and the correlation to FSH serum levels and sperm count. | Ghirelli-Filho M et al. | — | 2012 | → |
| Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. | Cope N et al. | — | 2012 | → |
| Variants of the human NR1I2 (PXR) locus in chronic periodontitis. | Folwaczny M et al. | — | 2012 | → |
| WNT2 locus is involved in genetic susceptibility of Peyronie's disease. | Dolmans GH et al. | — | 2012 | → |
| Absence of association between specific common variants of the obesity-related FTO gene and psychological and behavioral eating disorder phenotypes. | Jonassaint CR et al. | — | 2011 | → |
| A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population. | Yue W et al. | — | 2011 | → |
| A comprehensive analysis of the COL29A1 gene does not support a role in eczema. | Naumann A et al. | — | 2011 | → |
| A COMT gene haplotype associated with methamphetamine abuse. | Jugurnauth SK et al. | — | 2011 | → |
| ADIPOQ Gene Variants Associated with Susceptibility to Obesity and Low Serum Adiponectin Levels in Healthy Koreans. | Park JW et al. | — | 2011 | → |
| A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. | Bradfield JP et al. | — | 2011 | → |
| Analysis of genomewide association signals for nonsyndromic cleft lip/palate in a Kenya African Cohort. | Weatherley-White RC et al. | — | 2011 | → |
| Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. | Lillvis JH et al. | — | 2011 | → |
| An association analysis of Per2 with panic disorder in the Japanese population. | Otowa T et al. | — | 2011 | → |
| A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture. | Wang JZ et al. | — | 2011 | → |
| A polymorphism in the angiotensin II type 1 receptor gene has different effects on the risk of diabetic nephropathy in men and women. | Möllsten A et al. | — | 2011 | → |
| A polymorphism in the retinol binding protein 4 gene is not associated with gestational diabetes mellitus in several different ethnic groups. | Hiraoka M et al. | — | 2011 | → |
| A polymorphism of the ORAI1 gene is associated with the risk and recurrence of calcium nephrolithiasis. | Chou YH et al. | — | 2011 | → |
| A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. | Heath AC et al. | — | 2011 | → |
| Association Analysis of Nuclear Receptor Rev-erb Alpha Gene (NR1D1) and Japanese Methamphetamine Dependence. | Kishi T et al. | — | 2011 | → |
| Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population. | Yoshimura T et al. | — | 2011 | → |
| Association analysis of the LTA4H gene polymorphisms and pulmonary tuberculosis in 9115 subjects. | Curtis J et al. | — | 2011 | → |
| Association between major mood disorders and the hypocretin receptor 1 gene. | Rainero I et al. | — | 2011 | → |
| Association mapping. | Painter JN et al. | — | 2011 | → |
| Association of an IL-4 gene haplotype with Graves disease in children: experimental study and meta-analysis. | Lee YJ et al. | — | 2011 | → |
| Association of ANK3 with bipolar disorder confirmed in East Asia. | Takata A et al. | — | 2011 | → |
| Association of catechol-O-methyl transferase (COMT) gene -287A/G polymorphism with susceptibility to obsessive-compulsive disorder in Chinese Han population. | Liu S et al. | — | 2011 | → |
| Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. | Khalfallah A et al. | — | 2011 | → |
| Association of FCRL3 -169T/C polymorphism with endometriosis and identification of a protective haplotype against the development of the disease in Brazilian population. | Bianco B et al. | — | 2011 | → |
| Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis. | Teles JS et al. | — | 2011 | → |
| Association of genetic variations in the STAT4 and IRF7/KIAA1542 regions with systemic lupus erythematosus in a Northern Han Chinese population. | Li P et al. | — | 2011 | → |
| Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. | Cunninghame Graham DS et al. | — | 2011 | → |
| Association of polymorphisms in the Interleukin-18 gene with susceptibility to biliary atresia. | Lee HC et al. | — | 2011 | → |
| Association screening in the Epidermal Differentiation Complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczema. | Marenholz I et al. | — | 2011 | → |
| Association study of a variable-number tandem repeat polymorphism in the clock gene PERIOD3 and chronotype in Norwegian university students. | Osland TM et al. | — | 2011 | → |
| Association study of candidate gene polymorphisms and obesity in a young Mexican-American population from South Texas. | Duran-Gonzalez J et al. | — | 2011 | → |
| Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample. | Jitoku D et al. | — | 2011 | → |
| Association study of PDE4B with panic disorder in the Japanese population. | Otowa T et al. | — | 2011 | → |
| Association study of RELN polymorphisms with schizophrenia in Han Chinese population. | Li W et al. | — | 2011 | → |
| BRCA1 mutations do not increase prostate cancer risk: results from a meta-analysis including new data. | Fachal L et al. | — | 2011 | → |
| Challenges and recommendations for conducting epidemiological studies in the field of epilepsy pharmacogenetics. | Grover S et al. | — | 2011 | → |
| Childhood environmental and genetic predictors of adulthood obesity: the cardiovascular risk in young Finns study. | Juonala M et al. | — | 2011 | → |
| Clinical Implication of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation. | Lin MT et al. | — | 2011 | → |
| Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. | Petrovski S et al. | — | 2011 | → |
| Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype. | McGregor TL et al. | — | 2011 | → |
| Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP. | Birlea SA et al. | — | 2011 | → |
| Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. | Chen PL et al. | — | 2011 | → |
| Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis. | Bowes J et al. | — | 2011 | → |
| Consideration of the BDNF gene in relation to two phenotypes: hoarding and obesity. | Timpano KR et al. | — | 2011 | → |
| Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study. | Ribasés M et al. | — | 2011 | → |
| Dissection of genetic associations with language-related traits in population-based cohorts. | Paracchini S | — | 2011 | → |
| Do common variants play a role in risk for autism? Evidence and theoretical musings. | Devlin B et al. | — | 2011 | → |
| Effects of 16 genetic variants on fasting glucose and type 2 diabetes in South Asians: ADCY5 and GLIS3 variants may predispose to type 2 diabetes. | Rees SD et al. | — | 2011 | → |
| Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). | Hertel JK et al. | — | 2011 | → |
| Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk. | Simmons CR et al. | — | 2011 | → |
| Exonic DNA sequencing of ERBB4 in bipolar disorder. | Goes FS et al. | — | 2011 | → |
| Experimental designs for robust detection of effects in genome-wide case-control studies. | Ball RD | — | 2011 | → |
| Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations. | Sánchez-Mora C et al. | — | 2011 | → |
| Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study. | Hill LD et al. | — | 2011 | → |
| FTO and MC4R gene variants are associated with obesity in polycystic ovary syndrome. | Ewens KG et al. | — | 2011 | → |
| Gene-environment interaction in psychological traits and disorders. | Dick DM | — | 2011 | → |
| Genetic Association Analysis of NOS3 and Methamphetamine-Induced Psychosis Among Japanese. | Okochi T et al. | — | 2011 | → |
| Genetic diversity and population structure in cultivated sunflower and a comparison to its wild progenitor, Helianthus annuus L. | Mandel JR et al. | — | 2011 | → |
| Genetic evidence that vascular dementia is related to Alzheimer's disease: genetic association between tau polymorphism and vascular dementia in the Chinese population. | Ning M 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 | → |
| Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes. | Murea M et al. | — | 2011 | → |
| Genomewide association scan of suicidal thoughts and behaviour in major depression. | Schosser A et al. | — | 2011 | → |
| Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. | Painter JN et al. | — | 2011 | → |
| Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease. | Khor CC et al. | — | 2011 | → |
| Genome-wide association study identifies five new schizophrenia loci. | Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium | — | 2011 | → |
| Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations. | Noguchi E et al. | — | 2011 | → |
| Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population. | Hirota T et al. | — | 2011 | → |
| Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. | Freudenberg J et al. | — | 2011 | → |
| Genome-wide association study of the child behavior checklist dysregulation profile. | Mick E et al. | — | 2011 | → |
| Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. | Duncan EL et al. | — | 2011 | → |
| Glutamate cysteine ligase (GCL) and self reported depression: an association study from the HUNT. | Berk M et al. | — | 2011 | → |
| GWAPower: a statistical power calculation software for genome-wide association studies with quantitative traits. | Feng S et al. | — | 2011 | → |
| Haplotype-based analysis of ulcerative colitis risk loci identifies both IL2 and IL21 as susceptibility genes in Han Chinese. | Shi J et al. | — | 2011 | → |
| Haplotypes in the interleukin 8 gene and their association with chronic periodontitis susceptibility. | Scarel-Caminaga RM 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 ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. | Reilly MP et al. | — | 2011 | → |
| Identification of genes for bone mineral density variation by computational disease gene identification strategy. | Li GH et al. | — | 2011 | → |
| IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis. | Kelley JM 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 | → |
| IL3 variant on chromosomal region 5q31-33 and protection from recurrent malaria attacks. | Meyer CG et al. | — | 2011 | → |
| Imputation of genotypes from low- to high-density genotyping platforms and implications for genomic selection. | Berry DP et al. | — | 2011 | → |
| Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17. | Tintle N et al. | — | 2011 | → |
| Investigation of cytotoxic T-lymphocyte-associated protein 4 gene polymorphisms in symptomatic gallstone disease. | Shih SC et al. | — | 2011 | → |
| Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring. | Ainsworth HF et al. | — | 2011 | → |
| Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder. | Dwyer S et al. | — | 2011 | → |
| Lack of association between prokineticin 2 gene and Japanese methamphetamine dependence. | Kishi T et al. | — | 2011 | → |
| LINGO1 variants in the French-Canadian population. | Bourassa CV et al. | — | 2011 | → |
| Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease. | Lin CH et al. | — | 2011 | → |
| Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. | Haataja R et al. | — | 2011 | → |
| Missing heritability in the tails of quantitative traits? A simulation study on the impact of slightly altered true genetic models. | Pütter C et al. | — | 2011 | → |
| MMP-8 -799 C>T genetic polymorphism is associated with the susceptibility to chronic and aggressive periodontitis in Taiwanese. | Chou YH et al. | — | 2011 | → |
| Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations. | Einarsdottir E et al. | — | 2011 | → |
| Multiple testing and power calculations in genetic association studies. | So HC et al. | — | 2011 | → |
| Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. | Carroll LS et al. | — | 2011 | → |
| No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder. | Curran S et al. | — | 2011 | → |
| No association between bipolar disorder risk polymorphisms in ANK3 and CACNA1C and common migraine. | Wöber-Bingöl C et al. | — | 2011 | → |
| No evidence of IL21 association with multiple sclerosis in a Swedish population. | Lindén M et al. | — | 2011 | → |
| Nominal association between a polymorphism in DGKH and bipolar disorder detected in a meta-analysis of East Asian case-control samples. | Takata A et al. | — | 2011 | → |
| No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population. | He Y et al. | — | 2011 | → |
| No significant association between SIRT1 gene and methamphetamine-induced psychosis in the Japanese population. | Kishi T et al. | — | 2011 | → |
| Polymorphic locus rs10492972 of the KIF1B gene association with multiple sclerosis in Russia: case control study. | Kudryavtseva EA et al. | — | 2011 | → |
| Polymorphisms in folate-related enzyme genes in idiopathic infertile Brazilian men. | Gava MM et al. | — | 2011 | → |
| Polymorphisms of estrogen receptors alpha and beta in idiopathic, infertile Brazilian men: a case-control study. | Bianco B et al. | — | 2011 | → |
| Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma. | Ricci G et al. | — | 2011 | → |
| Possible association between ubiquitin-specific peptidase 46 gene and major depressive disorders in the Japanese population. | Fukuo Y et al. | — | 2011 | → |
| Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. | Guey LT et al. | — | 2011 | → |
| PPARα polymorphisms as risk factors for dyslipidemia in a Brazilian population. | Mazzotti DR et al. | — | 2011 | → |
| Predictive role of polymorphisms in interleukin-5 receptor alpha-subunit, lipoprotein lipase, integrin A2 and nitric oxide synthase genes on ischemic stroke in type 2 diabetes--an 8-year prospective cohort analysis of 1327 Chinese patients. | Luk AO et al. | — | 2011 | → |
| Promoter -817C>T variant of B lymphocyte stimulator gene (BLyS) and susceptibility to endometriosis-related infertility and idiopathic infertility in Brazilian population. | Christofolini DM et al. | — | 2011 | → |
| Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. | Bonilla C et al. | — | 2011 | → |
| Receptor for advanced glycation end-products (RAGE) provides a link between genetic susceptibility and environmental factors in type 1 diabetes. | Forbes JM et al. | — | 2011 | → |
| Relationship of 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase gene polymorphisms with metabolic syndrome and type 2 diabetes. | Moon SS et al. | — | 2011 | → |
| Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese. | Cheung BM et al. | — | 2011 | → |
| Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. | Rees SD et al. | — | 2011 | → |
| Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndrome. | Goodarzi MO et al. | — | 2011 | → |
| Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. | Das M et al. | — | 2011 | → |
| Significant association between common polymorphisms in the aromatase gene CYP19A1 and bone mineral density in postmenopausal women. | Mullin BH et al. | — | 2011 | → |
| SIRT1 gene, schizophrenia and bipolar disorder in the Japanese population: an association study. | Kishi T et al. | — | 2011 | → |
| SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. | Luciano M et al. | — | 2011 | → |
| Statistical issues and approaches in endophenotype research. | Sham PC et al. | — | 2011 | — |
| The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. | Rizzi TS et al. | — | 2011 | → |
| The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia. | Xiao J 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 expression of VEGF-A is down regulated in peripheral blood mononuclear cells of patients with secondary progressive multiple sclerosis. | Iacobaeus E et al. | — | 2011 | → |
| The factor XII -4C>T variant and risk of common thrombotic disorders: A HuGE review and meta-analysis of evidence from observational studies. | Johnson CY et al. | — | 2011 | → |
| The integration of 'omic' disciplines and systems biology in cattle breeding. | Berry DP et al. | — | 2011 | → |
| The neuronal transporter gene SLC6A15 confers risk to major depression. | Kohli MA et al. | — | 2011 | → |
| The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels. | Mehta NN et al. | — | 2011 | → |
| The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. | Min JL et al. | — | 2011 | → |
| TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. | van der Zee J et al. | — | 2011 | → |
| Transforming growth factor-{beta} gene polymorphisms in different phenotypes of sarcoidosis. | Pabst S et al. | — | 2011 | → |
| Type 2 diabetes susceptibility single-nucleotide polymorphisms are not associated with polycystic ovary syndrome. | Ewens KG et al. | — | 2011 | → |
| Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. | Been LF et al. | — | 2011 | → |
| Amyloid-β-related genes SORL1 and ACE are genetically associated with risk for late-onset Alzheimer disease in the Chinese population. | Ning M et al. | — | 2010 | → |
| Analysis of strain-dependent prepulse inhibition points to a role for Shmt1 (SHMT1) in mice and in schizophrenia. | Maekawa M et al. | — | 2010 | → |
| Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. | Shatunov A et al. | — | 2010 | → |
| Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. | Shen H et al. | — | 2010 | → |
| Genetic and functional analysis of the DLG4 gene encoding the post-synaptic density protein 95 in schizophrenia. | Cheng MC et al. | — | 2010 | → |
| Heme oxygenase 1 polymorphisms and plasma concentrations in critically ill patients. | Saukkonen K et al. | — | 2010 | → |
| IL-22RA2 associates with multiple sclerosis and macrophage effector mechanisms in experimental neuroinflammation. | Beyeen AD et al. | — | 2010 | → |
| Most common single-nucleotide polymorphisms associated with rheumatoid arthritis in persons of European ancestry confer risk of rheumatoid arthritis in African Americans. | Hughes LB et al. | — | 2010 | → |
| No association between FADS polymorphisms and atopic diseases in children from the GINI and LISA birth cohorts. | Singmann P et al. | — | 2010 | → |
| PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. | Beecham GW et al. | — | 2010 | → |
| Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. | Burdon KP et al. | — | 2010 | → |