A haplotype map of the human genome.
paper
Cited
Public
Unavailable
- Authors
- International HapMap Consortium
- Year
- 2005
- Journal
- Nature
- PMID
- 16255080
- DOI
- 10.1038/nature04226
- PMCID
- PMC1880871
Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. Here we report a public database of common variation in the human genome: more than one million single nucleotide polymorphisms (SNPs) for which accurate and complete genotypes have been obtained in 269 DNA samples from four populations, including ten 500-kilobase regions in which essentially all information about common DNA variation has been extracted. These data document the generality of recombination hotspots, a block-like structure of linkage disequilibrium and low haplotype diversity, leading to substantial correlations of SNPs with many of their neighbours. We show how the HapMap resource can guide the design and analysis of genetic association studies, shed light on structural variation and recombination, and identify loci that may have been subject to natural selection during human evolution.
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| Imputation disparities driven by recent selection and their impact on disease risk estimation in East and Southeast Asian populations. | Li D et al. | β | 2025 | β |
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| Proxy panels enable privacy-aware outsourcing of genotype imputation. | Zhi D et al. | β | 2025 | β |
| Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine. | Kansal R | β | 2025 | β |
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| The Impact of Ancestry on Genome-Wide Association Studies. | Jones SC et al. | β | 2025 | β |
| Twenty years of genome-wide association studies. | Southam L et al. | β | 2025 | β |
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| Chromosome-Level Haplotype Assembly for <i>Equus asinu</i>. | Miao X et al. | β | 2022 | β |
| Combinational Drug Repurposing from Genetic Networks Applied to Alzheimer's Disease. | Nabirotchkin S et al. | β | 2022 | β |
| Computational and experimental methods for classifying variants of unknown clinical significance. | Spielmann M et al. | β | 2022 | β |
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| Genomic medicine on the frontier of precision medicine. | Hasanzad M et al. | β | 2022 | β |
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| Inherent Nonlinear Distribution of High-Dimensional Genotypic Data Identified as a Possible Source of Confounding Factors in Population Structure Analysis. | Wang M | β | 2022 | β |
| Insights into AIM-InDel diversities in Yunnan Miao and Hani ethnic groups of China for forensic and population genetic purposes. | Cui W et al. | β | 2022 | β |
| Insights into the Genetic Architecture and Genomic Prediction of Powdery Mildew Resistance in Flax (<i>Linum usitatissimum</i> L.). | You FM et al. | β | 2022 | β |
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| Novel InDel variations of the Cry2 gene are associated with litter size in Australian White sheep. | Huang Y et al. | β | 2022 | β |
| Polycystic Ovary Syndrome: An Evolutionary Adaptation to Lifestyle and the Environment. | Parker J et al. | β | 2022 | β |
| Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association. | O'Sullivan JW et al. | β | 2022 | β |
| PopHumanVar: an interactive application for the functional characterization and prioritization of adaptive genomic variants in humans. | Colomer-Vilaplana A et al. | β | 2022 | β |
| Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. | Elhaik E | β | 2022 | β |
| Rapid Intraspecies Evolution of Fitness Effects of Yeast Genes. | Wang Y et al. | β | 2022 | β |
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| Ξeta-2-glycoprotein I exerts antithrombotic function through its domain V in mice. | Passam FH et al. | β | 2022 | β |
| A detection method for the capture of genomic signatures: From disease diagnosis to genome editing. | Benamozig O et al. | β | 2021 | β |
| Admixture with indigenous people helps local adaptation: admixture-enabled selection in Polynesians. | Isshiki M et al. | β | 2021 | β |
| Advances in Computational Methodologies for Classification and Sub-Cellular Locality Prediction of Non-Coding RNAs. | Asim MN et al. | β | 2021 | β |
| A HML6 endogenous retrovirus on chromosome 3 is upregulated in amyotrophic lateral sclerosis motor cortex. | Jones AR et al. | β | 2021 | β |
| Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. | Pinsach-Abuin ML et al. | β | 2021 | β |
| Analysis of genetic selection at insulin receptor substrate-2 gene loci. | Yoshiuchi I | β | 2021 | β |
| Association Between Hemostatic Profile and Migraine: A Mendelian Randomization Analysis. | Guo Y et al. | β | 2021 | β |
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| Determination of complete chromosomal haplotypes by bulk DNA sequencing. | Tourdot RW et al. | β | 2021 | β |
| Divergence in alternative polyadenylation contributes to gene regulatory differences between humans and chimpanzees. | Mittleman BE et al. | β | 2021 | β |
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| Effects of single nucleotide polymorphism ascertainment on population structure inferences. | Dokan K et al. | β | 2021 | β |
| Emerging Functions for snoRNAs and snoRNA-Derived Fragments. | Wajahat M et al. | β | 2021 | β |
| Evolutionary dynamics of the human pseudoautosomal regions. | Monteiro B et al. | β | 2021 | β |
| Fine-Scale Genetic Structure and Demographic History in the Miyako Islands of the Ryukyu Archipelago. | Matsunami M et al. | β | 2021 | β |
| Focused Strategies for Defining the Genetic Architecture of Congenital Heart Defects. | Martin LJ et al. | β | 2021 | β |
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| Genetic Risk Stratification: A Paradigm Shift in Prevention of Coronary Artery Disease. | Roberts R et al. | β | 2021 | β |
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| Genetic variations in medical research in the past, at present and in the future. | Kamatani Y et al. | β | 2021 | β |
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| Identification of natural selection in genomic data with deep convolutional neural network. | Nguembang Fadja A et al. | β | 2021 | β |
| Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass. | Feng GJ et al. | β | 2021 | β |
| Integrated Analysis of Whole Genome and Epigenome Data Using Machine Learning Technology: Toward the Establishment of Precision Oncology. | Asada K et al. | β | 2021 | β |
| Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs. | Sakurai-Yageta M et al. | β | 2021 | β |
| Joint Genome-Wide Association Analyses Identified 49 Novel Loci For Age at Natural Menopause. | Zhang L et al. | β | 2021 | β |
| Limitations of lymphoblastoid cell lines for establishing genetic reference datasets in the immunoglobulin loci. | Rodriguez OL et al. | β | 2021 | β |
| Loquat (Eriobotrya japonica (Thunb.) Lindl) population genomics suggests a two-staged domestication and identifies genes showing convergence/parallel selective sweeps with apple or peach. | Wang Y et al. | β | 2021 | β |
| Match statistics for sequence-based alleles in profiles from forensic PCR-mps kits. | Young B et al. | β | 2021 | β |
| Meiosis and beyond - understanding the mechanistic and evolutionary processes shaping the germline genome. | Bergero R et al. | β | 2021 | β |
| Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach. | Gupta JK et al. | β | 2021 | β |
| Molecular characterisation of osteoblasts from bone obtained from people of Polynesian and European ancestry undergoing joint replacement surgery. | Naot D et al. | β | 2021 | β |
| Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. | Kapoor A et al. | β | 2021 | β |
| Natural selection contributes to the myopia epidemic. | Long E et al. | β | 2021 | β |
| Noninvasive biomarkers for prediction and diagnosis of heart transplantation rejection. | Khachatoorian Y et al. | β | 2021 | β |
| On how to generalize species-specific conceptual schemes to generate a species-independent Conceptual Schema of the Genome. | GarcΓa S A et al. | β | 2021 | β |
| Pangenomics enables genotyping of known structural variants in 5202 diverse genomes. | SirΓ©n J et al. | β | 2021 | β |
| Personalized genome structure via single gamete sequencing. | Lyu R et al. | β | 2021 | β |
| Phenome-wide and expression quantitative trait locus associations of coronavirus disease 2019 genetic risk loci. | Moon CY et al. | β | 2021 | β |
| PIP-SNP: a pipeline for processing SNP data featured as linkage disequilibrium bin mapping, genotype imputing and marker synthesizing. | Zhang W et al. | β | 2021 | β |
| Points to Consider for Implementation of the ICH E17 Guideline: Learning from Past Multiregional Clinical Trials in Japan. | Asano K et al. | β | 2021 | β |
| Population genetic considerations for using biobanks as international resources in the pandemic era and beyond. | Carress H et al. | β | 2021 | β |
| Population genetics: past, present, and future. | Okazaki A et al. | β | 2021 | β |
| Promoter-interacting expression quantitative trait loci are enriched for functional genetic variants. | Chandra V et al. | β | 2021 | β |
| Reconstructing 50,000 years of human history from our DNA: lessons from modern genomics. | Rotival M et al. | β | 2021 | β |
| Response and Toxicity to Cytarabine Therapy in Leukemia and Lymphoma: From Dose Puzzle to Pharmacogenomic Biomarkers. | Di Francia R et al. | β | 2021 | β |
| Review on Databases and Bioinformatic Approaches on Pharmacogenomics of Adverse Drug Reactions. | Tong H et al. | β | 2021 | β |
| Revisiting the genome-wide significance threshold for common variant GWAS. | Chen Z et al. | β | 2021 | β |
| Scanning the human genome for "signatures" of positive selection: Transformative opportunities and ethical obligations. | Hernandez M et al. | β | 2021 | β |
| Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Lagou V et al. | β | 2021 | β |
| Single-molecule telomere length characterization by optical mapping in nano-channel array: Perspective and review on telomere length measurement. | Uppuluri L et al. | β | 2021 | β |
| So many Nigerians: why is Nigeria overrepresented as the ancestral genetic homeland of Legacy African North Americans? | Jackson FLC | β | 2021 | β |
| Structural and functional analysis of somatic coding and UTR indels in breast and lung cancer genomes. | Chen J et al. | β | 2021 | β |
| Technological readiness and implementation of genomic-driven precision medicine for complex diseases. | Franks PW et al. | β | 2021 | β |
| The Need for a Human Pangenome Reference Sequence. | Miga KH et al. | β | 2021 | β |
| Three decades of genetic privacy: a metaphoric journey. | Knoppers BM et al. | β | 2021 | β |
| Translating genetic association of lipid levels for biological and clinical application. | Crone B et al. | β | 2021 | β |
| What connectomics can learn from genomics. | Chen PB et al. | β | 2021 | β |
| Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. | Lin BM et al. | β | 2021 | β |
| A candidate intronic <i>CYP24A1</i> gene variant affects the risk of colorectal cancer. | Sadeghi H et al. | β | 2020 | β |
| Accurate assembly of the olive baboon (Papio anubis) genome using long-read and Hi-C data. | Batra SS et al. | β | 2020 | β |
| A comparison of humans and baboons suggests germline mutation rates do not track cell divisions. | Wu FL et al. | β | 2020 | β |
| Admixture and natural selection shaped genomes of an Austronesian-speaking population in the Solomon Islands. | Isshiki M et al. | β | 2020 | β |
| A fully integrated machine learning scan of selection in the chimpanzee genome. | Nye J et al. | β | 2020 | β |
| A Journey through Genetic Architecture and Predisposition of Coronary Artery Disease. | Roberts R et al. | β | 2020 | β |
| Alternative polyadenylation mediates genetic regulation of gene expression. | Mittleman BE et al. | β | 2020 | β |
| A Polygenic Risk Score for Breast Cancer in US Latinas and Latin American Women. | Shieh Y et al. | β | 2020 | β |
| A practical view of fine-mapping and gene prioritization in the post-genome-wide association era. | Broekema RV et al. | β | 2020 | β |
| Association between gene polymorphisms of voltage-dependent Ca<sup>2+</sup> channels and hypertension in the Dai people of China: a case-control study. | Huang L et al. | β | 2020 | β |
| Association of Vitamin D Metabolism Gene Polymorphisms with Autoimmunity: Evidence in Population Genetic Studies. | Ruiz-Ballesteros AI et al. | β | 2020 | β |
| A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions. | Garg P et al. | β | 2020 | β |
| A variant-centric perspective on geographic patterns of human allele frequency variation. | Biddanda A et al. | β | 2020 | β |
| Causal inference in genetic trio studies. | Bates S et al. | β | 2020 | β |
| Clustering of known low and moderate risk alleles rather than a novel recessive high-risk gene in non-BRCA1/2 sib trios affected with breast cancer. | Hilbers FS et al. | β | 2020 | β |
| Copy Number Variations and Expression Levels of Guanylate-Binding Protein 6 Gene Associated with Growth Traits of Chinese Cattle. | Hao D et al. | β | 2020 | β |
| CTLA-4 Expression Plays a Role in PSC and PBC Progression. | Meister P et al. | β | 2020 | β |
| De novo duplication on Chromosome 19 observed in nuclear family displaying neurodevelopmental disorders. | Sjaarda CP et al. | β | 2020 | β |
| Effects of <i>MACC1</i> polymorphisms on hepatocellular carcinoma development and clinical characteristics. | Lin CH et al. | β | 2020 | β |
| Egg transcriptome profile responds to maternal virus infection in honey bees, Apis mellifera. | Amiri E et al. | β | 2020 | β |
| Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leucocyte antigen locus. | Parks T et al. | β | 2020 | β |
| Epistasis between phenylethanolamine N-methyltransferase and Ξ²2-adrenergic receptor influences extracellular epinephrine level and associates with the susceptibility to allergic asthma. | Sio YY et al. | β | 2020 | β |
| From personalised nutrition to precision medicine: the rise of consumer genomics and digital health. | Moore JB | β | 2020 | β |
| Functional and population genetic features of copy number variations in two dairy cattle populations. | Lee YL et al. | β | 2020 | β |
| Genetic variants association with cancers in African-based populations: A systematic review. | Okoturo E et al. | β | 2020 | β |
| Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. | Hong S et al. | β | 2020 | β |
| Genome-wide pathogenesis interpretation using a heat diffusion-based systems genetics method and implications for gene function annotation. | Quan Y et al. | β | 2020 | β |
| Genomic predictions based on haplotypes fitted as pseudo-SNP for milk production and udder type traits and SCS in French dairy goats. | Teissier M et al. | β | 2020 | β |
| Genomics and Transcriptomics: The Powerful Technologies in Precision Medicine. | Khodadadian A et al. | β | 2020 | β |
| Haplotype-Based Genome-Wide Association Study and Identification of Candidate Genes Associated with Carcass Traits in Hanwoo Cattle. | Srivastava S et al. | β | 2020 | β |
| Human gene and disease associations for clinical-genomics and precision medicine research. | Ahmed Z et al. | β | 2020 | β |
| Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. | Trevino CE et al. | β | 2020 | β |
| Inference of Chromosome-Length Haplotypes Using Genomic Data of Three or a Few More Single Gametes. | Li R et al. | β | 2020 | β |
| Inference of differential gene regulatory networks based on gene expression and genetic perturbation data. | Zhou X et al. | β | 2020 | β |
| Interferon lambda 4 gene polymorphisms as a predicting tool of response to hepatitis C virus genotype 4 patients treated with Sofosbuvir and Ribavirin. | Sakr AA et al. | β | 2020 | β |
| Interindividual Differences in DNA Adduct Formation and Detoxification of 1,3-Butadiene-Derived Epoxide in Human HapMap Cell Lines. | Degner A et al. | β | 2020 | β |
| Legacy Data Confound Genomics Studies. | Anderson-TrocmΓ© L et al. | β | 2020 | β |
| MethHaplo: combining allele-specific DNA methylation and SNPs for haplotype region identification. | Zhou Q et al. | β | 2020 | β |
| MicroRNAs Determining Carcinogenesis by Regulating Oncogenes and Tumor Suppressor Genes During Cell Cycle. | Fasoulakis Z et al. | β | 2020 | β |
| MI-MAAP: marker informativeness for multi-ancestry admixed populations. | Chen S et al. | β | 2020 | β |
| Missing heritability of complex diseases: case solved? | GΓ©nin E | β | 2020 | β |
| Novel algorithms for efficient subsequence searching and mapping in nanopore raw signals towards targeted sequencing. | Han R et al. | β | 2020 | β |
| Pathway Analysis of Genes Identified through Post-GWAS to Underpin Prostate Cancer Aetiology. | Farashi S et al. | β | 2020 | β |
| Quantifying Influences on Intragenomic Mutation Rate. | Simon H et al. | β | 2020 | β |
| Recombination Rate Variation and Infrequent Sex Influence Genetic Diversity in Chlamydomonas reinhardtii. | Hasan AR et al. | β | 2020 | β |
| Simulation-Based Evaluation of Three Methods for Local Ancestry Deconvolution of Non-model Crop Species Genomes. | Cottin A et al. | β | 2020 | β |
| Statistically efficient association analysis of quantitative traits with haplotypes and untyped SNPs in family studies. | Diao G et al. | β | 2020 | β |
| Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci. | Neumeyer S et al. | β | 2020 | β |
| Studies of human twins reveal genetic variation that affects dietary fat perception. | Lin C et al. | β | 2020 | β |
| The contribution of rare genetic variants to the pathogenesis of polycystic ovary syndrome. | Dapas M et al. | β | 2020 | β |
| The Cystic Fibrosis Transmembrane Conductance Regulator 470 Met Allele Is Associated with an Increased Risk of Chronic Pancreatitis in Both Asian and Caucasian Populations: A Meta-Analysis. | Zhou D et al. | β | 2020 | β |
| The Earth BioGenome project: opportunities and challenges for plant genomics and conservation. | Exposito-Alonso M et al. | β | 2020 | β |
| The effect of kinship in re-identification attacks against genomic data sharing beacons. | Ayoz K et al. | β | 2020 | β |
| The genetic history of France. | Saint Pierre A et al. | β | 2020 | β |
| The pathogenesis of systemic lupus erythematosus: Harnessing big data to understand the molecular basis of lupus. | Catalina MD et al. | β | 2020 | β |
| Tools for teaching biochemistry and molecular biology: A parallel session at the IUBMB/PSBMB 2019 "Harnessing Interdisciplinary Education in Biochemistry and Molecular Biology" conference. | Chou CC et al. | β | 2020 | β |
| WITHDRAWN: Genetics of Parkinson's disease. | Lill CM | β | 2020 | β |
| A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene. | Hecker M et al. | β | 2019 | β |
| A greedy feature selection algorithm for Big Data of high dimensionality. | Tsamardinos I et al. | β | 2019 | β |
| Are SGLT2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis. | Drexel H et al. | β | 2019 | β |
| A ribonuclease-dependent cleavable beacon primer triggering DNA amplification for single nucleotide mutation detection with ultrahigh sensitivity and selectivity. | Ding X et al. | β | 2019 | β |
| Assessing the Evolutionary Conservation of Protein Disulphide Bonds. | Wong JWH | β | 2019 | β |
| A strategy for building and using a human reference pangenome. | Llamas B et al. | β | 2019 | β |
| Characterizing rare and low-frequency height-associated variants in the Japanese population. | Akiyama M et al. | β | 2019 | β |
| Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing. | Laks E et al. | β | 2019 | β |
| Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations. | Reisberg S et al. | β | 2019 | β |
| Composite kernel machine regression based on likelihood ratio test for joint testing of genetic and gene-environment interaction effect. | Zhao N et al. | β | 2019 | β |
| Confounding of linkage disequilibrium patterns in large scale DNA based gene-gene interaction studies. | Joiret M et al. | β | 2019 | β |
| Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population. | RamΓrez B et al. | β | 2019 | β |
| Diagnostic performance evaluation of sulfate-conjugated cholesterol metabolites as urinary biomarkers of Niemann-Pick disease type C. | Maekawa M et al. | β | 2019 | β |
| Differential HLA allele frequency in Mycobacterium africanum vs Mycobacterium tuberculosis in Mali. | Kone A et al. | β | 2019 | β |
| DNA identification of compromised samples with massive parallel sequencing. | Tillmar A et al. | β | 2019 | β |
| Evaluating and sharing global genetic ancestry in biomedical datasets. | Harismendy O et al. | β | 2019 | β |
| Extended HLA Haplotypes and Their Impact on DPB1 Matching of Unrelated Hematologic Stem Cell Transplant Donors. | Linjama T et al. | β | 2019 | β |
| Generalizing polygenic risk scores from Europeans to Hispanics/Latinos. | Grinde KE et al. | β | 2019 | β |
| Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. | Laufer VA et al. | β | 2019 | β |
| Genetic risk factors for the development of pulmonary disease identified by genome-wide association. | Hall R et al. | β | 2019 | β |
| Genetics of common complex kidney stone disease: insights from genome-wide association studies. | Palsson R et al. | β | 2019 | β |
| Genetics of narcolepsy. | Miyagawa T et al. | β | 2019 | β |
| Genetic variability analysis in a population from BogotΓ‘: Towards a haplotype map | Caicedo JD et al. | β | 2019 | β |
| Genetic variability of the ABCC2 gene and clinical outcomes in pancreatic cancer patients. | Gentiluomo M et al. | β | 2019 | β |
| Genetic variation in FCER1A predicts peginterferon alfa-2a-induced hepatitis B surface antigen clearance in East Asian patients with chronic hepatitis B. | Wei L et al. | β | 2019 | β |
| Genetic Variation of the Vitamin D Binding Protein Affects Vitamin D Status and Response to Supplementation in Infants. | Enlund-Cerullo M et al. | β | 2019 | β |
| Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patients. | Bhuvaneshwar K et al. | β | 2019 | β |
| Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2. | Hernandez Cordero AI et al. | β | 2019 | β |
| Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations. | Peterson RE et al. | β | 2019 | β |
| Genome-wide association study of Alzheimerβs disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset | Hong S et al. | β | 2019 | β |
| Genome-wide Significance Thresholds for Admixture Mapping Studies. | Grinde KE et al. | β | 2019 | β |
| Genomic Evidence for Local Adaptation of Hunter-Gatherers to the African Rainforest. | Lopez M et al. | β | 2019 | β |
| Genomic Medicine-Progress, Pitfalls, and Promise. | Shendure J et al. | β | 2019 | β |
| Haplotype matching in large cohorts using the Li and Stephens model. | Lunter G | β | 2019 | β |
| Haptoglobin-2 variant increases susceptibility to acute respiratory distress syndrome during sepsis. | Kerchberger VE et al. | β | 2019 | β |
| HLA*LA-HLA typing from linearly projected graph alignments. | Dilthey AT et al. | β | 2019 | β |
| Human collectin-11 (COLEC11) and its synergic genetic interaction with MASP2 are associated with the pathophysiology of Chagas Disease. | Sandri TL et al. | β | 2019 | β |
| Identification of 12 cancer types through genome deep learning. | Sun Y et al. | β | 2019 | β |
| Identification of loci associated with conception rate in primiparous Holstein cows. | Kiser JN et al. | β | 2019 | β |
| Identification of shared genomic aberrations between angiomatous and microcystic meningiomas. | Kuroi Y et al. | β | 2019 | β |
| Immune Gene Diversity in Archaic and Present-day Humans. | Reher D et al. | β | 2019 | β |
| INDEX-db: The Indian Exome Reference Database (Phase I). | Ahmed P H et al. | β | 2019 | β |
| International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. | Nievergelt CM et al. | β | 2019 | β |
| Leaving some behind: the growing gap in precision medicine for minority populations. | Perera M | β | 2019 | β |
| Links between age at menarche, antral follicle count, and body mass index in African American and European American women. | Schuh SM et al. | β | 2019 | β |
| Magnetic nanospheres for convenient and efficient capture and release of hepatitis B virus DNA. | Wen CY et al. | β | 2019 | β |
| Mapping Genome Variants Sheds Light on Genetic and Phenotypic Differentiation in Chinese. | Guo L et al. | β | 2019 | β |
| Mechanisms of immunogenicity in colorectal cancer. | Sillo TO et al. | β | 2019 | β |
| MHC Genomics and Disease: Looking Back to Go Forward. | Dawkins RL et al. | β | 2019 | β |
| Microhaplotypes in forensic genetics. | Oldoni F et al. | β | 2019 | β |
| Mouse Models and Online Resources for Functional Analysis of Osteoporosis Genome-Wide Association Studies. | Maynard RD et al. | β | 2019 | β |
| NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants. | Yoo SK et al. | β | 2019 | β |
| Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss. | Lenarduzzi S et al. | β | 2019 | β |
| Non-Coding RNAs and their Integrated Networks. | Zhang P et al. | β | 2019 | β |
| Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree. | Good DA et al. | β | 2019 | β |
| Pathogen Evasion of Chemokine Response Through Suppression of CXCL10. | Antonia AL et al. | β | 2019 | β |
| PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations. | Zhang C et al. | β | 2019 | β |
| Pharmacogenomics in IVF: A New Era in the Concept of Personalized Medicine. | Kalinderi K et al. | β | 2019 | β |
| PopHumanScan: the online catalog of human genome adaptation. | Murga-Moreno J et al. | β | 2019 | β |
| Predicting Polygenic Risk of Psychiatric Disorders. | Martin AR et al. | β | 2019 | β |
| Primers on nutrigenetics and nutri(epi)genomics: Origins and development of precision nutrition. | Bordoni L et al. | β | 2019 | β |
| Rare and common variant discovery in complex disease: the IBD case study. | Venkataraman GR et al. | β | 2019 | β |
| Recent advances and perspectives in next generation sequencing application to the genetic research of type 2 diabetes. | Nasykhova YA et al. | β | 2019 | β |
| Resequencing of cv CRI-12 family reveals haplotype block inheritance and recombination of agronomically important genes in artificial selection. | Lu X et al. | β | 2019 | β |
| Revisit Population-based and Family-based Genotype Imputation. | Liu CT et al. | β | 2019 | β |
| RSAT variation-tools: An accessible and flexible framework to predict the impact of regulatory variants on transcription factor binding. | Santana-Garcia W et al. | β | 2019 | β |
| scoreInvHap: Inversion genotyping for genome-wide association studies. | Ruiz-Arenas C et al. | β | 2019 | β |
| Statistical Association Mapping of Population-Structured Genetic Data. | Najafi A et al. | β | 2019 | β |
| Statistical inference of genetic pathway analysis in high dimensions. | Liu Y et al. | β | 2019 | β |
| Statistical methods for genome-wide association studies. | Wang MH et al. | β | 2019 | β |
| SureTypeSC-a Random Forest and Gaussian mixture predictor of high confidence genotypes in single-cell data. | Vogel I et al. | β | 2019 | β |
| Systematic comparison of germline variant calling pipelines cross multiple next-generation sequencers. | Chen J et al. | β | 2019 | β |
| The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? | MacInnes SJ et al. | β | 2019 | β |
| The advances in DNA mixture interpretation. | Yang J et al. | β | 2019 | β |
| The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data. | Zangwill LM et al. | β | 2019 | β |
| The Effect of <i>AMBP</i> SNPs, Their Haplotypes, and Gene-Environment Interactions on the Risk of Atherothrombotic Stroke Among the Chinese Population. | Liu H et al. | β | 2019 | β |
| The harmonic mean <i>p</i>-value for combining dependent tests. | Wilson DJ | β | 2019 | β |
| The myopia susceptibility locus vasoactive intestinal peptide receptor 2 (VIPR2) contains variants with opposite effects. | Leung KH et al. | β | 2019 | β |
| The Role of Chinese Medicine in Health Maintenance and Disease Prevention: Application of Constitution Theory. | Li L et al. | β | 2019 | β |
| Tissue typing for kidney transplantation for the general nephrologist. | Mulley WR et al. | β | 2019 | β |
| Validation of 46 loci associated with female fertility traits in cattle. | Kiser JN et al. | β | 2019 | β |
| Variant analysis of the chromodomain helicase DNA-binding protein 7 in pediatric disorders of sex development. | Zhang B et al. | β | 2019 | β |
| Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome. | Du Z et al. | β | 2019 | β |
| Whole-genome re-sequencing association study for direct genetic effects and social genetic effects of six growth traits in Large White pigs. | Wu P et al. | β | 2019 | β |
| Advances in understanding the genetic basis of diabetic kidney disease. | Li M et al. | β | 2018 | β |
| Adverse life events, psychiatric history, and biological predictors of postpartum depression in an ethnically diverse sample of postpartum women. | Guintivano J et al. | β | 2018 | β |
| ALPHLARD: a Bayesian method for analyzing HLA genes from whole genome sequence data. | Hayashi S et al. | β | 2018 | β |
| Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population. | Cyrus C et al. | β | 2018 | β |
| Analysis of type 2 diabetes and obesity genetic variants in Mexican Pima Indians: Marked allelic differentiation among Amerindians at HLA. | Hsueh WC et al. | β | 2018 | β |
| Ancestry and dental development: A geographic and genetic perspective. | Dhamo B et al. | β | 2018 | β |
| A new perspective on lipid research in age-related macular degeneration. | van Leeuwen EM et al. | β | 2018 | β |
| An imputation platform to enhance integration of rice genetic resources. | Wang DR et al. | β | 2018 | β |
| A One-Penny Imputed Genome from Next-Generation Reference Panels. | Browning BL et al. | β | 2018 | β |
| A reference haplotype panel for genome-wide imputation of short tandem repeats. | Saini S et al. | β | 2018 | β |
| A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations. | Duan Q et al. | β | 2018 | β |
| AROHap: An effective algorithm for single individual haplotype reconstruction based on asexual reproduction optimization. | Olyaee MH et al. | β | 2018 | β |
| A sensitive colorimetric DNA biosensor for specific detection of the HBV gene based on silver-coated glass slide and G-quadruplex-hemin DNAzyme. | Li Y et al. | β | 2018 | β |
| Assessing Rare Variation in Complex Traits. | Kuchenbaecker K et al. | β | 2018 | β |
| Assessment of the Genetic Architecture of Alzheimer's Disease Risk in Rate of Memory Decline. | Del-Aguila JL et al. | β | 2018 | β |
| Association between brain-derived neurotrophic factor gene polymorphisms and fibromyalgia in a Korean population: a multicenter study. | Park DJ et al. | β | 2018 | β |
| Association Between MALAT1 and THRIL Polymorphisms and Precancerous Cervical Lesions. | Wang Y et al. | β | 2018 | β |
| Association between Polymorphisms of Antioxidant Gene (MnSOD, CAT, and GPx1) and Risk of Coronary Artery Disease. | Yeh HL et al. | β | 2018 | β |
| Association of Vitamin D Receptor Gene Variation With Osteoporosis Risk in Belarusian and Lithuanian Postmenopausal Women. | Marozik PM et al. | β | 2018 | β |
| A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome. | Garg P et al. | β | 2018 | β |
| A unified genetic association test robust to latent population structure for a count phenotype. | Song M | β | 2018 | β |
| Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate. | Mostowska A et al. | β | 2018 | β |
| Computational pan-genomics: status, promises and challenges. | Computational Pan-Genomics Consortium | β | 2018 | β |
| Design of Arab Diabetes Gene-Centric Array (ADGCA) in population with an epidemic of Type 2 Diabetes: A population specific SNP evaluation. | Al-Rubeaan K et al. | β | 2018 | β |
| Effects of Demographic History on the Detection of Recombination Hotspots from Linkage Disequilibrium. | Dapper AL et al. | β | 2018 | β |
| Electronic health records: the next wave of complex disease genetics. | Wolford BN et al. | β | 2018 | β |
| Epidemiology of prostate cancer in Asian countries. | Kimura T et al. | β | 2018 | β |
| Factors Affecting Drug-Development Strategies in Asian Global Clinical Trials for Drug Approval in Japan. | Asano K et al. | β | 2018 | β |
| Finding associated variants in genome-wide association studies on multiple traits. | Gai L et al. | β | 2018 | β |
| From Genotype to Phenotype: A Primer on the Functional Follow-up of Genome-Wide Association Studies in Cardiovascular Disease. | Lin J et al. | β | 2018 | β |
| Genetic-Driven Druggable Target Identification and Validation. | Floris M et al. | β | 2018 | β |
| Genetics of Multiple Sclerosis: An Overview and New Directions. | Patsopoulos NA | β | 2018 | β |
| Genetic variants influencing phenotypic variance heterogeneity. | Ek WE et al. | β | 2018 | β |
| Genetic variations in the PI3K/PTEN/AKT/mTOR pathway predict tumor response and disease-free survival in locally advanced rectal cancer patients receiving preoperative chemoradiotherapy and radical surgery. | Peng J et al. | β | 2018 | β |
| Genome-Wide Association Studies. | Dehghan A | β | 2018 | β |
| Genome-Wide Association Studies for Pasmo Resistance in Flax (<i>Linum usitatissimum L</i>.). | He L et al. | β | 2018 | β |
| Genome-wide association studies of multiple sclerosis. | Cotsapas C et al. | β | 2018 | β |
| Genomewide association study reveals novel genetic loci associated with change in renal function in heart transplant recipients. | Asleh R et al. | β | 2018 | β |
| Genomics and pharmacogenomics of pediatric acute lymphoblastic leukemia. | Wu C et al. | β | 2018 | β |
| Genotype Imputation from Large Reference Panels. | Das S et al. | β | 2018 | β |
| GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits. | Huang D et al. | β | 2018 | β |
| Hidden genomic MHC disparity between HLA-matched sibling pairs in hematopoietic stem cell transplantation. | Koskela S et al. | β | 2018 | β |
| Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification. | Smieszek S et al. | β | 2018 | β |
| Identification of Prognostic and Susceptibility Markers in Chronic Myeloid Leukemia Using Next Generation Sequencing. | Shokeen Y et al. | β | 2018 | β |
| Impact of Genetic Variation on CRISPR-Cas Targeting. | Canver MC et al. | β | 2018 | β |
| Integrated genome sizing (IGS) approach for the parallelization of whole genome analysis. | Sona P et al. | β | 2018 | β |
| Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits. | Wu Y et al. | β | 2018 | β |
| Interdisciplinary Models for Research and Clinical Endeavors in Genomic Medicine: A Scientific Statement From the American Heart Association. | Musunuru K et al. | β | 2018 | β |
| Intrinsic and Extrinsic Factors Impacting Absorption, Metabolism, and Health Effects of Dietary Carotenoids. | Moran NE et al. | β | 2018 | β |
| Is the rs1801282 (G/C) Polymorphism of <i>PPAR - Gamma</i> Gene Associated with T2DM in Iraqi People? | Al-Naemi AH et al. | β | 2018 | β |
| <i>UBD</i> modifies <i>APOL1</i>-induced kidney disease risk. | Zhang JY et al. | β | 2018 | β |
| Kernel machine methods for integrative analysis of genome-wide methylation and genotyping studies. | Zhao N et al. | β | 2018 | β |
| Kourami: graph-guided assembly for novel human leukocyte antigen allele discovery. | Lee H et al. | β | 2018 | β |
| Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. | Floyd JS et al. | β | 2018 | β |
| Leveraging human genetic and adverse outcome pathway (AOP) data to inform susceptibility in human health risk assessment. | Mortensen HM et al. | β | 2018 | β |
| Mating Design and Genetic Structure of a Multi-Parent Advanced Generation Intercross (MAGIC) Population of Sorghum (<i>Sorghum bicolor</i> (L.) Moench). | Ongom PO et al. | β | 2018 | β |
| Measuring Genetic Differentiation from Pool-seq Data. | Hivert V et al. | β | 2018 | β |
| Medical genetics and genomic medicine in Nigeria. | Adeyemo AA et al. | β | 2018 | β |
| Meta-Analysis of Common and Rare Variants. | Michailidou K | β | 2018 | β |
| Microarray study of gene expression profile to identify new candidate genes involved in the molecular mechanism of leptin-induced knee joint osteoarthritis in rat. | Fan Q et al. | β | 2018 | β |
| MP-LAMP: parallel detection of statistically significant multi-loci markers on cloud platforms. | Yoshizoe K et al. | β | 2018 | β |
| Multiple sclerosis. | Cotsapas C et al. | β | 2018 | β |
| Mycophenolic Acid and Its Metabolites in Kidney Transplant Recipients: A Semimechanistic Enterohepatic Circulation Model to Improve Estimating Exposure. | Okour M et al. | β | 2018 | β |
| No Evidence for Recent Selection at FOXP2 among Diverse Human Populations. | Atkinson EG et al. | β | 2018 | β |
| Nonparametric approaches for population structure analysis. | Alhusain L et al. | β | 2018 | β |
| One Hundred Years of Linkage Disequilibrium. | Sved JA et al. | β | 2018 | β |
| Pedigree Selection and Information Content. | Vardarajan BN et al. | β | 2018 | β |
| Personalised Medicine and Medical Imaging: Opportunities and Challenges for Contemporary Health Care. | Atutornu J et al. | β | 2018 | β |
| Personalised Medicine: The Odyssey from Hope to Practice. | Visvikis-Siest S et al. | β | 2018 | β |
| Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology. | Seyerle AA et al. | β | 2018 | β |
| PopHuman: the human population genomics browser. | Casillas S et al. | β | 2018 | β |
| POPSTR: Inference of Admixed Population Structure Based on Single-Nucleotide Polymorphisms and Copy Number Variations. | Ahn J et al. | β | 2018 | β |
| Precise detection of de novo single nucleotide variants in human genomes. | GΓ³mez-Romero L et al. | β | 2018 | β |
| Racial/ethnic disparities in the adjuvant chemotherapy of locally advanced colon cancer patients. | Zhong X et al. | β | 2018 | β |
| Rare-Variant Studies to Complement Genome-Wide Association Studies. | Sazonovs A et al. | β | 2018 | β |
| Rigor and reproducibility in genetic research on eating disorders. | HΓΌbel C et al. | β | 2018 | β |
| Role of Germline Genetics in Identifying Survivors at Risk for Adverse Effects of Cancer Treatment. | Morton LM et al. | β | 2018 | β |
| Structural Prediction of Protein-Protein Interactions by Docking: Application to Biomedical Problems. | Barradas-Bautista D et al. | β | 2018 | β |
| Success and failure in replication of genotype-phenotype associations: How does replication help in understanding the genetic basis of phenotypic variation in outbred populations? | Schielzeth H et al. | β | 2018 | β |
| The collaborative effect of scientific meetings: A study of the International Milk Genomics Consortium. | Kwok E et al. | β | 2018 | β |
| The Comoros Show the Earliest Austronesian Gene Flow into the Swahili Corridor. | Brucato N et al. | β | 2018 | β |
| The genomics of selenium: Its past, present and future. | Davy T et al. | β | 2018 | β |
| The UK Biobank resource with deep phenotyping and genomic data. | Bycroft C et al. | β | 2018 | β |
| Understanding the Hidden Complexity of Latin American Population Isolates. | Mooney JA et al. | β | 2018 | β |
| Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies. | Song M et al. | β | 2018 | β |
| VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study. | Mili FD et al. | β | 2018 | β |
| A Breakthrough in Genetics and its Relevance to Prevention of Coronary Artery Disease in LMIC. | Roberts R | β | 2017 | β |
| A missense variant of the ABCC11 gene is associated with Axillary Osmidrosis susceptibility and clinical phenotypes in the Chinese Han Population. | Ren Y et al. | β | 2017 | β |
| Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion. | Huang LO et al. | β | 2017 | β |
| An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression. | Akiyama T et al. | β | 2017 | β |
| An Expanded View of Complex Traits: From Polygenic to Omnigenic. | Boyle EA et al. | β | 2017 | β |
| A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, Japan. | Kanzawa-Kiriyama H et al. | β | 2017 | β |
| Association Analysis of Nonsyndromic Congenital Heart Disease and Tag Single Nucleotide Polymorphisms of TBX20 and Genes in the Ras-MAPK Pathway. | Luo Z et al. | β | 2017 | β |
| Association of Posttraumatic Stress Disorder With rs2267735 in the ADCYAP1R1 Gene: A Meta-Analysis. | Lind MJ et al. | β | 2017 | β |
| Autoimmune aspects of psoriasis: Heritability and autoantigens. | Prinz JC | β | 2017 | β |
| Batch effects and the effective design of single-cell gene expression studies. | Tung PY et al. | β | 2017 | β |
| Beliefs about Genetically Targeted Care in African Americans. | Halbert CH et al. | β | 2017 | β |
| Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. | McDonald MN et al. | β | 2017 | β |
| Cancer is an adaptation that selects in animals against energy dissipation. | Muller AWJ | β | 2017 | β |
| Cardiovascular pharmacogenetics: a promise for genomically-guided therapy and personalized medicine. | Zaiou M et al. | β | 2017 | β |
| CD4+ T cells from patients with primary sclerosing cholangitis exhibit reduced apoptosis and down-regulation of proapoptotic Bim in peripheral blood. | Schoknecht T et al. | β | 2017 | β |
| Characterization of noncoding regulatory DNA in the human genome. | Elkon R et al. | β | 2017 | β |
| Clinical interpretation of copy number variants in the human genome. | Nowakowska B | β | 2017 | β |
| Cluster ensemble based on Random Forests for genetic data. | Alhusain L et al. | β | 2017 | β |
| Comparative analysis of the EGFR, HER2, c-MYC, and MET variations in colorectal cancer determined by three different measures: gene copy number gain, amplification status and the 2013 ASCO/CAP guideline criterion for HER2 testing of breast cancer. | Kwak Y et al. | β | 2017 | β |
| Copy Number Variations Detection: Unravelling the Problem in Tangible Aspects. | do Nascimento F et al. | β | 2017 | β |
| Detailed analysis of inversions predicted between two human genomes: errors, real polymorphisms, and their origin and population distribution. | Vicente-Salvador D et al. | β | 2017 | β |
| Detecting gene subnetworks under selection in biological pathways. | Gouy A et al. | β | 2017 | β |
| Diagnosis and clinical management of duplications and deletions. | Capalbo A et al. | β | 2017 | β |
| Differences in the rare variant spectrum among human populations. | Mathieson I et al. | β | 2017 | β |
| Differential analysis of mutations in the Jewish population and their implications for diseases. | Einhorn Y et al. | β | 2017 | β |
| Discerning the Origins of the Negritos, First Sundaland People: Deep Divergence and Archaic Admixture. | Jinam TA et al. | β | 2017 | β |
| Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing. | Leiva-Torres GA et al. | β | 2017 | β |
| DNA origami-based shape IDs for single-molecule nanomechanical genotyping. | Zhang H et al. | β | 2017 | β |
| Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. | Schneider VA et al. | β | 2017 | β |
| Expression of long non-coding RNAs in autoimmunity and linkage to enhancer function and autoimmune disease risk genetic variants. | Aune TM et al. | β | 2017 | β |
| Family studies to find rare high risk variants in migraine. | Hansen RD et al. | β | 2017 | β |
| Fast admixture analysis and population tree estimation for SNP and NGS data. | Cheng JY et al. | β | 2017 | β |
| Fine mapping by composite genome-wide association analysis. | Casellas J et al. | β | 2017 | β |
| Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection. | Huang H et al. | β | 2017 | β |
| From typical sequences to typical genotypes. | Tal O et al. | β | 2017 | β |
| G allele at -924 AΒ >Β G position of FoxP3 gene promoter as a risk factor for tuberculosis. | Beiranvand E et al. | β | 2017 | β |
| geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation. | Wuster A et al. | β | 2017 | β |
| Genetic Association of Hematopoietic Stem Cell Transplantation Outcome beyond Histocompatibility Genes. | Gam R et al. | β | 2017 | β |
| Genetic association studies in cardiovascular diseases: Do we have enough power? | Auer PL et al. | β | 2017 | β |
| Genetic effects influencing risk for major depressive disorder in China and Europe. | Bigdeli TB et al. | β | 2017 | β |
| Genetic polymorphisms of non-coding RNAs associated with increased head and neck cancer susceptibility: a systematic review and meta-analysis. | Pan W et al. | β | 2017 | β |
| Genetic predisposition to bevacizumab-induced hypertension. | Frey MK et al. | β | 2017 | β |
| Genetics-directed drug discovery for combating Mycobacterium tuberculosis infection. | Quan Y et al. | β | 2017 | β |
| Genetics of common complex diseases: a view from Iceland. | Arnar DO et al. | β | 2017 | β |
| Genetic studies of alcohol dependence in the context of the addiction cycle. | Reilly MT et al. | β | 2017 | β |
| Genetic variants associated with risk of Alzheimer's disease contribute to cognitive change in midlife: The Atherosclerosis Risk in Communities Study. | Bressler J et al. | β | 2017 | β |
| Genetic variation in the eicosanoid pathway is associated with non-small-cell lung cancer (NSCLC) survival. | Sausville LN et al. | β | 2017 | β |
| Genome Annotation. | Abugessaisa I et al. | β | 2017 | β |
| Genome annotation for clinical genomic diagnostics: strengths and weaknesses. | Steward CA et al. | β | 2017 | β |
| Genome-Wide Association Studies for Idiosyncratic Drug-Induced Hepatotoxicity: Looking Back-Looking Forward to Next-Generation Innovation. | Petros Z et al. | β | 2017 | β |
| Genome-wide association studies of cancer: current insights and future perspectives. | Sud A et al. | β | 2017 | β |
| Genome-wide screening for highly discriminative SNPs for personal identification and their assessment in world populations. | Li L et al. | β | 2017 | β |
| Genome-wide study of an elite rice pedigree reveals a complex history of genetic architecture for breeding improvement. | Chen S et al. | β | 2017 | β |
| Genomic admixture tracks pulses of economic activity over 2,000 years in the Indian Ocean trading network. | Brucato N et al. | β | 2017 | β |
| Genomic translational research: Paving the way to individualized cardiac functional analyses and personalized cardiology. | Pasipoularides A | β | 2017 | β |
| Glutathione peroxidase 3 gene polymorphisms and the risk of sudden sensorineural hearing loss. | Chien CY et al. | β | 2017 | β |
| Haplotype-resolved sweet potato genome traces back its hexaploidization history. | Yang J et al. | β | 2017 | β |
| HLA-HD: An accurate HLA typing algorithm for next-generation sequencing data. | Kawaguchi S et al. | β | 2017 | β |
| Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk. | Galarza-MuΓ±oz G et al. | β | 2017 | β |
| Human genetic variation in <i>VAC14</i> regulates <i>Salmonella</i> invasion and typhoid fever through modulation of cholesterol. | Alvarez MI et al. | β | 2017 | β |
| Identification of polymorphisms in cancer patients that differentially affect survival with age. | Doherty A et al. | β | 2017 | β |
| "I don't have to know why it snows, I just have to shovel it!": Addiction Recovery, Genetic Frameworks, and Biological Citizenship. | Dingel MJ et al. | β | 2017 | β |
| Intergenic disease-associated regions are abundant in novel transcripts. | Bartonicek N et al. | β | 2017 | β |
| Is There a Role for Genomics in the Management of Hypertension? | Burrello J et al. | β | 2017 | β |
| Lack of association of mortalin (HSPA9) and other mitochondria-related genes with risk of Parkinson's and Alzheimer's diseases. | Chung SJ et al. | β | 2017 | β |
| Mathematical Constraints on <i>F</i><sub>ST</sub>: Biallelic Markers in Arbitrarily Many Populations. | Alcala N et al. | β | 2017 | β |
| MHC class I diversity in chimpanzees and bonobos. | Maibach V et al. | β | 2017 | β |
| Multiple Testing in the Context of Gene Discovery in Sickle Cell Disease Using Genome-Wide Association Studies. | Kuo KHM | β | 2017 | β |
| Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis. | Martin-Fernandez L et al. | β | 2017 | β |
| NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types. | Lee S et al. | β | 2017 | β |
| Partial replication of two rumination-related candidate gene studies. | Van Hulle CA et al. | β | 2017 | β |
| PEMapper and PECaller provide a simplified approach to whole-genome sequencing. | Johnston HR et al. | β | 2017 | β |
| Personalized Medicine: New Perspectives for the Diagnosis and the Treatment of Renal Diseases. | Gluba-BrzΓ³zka A et al. | β | 2017 | β |
| Prediction of genome-wide DNA methylation in repetitive elements. | Zheng Y et al. | β | 2017 | β |
| Prioritising Causal Genes at Type 2 Diabetes Risk Loci. | Grotz AK et al. | β | 2017 | β |
| Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data. | Wu Y et al. | β | 2017 | β |
| Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS). | Daneshpour MS et al. | β | 2017 | β |
| Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO). | Cox AJ et al. | β | 2017 | β |
| Revealing phenotype-associated functional differences by genome-wide scan of ancient haplotype blocks. | Onuki R et al. | β | 2017 | β |
| Rising Strengths Hong Kong SAR in Bioinformatics. | Chakraborty C et al. | β | 2017 | β |
| Role of major histocompatibility complex variation in graft-versus-host disease after hematopoietic cell transplantation. | Petersdorf EW | β | 2017 | β |
| Scalable whole-genome single-cell library preparation without preamplification. | Zahn H et al. | β | 2017 | β |
| SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patients. | Sun J et al. | β | 2017 | β |
| Securing the use of existing sample collections for future human genetic research. | Kanoungi G et al. | β | 2017 | β |
| Sensorimotor Learning: Neurocognitive Mechanisms and Individual Differences. | Seidler RD et al. | β | 2017 | β |
| Sequence robust association test for familial data. | Dai W et al. | β | 2017 | β |
| Signatures of co-evolutionary host-pathogen interactions in the genome of the entomopathogenic nematode Steinernema carpocapsae. | Flores-Ponce M et al. | β | 2017 | β |
| State of Art of Cancer Pharmacogenomics in Latin American Populations. | LΓ³pez-CortΓ©s A et al. | β | 2017 | β |
| Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration. | Yaspan BL et al. | β | 2017 | β |
| The association of insertions/deletions (INDELs) and variable number tandem repeats (VNTRs) with obesity and its related traits and complications. | Say YH et al. | β | 2017 | β |
| The genomic landscape of human cellular circadian variation points to a novel role for the signalosome. | Gaspar L et al. | β | 2017 | β |
| The haploinsufficient tumor suppressor, CUX1, acts as an analog transcriptional regulator that controls target genes through distal enhancers that loop to target promoters. | Arthur RK et al. | β | 2017 | β |
| The impact of common dopamine D2 receptor gene polymorphisms on D2/3 receptor availability: C957T as a key determinant in putamen and ventral striatum. | Smith CT et al. | β | 2017 | β |
| The impact of rare and low-frequency genetic variants in common disease. | Bomba L et al. | β | 2017 | β |
| The impact of recombination on human mutation load and disease. | Alves I et al. | β | 2017 | β |
| Tour de France Champions born or made: where do we take the genetics of performance? | Moran CN et al. | β | 2017 | β |
| What can time-frequency and phase coherence measures tell us about the genetic basis of P3 amplitude? | Malone SM et al. | β | 2017 | β |
| Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans. | Choudhury A et al. | β | 2017 | β |
| A Cellular GWAS Approach to Define Human Variation in Cellular Pathways Important to Inflammation. | Miller SI et al. | β | 2016 | β |
| Adaptive Set-Based Methods for Association Testing. | Su YC et al. | β | 2016 | β |
| A genome-wide association study in multiple system atrophy. | Sailer A et al. | β | 2016 | β |
| Age-related macular degeneration: genome-wide association studies to translation. | Black JR et al. | β | 2016 | β |
| A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals. | Sobota RS et al. | β | 2016 | β |
| A model for the clustered distribution of SNPs in the human genome. | Lee CY | β | 2016 | β |
| Analysis of Case-Parent Trios Using a Loglinear Model with Adjustment for Transmission Ratio Distortion. | Huang LO et al. | β | 2016 | β |
| Analysis of optimal alignments unfolds aligners' bias in existing variant profiles. | Tran Q et al. | β | 2016 | β |
| Analytical Complexity in Detection of Gene Variant-by-Environment Exposure Interactions in High-Throughput Genomic and Exposomic Research. | Patel CJ | β | 2016 | β |
| A network of synaptic genes associated with schizophrenia and bipolar disorder. | Forero DA et al. | β | 2016 | β |
| An exome-wide analysis of low frequency and rare variants in relation to risk of breast cancer in African American Women: the AMBER Consortium. | Haddad SA et al. | β | 2016 | β |
| An expanded sequence context model broadly explains variability in polymorphism levels across the human genome. | Aggarwala V et al. | β | 2016 | β |
| AP-SKAT: highly-efficient genome-wide rare variant association test. | Hasegawa T et al. | β | 2016 | β |
| A Simple Algorithm for Population Classification. | Hu P et al. | β | 2016 | β |
| Assessment of PAX6 alleles in 66 families with aniridia. | Bobilev AM et al. | β | 2016 | β |
| Association of BAK1 single nucleotide polymorphism with a risk for dengue hemorrhagic fever. | Dang TN et al. | β | 2016 | β |
| Association of genetic variants with skin pigmentation phenotype among populations of west Maharashtra, India. | Jonnalagadda M et al. | β | 2016 | β |
| Association of HOMER1 rs2290639 with suicide attempts in Hong Kong Chinese and the potentially functional role of this polymorphism. | Rao S et al. | β | 2016 | β |
| Association of polymorphisms in the MyD88, IRAK4 and TRAF6 genes and susceptibility to type 2 diabetes mellitus and diabetic nephropathy in a southern Han Chinese population. | Guo C et al. | β | 2016 | β |
| Associations of genetic variants for adult lipid levels with lipid levels in children. The Generation R Study. | Latsuzbaia A et al. | β | 2016 | β |
| Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI). | Nalls MA et al. | β | 2016 | β |
| Beyond Endometriosis Genome-Wide Association Study: From Genomics to Phenomics to the Patient. | Zondervan KT et al. | β | 2016 | β |
| Bithionol blocks pathogenicity of bacterial toxins, ricin, and Zika virus. | Leonardi W et al. | β | 2016 | β |
| BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers. | Meeks HD et al. | β | 2016 | β |
| CCSI: a database providing chromatin-chromatin spatial interaction information. | Xie X et al. | β | 2016 | β |
| Characterisation of the global transcriptional response to heat shock and the impact of individual genetic variation. | Humburg P et al. | β | 2016 | β |
| Clinical and genetic predictors of dipeptidyl peptidase-4 inhibitor treatment response in Type 2 diabetes mellitus. | Jamaluddin JL et al. | β | 2016 | β |
| Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion. | Troyanov S et al. | β | 2016 | β |
| Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies. | Mieth B et al. | β | 2016 | β |
| Common SIRT1 variants modify the effect of abdominal adipose tissue on aging-related lung function decline. | Curjuric I et al. | β | 2016 | β |
| Comparative physiogenomic analyses of weight loss in response to 2 modes of bariatric surgery: demonstration with candidate neuropsychiatric and cardiometabolic genes. | Seip RL et al. | β | 2016 | β |
| Comparing performance of modern genotype imputation methods in different ethnicities. | Roshyara NR et al. | β | 2016 | β |
| Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe. | Blauwendraat C et al. | β | 2016 | β |
| Concepts and relevance of genome-wide association studies. | Scherer A et al. | β | 2016 | β |
| Conserved 33-kb haplotype in the MHC class III region regulates chronic arthritis. | Yau AC et al. | β | 2016 | β |
| CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk. | Garcia-Albeniz X et al. | β | 2016 | β |
| DEFB1 gene polymorphisms and tuberculosis in a Northeastern Brazilian population. | Celerino da Silva R et al. | β | 2016 | β |
| Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive. | Mishra S et al. | β | 2016 | β |
| Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. | Smith JG et al. | β | 2016 | β |
| DMETβ’ (Drug Metabolism Enzymes and Transporters): a pharmacogenomic platform for precision medicine. | Arbitrio M et al. | β | 2016 | β |
| Embracing Complex Associations in Common Traits: Critical Considerations for Precision Medicine. | Hall MA et al. | β | 2016 | β |
| Epigenetic and genetic variation in GATA5 is associated with gastric disease risk. | Sobota RS et al. | β | 2016 | β |
| Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. | MΓΆller M et al. | β | 2016 | β |
| Evaluation of the association of single nucleotide polymorphisms in the PRPH2 gene with adult-onset foveomacular vitelliform dystrophy. | Grunin M et al. | β | 2016 | β |
| Evidence for natural selection at the melanocortin-3 receptor gene in European and African populations. | Yoshiuchi I | β | 2016 | β |
| Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes. | Sudhaman S et al. | β | 2016 | β |
| Fifteen years of genomewide scans for selection: trends, lessons and unaddressed genetic sources of complication. | Haasl RJ et al. | β | 2016 | β |
| From Single Variants to Protein Cascades: MULTISCALE MODELING OF SINGLE NUCLEOTIDE VARIANT SETS IN GENETIC DISORDERS. | Mueller SC et al. | β | 2016 | β |
| Galectin-3 and Its Genetic Variation rs4644 Modulate Enterovirus 71 Infection. | Huang WC et al. | β | 2016 | β |
| Gene copy number variation analysis reveals dosage-insensitive expression of CYP2E1. | Tremmel R et al. | β | 2016 | β |
| Gene regulation and genetics in neurochemistry, past to future. | Barger SW | β | 2016 | β |
| Genetic analysis of the aquaporin-4 gene for anti-AQP4 antibody-positive neuromyelitis optica in a Japanese population. | Ogasawara M et al. | β | 2016 | β |
| Genetic Association Studies of Suicidal Behavior: A Review of the Past 10βYears, Progress, Limitations, and Future Directions. | Mirkovic B et al. | β | 2016 | β |
| Genetic components in diabetic retinopathy. | Mishra B et al. | β | 2016 | β |
| Genetic predisposition to prostate cancer. | Benafif S et al. | β | 2016 | β |
| Genetics of Diabetic Kidney Disease. | Florez JC | β | 2016 | β |
| Genetics of Parkinson's disease. | Lill CM | β | 2016 | β |
| Genetic Studies on Polycystic Ovary Syndrome. | Zhao H et al. | β | 2016 | β |
| Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility. | Ye BD et al. | β | 2016 | β |
| Genetic variations in the PI3K-PTEN-AKT-mTOR pathway are associated with distant metastasis in nasopharyngeal carcinoma patients treated with intensity-modulated radiation therapy. | Guo Q et al. | β | 2016 | β |
| Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer. | Gong J et al. | β | 2016 | β |
| Genotype Imputation with Millions of Reference Samples. | Browning BL et al. | β | 2016 | β |
| Germline genetic profiling in prostate cancer: latest developments and potential clinical applications. | Ahmed M et al. | β | 2016 | β |
| High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. | Dilthey AT et al. | β | 2016 | β |
| High plasma chemerin is associated with renal dysfunction and predictive for cardiovascular events - Insights from phenotype and genotype characterization. | Leiherer A et al. | β | 2016 | β |
| Hirschsprung's disease: A bridge for science and surgery. | Tam PK | β | 2016 | β |
| How many biological replicates are needed in an RNA-seq experiment and which differential expression tool should you use? | Schurch NJ et al. | β | 2016 | β |
| Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype. | Pasterkamp G et al. | β | 2016 | β |
| Identification of selective sweeps reveals divergent selection between Chinese Holstein and Simmental cattle populations. | Chen M et al. | β | 2016 | β |
| Information recovery from low coverage whole-genome bisulfite sequencing. | Libertini E et al. | β | 2016 | β |
| Interaction between susceptibility loci in cGAS-STING pathway, MHC gene and HPV infection on the risk of cervical precancerous lesions in Chinese population. | Xiao D et al. | β | 2016 | β |
| Linking short tandem repeat polymorphisms with cytosine modifications in human lymphoblastoid cell lines. | Zhang Z et al. | β | 2016 | β |
| MC3R gene polymorphisms are associated with early childhood adiposity gain and infant appetite in an Asian population. | Aris IM et al. | β | 2016 | β |
| Migration Route Out of Africa Unresolved by 225 Egyptian and Ethiopian Whole Genome Sequences. | Shriner D et al. | β | 2016 | β |
| Million Veteran Program: A mega-biobank to study genetic influences on health and disease. | Gaziano JM et al. | β | 2016 | β |
| Molecular genetics of coronary artery disease. | Ozaki K et al. | β | 2016 | β |
| Navigating pleiotropy in precision medicine: pharmacogenes from trauma to behavioral health. | Oberg V et al. | β | 2016 | β |
| Next generation sequencing: implications in personalized medicine and pharmacogenomics. | Rabbani B et al. | β | 2016 | β |
| Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data. | Dunkhase E et al. | β | 2016 | β |
| No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. | Johnson EC et al. | β | 2016 | β |
| Obesity, More than a 'Cosmetic' Problem. Current Knowledge and Future Prospects of Human Obesity Genetics. | Shabana et al. | β | 2016 | β |
| Opportunities and challenges of big data for the social sciences: The case of genomic data. | Liu H et al. | β | 2016 | β |
| Personalized Proteomics: The Future of Precision Medicine. | Duarte TT et al. | β | 2016 | β |
| Perspectives in Polycystic Ovary Syndrome: From Hair to Eternity. | Dunaif A | β | 2016 | β |
| Phasing for medical sequencing using rare variants and large haplotype reference panels. | Sharp K et al. | β | 2016 | β |
| Polymorphisms in the TMEM132D region are associated with panic disorder in HLA-DRB1*13:02-negative individuals of a Japanese population. | Shimada-Sugimoto M et al. | β | 2016 | β |
| Polymorphisms of the TRPV2 and TRPV3 genes associated with fibromyalgia in a Korean population. | Park DJ et al. | β | 2016 | β |
| Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray. | Coleman JR et al. | β | 2016 | β |
| Rapid phenotyping of knockout mice to identify genetic determinants of bone strength. | Freudenthal B et al. | β | 2016 | β |
| Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels. | Boettger LM et al. | β | 2016 | β |
| Research and drug development activities in rare diseases: differences between Japan and Europe regarding influence of prevalence. | Mizoguchi H et al. | β | 2016 | β |
| Signaling in Host-Associated Microbial Communities. | Fischbach MA et al. | β | 2016 | β |
| Single nucleotide polymorphisms in clinics: Fantasy or reality for cancer? | Srinivasan S et al. | β | 2016 | β |
| SLCO1B1 Gene Variations Among Tanzanians, Ethiopians, and Europeans: Relevance for African and Worldwide Precision Medicine. | Aklillu E et al. | β | 2016 | β |
| Sparse Exponential Family Principal Component Analysis. | Lu M et al. | β | 2016 | β |
| Sporadic, Global Linkage Disequilibrium Between Unlinked Segregating Sites. | Skelly DA et al. | β | 2016 | β |
| Structural basis for human PRDM9 action at recombination hot spots. | Patel A et al. | β | 2016 | β |
| The Challenges of Precision Medicine in Obstructive Sleep Apnea. | Khalyfa A et al. | β | 2016 | β |
| The Future of Cardiovascular Epidemiology. | Vasan RS et al. | β | 2016 | β |
| The Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics Approach. | Saeb AT et al. | β | 2016 | β |
| The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants. | Fadista J et al. | β | 2016 | β |
| The Time Scale of Recombination Rate Evolution in Great Apes. | Stevison LS et al. | β | 2016 | β |
| Tools for Predicting the Functional Impact of Nonsynonymous Genetic Variation. | Tang H et al. | β | 2016 | β |
| Toward Optimum Benefit-Risk and Reduced Access Lag For Cancer Drugs in Asia: A Global Development Framework Guided by Clinical Pharmacology Principles. | Venkatakrishnan K et al. | β | 2016 | β |
| Towards precision medicine. | Ashley EA | β | 2016 | β |
| Transcriptional similarity in couples reveals the impact of shared environment and lifestyle on gene regulation through modified cytosines. | Tang K et al. | β | 2016 | β |
| Translating Lung Function Genome-Wide Association Study (GWAS) Findings: New Insights for Lung Biology. | Kheirallah AK et al. | β | 2016 | β |
| Type 2 diabetes: genetic data sharing to advance complex disease research. | Flannick J et al. | β | 2016 | β |
| Uromodulin gene variants and their association with renal function and blood pressure in cats: a pilot study. | Jepson RE et al. | β | 2016 | β |
| Variable Autosomal and X Divergence Near and Far from Genes Affects Estimates of Male Mutation Bias in Great Apes. | Narang P et al. | β | 2016 | β |
| Accurate estimation of haplotype frequency from pooled sequencing data and cost-effective identification of rare haplotype carriers by overlapping pool sequencing. | Cao CC et al. | β | 2015 | β |
| A coalescent-based method for population tree inference with haplotypes. | Wu Y | β | 2015 | β |
| A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population. | Amy M et al. | β | 2015 | β |
| A copy number variation map of the human genome. | Zarrei M et al. | β | 2015 | β |
| Activity of coagulation factor XI in patients with spontaneous miscarriage: the presence of risk alleles. | Sokol J et al. | β | 2015 | β |
| Addressing population-specific multiple testing burdens in genetic association studies. | Sobota RS et al. | β | 2015 | β |
| A genome-wide scan reveals important roles of DNA methylation in human longevity by regulating age-related disease genes. | Xiao FH et al. | β | 2015 | β |
| A genomic portrait of haplotype diversity and signatures of selection in indigenous southern African populations. | Chimusa ER et al. | β | 2015 | β |
| A haplotype map of allohexaploid wheat reveals distinct patterns of selection on homoeologous genomes. | Jordan KW et al. | β | 2015 | β |
| Allele-Selective Transcriptome Recruitment to Polysomes Primed for Translation: Protein-Coding and Noncoding RNAs, and RNA Isoforms. | Mascarenhas R et al. | β | 2015 | β |
| A method to predict the impact of regulatory variants from DNA sequence. | Lee D et al. | β | 2015 | β |
| A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians. | Shim H et al. | β | 2015 | β |
| Analysis of WNT4 polymorphism in Chinese Han women with endometriosis. | Wu Z et al. | β | 2015 | β |
| An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults. | Tong JH et al. | β | 2015 | β |
| An efficient weighted tag SNP-set analytical method in genome-wide association studies. | Yan B et al. | β | 2015 | β |
| A new tool called DISSECT for analysing large genomic data sets using a Big Data approach. | Canela-Xandri O et al. | β | 2015 | β |
| An integrated map of structural variation in 2,504 human genomes. | Sudmant PH et al. | β | 2015 | β |
| A Population Based Study of the Genetic Association between Catecholamine Gene Variants and Spontaneous Low-Frequency Fluctuations in Reaction Time. | Bastiaansen JA et al. | β | 2015 | β |
| A selective review of robust variable selection with applications in bioinformatics. | Wu C et al. | β | 2015 | β |
| A simple procedure for directly obtaining haplotype sequences of diploid genomes. | Noyes HA et al. | β | 2015 | β |
| Association between IPTA gene polymorphisms and hematological abnormalities in hepatitis C virus-infected patients receiving combination therapy. | Hwang JJ et al. | β | 2015 | β |
| Association between the Interaction of Key Genes Involved in Effector T-Cell Pathways and Susceptibility to Develop allergic Rhinitis: A Population-Based Case-Control Association Study. | Zhang Y et al. | β | 2015 | β |
| Association of joint erosion with SLC22A4 gene polymorphisms inconsistently associated with rheumatoid arthritis susceptibility. | Han TU et al. | β | 2015 | β |
| Association of PELI1 polymorphisms in systemic lupus erythematosus susceptibility in a Chinese population. | Chen FR et al. | β | 2015 | β |
| Association of symptoms and severity of rift valley fever with genetic polymorphisms in human innate immune pathways. | Hise AG et al. | β | 2015 | β |
| Association of type 2 diabetes GWAS loci and the risk of Parkinson's and Alzheimer's diseases. | Chung SJ et al. | β | 2015 | β |
| Big data challenges in bone research: genome-wide association studies and next-generation sequencing. | Alonso N et al. | β | 2015 | β |
| Bioinformatics tools for discovery and functional analysis of single nucleotide polymorphisms. | Li L et al. | β | 2015 | β |
| BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures. | Medina-GΓ³mez C et al. | β | 2015 | β |
| Calcineurin orchestrates dimorphic transitions, antifungal drug responses and host-pathogen interactions of the pathogenic mucoralean fungus Mucor circinelloides. | Lee SC et al. | β | 2015 | β |
| Cardiovascular pharmacogenomics; state of current knowledge and implementation in practice. | Shahabi P et al. | β | 2015 | β |
| Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations. | Wu L et al. | β | 2015 | β |
| Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study. | Medina-Gomez C et al. | β | 2015 | β |
| Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest Leaf. | Kang JT et al. | β | 2015 | β |
| Climatic variability, plasticity, and dispersal: A case study from Lake Tana, Ethiopia. | Grove M et al. | β | 2015 | β |
| Clinical implications of copy number variations in autoimmune disorders. | Yim SH et al. | β | 2015 | β |
| Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication. | Beck CR et al. | β | 2015 | β |
| Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. | Nead KT et al. | β | 2015 | β |
| dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsets. | Baron RV et al. | β | 2015 | β |
| De novo assembly of a haplotype-resolved human genome. | Cao H et al. | β | 2015 | β |
| Detecting Genetic Risk Factors for Alzheimer's Disease in Whole Genome Sequence Data via Lasso Screening. | Yang T et al. | β | 2015 | β |
| Development of a forensic identity SNP panel for Indonesia. | Augustinus D et al. | β | 2015 | β |
| DISEASES: text mining and data integration of disease-gene associations. | Pletscher-Frankild S et al. | β | 2015 | β |
| Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. | Cutler DJ et al. | β | 2015 | β |
| Dissecting the genetic structure and admixture of four geographical Malay populations. | Deng L et al. | β | 2015 | β |
| Distinct Transcript Isoforms of the Atypical Chemokine Receptor 1 (ACKR1)/Duffy Antigen Receptor for Chemokines (DARC) Gene Are Expressed in Lymphoblasts and Altered Isoform Levels Are Associated with Genetic Ancestry and the Duffy-Null Allele. | Davis MB et al. | β | 2015 | β |
| Diversity of Mycobacterium tuberculosis across Evolutionary Scales. | O'Neill MB et al. | β | 2015 | β |
| DVWA gene polymorphisms and osteoarthritis. | BravatΓ V et al. | β | 2015 | β |
| Entropic cages for trapping DNA near a nanopore. | Liu X et al. | β | 2015 | β |
| Epidermal growth factor receptor pathway polymorphisms and the prognosis of hepatocellular carcinoma. | Wang W et al. | β | 2015 | β |
| Estimating copy numbers of alleles from population-scale high-throughput sequencing data. | Mimori T et al. | β | 2015 | β |
| Evaluating historical candidate genes for schizophrenia. | Farrell MS et al. | β | 2015 | β |
| Evaluating intra- and inter-individual variation in the human placental transcriptome. | Hughes DA et al. | β | 2015 | β |
| Evaluating the role of admixture in cancer therapy via in vitro drug response and multivariate genome-wide associations. | Jack J et al. | β | 2015 | β |
| Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes. | Li YS et al. | β | 2015 | β |
| Exploring Genetic Susceptibility to Fibromyalgia. | Park DJ et al. | β | 2015 | β |
| Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. | Croteau-Chonka DC et al. | β | 2015 | β |
| Extendable blocking probe in reverse transcription for analysis of RNA variants with superior selectivity. | Ho TH et al. | β | 2015 | β |
| Family-Based Benchmarking of Copy Number Variation Detection Software. | Nutsua ME et al. | β | 2015 | β |
| Genetic analysis of schizophrenia and bipolar disorder reveals polygenicity but also suggests new directions for molecular interrogation. | Neale BM et al. | β | 2015 | β |
| Genetic association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population. | Zhang Y et al. | β | 2015 | β |
| Genetic Diversity and Societally Important Disparities. | Rosenberg NA et al. | β | 2015 | β |
| Genetic epidemiology of coronary artery disease: an Asian Indian perspective. | Jayashree S et al. | β | 2015 | β |
| Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke. | Hanscombe KB et al. | β | 2015 | β |
| Genetic insight into the role of MRAS in coronary artery disease risk. | Liu L et al. | β | 2015 | β |
| Genetic investigations on intracranial aneurysm: update and perspectives. | Bourcier R et al. | β | 2015 | β |
| Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. | Grondin Y et al. | β | 2015 | β |
| Genetic Polymorphisms of IL-17F and TRAF3IP2 Could Be Predictive Factors of the Long-Term Effect of Infliximab against Crohn's Disease. | Urabe S et al. | β | 2015 | β |
| Genetic polymorphisms of PCSK2 are associated with glucose homeostasis and progression to type 2 diabetes in a Chinese population. | Chang TJ et al. | β | 2015 | β |
| [Genetic predisposition and Pediatric Acute Respiratory Distress Syndrome: New tools for genetic study]. | Erranz MB et al. | β | 2015 | β |
| Genetics and brain morphology. | Strike LT et al. | β | 2015 | β |
| Genetics of allergic diseases. | Ortiz RA et al. | β | 2015 | β |
| Genetics of endometriosis. | Rahmioglu N et al. | β | 2015 | β |
| Genetic variants of OCT1 influence glycemic response to metformin in Han Chinese patients with type-2 diabetes mellitus in Shanghai. | Zhou Y et al. | β | 2015 | β |
| Genetic Variations in MicroRNA-Binding Sites Affect MicroRNA-Mediated Regulation of Several Genes Associated With Cardio-metabolic Phenotypes. | Ghanbari M et al. | β | 2015 | β |
| Genetic Variations in the TP53 Pathway in Native Americans Strongly Suggest Adaptation to the High Altitudes of the Andes. | Jacovas VC et al. | β | 2015 | β |
| Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. | Chan Y et al. | β | 2015 | β |
| Genome-wide association of drought-related and biomass traits with HapMap SNPs in Medicago truncatula. | Kang Y et al. | β | 2015 | β |
| Genome-Wide Association Studies and Liver Disease. | Speliotes EK | β | 2015 | β |
| Genome-wide association study in an admixed case series reveals IL12A as a new candidate in BehΓ§et disease. | Kappen JH et al. | β | 2015 | β |
| Genome-wide homozygosity signature and risk of Hodgkin lymphoma. | Sud A et al. | β | 2015 | β |
| Genomic consequences of selection and genome-wide association mapping in soybean. | Wen Z et al. | β | 2015 | β |
| Genomic population structure and prevalence of copy number variations in South African Nguni cattle. | Wang MD et al. | β | 2015 | β |
| Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations. | Hu XS et al. | β | 2015 | β |
| Genomics in rugby union: A review and future prospects. | Heffernan SM et al. | β | 2015 | β |
| Genotyping of common SIRPB1 copy number variant using Paralogue Ratio Test coupled to MALDI-MS quantification. | Royo JL et al. | β | 2015 | β |
| Heterospecific SNP diversity in humans and rhesus macaque (Macaca mulatta). | Ng J et al. | β | 2015 | β |
| High-resolution HLA-A, HLA-B, and HLA-DRB1 haplotype frequencies from the French Bone Marrow Donor Registry. | Gourraud PA et al. | β | 2015 | β |
| Hormone-related pathways and risk of breast cancer subtypes in African American women. | Haddad SA et al. | β | 2015 | β |
| Human aging in the post-GWAS era: further insights reveal potential regulatory variants. | Haider SA et al. | β | 2015 | β |
| Human genetic diversity in the Japanese Archipelago: dual structure and beyond. | Jinam TA et al. | β | 2015 | β |
| Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder. | Tong J et al. | β | 2015 | β |
| Identifying rhesus macaque gene orthologs using heterospecific human CNV probes. | Ng J et al. | β | 2015 | β |
| iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing. | Yamaguchi-Kabata Y et al. | β | 2015 | β |
| Immunogenetic influences on acquisition of HIV-1 infection: consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2). | Li X et al. | β | 2015 | β |
| Immunogenetics of rheumatoid arthritis: Understanding functional implications. | Messemaker TC et al. | β | 2015 | β |
| Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine. | Yang C et al. | β | 2015 | β |
| Improved genome inference in the MHC using a population reference graph. | Dilthey A et al. | β | 2015 | β |
| Inference of gorilla demographic and selective history from whole-genome sequence data. | McManus KF et al. | β | 2015 | β |
| Inferring positive selection in humans from genomic data. | Wollstein A et al. | β | 2015 | β |
| Integrating phenotypic small-molecule profiling and human genetics: the next phase in drug discovery. | Johannessen CM et al. | β | 2015 | β |
| Jackknife-based gene-gene interactiontests for untyped SNPs. | Song M | β | 2015 | β |
| Leveraging Multi-ethnic Evidence for Mapping Complex Traits in Minority Populations: An Empirical Bayes Approach. | Coram MA et al. | β | 2015 | β |
| Linkage disequilibrium network analysis (LDna) gives a global view of chromosomal inversions, local adaptation and geographic structure. | Kemppainen P et al. | β | 2015 | β |
| Linking Genes to Cardiovascular Diseases: Gene Action and Gene-Environment Interactions. | Pasipoularides A | β | 2015 | β |
| Mapping asthma-associated variants in admixed populations. | Mersha TB | β | 2015 | β |
| Methods: for studying pharmacogenetic profiles of combination chemotherapeutic drugs. | Di Paolo A et al. | β | 2015 | β |
| Mitochondrial Aging and Physical Decline: Insights From Three Generations of Women. | Hebert SL et al. | β | 2015 | β |
| Museum samples reveal rapid evolution by wild honey bees exposed to a novel parasite. | Mikheyev AS et al. | β | 2015 | β |
| Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease. | Al-Allaf FA et al. | β | 2015 | β |
| NNK reduction pathway gene polymorphisms and risk of lung cancer. | Modesto JL et al. | β | 2015 | β |
| Obesity-Related Genetic Variants and their Associations with Physical Activity. | Lee H et al. | β | 2015 | β |
| Penalized multimarker vs. single-marker regression methods for genome-wide association studies of quantitative traits. | Yi H et al. | β | 2015 | β |
| Pharmacogenomic assessment of Mexican and Peruvian populations. | Marsh S et al. | β | 2015 | β |
| PIK3CA rs7640662 (C/G) single nucleotide polymorphism lacks association with breast cancer cases in Persians. | Mir A et al. | β | 2015 | β |
| Posterior predictive checks to quantify lack-of-fit in admixture models of latent population structure. | Mimno D et al. | β | 2015 | β |
| Precision Medicine and Non-Colorectal Cancer Liver Metastases: Fiction or Reality? | Liakopoulou E et al. | β | 2015 | β |
| Predicting genome-wide DNA methylation using methylation marks, genomic position, and DNA regulatory elements. | Zhang W et al. | β | 2015 | β |
| Progress and promise in understanding the genetic basis of common diseases. | Price AL et al. | β | 2015 | β |
| Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations. | Zeevi DA et al. | β | 2015 | β |
| Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent. | Kuo JZ et al. | β | 2015 | β |
| Rare variant association studies: considerations, challenges and opportunities. | Auer PL et al. | β | 2015 | β |
| Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals. | Nagasaki M et al. | β | 2015 | β |
| Receptor Polymorphism and Genomic Structure Interact to Shape Bitter Taste Perception. | Roudnitzky N et al. | β | 2015 | β |
| RiceVarMap: a comprehensive database of rice genomic variations. | Zhao H et al. | β | 2015 | β |
| Role of six single nucleotide polymorphisms, risk factors in coronary disease, in OLR1 alternative splicing. | Tejedor JR et al. | β | 2015 | β |
| SCAN database: facilitating integrative analyses of cytosine modification and expression QTL. | Zhang W et al. | β | 2015 | β |
| Selecting causal genes from genome-wide association studies via functionally coherent subnetworks. | TaΕan M et al. | β | 2015 | β |
| Sex hormones and macronutrient metabolism. | Comitato R et al. | β | 2015 | β |
| Sex-Specific Parental Effects on Offspring Lipid Levels. | Predazzi IM et al. | β | 2015 | β |
| Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. | Moser G et al. | β | 2015 | β |
| Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications. | Huang L et al. | β | 2015 | β |
| Single-molecule super-resolution imaging of chromosomes and in situ haplotype visualization using Oligopaint FISH probes. | Beliveau BJ et al. | β | 2015 | β |
| Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing. | Jiang Y et al. | β | 2015 | β |
| SNP imputation bias reduces effect size determination. | Khankhanian P et al. | β | 2015 | β |
| TAS2R bitter taste receptors regulate thyroid function. | Clark AA et al. | β | 2015 | β |
| The genetic architecture of gene expression levels in wild baboons. | Tung J et al. | β | 2015 | β |
| The genetic basis of population fecundity prediction across multiple field populations of Nilaparvata lugens. | Sun ZX et al. | β | 2015 | β |
| The genome as pharmacopeia: association of genetic dose with phenotypic response. | Wadhawan S et al. | β | 2015 | β |
| The genomic landscape of human immune-mediated diseases. | Wu X et al. | β | 2015 | β |
| The Mouse Universal Genotyping Array: From Substrains to Subspecies. | Morgan AP et al. | β | 2015 | β |
| The relationships between IFNL4 genotype, intrahepatic interferon-stimulated gene expression and interferon treatment response differs in HCV-1 compared with HCV-3. | Holmes JA et al. | β | 2015 | β |
| The role of genetic variation across IL-1Ξ², IL-2, IL-6, and BDNF in antipsychotic-induced weight gain. | Fonseka TM et al. | β | 2015 | β |
| Toll-like receptor (TLR4) Asp299Gly and Thr399Ile polymorphisms in relation to clinical falciparum malaria among Nigerian children: a multisite cross-sectional immunogenetic study in Lagos. | Iwalokun BA et al. | β | 2015 | β |
| Understanding inflammatory bowel disease via immunogenetics. | de Lange KM et al. | β | 2015 | β |
| Unique characteristics of the Ainu population in Northern Japan. | Jinam TA et al. | β | 2015 | β |
| Unravelling the genetic history of Negritos and indigenous populations of Southeast Asia. | Aghakhanian F et al. | β | 2015 | β |
| What is the Contribution of Genetics to Periodontal Risk? | Loos BG et al. | β | 2015 | β |
| 2013 William Allan Award: My multifactorial journey. | Chakravarti A | β | 2014 | β |
| A bioinformatics workflow for detecting signatures of selection in genomic data. | Cadzow M et al. | β | 2014 | β |
| A Comparison of the Pharmacokinetics and Drug Safety Among East Asian Populations. | Oishi M et al. | β | 2014 | β |
| A comprehensive association analysis confirms ZMIZ1 to be a susceptibility gene for vitiligo in Chinese population. | Sun Y et al. | β | 2014 | β |
| Advances in individualized and regenerative medicine. | Blum HE | β | 2014 | β |
| A general approach for haplotype phasing across the full spectrum of relatedness. | O'Connell J et al. | β | 2014 | β |
| A genome-wide association meta-analysis of preschool internalizing problems. | Benke KS et al. | β | 2014 | β |
| A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease. | Hanchard NA et al. | β | 2014 | β |
| Ancestry-informative markers for African Americans based on the Affymetrix Pan-African genotyping array. | Zhang X et al. | β | 2014 | β |
| An effective haplotype assembly algorithm based on hypergraph partitioning. | Chen X et al. | β | 2014 | β |
| An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval. | Kapoor A et al. | β | 2014 | β |
| Angiopoietin-like protein 4 significantly predicts future cardiovascular events in coronary patients. | Muendlein A et al. | β | 2014 | β |
| Applying genome-wide gene-based expression quantitative trait locus mapping to study population ancestry and pharmacogenetics. | Yang HC et al. | β | 2014 | β |
| ArchiLD: hierarchical visualization of linkage disequilibrium in human populations. | Melchiotti R et al. | β | 2014 | β |
| A reference genome for common bean and genome-wide analysis of dual domestications. | Schmutz J et al. | β | 2014 | β |
| A replication study confirms the association of GWAS-identified SNPs at MICB and PLCE1 in Thai patients with dengue shock syndrome. | Dang TN et al. | β | 2014 | β |
| Association between the melanopsin gene polymorphism OPN4*Ile394Thr and sleep/wake timing in Japanese university students. | Lee SI et al. | β | 2014 | β |
| Association claims in the sequencing era. | Pulit SL et al. | β | 2014 | β |
| Association of CD209 and CD209L polymorphisms with tuberculosis infection in a Northeastern Brazilian population. | da Silva RC et al. | β | 2014 | β |
| Association of IL33-IL-1 receptor-like 1 (IL1RL1) pathway polymorphisms with wheezing phenotypes and asthma in childhood. | Savenije OE et al. | β | 2014 | β |
| Association of leptin/receptor and TNF-Ξ± gene variants with adolescent obesity in Malaysia. | Ng ZY et al. | β | 2014 | β |
| Association of the endothelial protein C receptor (PROCR) rs867186-G allele with protection from severe malaria. | Naka I et al. | β | 2014 | β |
| Autoimmune diseases association study with the KIAA1109-IL2-IL21 region in a Tunisian population. | Bouzid D et al. | β | 2014 | β |
| Bayesian inference of local trees along chromosomes by the sequential Markov coalescent. | Zheng C et al. | β | 2014 | β |
| Characterizing genetic variants for clinical action. | Ramos EM et al. | β | 2014 | β |
| Chemistry, biology, and medicine of fluorescent nanomaterials and related systems: new insights into biosensing, bioimaging, genomics, diagnostics, and therapy. | Yao J et al. | β | 2014 | β |
| Clinical utility of pharmacogenomics in the management of hepatitis C. | Trinks J et al. | β | 2014 | β |
| Comparison of genotype clustering tools with rare variants. | Perreault LP et al. | β | 2014 | β |
| Comprehensive assessment of the association between XPD rs13181 polymorphism and lung cancer risk. | Wu HY et al. | β | 2014 | β |
| Computational identification and analysis of functional polymorphisms involved in the activation and detoxification genes implicated in endometriosis. | Panda R et al. | β | 2014 | β |
| Contrasting X-linked and autosomal diversity across 14 human populations. | Arbiza L et al. | β | 2014 | β |
| CR1, ABCA7, and APOE genes affect the features of cognitive impairment in Alzheimer's disease. | Chung SJ et al. | β | 2014 | β |
| Crossing-over in a hypervariable species preferentially occurs in regions of high local similarity. | Seplyarskiy VB et al. | β | 2014 | β |
| Digging up the human genome: current progress in deciphering adverse drug reactions. | Su SC et al. | β | 2014 | β |
| Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing. | Liu Y et al. | β | 2014 | β |
| Disrupted human-pathogen co-evolution: a model for disease. | Kodaman N et al. | β | 2014 | β |
| DNA mismatch repair MSH2 gene-based SNP associated with different populations. | Abduljaleel Z et al. | β | 2014 | β |
| Elucidating the genotype-phenotype relationships and network perturbations of human shared and specific disease genes from an evolutionary perspective. | Begum T et al. | β | 2014 | β |
| eMERGEing progress in genomics-the first seven years. | Crawford DC et al. | β | 2014 | β |
| Empirical prediction of genomic susceptibilities for multiple cancer classes. | Kim M et al. | β | 2014 | β |
| Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. | Fang H et al. | β | 2014 | β |
| Estrogen receptor 2 gene polymorphism in idiopathic scoliosis. | Kotwicki T et al. | β | 2014 | β |
| Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in Japan. | Minari J et al. | β | 2014 | β |
| Exploiting population samples to enhance genome-wide association studies of disease. | Kaufman S et al. | β | 2014 | β |
| Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. | Tomlinson MJ et al. | β | 2014 | β |
| FLAGS, frequently mutated genes in public exomes. | Shyr C et al. | β | 2014 | β |
| Genetic analysis of an allergic rhinitis cohort reveals an intercellular epistasis between FAM134B and CD39. | Melchiotti R et al. | β | 2014 | β |
| Genetic ancestry of participants in the National Children's Study. | Smith EN et al. | β | 2014 | β |
| Genetic bio-ancestry and social construction of racial classification in social surveys in the contemporary United States. | Guo G et al. | β | 2014 | β |
| Genetic determinants of pulmonary fibrosis: evolving concepts. | Spagnolo P et al. | β | 2014 | β |
| Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians. | Figueiredo JC et al. | β | 2014 | β |
| Genetics of cognition in epilepsy. | Busch RM et al. | β | 2014 | β |
| Genetics of polycystic ovary syndrome. | Welt CK et al. | β | 2014 | β |
| Genetic susceptibility to type 2 diabetes and obesity: follow-up of findings from genome-wide association studies. | Basile KJ et al. | β | 2014 | β |
| Genetic variant in IL33 is associated with susceptibility to rheumatoid arthritis. | Li C et al. | β | 2014 | β |
| Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. | Rahmioglu N et al. | β | 2014 | β |
| Genetic variation and adaptation in Africa: implications for human evolution and disease. | Gomez F et al. | β | 2014 | β |
| Genetic variation of the whole ICAM4 gene in Caucasians and African Americans. | Srivastava K et al. | β | 2014 | β |
| Genome evolution by matrix algorithms: cellular automata approach to population genetics. | Qiu S et al. | β | 2014 | β |
| Genome-scale neurogenetics: methodology and meaning. | McCarroll SA et al. | β | 2014 | β |
| Genome-wide analysis of cold adaptation in indigenous Siberian populations. | Cardona A et al. | β | 2014 | β |
| Genome-wide association studies of atopic dermatitis. | Tamari M et al. | β | 2014 | β |
| Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania. | Mtatiro SN et al. | β | 2014 | β |
| Genome-wide detection of copy number variations among diverse horse breeds by array CGH. | Wang W et al. | β | 2014 | β |
| Genome-wide diet-gene interaction analyses for risk of colorectal cancer. | Figueiredo JC et al. | β | 2014 | β |
| Genome-wide scans of genetic variants for psychophysiological endophenotypes: a methodological overview. | Iacono WG et al. | β | 2014 | β |
| Genomic medicine: health care issues and the unresolved ethical and social dilemmas. | Idemyor V | β | 2014 | β |
| Guidelines for the tetra-primer ARMS-PCR technique development. | Medrano RF et al. | β | 2014 | β |
| GWAS to Sequencing: Divergence in Study Design and Analysis. | King CR et al. | β | 2014 | β |
| Human genetic research, race, ethnicity and the labeling of populations: recommendations based on an interdisciplinary workshop in Japan. | Takezawa Y et al. | β | 2014 | β |
| Human genetics' 50th anniversary issue. | Hudson TJ | β | 2014 | β |
| Human genetics of diabetic retinopathy. | Tang ZH et al. | β | 2014 | β |
| Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. | Colonna V et al. | β | 2014 | β |
| Identification of allelic imbalance with a statistical model for subtle genomic mosaicism. | Xia R et al. | β | 2014 | β |
| Identification of APOH polymorphisms as common genetic risk factors for venous thrombosis in the Chinese population. | Tang L et al. | β | 2014 | β |
| Impact of range expansions on current human genomic diversity. | Sousa V et al. | β | 2014 | β |
| Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus. | Black HA et al. | β | 2014 | β |
| Innate and adaptive immune responses in HCV infections. | Heim MH et al. | β | 2014 | β |
| Insertion-deletions burden in copy number polymorphisms of the Tibetan population. | Veerappa AM et al. | β | 2014 | β |
| Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. | Cabrera S et al. | β | 2014 | β |
| Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 1. Fundamental Concepts in Molecular Genetics. | Li A et al. | β | 2014 | β |
| Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. | Mokry FB et al. | β | 2014 | β |
| Linking the genetic architecture of cytosine modifications with human complex traits. | Zhang X et al. | β | 2014 | β |
| Maximum likelihood model based on minor allele frequencies and weighted Max-SAT formulation for haplotype assembly. | Mousavi SR et al. | β | 2014 | β |
| Methylation potential associated with diet, genotype, protein, and metabolite levels in the Delta Obesity Vitamin Study. | Monteiro JP et al. | β | 2014 | β |
| Molecular and genetic epidemiology of cancer in low- and medium-income countries. | Malhotra J | β | 2014 | β |
| Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives. | Caignard G et al. | β | 2014 | β |
| NOD2 and CCDC122-LACC1 genes are associated with leprosy susceptibility in Brazilians. | Sales-Marques C et al. | β | 2014 | β |
| Novel H3K4me3 marks are enriched at human- and chimpanzee-specific cytogenetic structures. | Giannuzzi G et al. | β | 2014 | β |
| Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia. | Mokhtar SS et al. | β | 2014 | β |
| Obesity-associated gene FTO rs9939609 polymorphism in relation to the risk of tuberculosis. | Feng Y et al. | β | 2014 | β |
| On the unfounded enthusiasm for soft selective sweeps. | Jensen JD | β | 2014 | β |
| OptiType: precision HLA typing from next-generation sequencing data. | Szolek A et al. | β | 2014 | β |
| Ovarian aging and premature ovarian failure. | SΓΌkΓΌr YE et al. | β | 2014 | β |
| Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. | PΓ©rez-Palma E et al. | β | 2014 | β |
| Phenotype-based cell-specific metabolic modeling reveals metabolic liabilities of cancer. | Yizhak K et al. | β | 2014 | β |
| Polymorphisms in the DNA repair gene ERCC2/XPD and breast cancer risk: a HapMap-based case-control study among Han Women in a Chinese less-developed area. | Wang T et al. | β | 2014 | β |
| Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance. | Choudhury A et al. | β | 2014 | β |
| Predicting DNA methylation level across human tissues. | Ma B et al. | β | 2014 | β |
| Purifying selection in deeply conserved human enhancers is more consistent than in coding sequences. | De Silva DR et al. | β | 2014 | β |
| Race, common genetic variation, and therapeutic response disparities in heart failure. | Taylor MR et al. | β | 2014 | β |
| Rare and low-frequency variants in human common diseases and other complex traits. | Lettre G | β | 2014 | β |
| Rare-variant association analysis: study designs and statistical tests. | Lee S et al. | β | 2014 | β |
| Single Nucleotide Polymorphisms in Osteogenic Genes in Atrophic Delayed Fracture-Healing: A Preliminary Investigation. | Sathyendra V et al. | β | 2014 | β |
| Statistical power and significance testing in large-scale genetic studies. | Sham PC et al. | β | 2014 | β |
| Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection. | Herrera-Ramos E et al. | β | 2014 | β |
| Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. | Woltmann A et al. | β | 2014 | β |
| The challenges, advantages and future of phenome-wide association studies. | Hebbring SJ | β | 2014 | β |
| The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort. | Shigemizu D et al. | β | 2014 | β |
| The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and geneβenvironment interactions. | Angstadt AY et al. | β | 2014 | β |
| The effects of socioeconomic status, clinical factors, and genetic ancestry on pulmonary tuberculosis disease in northeastern Mexico. | Young BN et al. | β | 2014 | β |
| The evolution of comparative genomics. | Mullikin JC | β | 2014 | β |
| The genomic architecture of population divergence between subspecies of the European rabbit. | Carneiro M et al. | β | 2014 | β |
| The impact of large-scale genomic methods in orthopaedic disorders: insights from genome-wide association studies. | Paria N et al. | β | 2014 | β |
| The impact of the human genome project on complex disease. | Bailey JN et al. | β | 2014 | β |
| The marriage of quantitative genetics and cell biology: a novel screening approach reveals people have genetically encoded variation in microtubule stability. | Ko DC et al. | β | 2014 | β |
| The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia. | Deng L et al. | β | 2014 | β |
| The synapse in schizophrenia. | Pocklington AJ et al. | β | 2014 | β |
| Variants of a Thermus aquaticus DNA polymerase with increased selectivity for applications in allele- and methylation-specific amplification. | Drum M et al. | β | 2014 | β |
| Variation block-based genomics method for crop plants. | Kim YH et al. | β | 2014 | β |
| Variation in genes related to hepatic lipid metabolism and changes in waist circumference and body weight. | Meidtner K et al. | β | 2014 | β |
| Who are the Okinawans? Ancestry, genome diversity, and implications for the genetic study of human longevity from a geographically isolated population. | Bendjilali N et al. | β | 2014 | β |
| Whole-genome sequence variation, population structure and demographic history of the Dutch population. | Genome of the Netherlands Consortium | β | 2014 | β |
| Widespread signals of convergent adaptation to high altitude in Asia and america. | Foll M et al. | β | 2014 | β |