The International HapMap Project.
paper
Cited
Public
Unavailable
- Authors
- International HapMap Consortium
- Year
- 2003
- Journal
- Nature
- PMID
- 14685227
- DOI
- 10.1038/nature02168
The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with ancestry from parts of Africa, Asia and Europe. The HapMap will allow the discovery of sequence variants that affect common disease, will facilitate development of diagnostic tools, and will enhance our ability to choose targets for therapeutic intervention.
No figures extracted from this document.
No chunks β full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
Not in any collection.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Association of MMP-2 and MMP-9 Polymorphisms and the Pathogenesis of Childhood Burkitt's Lymphoma. | da Silva EF et al. | β | 2026 | β |
| Databases, Biobanks and International Consortia: Major Resources for Human Population Genomics and Biological Anthropology. | Aguado S et al. | β | 2026 | β |
| Defining Genetic Ancestry: Implications for Nurses. | Jimenez A et al. | β | 2026 | β |
| eQTL analysis: A bridge from genome to mechanism. | Jia Z et al. | β | 2026 | β |
| Exploring the Genetic Overlap Between Metabolic Traits and Anorexia Nervosa. | Adams DM et al. | β | 2026 | β |
| Functional significance of NLRP3 polymorphisms in mild cognitive impairment. | Gao R et al. | β | 2026 | β |
| GPU-accelerated linkage disequilibrium scans reveal non-independent assortment of human non-homologous chromosomes. | Lv W et al. | β | 2026 | β |
| Large-scale dependent multiple testing via higher-order hidden Markov models. | Li C et al. | β | 2026 | β |
| Leveraging low-cost short-read sequencing: revolutionizing complex trait genetics. | Ruckman SN et al. | β | 2026 | β |
| Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity. | Cappadona C et al. | β | 2026 | β |
| Multiple-testing corrections in case-control studies using identity-by-descent segments. | Temple SD et al. | β | 2026 | β |
| Population-scale sequencing resolves determinants of persistent EBV DNA. | Nyeo SS et al. | β | 2026 | β |
| Predicting enviromically adapted varieties with big data. | Gogna A et al. | β | 2026 | β |
| rs6971 TSPO polymorphism in Parkinson's disease. | Patel B et al. | β | 2026 | β |
| Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic review. | Liu S et al. | β | 2025 | β |
| An Ocular Gene-Set Expression Library for Heritability Partition and Cell Line Enrichment Analyses. | Hysi PG et al. | β | 2025 | β |
| A polygenic score for height identifies an unmeasured genetic predisposition among pediatric patients with idiopathic short stature. | Shelley JP et al. | β | 2025 | β |
| A privacy-preserving HLA imputation method with homomorphic encryption. | Kim H et al. | β | 2025 | β |
| A reinforcement learning-based approach for dynamic privacy protection in genomic data sharing beacons. | Poorghaffar Aghdam M et al. | β | 2025 | β |
| A structured coalescent model reveals deep ancestral structure shared by all modern humans. | Cousins T et al. | β | 2025 | β |
| Beacon Reconstruction Attack: Reconstruction of genomes in genomic data-sharing beacons using summary statistics. | Saleem K et al. | β | 2025 | β |
| Boosting the Power of Rare Variant Association Studies by Imputation Using Large-scale Sequencing Population. | Dai ζ΄ζ―ε² J et al. | β | 2025 | β |
| Brain-wide pleiotropy investigation of alcohol drinking and tobacco smoking behaviors. | Deiana G et al. | β | 2025 | β |
| Characterisation of identity-informative genetic markers in the Australian population with European ancestry. | Watson JL et al. | β | 2025 | β |
| Characterizing features affecting local ancestry inference performance in admixed populations. | Honorato-Mauer J et al. | β | 2025 | β |
| Community and bioethicists' perspectives on iPSC research with biobanked samples collected using broad consent. | Ikhane PA et al. | β | 2025 | β |
| Complex genetic variation in nearly complete human genomes. | Logsdon GA et al. | β | 2025 | β |
| Determinant-based grouping of SNPs and its application for detecting disease-associated genomic loci. | Khvorykh G et al. | β | 2025 | β |
| Direct assessment of hereditary hemochromatosis in preimplantation genetic testing. | Zhang Q et al. | β | 2025 | β |
| Dynamic clustering of genomics cohorts beyond race, ethnicity-and ancestry. | Mohsen H et al. | β | 2025 | β |
| EQTL analyses are a formidable tool to define the immunogenetic mechanisms underpinning Spondyloarthropathies. | Vecellio M et al. | β | 2025 | β |
| Estimating disorder probability based on polygenic prediction using the BPC approach. | Uffelmann E et al. | β | 2025 | β |
| Estimating effective population size trajectories from time-series identity-by-descent segments. | Huang Y et al. | β | 2025 | β |
| Evaluating Kinship Estimation Methods for Reduced-Representation SNP Data in Non-model Species. | McMaster ES et al. | β | 2025 | β |
| Expanding biobank pharmacogenomics through machine learning calls of structural variation. | Vanderwerff B et al. | β | 2025 | β |
| FoundationOne CDx and FoundationOne Heme Detect Epstein-Barr Virus with High Sensitivity and Specificity. | Honecker J et al. | β | 2025 | β |
| Functional Polymorphisms Regulate FOXO1 Transcript Expression and Contribute to the Risk and Symptom Severity of HDM-Induced Allergic Rhinitis. | Sio YY et al. | β | 2025 | β |
| Genetic and environmental contributions to individual differences in visual attention and oculomotor control in early infancy. | Siqueiros-Sanchez M et al. | β | 2025 | β |
| Genetic Similarity Clustering Using the UK Biobank as a Reference Dataset. | Le NQ et al. | β | 2025 | β |
| Genetic variants in the CD59 gene: An exploratory study of large genome databases. | Srivastava K et al. | β | 2025 | β |
| Human de novo mutation rates from a four-generation pedigree reference. | Porubsky D et al. | β | 2025 | β |
| IGLoo enables comprehensive analysis and assembly of immunoglobulin heavy-chain loci in lymphoblastoid cell lines using PacBio high-fidelity reads. | Lin MJ et al. | β | 2025 | β |
| Importance of genetic ancestry in pharmacogenomics for precision medicine. | Venkatesh R et al. | β | 2025 | β |
| Interaction Between the <i>UCP2</i> rs659366 Polymorphism and Dietary Capsaicin Intake in Relation to the Inflammatory State in Mexican Adults. | Sobrevilla-Navarro AA et al. | β | 2025 | β |
| Knockoff procedure improves susceptibility gene identifications in conditional transcriptome-wide association studies. | Zhang X et al. | β | 2025 | β |
| Local ancestry-informed GWAS of warfarin dose requirement in African Americans identifies a CYP2C19 splicing QTL. | Singh A et al. | β | 2025 | β |
| Male infertility and its ties to next generation sequencing as a new forward path to definite diagnoses. | Afkari M et al. | β | 2025 | β |
| Methods for Chromosome-Scale Haplotype Reconstruction. | Garg S | β | 2025 | β |
| Multiancestry Transcriptome-Wide Association Study Identifies Candidate Genes Associated with Hepatoblastoma. | Xie T et al. | β | 2025 | β |
| Multi-omics in Allergic Rhinitis: Mechanism Dissection and Precision Medicine. | Hao Y et al. | β | 2025 | β |
| Multiple-testing corrections in selection scans using identity-by-descent segments. | Temple SD et al. | β | 2025 | β |
| NLRP3 genetic variants and their impact on psoriasis susceptibility, severity, and risk of psoriatic arthritis. | Moreira CR et al. | β | 2025 | β |
| No evidence of a causal relationship between negative emotions and glaucoma: evidence triangulation from genetic correlation, Mendelian randomisation and colocalisation. | Qi J et al. | β | 2025 | β |
| ntRoot: computational inference of human ancestry at scale from genomic data. | Warren RL et al. | β | 2025 | β |
| Obstructive sleep apnea mediates genetic risk of Diabetes Mellitus in Hispanic and Latino communities. | Hrytsenko Y et al. | β | 2025 | β |
| Order from entropy: big data from FAIR data cohorts in the digital age of plant breeding. | Gogna A et al. | β | 2025 | β |
| Perspectives and opportunities in forensic human, animal, and plant integrative genomics in the Pangenome era. | He G et al. | β | 2025 | β |
| Phased genome assemblies and pangenome graphs of human populations of Japan and Saudi Arabia. | Kulmanov M et al. | β | 2025 | β |
| Polaris: Polarization of ancestral and derived polymorphic alleles for inferences of extended haplotype homozygosity in human populations. | Lisi A et al. | β | 2025 | β |
| Proteogenomic Profiling of Treatment-NaΓ―ve Metastatic Malignant Melanoma. | Kuras M et al. | β | 2025 | β |
| Sparse multitask group Lasso for genome-wide association studies. | Nouira A et al. | β | 2025 | β |
| Striving Towards Equity in Cardiovascular Genomics Research. | Jurado VΓ©lez J et al. | β | 2025 | β |
| The evolution of dbSNP: 25 years of impact in genomic research. | Phan L et al. | β | 2025 | β |
| The evolution of interdisciplinarity and internationalization in scientific journals. | Zhou H et al. | β | 2025 | β |
| The Fortunes of Genomic Medicine: A Quarter Century of Promise. | Sturdy S | β | 2025 | β |
| The genetics of motor neuron disease in New Zealand. | Mrkela M et al. | β | 2025 | β |
| The Genomics Revolution Drives a New Era in Entomology. | Li F et al. | β | 2025 | β |
| The impact of long non-coding RNA <i>HOTTIP</i> genetic variants on oral cancer progression and clinicopathological characteristics. | Chen PJ et al. | β | 2025 | β |
| The mutational landscape and functional effects of noncoding ultraconserved elements in human cancers. | Bayraktar R et al. | β | 2025 | β |
| The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals. | Wang LY et al. | β | 2025 | β |
| The proteogenomic landscape of the human kidney and implications for cardio-kidney-metabolic health. | Hirohama D et al. | β | 2025 | β |
| Transcriptomic analysis of iPSC-derived endothelium reveals adaptations to high altitude hypoxia in energy metabolism and inflammation. | Gray OA et al. | β | 2025 | β |
| Uterine fibroids show evidence of shared genetic architecture with blood pressure traits. | Akerele AT et al. | β | 2025 | β |
| Voices of Nanomedicine: Blueprint Guidelines for Collaboration in Addressing Global Unmet Medical Needs. | Prasad R et al. | β | 2025 | β |
| Workforce Development in Genomic Data Science for Health: A Worldview. | Lukhele ST et al. | β | 2025 | β |
| X-cross/over: a web tool for graph-based estimation of meiotic crossover events in plants. | Makai S et al. | β | 2025 | β |
| A genetic survey of patients with familial idiopathic intracranial hypertension residing in a Middle Eastern village: genetic association study. | Berkowitz E et al. | β | 2024 | β |
| A genome-wide association study of neonatal metabolites. | He Q et al. | β | 2024 | β |
| A genotype imputation reference panel specific for native Southeast Asian populations. | Cengnata A et al. | β | 2024 | β |
| AGIDB: a versatile database for genotype imputation and variant decoding across species. | Zhang K et al. | β | 2024 | β |
| Allele-specific DNA demethylation editing leads to stable upregulation of allele-specific gene expression. | Rajaram N et al. | β | 2024 | β |
| A multi-regional human brain atlas of chromatin accessibility and gene expression facilitates promoter-isoform resolution genetic fine-mapping. | Dong P et al. | β | 2024 | β |
| Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population. | Nasir Hashmi A et al. | β | 2024 | β |
| Association of tyrosine kinase 2 polymorphisms with susceptibility to microscopic polyangiitis in a Guangxi population. | Yang B et al. | β | 2024 | β |
| A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. | Jermy B et al. | β | 2024 | β |
| BEATRICE: Bayesian fine-mapping from summary data using deep variational inference. | Ghosal S et al. | β | 2024 | β |
| Beyond genes-for-behaviour: The potential for genomics to resolve long-standing questions in avian brood parasitism. | RΓΆnkΓ€ K et al. | β | 2024 | β |
| Beyond the Human Genome Project: The Age of Complete Human Genome Sequences and Pangenome References. | Taylor DJ et al. | β | 2024 | β |
| Biological basis of extensive pleiotropy between blood traits and cancer risk. | Pardo-Cea MA et al. | β | 2024 | β |
| Biostatistical Aspects of Whole Genome Sequencing Studies: Preprocessing and Quality Control. | Betschart RO et al. | β | 2024 | β |
| Carl von LinnΓ©: The Development of the Idea of Binomial Nomenclature. | Yucesan E | β | 2024 | β |
| Cell-Based Therapy and Genome Editing as Emerging Therapeutic Approaches to Treat Rheumatoid Arthritis. | Chasov V et al. | β | 2024 | β |
| Cell type and dynamic state govern genetic regulation of gene expression in heterogeneous differentiating cultures. | Popp JM et al. | β | 2024 | β |
| Collecting baleen whale blow samples by drone: A minimally intrusive tool for conservation genetics. | O'Mahony ΓN et al. | β | 2024 | β |
| Convergence of the dysregulated regulome in schizophrenia with polygenic risk and evolutionarily constrained enhancers. | Dong P et al. | β | 2024 | β |
| Cross-population applications of genomics to understand the risk of multifactorial traits involving inflammation and immunity. | Alamad B et al. | β | 2024 | β |
| Data sharing ethics toolkit: The Human Cell Atlas. | Kirby E et al. | β | 2024 | β |
| Detection of circulating tumor DNA by tumor-informed whole-genome sequencing enables prediction of recurrence in stage III colorectal cancer patients. | Frydendahl A et al. | β | 2024 | β |
| Dopamine signaling enriched striatal gene set predicts striatal dopamine synthesis and physiological activity in vivo. | Sportelli L et al. | β | 2024 | β |
| Endotypes of Paediatric Cough-Do They Exist and Finding New Techniques to Improve Clinical Outcomes. | O'Farrell HE et al. | β | 2024 | β |
| Evaluation of the Copy Number Variants and Single-Nucleotide Polymorphisms of <i>ABCA3</i> in Newborns with Respiratory Distress Syndrome-A Pilot Study. | Anciuc-Crauciuc M et al. | β | 2024 | β |
| Exploring factors impacting haplotype-based noninvasive prenatal diagnosis for single-gene recessive disorders. | Kong L et al. | β | 2024 | β |
| Flexible and cost-effective genomic surveillance of P. falciparum malaria with targeted nanopore sequencing. | de Cesare M et al. | β | 2024 | β |
| From Omics to Multi-Omics: A Review of Advantages and Tradeoffs. | Hayes CN et al. | β | 2024 | β |
| Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. | Suzuki K et al. | β | 2024 | β |
| Genetic variation analysis of Guanling cattle based on whole-genome resequencing. | Xu L et al. | β | 2024 | β |
| Genome-wide association meta-analysis identifies two novel loci associated with dental caries. | Nogawa S et al. | β | 2024 | β |
| Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors. | Olofsson IA et al. | β | 2024 | β |
| Genome-Wide Genetic Associations Prioritize Evaluation of Causal Mechanisms of Atherosclerotic Disease Risk. | Quertermous T et al. | β | 2024 | β |
| Genomic and physiological mechanisms of high-altitude adaptation in Ethiopian highlanders: a comparative perspective. | Seifu WD et al. | β | 2024 | β |
| Genomic reproducibility in the bioinformatics era. | Baykal PI et al. | β | 2024 | β |
| Genotype-based "virtual" metabolomics in a clinical biobank identifies novel metabolite-disease associations. | Bagheri M et al. | β | 2024 | β |
| Higher Genetic Risk for Type 2 Diabetes Is Associated With a Faster Decline of Ξ²-Cell Function in an East Asian Population. | Lee H et al. | β | 2024 | β |
| Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma. | Ma M et al. | β | 2024 | β |
| Host genetics and microbiota data analysis in colorectal cancer research. | GonzΓ‘lez A et al. | β | 2024 | β |
| Human gene regulatory evolution is driven by the divergence of regulatory element function in both cis and trans. | Hansen TJ et al. | β | 2024 | β |
| Human genetics and epigenetics of alcohol use disorder. | Zhou H et al. | β | 2024 | β |
| Hypobaric hypoxia drives selection of altitude-associated adaptative alleles in the Himalayan population. | Sharma S et al. | β | 2024 | β |
| Incorporating genotype information in a precise prediction model for platinum sensitivity in epithelial ovarian cancer. | Du NY et al. | β | 2024 | β |
| Integration of risk factor polygenic risk score with disease polygenic risk score for disease prediction. | Jung H et al. | β | 2024 | β |
| Interactive data sharing for multiple questionnaire-based exposome-wide association studies and exposome correlations in the Personalized Environment and Genes Study. | Lloyd D et al. | β | 2024 | β |
| LDER-GE estimates phenotypic variance component of gene-environment interactions in human complex traits accurately with GE interaction summary statistics and full LD information. | Dong Z et al. | β | 2024 | β |
| Mitochondrial complex I deficiency stratifies idiopathic Parkinson's disease. | FlΓΈnes IH et al. | β | 2024 | β |
| Novel insight into the etiology of ischemic stroke gained by integrative multiome-wide association study. | Jung J et al. | β | 2024 | β |
| ntsm: an alignment-free, ultra-low-coverage, sequencing technology agnostic, intraspecies sample comparison tool for sample swap detection. | Chu J et al. | β | 2024 | β |
| Overcoming barriers to single-cell RNA sequencing adoption in low- and middle-income countries. | Boakye Serebour T et al. | β | 2024 | β |
| Perspective on the Coevolutionary Role of Host and Gut Microbiota in Polyphenol Health Effects: Metabotypes and Precision Health. | EspΓn JC et al. | β | 2024 | β |
| Pharmacogenomics: A Genetic Approach to Drug Development and Therapy. | Qahwaji R et al. | β | 2024 | β |
| Phenotypic Associations With the HMOX1 GT(n) Repeat in European Populations. | Hamilton F et al. | β | 2024 | β |
| Principles and methods for transferring polygenic risk scores across global populations. | Kachuri L et al. | β | 2024 | β |
| Removing unwanted variation between samples in Hi-C experiments. | Fletez-Brant K et al. | β | 2024 | β |
| Research Progress and Applications of Bovine Genome in the Tribe <i>Bovini</i>. | Du X et al. | β | 2024 | β |
| Sex differences in the pleiotropy of hearing difficulty with imaging-derived phenotypes: a brain-wide investigation. | He J et al. | β | 2024 | β |
| Sources of gene expression variation in a globally diverse human cohort. | Taylor DJ et al. | β | 2024 | β |
| Spatiotemporal omics for biology and medicine. | Liu L et al. | β | 2024 | β |
| St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors. | Matt GY et al. | β | 2024 | β |
| The commitment of the human cell atlas to humanity. | Amit I et al. | β | 2024 | β |
| The Human 8-oxoG DNA Glycosylase 1 (<i>OGG1</i>) <i>Ser</i>326<i>Cys</i> Polymorphism in Infertile Men. | GonzΓ‘lez-DΓaz CA et al. | β | 2024 | β |
| The Role of Genetics in Managing Peripheral Arterial Disease. | Biagetti G et al. | β | 2024 | β |
| The Role of Patient Organizations in Shaping Research, Health Policies, and Health Services for Rare Genetic Diseases: The Dutch Experience. | Poortman Y et al. | β | 2024 | β |
| Three decades of osteoarthritis molecular genetics research: From early discussions to impressive breakthroughs. | Loughlin J | β | 2024 | β |
| Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives. | VilΓ -Valls L et al. | β | 2024 | β |
| Utility of long-read sequencing for All of Us. | Mahmoud M et al. | β | 2024 | β |
| Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs. | Γ s J et al. | β | 2024 | β |
| A Comprehensive Analysis of 21 Actionable Pharmacogenes in the Spanish Population: From Genetic Characterisation to Clinical Impact. | Nunez-Torres R et al. | β | 2023 | β |
| Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. | Horimoto ARVR et al. | β | 2023 | β |
| A global view of aging and Alzheimer's pathogenesis-associated cell population dynamics and molecular signatures in human and mouse brains. | Sziraki A et al. | β | 2023 | β |
| Alzheimer's disease genetic burden is associated with mid-life depression among persons with normal cognition. | Wingo TS et al. | β | 2023 | β |
| AmelHap: Leveraging drone whole-genome sequence data to create a honey bee HapMap. | Parejo M et al. | β | 2023 | β |
| A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease. | Patel AP et al. | β | 2023 | β |
| A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. | Xu L et al. | β | 2023 | β |
| An Overview of Deep Generative Models in Functional and Evolutionary Genomics. | Yelmen B et al. | β | 2023 | β |
| Aryl Hydrocarbon Receptor Agonism Antagonizes the Hypoxia-driven Inflammation in Cystic Fibrosis. | Pariano M et al. | β | 2023 | β |
| Assessing and mitigating privacy risks of sparse, noisy genotypes by local alignment to haplotype databases. | Emani PS et al. | β | 2023 | β |
| Association of the polymorphisms of the cholesteryl ester transfer protein gene with coronary artery disease: a meta-analysis. | Zhang R et al. | β | 2023 | β |
| Benchmarking of local genetic correlation estimation methods using summary statistics from genome-wide association studies. | Zhang C et al. | β | 2023 | β |
| Benchmarking RNA Editing Detection Tools. | Morales DR et al. | β | 2023 | β |
| Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). | Matalon DR et al. | β | 2023 | β |
| CMDB: the comprehensive population genome variation database of China. | Li Z et al. | β | 2023 | β |
| Completing a genomic characterisation of microscopic tumour samples with copy number. | Nulsen J et al. | β | 2023 | β |
| Comprehensive variant discovery in the era of complete human reference genomes. | Cechova M et al. | β | 2023 | β |
| Creating a Surgical Biobank: The Hershey Medical Center Experience. | Mankarious MM et al. | β | 2023 | β |
| Current Landscape of Genome-Wide Association Studies in Acute Myeloid Leukemia: A Review. | Marrero RJ et al. | β | 2023 | β |
| Current Status and Future Prospects of Inflammatory Bowel Disease Genetics. | Kakuta Y et al. | β | 2023 | β |
| Development of super-specific epigenome editing by targeted allele-specific DNA methylation. | Rajaram N et al. | β | 2023 | β |
| Effect of ERCC1 polymorphisms on the response to platinum-based chemotherapy: A systematic review and meta-analysis based on Asian population. | Wu X et al. | β | 2023 | β |
| Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation. | Zakaria WNA et al. | β | 2023 | β |
| Ethnic-specific predictors of neurotoxicity among patients with pediatric acute lymphoblastic leukemia after high-dose methotrexate. | Harris RD et al. | β | 2023 | β |
| Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups. | Kurniansyah N et al. | β | 2023 | β |
| Functional Polymorphisms of the Arachidonic Acid Pathway Associate with Risks and Clinical Outcomes of Allergic Diseases. | Sio YY et al. | β | 2023 | β |
| Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization. | Zakaria WNA et al. | β | 2023 | β |
| Genetic Influence of Fracture Nonunion (FNU): A Systematic Review. | Sadat-Ali M et al. | β | 2023 | β |
| Genetic interaction in the association between oxidative stress and diabetes in the Spanish population. | Melero R et al. | β | 2023 | β |
| Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. | Martinez-Carrasco A et al. | β | 2023 | β |
| Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage. | Gaastra B et al. | β | 2023 | β |
| Genome and haplotype provide insights into the population differentiation and breeding improvement of Gossypium barbadense. | Wang N et al. | β | 2023 | β |
| Genome-wide association studies of cardiovascular disease. | Walsh R et al. | β | 2023 | β |
| Genomic Insights into the Population History of the Resande or Swedish Travelers. | VilΓ -Valls L et al. | β | 2023 | β |
| Genotype andΒ phenotype data standardization, utilization andΒ integration inΒ the big data era forΒ agricultural sciences. | Deng CH et al. | β | 2023 | β |
| GWAs Identify DNA Variants Influencing Eyebrow Thickness Variation in Europeans and Across Continental Populations. | Peng F et al. | β | 2023 | β |
| Hybrid autoencoder with orthogonal latent space for robust population structure inference. | Yuan M et al. | β | 2023 | β |
| <i>CLEC16A</i>-An Emerging Master Regulator of Autoimmunity and Neurodegeneration. | Pandey R et al. | β | 2023 | β |
| Identification by whole genome sequencing of genes associated with delayed postoperative hemorrhage in Scottish deerhounds. | Court MH et al. | β | 2023 | β |
| Identification of a RAD51B enhancer variant for susceptibility and progression to glioma. | Huang L et al. | β | 2023 | β |
| Identification of region-specific splicing QTLs in human hippocampal tissue and its distinctive role in brain disorders. | Li X et al. | β | 2023 | β |
| Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. | Wu Y et al. | β | 2023 | β |
| Importance of Diversity in Precision Medicine: Generalizability of Genetic Associations Across Ancestry Groups Toward Better Identification of Disease Susceptibility Variants. | Cruz LA et al. | β | 2023 | β |
| Increased mutation and gene conversion within human segmental duplications. | Vollger MR et al. | β | 2023 | β |
| Integrative genetic analysis illuminates ALS heritability and identifies risk genes. | Megat S et al. | β | 2023 | β |
| Investigation of heteroscedasticity in polygenic risk scores across 15 quantitative traits. | Jung H et al. | β | 2023 | β |
| Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. | Bhattacharya A et al. | β | 2023 | β |
| Latest Development on Genetics of Common Retinal Diseases. | Chen LJ et al. | β | 2023 | β |
| Lineage specific 3D genome structure in the adult human brain and neurodevelopmental changes in the chromatin interactome. | Rahman S et al. | β | 2023 | β |
| Localized assembly for long reads enables genome-wide analysis of repetitive regions at single-base resolution in human genomes. | Ikemoto K et al. | β | 2023 | β |
| Microsatellites used in forensics are in regions enriched for trait-associated variants. | Link V et al. | β | 2023 | β |
| Multi-environment Genomic Selection in Rice Elite Breeding Lines. | Nguyen VH et al. | β | 2023 | β |
| Multi-Omics Studies in Historically Excluded Populations: The Road to Equity. | Yang G et al. | β | 2023 | β |
| Multiple sclerosis risk variants influence the peripheral B-cell compartment early in life in the general population. | de Mol CL et al. | β | 2023 | β |
| New insights from the last decade of research in psychiatric genetics: discoveries, challenges and clinical implications. | Andreassen OA et al. | β | 2023 | β |
| Ophthalmic genetic counselling: emerging trends in practice perspectives in Asia. | Hui EKY et al. | β | 2023 | β |
| Outer dynein arm docking complex subunit 2 polymorphism rs7893462 modulates hepatocellular carcinoma susceptibility and can serve as an overall survival biomarker for hepatitis B virus-related hepatocellular carcinoma after hepatectomy: a cohort study with a long-term follow-up. | Zeng Z et al. | β | 2023 | β |
| Pharmacovariome scanning using whole pharmacogene resequencing coupled with deep computational analysis and machine learning for clinical pharmacogenomics. | Tafazoli A et al. | β | 2023 | β |
| Population diversity and equity in the genomic era: going global to return to the local. | Ruderman A | β | 2023 | β |
| Positive personality traits moderate persistent high alcohol consumption, determined by polygenic risk in U.S. military veterans: results from a 10-year, population-based, observational cohort study. | Na P et al. | β | 2023 | β |
| Predicting the molecular mechanism-driven progression of breast cancer through comprehensive network pharmacology and molecular docking approach. | Vyas B et al. | β | 2023 | β |
| Repeated evolution of herbicide resistance in <i>Lolium multiflorum</i> revealed by haplotype-resolved analysis of acetyl-CoA carboxylase. | Brunharo CACG et al. | β | 2023 | β |
| SAMHD1 single nucleotide polymorphisms impact outcome in children with newly diagnosed acute myeloid leukemia. | Marrero RJ et al. | β | 2023 | β |
| Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia. | Henden L et al. | β | 2023 | β |
| Simultaneous detection of DNA variation and methylation at HLA class II locus and immune gene promoters using targeted SureSelect Methyl-Sequencing. | Kalomoiri M et al. | β | 2023 | β |
| Single-cell multiomics of the human retina reveals hierarchical transcription factor collaboration in mediating cell type-specific effects of genetic variants on gene regulation. | Wang J et al. | β | 2023 | β |
| Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations. | Liegel RP et al. | β | 2023 | β |
| Systemic interindividual epigenetic variation in humans is associated with transposable elements and under strong genetic control. | Gunasekara CJ et al. | β | 2023 | β |
| The Extent of Edgetic Perturbations in the Human Interactome Caused by Population-Specific Mutations. | Cui H et al. | β | 2023 | β |
| The genetics of autism spectrum disorder in an East African familial cohort. | Tuncay IO et al. | β | 2023 | β |
| The genetics of incontinence: A scoping review. | Breinbjerg A et al. | β | 2023 | β |
| The human pangenome reference anticipates equitable and fundamental genomic insights. | Frazer KA et al. | β | 2023 | β |
| The <i>KL</i> genetic polymorphisms Associated with type 2 diabetes Mellitus. | Jin HS et al. | β | 2023 | β |
| The impact of <i>FOXP3</i> polymorphisms on oral cancer progression and clinicopathological characteristics. | Chen PJ et al. | β | 2023 | β |
| The landscape of somatic mutations in lymphoblastoid cell lines. | Caballero M et al. | β | 2023 | β |
| The Legacy of Infectious Disease Exposure on the Genomic Diversity of Indigenous Southern Mexicans. | Garcia OA et al. | β | 2023 | β |
| The mitochondrial protein TSPO in Alzheimer's disease: relation to the severity of AD pathology and the neuroinflammatory environment. | Garland EF et al. | β | 2023 | β |
| Toward Inclusivity in Preclinical Drug Development: A Proposition to Start with Intestinal Organoids. | Co JY et al. | β | 2023 | β |
| Whole-exome sequencing of oral epithelial dysplasia samples reveals an association with new genes. | Adorno-Farias D et al. | β | 2023 | β |
| Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria. | Joshi E et al. | β | 2023 | β |
| 17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson's disease are associated with LRRC37A/2 expression in astrocytes. | Bowles KR et al. | β | 2022 | β |
| A Comparison of Methods for Gene-Based Testing That Account for Linkage Disequilibrium. | Cinar O et al. | β | 2022 | β |
| A comprehensive evaluation of polygenic score and genotype imputation performances of human SNP arrays in diverse populations. | Nguyen DT et al. | β | 2022 | β |
| Alcohol intake and stomach cancer risk in Japan: A pooled analysis of six cohort studies. | Tamura T et al. | β | 2022 | β |
| An adipose lncRAP2-Igf2bp2 complex enhances adipogenesis and energy expenditure by stabilizing target mRNAs. | Alvarez-Dominguez JR et al. | β | 2022 | β |
| A Poisson reduced-rank regression model for association mapping in sequencing data. | Fitzgerald T et al. | β | 2022 | β |
| Assessing reproducibility of inherited variants detected with short-read whole genome sequencing. | Pan B et al. | β | 2022 | β |
| Association of Common Polymorphisms in the Interleukin-1 Beta Gene with Hepatocellular Carcinoma in Caucasian Patients with Chronic Hepatitis B. | Fischer J et al. | β | 2022 | β |
| Blood Group Genotyping. | Cone Sullivan JK et al. | β | 2022 | β |
| Breathing new life into clinical testing and diagnostics: perspectives on volatile biomarkers from breath. | Haworth JJ et al. | β | 2022 | β |
| Causal Graph Among Serum Lipids and Glycemic Traits: A Mendelian Randomization Study. | Zhu Z et al. | β | 2022 | β |
| Characterization of Arabian Peninsula whole exomes: Contributing to the catalogue of human diversity. | Ferreira JC et al. | β | 2022 | β |
| Characterizing gene expression in anΒ in vitro biomechanical strain model of joint health | Hung A et al. | β | 2022 | β |
| Combined effects of nucleotide-binding domain-like receptor protein 3 polymorphisms and environmental metals exposure on chronic kidney disease. | Hsueh YM et al. | β | 2022 | β |
| Comprehensive characterization genetic regulation and chromatin landscape of enhancer-associated long non-coding RNAs and their implication in human cancer. | Li X et al. | β | 2022 | β |
| Computational approaches for predicting variant impact: An overview from resources, principles to applications. | Liu Y et al. | β | 2022 | β |
| Computational Drug Repurposing Based on a Recommendation System and Drug-Drug Functional Pathway Similarity. | Shao M et al. | β | 2022 | β |
| Copy number alteration signatures as biomarkers in cancer: a review. | Giles Doran C et al. | β | 2022 | β |
| CYP4 subfamily V member 2 (CYP4V2) polymorphisms were associated with ischemic stroke in Chinese Han population. | Long F et al. | β | 2022 | β |
| Deconstructing a Syndrome: Genomic Insights Into PCOS Causal Mechanisms and Classification. | Dapas M et al. | β | 2022 | β |
| Deep learning-based integration of genetics with registry data for stratification of schizophrenia and depression. | AllesΓΈe RL et al. | β | 2022 | β |
| Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. | Castaneda-Garcia C et al. | β | 2022 | β |
| de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project. | Ng JK et al. | β | 2022 | β |
| Determinants in Tailoring Antidiabetic Therapies: A Personalized Approach. | Rizvi AA et al. | β | 2022 | β |
| Dynamics of Viral and Host 3D Genome Structure upon Infection. | Friedman MJ et al. | β | 2022 | β |
| From Genome-Wide to Environment-Wide: Capturing the Environome. | von Stumm S et al. | β | 2022 | β |
| Genetic determinants of cardiometabolic and pulmonary phenotypes and obstructive sleep apnoea in HCHS/SOL. | Zhang Y et al. | β | 2022 | β |
| Genetic Modifiers of Sickle Cell Disease. | Pincez T et al. | β | 2022 | β |
| Genetic polymorphism in <i>Methylenetetrahydrofolate Reductase chloride transport protein 6</i> (<i>MTHFR CLCN6</i>) gene is associated with keratinocyte skin cancer in a cohort of renal transplant recipients. | Griffin L et al. | β | 2022 | β |
| Genetics of the human microglia regulome refines Alzheimer's disease risk loci. | Kosoy R et al. | β | 2022 | β |
| Genome and transcriptome profiling of spontaneous preterm birth phenotypes. | Gupta JK et al. | β | 2022 | β |
| Genome interpretation using in silico predictors of variant impact. | Katsonis P et al. | β | 2022 | β |
| Genomic data integration and user-defined sample-set extraction for population variant analysis. | Alfonsi T et al. | β | 2022 | β |
| Genomic Data Sharing under Dependent Local Differential Privacy. | Yilmaz E et al. | β | 2022 | β |
| Genomic medicine on the frontier of precision medicine. | Hasanzad M et al. | β | 2022 | β |
| Global and local ancestry modulate APOE association with Alzheimer's neuropathology and cognitive outcomes in an admixed sample. | Naslavsky MS et al. | β | 2022 | β |
| GTQC: Automated Genotyping Array Quality Control and Report. | Zhao S et al. | β | 2022 | β |
| hapCon: estimating contamination of ancient genomes by copying from reference haplotypes. | Huang Y et al. | β | 2022 | β |
| HAPPE: A Tool for Population Haplotype Analysis and Visualization in Editable Excel Tables. | Feng C et al. | β | 2022 | β |
| HKG: an open genetic variant database of 205 Hong Kong cantonese exomes. | Ou M et al. | β | 2022 | β |
| Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types. | Rhodes K et al. | β | 2022 | β |
| Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data. | Lee H et al. | β | 2022 | β |
| Impact of Clinicopathological Characteristics and Tissue Inhibitor of Metalloproteinase-3 Polymorphism Rs9619311 on Biochemical Recurrence in Taiwanese Patients with Prostate Cancer. | Hsieh CY et al. | β | 2022 | β |
| Impact of EFEMP1 on the survival outcome of biliary atresia in Thai infants. | Laochareonsuk W et al. | β | 2022 | β |
| Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort. | Brolin K et al. | β | 2022 | β |
| Interaction Effects of DRD2 Genetic Polymorphism and Interpersonal Stress on Problematic Gaming in College Students. | Kim E et al. | β | 2022 | β |
| Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort. | Grigoriadis D et al. | β | 2022 | β |
| Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations. | Taraszka K et al. | β | 2022 | β |
| Limb development genes underlie variation in human fingerprint patterns. | Li J et al. | β | 2022 | β |
| MicroRNA Processing Pathway-Based Polygenic Score for Clear Cell Renal Cell Carcinoma in the Volga-Ural Region Populations of Eurasian Continent. | Ivanova E et al. | β | 2022 | β |
| Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies. | Lu Z et al. | β | 2022 | β |
| Multiple haplotype-based analyses provide genetic and evolutionary insights into tomato fruit weight and composition. | Zhao J et al. | β | 2022 | β |
| NGS allele counts versus called genotypes for testing genetic association. | GonzΓ‘lez Silos R et al. | β | 2022 | β |
| Nonsynonymous amino acid changes in the Ξ±-chain of complement component 5 influence longitudinal susceptibility to <i>Plasmodium falciparum</i> infections and severe malarial anemia in kenyan children. | Raballah E et al. | β | 2022 | β |
| Population-level variation in enhancer expression identifies disease mechanisms in the human brain. | Dong P et al. | β | 2022 | β |
| Profiling genes encoding the adaptive immune receptor repertoire with gAIRR Suite. | Lin MJ et al. | β | 2022 | β |
| Prospects of Non-Coding Elements in Genomic DNA Based Gene Therapy. | Simna SP et al. | β | 2022 | β |
| Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation. | Doleschall M et al. | β | 2022 | β |
| Rare diseases: human genome research is coming home. | Ropers HH et al. | β | 2022 | β |
| Review of the Forensic Applicability of Biostatistical Methods for Inferring Ancestry from Autosomal Genetic Markers. | Tvedebrink T | β | 2022 | β |
| Single Nucleotide Polymorphism of TWIST2 May Be a Modifier for the Association between High-Density Lipoprotein Cholesterol and Blood Lead (Pb) Level. | Yang CC et al. | β | 2022 | β |
| Somatic XIST activation and features of X chromosome inactivation in male human cancers. | Sadagopan A et al. | β | 2022 | β |
| SYNPRED: prediction of drug combination effects in cancer using different synergy metrics and ensemble learning. | Preto AJ et al. | β | 2022 | β |
| Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research. | Lee SS et al. | β | 2022 | β |
| Ten simple rules for a successful international consortium in big data omics. | Stobbe MD et al. | β | 2022 | β |
| The Analysis of a Genome-Wide Association Study (GWAS) of Overweight and Obesity in Psoriasis. | Kisielnicka A et al. | β | 2022 | β |
| The genetic determinants of oral diseases in Africa: The gaps should be filled. | Sudi SM et al. | β | 2022 | β |
| The Impact of Matrix Metalloproteinase-11 Polymorphisms on Colorectal Cancer Progression and Clinicopathological Characteristics. | Huang HC et al. | β | 2022 | β |
| The Past and Future of Rare Skin Disease Research and Therapy. | Onoufriadis A et al. | β | 2022 | β |
| The Peopling and Migration History of the Natives in Peninsular Malaysia and Borneo: A Glimpse on the Studies Over the Past 100 years. | Hoh BP et al. | β | 2022 | β |
| The Thousand Polish Genomes-A Database of Polish Variant Allele Frequencies. | Kaja E et al. | β | 2022 | β |
| Translocator Protein (18 kDa) Polymorphism (rs6971) in the Korean Population. | Lee H et al. | β | 2022 | β |
| Vitamin D Receptor Gene Polymorphisms, Ξ²-cell Function, and Vitamin D Status in Non-obese Mexican Adults. | PiΓ±a-Aguero MI et al. | β | 2022 | β |
| White matter microstructural differences in children and genetic risk for multiple sclerosis: A population-based study. | de Mol CL et al. | β | 2022 | β |
| Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms. | Maegawa T et al. | β | 2022 | β |
| Accurate imputation of human leukocyte antigens with CookHLA. | Cook S et al. | β | 2021 | β |
| Admixture Has Shaped Romani Genetic Diversity in Clinically Relevant Variants. | Font-Porterias N et al. | β | 2021 | β |
| A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis. | Hayashi S et al. | β | 2021 | β |
| Analysis and Interpretation of the Impact of Missense Variants in Cancer. | Petrosino M et al. | β | 2021 | β |
| Analytical Performance of NGS-Based Molecular Genetic Tests Used in the Diagnostic Workflow of Pheochromocytoma/Paraganglioma. | Sarkadi B et al. | β | 2021 | β |
| Application of CRISPR-Cas9 gene editing for congenital heart disease. | Seok H et al. | β | 2021 | β |
| A prospective trial of abiraterone acetate plus prednisone in Black and White men with metastatic castrate-resistant prostate cancer. | George DJ et al. | β | 2021 | β |
| Assessing Autosomal InDel Loci With Multiple Insertions or Deletions of Random DNA Sequences in Human Genome. | Yao Y et al. | β | 2021 | β |
| Assessment of ANG variants in Parkinson's disease. | Grenn FP et al. | β | 2021 | β |
| Association between interleukin-10 polymorphisms and CD4<sup>+</sup>CD25<sup>+</sup>FOXP3<sup>+</sup> T cells in asthmatic children. | Mocellin M et al. | β | 2021 | β |
| Association of Genetic West African Ancestry, Blood Pressure Response to Therapy, and Cardiovascular Risk Among Self-reported Black Individuals in the Systolic Blood Pressure Reduction Intervention Trial (SPRINT). | Rao S et al. | β | 2021 | β |
| Association of TERT gene polymorphisms with clinical benign prostatic hyperplasia in a Chinese Han population of the Northwest region. | Fan G et al. | β | 2021 | β |
| Association of Vitamin D Receptor Gene Polymorphisms with Serum Vitamin D Levels in a Greek Rural Population (Velestino Study). | Divanoglou N et al. | β | 2021 | β |
| Associations between inflammasome-related gene NLRP3 Polymorphisms (rs10754558 and rs35829419) and risk of bladder cancer in a Chinese population. | Xu G et al. | β | 2021 | β |
| A wealth of discovery built on the Human Genome Project - by the numbers. | Gates AJ et al. | β | 2021 | β |
| <b>Emerging Roles of the Human Solute Carrier 22 Family</b>. | Yee SW et al. | β | 2021 | β |
| Bench Research Informed by GWAS Results. | Kondratyev NV et al. | β | 2021 | β |
| Breeding for Climate Change Resilience: A Case Study of Loblolly Pine (<i>Pinus taeda</i> L.) in North America. | Matallana-Ramirez LP et al. | β | 2021 | β |
| Cas9 targeted enrichment of mobile elements using nanopore sequencing. | McDonald TL et al. | β | 2021 | β |
| Cataloguing experimentally confirmed 80.7Β kb-long ACKR1 haplotypes from the 1000 Genomes Project database. | Srivastava K et al. | β | 2021 | β |
| Challenges and Opportunities in Understanding Genetics of Fungal Diseases: Towards a Functional Genomics Approach. | Bruno M et al. | β | 2021 | β |
| Characterizing the Genetic Architecture of Parkinson's Disease in Latinos. | Loesch DP et al. | β | 2021 | β |
| Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci. | Perrin HJ et al. | β | 2021 | β |
| Comprehensive analysis of important pharmacogenes in Koreans using the DMETβ’ platform. | Kim B et al. | β | 2021 | β |
| Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts. | Woo XY et al. | β | 2021 | β |
| Data Integration Challenges for Machine Learning in Precision Medicine. | MartΓnez-GarcΓa M et al. | β | 2021 | β |
| Diabetes and Genetics: A Relationship Between Genetic Risk Alleles, Clinical Phenotypes and Therapeutic Approaches. | Sayed S et al. | β | 2021 | β |
| Distinguishing HapMap Accessions Through Recursive Set Partitioning in Hierarchical Decision Trees. | Zhang W et al. | β | 2021 | β |
| Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome. | Douard E et al. | β | 2021 | β |
| Effects of single nucleotide polymorphism ascertainment on population structure inferences. | Dokan K et al. | β | 2021 | β |
| Exome Sequencing Identifies Abnormalities in Glycosylation and ANKRD36C in Patients with Immune-Mediated Thrombotic Thrombocytopenic Purpura. | Basu MK et al. | β | 2021 | β |
| Family-based gene-environment interaction using sequence kernel association test (FGE-SKAT) for complex quantitative traits. | Guo CY et al. | β | 2021 | β |
| Founder variants and population genomes-Toward precision medicine. | Jain A et al. | β | 2021 | β |
| From one human genome to a complex tapestry of ancestry. | Rotimi CN et al. | β | 2021 | β |
| Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. | Mulford AJ et al. | β | 2021 | β |
| Genetic origins, singularity, and heterogeneity of Basques. | Flores-Bello A et al. | β | 2021 | β |
| Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife). | Neustaeter A et al. | β | 2021 | β |
| Genetic Risk Stratification: A Paradigm Shift in Prevention of Coronary Artery Disease. | Roberts R et al. | β | 2021 | β |
| Genetics of Polycystic Ovary Syndrome: What is New? | Welt CK | β | 2021 | β |
| Genetic variations in medical research in the past, at present and in the future. | Kamatani Y et al. | β | 2021 | β |
| Genome Reconstruction Attacks Against Genomic Data-Sharing Beacons. | Ayoz K et al. | β | 2021 | β |
| Haplotype diversity and sequence heterogeneity of human telomeres. | Grigorev K et al. | β | 2021 | β |
| How imputation can mitigate SNP ascertainment Bias. | Geibel J et al. | β | 2021 | β |
| Identification of pleiotropy at the gene level between psychiatric disorders and related traits. | Polushina T et al. | β | 2021 | β |
| Identifying causal variants by fine mapping across multiple studies. | LaPierre N et al. | β | 2021 | β |
| Impact of Genetic Variation in Gene Regulatory Sequences: A Population Genomics Perspective. | Joshi M et al. | β | 2021 | β |
| Infant Metabolome in Relation to Prenatal DHA Supplementation and Maternal Single-Nucleotide Polymorphism rs174602: Secondary Analysis of a Randomized Controlled Trial in Mexico. | Tandon S et al. | β | 2021 | β |
| In Silico Analysis of the Molecular-Level Impact of SMPD1 Variants on Niemann-Pick Disease Severity. | Ancien F et al. | β | 2021 | β |
| Integrating disease and drug-related phenotypes for improved identification of pharmacogenomic variants. | Ouellette TW et al. | β | 2021 | β |
| International strategy in cancer epidemiology: Japan's involvement in global projects and future role. | Matsuda T et al. | β | 2021 | β |
| Intronic Variant of MUTYH Gene Exhibits A Strong Association with Early Onset of Breast Cancer Susceptibility in Indonesian Women Population. | Panigoro SS et al. | β | 2021 | β |
| JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene-variant discovery, annotation, prediction, and genotyping. | Ahmed Z et al. | β | 2021 | β |
| LncRBase V.2: an updated resource for multispecies lncRNAs and ClinicLSNP hosting genetic variants in lncRNAs for cancer patients. | Das T et al. | β | 2021 | β |
| Local and Systemic Cytokine, Chemokine, and FGF Profile in Bacterial Chondronecrosis with Osteomyelitis (BCO)-Affected Broilers. | Ramser A et al. | β | 2021 | β |
| Longitudinal data reveal strong genetic and weak non-genetic components of ethnicity-dependent blood DNA methylation levels. | McKennan C et al. | β | 2021 | β |
| Machine learning based disease prediction from genotype data. | Katsaouni N et al. | β | 2021 | β |
| Making Sense of Genetic Information: The Promising Evolution of Clinical Stratification and Precision Oncology Using Machine Learning. | Baptiste M et al. | β | 2021 | β |
| MARS: leveraging allelic heterogeneity to increase power of association testing. | Hormozdiari F 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 |
| Minor Allele Frequencies and Molecular Pathways Differences for SNPs Associated with Amyotrophic Lateral Sclerosis in Subjects Participating in the UKBB and 1000 Genomes Project. | D'Antona S et al. | β | 2021 | β |
| Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy. | Santos RO et al. | β | 2021 | β |
| On the inference of complex phylogenetic networks by Markov Chain Monte-Carlo. | Rabier CE et al. | β | 2021 | β |
| Pharmacogenomic considerations for repurposing of dexamethasone as a potential drug against SARS-CoV-2 infection. | Vohra M et al. | β | 2021 | β |
| Pharmacogenomics and Personalized Medicine in Type 2 Diabetes Mellitus: Potential Implications for Clinical Practice. | Venkatachalapathy P et al. | β | 2021 | β |
| Planning and Conducting a Pharmacogenetics Association Study. | Hertz DL et al. | β | 2021 | β |
| Polygenic risk scores: the future of cancer risk prediction, screening, and precision prevention. | Wang Y et al. | β | 2021 | β |
| Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population. | He C et al. | β | 2021 | β |
| Prevalence of SLCO1B1 single nucleotide variations and their association with hypercholesterolaemia in hypercholesterolemic patients in Gauteng, South Africa. | de Beer R et al. | β | 2021 | β |
| Problems and promises: How to tell the story of a Genome Wide Association Study? | Heeney C | β | 2021 | β |
| Racial Disparity in Drug Disposition in the Digestive Tract. | Gao S et al. | β | 2021 | β |
| Recessive/dominant model: Alternative choice in case-control-based genome-wide association studies. | Liu HM 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 |
| SeeCiTe: a method to assess CNV calls from SNP arrays using trio data. | Lavrichenko K et al. | β | 2021 | β |
| Single nucleotide polymorphisms in sweet, fat, umami, salt, bitter and sour taste receptor genes are associated with gustatory function and taste preferences in young adults. | Chamoun E et al. | β | 2021 | β |
| SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression. | Hou G et al. | β | 2021 | β |
| SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population. | Chen JH et al. | β | 2021 | β |
| Soybean (Glycine max) Haplotype Map (GmHapMap): a universal resource for soybean translational and functional genomics. | Torkamaneh D et al. | β | 2021 | β |
| Status and prospects of genome-wide association studies in plants. | Tibbs Cortes L et al. | β | 2021 | β |
| T cell composition and polygenic multiple sclerosis risk: A population-based study in children. | de Mol CL et al. | β | 2021 | β |
| The Counteracting Effects of Demography on Functional Genomic Variation: The Roma Paradigm. | Font-Porterias N et al. | β | 2021 | β |
| The first insight into the genetic structure of the population of modern Serbia. | Drljaca T et al. | β | 2021 | β |
| The genetic scenario of Mercheros: an under-represented group within the Iberian Peninsula. | Flores-Bello A et al. | β | 2021 | β |
| The impact of receptor of advanced glycation end-products polymorphisms on prostate cancer progression and clinicopathological characteristics. | Chou YE et al. | β | 2021 | β |
| The influence of nutrigenetics on biomarkers of selenium nutritional status. | Donadio JLS et al. | β | 2021 | β |
| The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association. | Chen TH et al. | β | 2021 | β |
| The Need for a Human Pangenome Reference Sequence. | Miga KH et al. | β | 2021 | β |
| Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. | Atkinson EG et al. | β | 2021 | β |
| Translating genetic association of lipid levels for biological and clinical application. | Crone B et al. | β | 2021 | β |
| Tripartite Motif 22 (TRIM22) protein restricts herpes simplex virus 1 by epigenetic silencing of viral immediate-early genes. | Reddi TS et al. | β | 2021 | β |
| Ultrafast homomorphic encryption models enable secure outsourcing of genotype imputation. | Kim M et al. | β | 2021 | β |
| Weak Association Between the Glutamate Decarboxylase 1 Gene (GAD1) and Schizophrenia in Han Chinese Population. | Zhang L et al. | β | 2021 | β |
| Whole genome copy number analyses reveal a highly aberrant genome in TP53 mutant lung adenocarcinoma tumors. | BjaanΓ¦s MM et al. | β | 2021 | β |
| Whole genome sequencing of low input circulating cell-free DNA obtained from normal human subjects. | Foley JF et al. | β | 2021 | β |
| Whole genome variation in 27 Mexican indigenous populations, demographic and biomedical insights. | Aguilar-OrdoΓ±ez I et al. | β | 2021 | β |
| A brief history of human disease genetics. | Claussnitzer M 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 |
| A decision tree to improve identification of pathogenic mutations in clinical practice. | do Nascimento PM et al. | β | 2020 | β |
| A genetic variant in microRNA-146a is associated with sporadic breast cancer in a Southern Brazilian Population. | Brincas HM et al. | β | 2020 | β |
| A Journey through Genetic Architecture and Predisposition of Coronary Artery Disease. | Roberts R et al. | β | 2020 | β |
| A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1. | Deng M et al. | β | 2020 | β |
| A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson's disease. | Boussaad I et al. | β | 2020 | β |
| A positively selected FBN1 missense variant reduces height in Peruvian individuals. | Asgari S et al. | β | 2020 | β |
| Association between genetic variations in GSH-related and MT genes and low-dose methylmercury exposure in children and women of childbearing age: a pilot study. | Chan PHY et al. | β | 2020 | β |
| Association of 11Ξ²-hydroxysteroid dehydrogenase type1 (HSD11b1) gene polymorphisms with outcome of antidepressant therapy and suicide attempts. | Figaro-Drumond FV et al. | β | 2020 | β |
| Association of Genetic Polymorphisms With Hepatitis C Virus-related Liver Cirrhosis in Japan. | Kamimura S et al. | β | 2020 | β |
| Authentication, characterization and contamination detection of cell lines, xenografts and organoids by barcode deep NGS sequencing. | Chen X et al. | β | 2020 | β |
| Cannabinoids and psychotic symptoms: A potential role for a genetic variant in the P2X purinoceptor 7 (P2RX7) gene. | Boks MP et al. | β | 2020 | β |
| Citizens' Attitudes, Knowledge, and Educational Needs in the Field of Omics Sciences: A Systematic Literature Review. | CalabrΓ² GE et al. | β | 2020 | β |
| Comprehensive identification and characterization of somatic copy number alterations in tripleβnegative breast cancer. | Li Z et al. | β | 2020 | β |
| Contrasting DCIS and invasive breast cancer by subtype suggests basal-like DCIS as distinct lesions. | Bergholtz H et al. | β | 2020 | β |
| Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates. | Sul JH et al. | β | 2020 | β |
| Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus. | Raj P et al. | β | 2020 | β |
| Determinants of transcription factor regulatory range. | Chen CH et al. | β | 2020 | β |
| DNA copy number motifs are strong and independent predictors of survival in breast cancer. | Pladsen AV et al. | β | 2020 | β |
| Efficient logging and querying for blockchain-based cross-site genomic dataset access audit. | Ma S 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 |
| Erosion of Gene Co-expression Networks Reveal Deregulation of Immune System Processes in Late-Onset Alzheimer's Disease. | Malamon JS et al. | β | 2020 | β |
| Evaluation of population stratification adjustment using genome-wide or exonic variants. | Chen Y et al. | β | 2020 | β |
| Evolutionary history of modern Samoans. | Harris DN et al. | β | 2020 | β |
| Evolutionary perspectives on polygenic selection, missing heritability, and GWAS. | Uricchio LH | β | 2020 | β |
| Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk. | Bobbili DR et al. | β | 2020 | β |
| Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. | Ratnapriya R et al. | β | 2020 | β |
| Fostering Ethical, Legal, and Social Implications Research in Tribal Communities: The Center for the Ethics of Indigenous Genomic Research. | Hiratsuka VY et al. | β | 2020 | β |
| From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases. | Cano-Gamez E et al. | β | 2020 | β |
| Gene editing and CRISPR in the clinic: current and future perspectives. | Hirakawa MP et al. | β | 2020 | β |
| Gene-Environment Interaction between the <i>IL1RN</i> Variants and Childhood Environmental Tobacco Smoke Exposure in Asthma Risk. | Shao Y et al. | β | 2020 | β |
| Gene-Environment Interaction in the Era of Precision Medicine - Filling the Potholes Rather Than Starting to Build a New Road. | Γlvarez-Castro JM | β | 2020 | β |
| Genetic Association of Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy. | Chen LJ | β | 2020 | β |
| Genetic Predisposition to Glioma Mediated by a MAPKAP1 Enhancer Variant. | Huang L et al. | β | 2020 | β |
| Gene Variants Associated With Venous Thrombosis: A Replication Study in a Brazilian Multicentre Study. | Romano AVC et al. | β | 2020 | β |
| Genome-wide association studies of cardiac electrical phenotypes. | Glinge C et al. | β | 2020 | β |
| Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. | Cha PC et al. | β | 2020 | β |
| Genome-wide association study of genetic variations associated with treatment failure after intravesical bacillus Calmette-GuΓ©rin therapy for non-muscle invasive bladder cancer. | Shiota M et al. | β | 2020 | β |
| Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity. | Choquet H et al. | β | 2020 | β |
| Genome-wide linkage analysis of families with primary hyperhidrosis. | Schote AB et al. | β | 2020 | β |
| Genome-wide meta-analysis associates GPSM1 with type 2 diabetes, a plausible gene involved in skeletal muscle function. | Ding Q et al. | β | 2020 | β |
| Genomics and Liver Transplantation: Genomic Biomarkers for the Diagnosis of Acute Cellular Rejection. | Kohut TJ et al. | β | 2020 | β |
| Genomics in Personalized Nutrition: Can You "Eat for Your Genes"? | Mullins VA et al. | β | 2020 | β |
| Genomic Underpinnings of Tumor Behavior in <i>In Situ</i> and Early Lung Adenocarcinoma. | Qian J et al. | β | 2020 | β |
| Genomic Variation, Evolvability, and the Paradox of Mental Illness. | Gualtieri CT | β | 2020 | β |
| GWAS in cancer: progress and challenges. | Liang B et al. | β | 2020 | β |
| Hepatic NADH reductive stress underlies common variation in metabolic traits. | Goodman RP et al. | β | 2020 | β |
| Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition. | Gupta H et al. | β | 2020 | β |
| Human transposon insertion profiling by sequencing (TIPseq) to map LINE-1 insertions in single cells. | McKerrow W et al. | β | 2020 | β |
| Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology. | Zhou W et al. | β | 2020 | β |
| Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults. | Kong SH et al. | β | 2020 | β |
| Identification of PIEZO1 polymorphisms for human bone mineral density. | Bai WY et al. | β | 2020 | β |
| Identification of therapeutic targets from genetic association studies using hierarchical component analysis. | Lee HC et al. | β | 2020 | β |
| Identifying disease-causing mutations in genomes of single patients by computational approaches. | Sevim Bayrak C et al. | β | 2020 | β |
| Impact of Matrix Metalloproteinase-11 Gene Polymorphisms on Biochemical Recurrence and Clinicopathological Characteristics of Prostate Cancer. | Hsieh CY et al. | β | 2020 | β |
| Impact of Matrix Metalloproteinases 11 Gene Variants on Urothelial Cell Carcinoma Development and Clinical Characteristics. | Li CC et al. | β | 2020 | β |
| Improved haplotype inference by exploiting long-range linking and allelic imbalance in RNA-seq datasets. | Berger E et al. | β | 2020 | β |
| Inauguration of the Tanzania Society of Human Genetics: Biomedical Research in Tanzania with Emphasis on Human Genetics and Genomics. | Alimohamed MZ et al. | β | 2020 | β |
| Integration of GWAS Summary Statistics and Gene Expression Reveals Target Cell Types Underlying Kidney Function Traits. | Li Y 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 |
| LDpop: an interactive online tool to calculate and visualize geographic LD patterns. | Alexander TA et al. | β | 2020 | β |
| Life History Effects on Neutral Diversity Levels of Autosomes and Sex Chromosomes. | Amster G et al. | β | 2020 | β |
| Location deviations of DNA functional elements affected SNP mapping in the published databases and references. | Zheng H et al. | β | 2020 | β |
| Long-Term Consumption of Anthocyanin-Rich Fruit Juice: Impact on Gut Microbiota and Antioxidant Markers in Lymphocytes of Healthy Males. | Groh IAM et al. | β | 2020 | β |
| Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits. | Glastonbury CA et al. | β | 2020 | β |
| Mannose-binding lectin 2 gene polymorphisms and their association with tuberculosis in a Chinese population. | Zhang JX et al. | β | 2020 | β |
| Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. | Gaare JJ et al. | β | 2020 | β |
| MI-MAAP: marker informativeness for multi-ancestry admixed populations. | Chen S et al. | β | 2020 | β |
| Mitochondrial GWAS and association of nuclear - mitochondrial epistasis with BMI in T1DM patients. | Ludwig-SΕomczyΕska AH et al. | β | 2020 | β |
| Molecular Discordance between Myeloid Sarcomas and Concurrent Bone Marrows Occurs in Actionable Genes and Is Associated with Worse Overall Survival. | Werstein B et al. | β | 2020 | β |
| Molecular genetics in psychology and personality neuroscience: On candidate genes, genome wide scans, and new research strategies. | Montag C et al. | β | 2020 | β |
| NCMHap: a novel method for haplotype reconstruction based on Neutrosophic c-means clustering. | Zamani F et al. | β | 2020 | β |
| NG-Circos: next-generation Circos for data visualization and interpretation. | Cui Y et al. | β | 2020 | β |
| Novel rare frameshift variation in aggressive periodontitis: Exomic and familial-screening analysis. | Taiete T et al. | β | 2020 | β |
| Overcoming the challenges of imputation of rare variants in a Taiwanese cohort. | Chattopadhyay A et al. | β | 2020 | β |
| Overlapping genetic architecture between Parkinson disease and melanoma. | Dube U et al. | β | 2020 | β |
| Polygenic Multiple Sclerosis Risk and Population-Based Childhood Brain Imaging. | de Mol CL et al. | β | 2020 | β |
| Polygenic risk scoring in the human embryo: reproductive genetics, final frontier? | Treff NR | β | 2020 | β |
| Positive selection in admixed populations from Ethiopia. | Walsh S et al. | β | 2020 | β |
| Predicting geographic location from genetic variation with deep neural networks. | Battey CJ et al. | β | 2020 | β |
| Prediction and management of CAD risk based on genetic stratification. | Roberts R et al. | β | 2020 | β |
| Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs. | Treff NR et al. | β | 2020 | β |
| Refining the "double two-thirds" rule: Genotype-based breed grouping and clinical presentation help predict the diagnosis of canine splenic mass lesions in 288 dogs. | Davies O et al. | β | 2020 | β |
| RETRACTED: CGVD: a genomic variation database for Chinese populations. | Zeng J et al. | β | 2020 | β |
| Role of long non-coding RNA in DEET- and fipronil-mediated alteration of transcripts associated with Phase I and Phase II xenobiotic metabolism in human primary hepatocytes. | Lawrie RD et al. | β | 2020 | β |
| Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases. | Yamasaki M et al. | β | 2020 | β |
| Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery. | Varner MW et al. | β | 2020 | β |
| Spatiotemporal DNA methylome dynamics of the developing mouse fetus. | He Y et al. | β | 2020 | β |
| Structural variation in the sequencing era. | Ho SS et al. | β | 2020 | β |
| The Birth of Bio-data Science: Trends, Expectations, and Applications. | Goh WWB et al. | β | 2020 | β |
| The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations. | Rocha CS et al. | β | 2020 | β |
| The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals. | Cao Y 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 gut microbiome but not the resistome is associated with urogenital schistosomiasis in preschool-aged children. | Osakunor DNM et al. | β | 2020 | β |
| The Human Genome Project changed everything. | Gibbs RA | β | 2020 | β |
| The Impact of <i>HMGB1</i> Polymorphisms on Prostate Cancer Progression and Clinicopathological Characteristics. | Chou YE et al. | β | 2020 | β |
| The Impact of Pharmacogenomics in Personalized Medicine. | Singh DB | β | 2020 | β |
| The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. | Li D et al. | β | 2020 | β |
| The Nigerian Bioinformatics and Genomics Network (NBGN): a collaborative platform to advance bioinformatics and genomics in Nigeria. | Fatumo S 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 |
| TraPS-VarI: Identifying genetic variants altering phosphotyrosine based signalling motifs. | Ulaganathan VK | β | 2020 | β |
| Turning strains into strengths for understanding psychiatric disorders. | Moore SJ et al. | β | 2020 | β |
| VEF: a variant filtering tool based on ensemble methods. | Zhang C et al. | β | 2020 | β |
| XPA: DNA Repair Protein of Significant Clinical Importance. | BorszΓ©kovΓ‘ PulzovΓ‘ L et al. | β | 2020 | β |
| 1k-RiCA (1K-Rice Custom Amplicon) a novel genotyping amplicon-based SNP assay for genetics and breeding applications in rice. | Arbelaez JD et al. | β | 2019 | β |
| A Bayesian approach to Mendelian randomisation with dependent instruments. | Shapland CY et al. | β | 2019 | β |
| Allele-specific binding of RNA-binding proteins reveals functional genetic variants in the RNA. | Yang EW et al. | β | 2019 | β |
| Analysis of differences in human leukocyte antigen between the two Wellcome Trust Case Control Consortium control datasets. | Jang CS et al. | β | 2019 | β |
| An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations. | Dube U et al. | β | 2019 | β |
| Ancestry informative markers (AIMs) for Korean and other East Asian and South East Asian populations. | Jung JY et al. | β | 2019 | β |
| Application of Chaotic Laws to Improve Haplotype Assembly Using Chaos Game Representation. | Olyaee MH et al. | β | 2019 | β |
| Applications of Genomic Technologies in Retinal Degenerative Diseases. | Ratnapriya R | β | 2019 | β |
| A Screening Test for <i>HLA-B<sup>β</sup>15:02</i> in a Large United States Patient Cohort Identifies Broader Risk of Carbamazepine-Induced Adverse Events. | Fang H et al. | β | 2019 | β |
| A single-nucleotide polymorphism in a gene modulating glucocorticoid sensitivity is associated with the decline in total lung capacity after lung transplantation. | Yamamoto H et al. | β | 2019 | β |
| Association between CD53 genetic polymorphisms and tuberculosis cases. | Jin HS et al. | β | 2019 | β |
| Association between <i>SLCO1B1</i> rs4149056 and tegafur-uracil-induced hepatic dysfunction in breast cancer. | Kamio H et al. | β | 2019 | β |
| Association Between rs3833912/rs16944 SNPs and Risk for Cerebral Palsy in Mexican Children. | Torres-Merino S et al. | β | 2019 | β |
| Bayesian multivariate reanalysis of large genetic studies identifies many new associations. | Turchin MC et al. | β | 2019 | β |
| Biomedical Research Cohort Membership Disclosure on Social Media. | Liu Y et al. | β | 2019 | β |
| CERENKOV2: improved detection of functional noncoding SNPs using data-space geometric features. | Yao Y et al. | β | 2019 | β |
| Common DNA sequence variation influences 3-dimensional conformation of the human genome. | Gorkin DU et al. | β | 2019 | β |
| Construction of JRG (Japanese reference genome) with single-molecule real-time sequencing. | Nagasaki M et al. | β | 2019 | β |
| Copy number variation is highly correlated with differential gene expression: a pan-cancer study. | Shao X et al. | β | 2019 | β |
| Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in African Americans. | Jones CC et al. | β | 2019 | β |
| CYP2C19 and STAT6 Variants Influence the Outcome of Proton Pump Inhibitor Therapy in Pediatric Eosinophilic Esophagitis. | Mougey EB et al. | β | 2019 | β |
| Detecting latent exposure in genome-wide association studies using a breakpoint model for logistic regression. | Alarcon F et al. | β | 2019 | β |
| Detecting Population-Differentiation Copy Number Variants in Human Population Tree by Sparse Group Selection. | Zhang H et al. | β | 2019 | β |
| Dissecting human North African gene-flow into its western coastal surroundings. | Arauna LR et al. | β | 2019 | β |
| Effects of teriparatide in Chinese and Caucasian women with osteoporosis: bridging study on efficacy. | Xie Z et al. | β | 2019 | β |
| Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. | Budde M et al. | β | 2019 | β |
| Emerging Roles for NLRC5 in Immune Diseases. | Wang JQ et al. | β | 2019 | β |
| Established and emerging strategies to crack the genetic code of obesity. | Tam V et al. | β | 2019 | β |
| Establishment of Integrated Biobank for Precision Medicine and Personalized Healthcare: The Tohoku Medical Megabank Project. | Fuse N et al. | β | 2019 | β |
| European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin. | Font-Porterias N et al. | β | 2019 | β |
| Evidence of Assortative Mating in Autism Spectrum Disorder. | Connolly S et al. | β | 2019 | β |
| Facial recognition from DNA using face-to-DNA classifiers. | Sero D et al. | β | 2019 | β |
| FcΞ³RIIIa receptor polymorphism influences NK cell mediated ADCC activity against HIV. | Talathi SP et al. | β | 2019 | β |
| Fine-mapping scan of bipolar disorder susceptibility loci in Latino pedigrees. | Gonzalez S et al. | β | 2019 | β |
| Fish intake interacts with TM6SF2 gene variant to affect NAFLD risk: results of a case-control study. | Kalafati IP et al. | β | 2019 | β |
| ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest. | Li J et al. | β | 2019 | β |
| Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus. | Buckley MA et al. | β | 2019 | β |
| Genetic analysis of pharmacogenomic VIP variants in the Blang population from Yunnan Province of China. | Zhang C et al. | β | 2019 | β |
| Genetic comparison of sickle cell anaemia cohorts from Brazil andΒ the United States reveals high levels of divergence. | Cruz PRS et al. | β | 2019 | β |
| Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms. | Walker RL et al. | β | 2019 | β |
| Genetic Polymorphisms Affecting IDO1 or IDO2 Activity Differently Associate With Aspergillosis in Humans. | Napolioni V et al. | β | 2019 | β |
| Genetics of rheumatoid arthritis: 2018 status. | Okada Y et al. | β | 2019 | β |
| Genetic Support for Longevity-Enhancing Drug Targets: Issues, Preliminary Data, and Future Directions. | McCorrison J 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 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 |
| Genome-Wide Association Analysis Reveals Key Genes Responsible for Egg Production of Lion Head Goose. | Zhao Q et al. | β | 2019 | β |
| Genome-wide expression profiling-based copy number variations and colorectal cancer risk in Chinese. | Wang K et al. | β | 2019 | β |
| Genomic and Phenomic Research in the 21st Century. | Hebbring S | β | 2019 | β |
| Genomic data analysis workflows for tumors from patient-derived xenografts (PDXs): challenges and guidelines. | Woo XY et al. | β | 2019 | β |
| Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. | Grotzinger AD et al. | β | 2019 | β |
| Gigwa v2-Extended and improved genotype investigator. | SempΓ©rΓ© G et al. | β | 2019 | β |
| GWAS of Behavioral Traits. | Mehta D et al. | β | 2019 | β |
| High-efficiency genomic editing in Epstein-Barr virus-transformed lymphoblastoid B cells using a single-stranded donor oligonucleotide strategy. | Johnston AD et al. | β | 2019 | β |
| Identification of novel genetic variants predisposing to familial oral squamous cell carcinomas. | Huang Y et al. | β | 2019 | β |
| IMI - Myopia Genetics Report. | Tedja MS et al. | β | 2019 | β |
| Improving Community Advisory Board Engagement in Precision Medicine Research to Reduce Health Disparities. | Connors E et al. | β | 2019 | β |
| Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer. | Ferreira EN et al. | β | 2019 | β |
| Informativeness of dental morphology in ancestry estimation in African Americans. | Gross JM et al. | β | 2019 | β |
| Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits. | Massrali A et al. | β | 2019 | β |
| Interactions between <i>DRD2/ANKK1</i> TaqIA Polymorphism and Dietary Factors Influence Plasma Triglyceride Concentrations in Diabetic Patients from Western Mexico: A Cross-sectional Study. | Ramos-Lopez O et al. | β | 2019 | β |
| Investigating skewness to understand gene expression heterogeneity in large patient cohorts. | Church BV et al. | β | 2019 | β |
| IPCAPS: an R package for iterative pruning to capture population structure. | Chaichoompu K et al. | β | 2019 | β |
| Iron Matryoshka-Haemochromatosis nested in Ferroportin Disease? | Viveiros A et al. | β | 2019 | β |
| Is it time to change the reference genome? | Ballouz S et al. | β | 2019 | β |
| Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. | Sasani TA et al. | β | 2019 | β |
| Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves' Disease in the Chinese Han Population. | Li J et al. | β | 2019 | β |
| Linking of genetic risk variants to disease-specific gene expression via multi-omics studies in rheumatoid arthritis. | Suzuki A et al. | β | 2019 | β |
| Mechanisms of B-Cell Oncogenesis Induced by Epstein-Barr Virus. | Saha A et al. | β | 2019 | β |
| Meta-analysis of genome-wide association studies for body fat distribution in 694Β 649 individuals of European ancestry. | Pulit SL 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 |
| Network Medicine in the Age of Biomedical Big Data. | Sonawane AR et al. | β | 2019 | β |
| No Association of Variants of the NPY-System With Obsessive-Compulsive Disorder in Children and Adolescents. | Franke M et al. | β | 2019 | β |
| Odyssey: a semi-automated pipeline for phasing, imputation, and analysis of genome-wide genetic data. | Eller RJ et al. | β | 2019 | β |
| OPATs: Omnibus P-value association tests. | Chen CW et al. | β | 2019 | β |
| Opportunities, resources, and techniques for implementing genomics in clinical care. | Manolio TA et al. | β | 2019 | β |
| Pedigree-based estimation of human mobile element retrotransposition rates. | Feusier J et al. | β | 2019 | β |
| Personalized Medicine and the Power of Electronic Health Records. | Abul-Husn NS et al. | β | 2019 | β |
| Pervasive Inter-Individual Variation in Allele-Specific Expression in Monozygotic Twins. | da Silva Francisco Junior R et al. | β | 2019 | β |
| Pharmacogenetics of anticancer monoclonal antibodies. | Shek D et al. | β | 2019 | β |
| Pharmacogenomics of amlodipine and hydrochlorothiazide therapy and the quest for improved control of hypertension: a mini review. | Johnson R et al. | β | 2019 | β |
| Polygenic risk for psychiatric disorders correlates with executive function in typical development. | Schork AJ et al. | β | 2019 | β |
| Polymorphism in the PBX1 gene is related to cystinuria in Brazilian families. | Reis ST et al. | β | 2019 | β |
| Population Structure and Implications on the Genetic Architecture of HIV-1 Phenotypes Within Southern Africa. | Thami PK et al. | β | 2019 | β |
| Precision epidemiology for infectious disease control. | Ladner JT et al. | β | 2019 | β |
| Radiation-Induced Chromosomal Breaks may be DNA Repair Fragile Sites with Larger-scale Correlations to Eight Double-Strand-Break Related Data Sets over the Human Genome. | Brahme A et al. | β | 2019 | β |
| Re-identification of individuals in genomic data-sharing beacons via allele inference. | von Thenen N et al. | β | 2019 | β |
| Replicability analysis in genome-wide association studies via Cartesian hidden Markov models. | Wang P et al. | β | 2019 | β |
| Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. | Wang M 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 |
| Salivary Ξ±-amylase copy number is not associated with weight trajectories and glycemic improvements following clinical weight loss: results from a 2-phase dietary intervention study. | Valsesia A et al. | β | 2019 | β |
| Selective Sweeps. | Stephan W | β | 2019 | β |
| Shades of complexity: New perspectives on the evolution and genetic architecture of human skin. | Quillen EE et al. | β | 2019 | β |
| Shared additive genetic variation for alcohol dependence among subjects of African and European ancestry. | Brick LA et al. | β | 2019 | β |
| Single nucleotide polymorphisms of let-7-related genes increase susceptibility to breast cancer. | Du Y et al. | β | 2019 | β |
| SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. | FernΓ‘ndez-Santiago R et al. | β | 2019 | β |
| Sparse Convolutional Denoising Autoencoders for Genotype Imputation. | Chen J et al. | β | 2019 | β |
| Statistical Association Mapping of Population-Structured Genetic Data. | Najafi A et al. | β | 2019 | β |
| Step-Up Therapy in Black Children and Adults with Poorly Controlled Asthma. | Wechsler ME et al. | β | 2019 | β |
| Surveying Gut Microbiome Research in Africans: Toward Improved Diversity and Representation. | Brewster R et al. | β | 2019 | β |
| Target 2035: probing the human proteome. | Carter AJ et al. | β | 2019 | β |
| Targeting BCAA Catabolism to Treat Obesity-Associated Insulin Resistance. | Zhou M et al. | β | 2019 | β |
| The Continuing Evolution of Precision Health in Type 2 Diabetes: Achievements and Challenges. | Lin Y et al. | β | 2019 | β |
| The Era of the Genome and Dental Medicine. | Divaris K | β | 2019 | β |
| The Evolving Field of Genetic Epidemiology: From Familial Aggregation to Genomic Sequencing. | Duggal P et al. | β | 2019 | β |
| The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE. | Bien SA et al. | β | 2019 | β |
| The Influence of FTO Polymorphism rs9939609 on Obesity, Some Clinical Features, and Disturbance of Carbohydrate Metabolism in Patients with Psoriasis. | Tupikowska-Marzec M et al. | β | 2019 | β |
| The Medical Genome Reference Bank: a whole-genome data resource of 4000 healthy elderly individuals. Rationale and cohort design. | Lacaze P et al. | β | 2019 | β |
| The MHC in the era of next-generation sequencing: Implications for bridging structure with function. | Petersdorf EW et al. | β | 2019 | β |
| The NCATS BioPlanet - An Integrated Platform for Exploring the Universe of Cellular Signaling Pathways for Toxicology, Systems Biology, and Chemical Genomics. | Huang R et al. | β | 2019 | β |
| The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019. | Buniello A et al. | β | 2019 | β |
| The Single Nucleotide Polymorphism Mal-D96N Mice Provide New Insights into Functionality of Mal in TLR Immune Responses. | Dowling JK et al. | β | 2019 | β |
| Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis. | Hao L et al. | β | 2019 | β |
| Whole-genome re-sequencing reveals the impact of the interaction of copy number variants of the rhg1 and Rhg4 genes on broad-based resistance to soybean cyst nematode. | Patil GB et al. | β | 2019 | β |
| A common regulatory variant in SLC35B4 influences the recurrence and survival of prostate cancer. | Huang EY et al. | β | 2018 | β |
| A decade of genome-wide association studies for coronary artery disease: the challenges ahead. | Erdmann J et al. | β | 2018 | β |
| A Genome-Wide Association Study Identifies a Candidate Gene Associated With Atazanavir Exposure Measured in Hair. | Tamraz B et al. | β | 2018 | β |
| A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci. | Hamdi Y et al. | β | 2018 | β |
| Agronomic Linked Data (AgroLD): A knowledge-based system to enable integrative biology in agronomy. | Venkatesan A et al. | β | 2018 | β |
| A Likelihood-Free Inference Framework for Population Genetic Data using Exchangeable Neural Networks. | Chan J et al. | β | 2018 | β |
| A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease. | Williams LM et al. | β | 2018 | β |
| A Methodological Assessment and Characterization of Genetically-Driven Variation in Three Human Phosphoproteomes. | Engelmann BW et al. | β | 2018 | β |
| A modified response of NAFLD patients with non-significant fibrosis in nutritional counseling according to GCKR rs1260326. | Kaliora AC et al. | β | 2018 | β |
| Ancestry and dental development: A geographic and genetic perspective. | Dhamo B et al. | β | 2018 | β |
| A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs. | Kim SA et al. | β | 2018 | β |
| A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia. | Rydning SL et al. | β | 2018 | β |
| A nursing theory-guided framework for genetic and epigenetic research. | Maki KA et al. | β | 2018 | β |
| A pleiotropic effect of the APOE gene: association of APOE polymorphisms with multibacillary leprosy in Han Chinese from Southwest China. | Wang D et al. | β | 2018 | β |
| APOE gene and neuropsychiatric disorders and endophenotypes: A comprehensive review. | Forero DA et al. | β | 2018 | β |
| A remark on copy number variation detection methods. | Li S et al. | β | 2018 | β |
| A review of bioinformatic methods for forensic DNA analyses. | Liu YY et al. | β | 2018 | β |
| A review of the associations between single nucleotide polymorphisms in taste receptors, eating behaviors, and health. | Chamoun E et al. | β | 2018 | β |
| A single-nucleotide polymorphism of the beta 2-adrenergic receptor gene can predict pathological complete response to taxane- and platinum-based neoadjuvant chemotherapy in breast cancer. | Du Y et al. | β | 2018 | β |
| Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability. | Sokol J et al. | β | 2018 | β |
| A tutorial on conducting genome-wide association studies: Quality control and statistical analysis. | Marees AT et al. | β | 2018 | β |
| Bioavailability of Fat-Soluble Vitamins and Phytochemicals in Humans: Effects of Genetic Variation. | Borel P et al. | β | 2018 | β |
| Bioinformatics and genomic databases. | Chen J et al. | β | 2018 | β |
| Breast cancer: The translation of big genomic data to cancer precision medicine. | Low SK et al. | β | 2018 | β |
| Causal Inference in Cancer Epidemiology: What Is the Role of Mendelian Randomization? | Yarmolinsky J et al. | β | 2018 | β |
| Characterization of copy number variants in a large multibreed population of beef and dairy cattle using high-density single nucleotide polymorphism genotype data. | Rafter P et al. | β | 2018 | β |
| Codon based co-occurrence network motifs in human mitochondria. | Shinde P et al. | β | 2018 | β |
| Conserved and species-specific transcription factor co-binding patterns drive divergent gene regulation in human and mouse. | Diehl AG et al. | β | 2018 | β |
| Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort. | Carvalho SDCES et al. | β | 2018 | β |
| Copy Number Variation. | MacΓ© A et al. | β | 2018 | β |
| CRISPR/Cas9-Mediated Genome Editing in Epstein-Barr Virus-Transformed Lymphoblastoid B-Cell Lines. | Jiang S et al. | β | 2018 | β |
| Deciphering DMET genetic data: comprehensive assessment of Northwestern Han, Tibetan, Uyghur populations and their comparison to eleven 1000 genome populations. | Zhang J et al. | β | 2018 | β |
| Deciphering the fine nucleotide diversity of full HLA class I and class II genes in a well-documented population from sub-Saharan Africa. | Goeury T et al. | β | 2018 | β |
| De novo assembly of haplotype-resolved genomes with trio binning. | Koren S et al. | β | 2018 | β |
| Detecting, quantifying, and discriminating the mechanism of mosaic chromosomal aneuploidies using MAD-seq. | Kong Y et al. | β | 2018 | β |
| DNMT1 and DNMT3A haplotypes associated with noise-induced hearing loss in Chinese workers. | Ding E et al. | β | 2018 | β |
| Epidemiology of prostate cancer in Asian countries. | Kimura T et al. | β | 2018 | β |
| Exploiting next-generation sequencing to solve the haplotyping puzzle in polyploids: a simulation study. | Motazedi E et al. | β | 2018 | β |
| EXPOsOMICS: final policy workshop and stakeholder consultation. | Turner MC et al. | β | 2018 | β |
| Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes. | Quan Y et al. | β | 2018 | β |
| Fast Ordered Sampling of DNA Sequence Variants. | Greenberg AJ | β | 2018 | β |
| Fast score test with global null estimation regardless of missing genotypes. | Sato S et al. | β | 2018 | β |
| Forensic SNP Genotyping with SNaPshot: Development of a Novel In-house SBE Multiplex SNP Assay. | Zar MS et al. | β | 2018 | β |
| Frequency of PAR4 Ala120Thr variant associated with platelet reactivity significantly varies across sub-Saharan African populations. | Heenkenda MK et al. | β | 2018 | β |
| From genome-wide association studies to Mendelian randomization: novel opportunities for understanding cardiovascular disease causality, pathogenesis, prevention, and treatment. | Benn M et al. | β | 2018 | β |
| Functional genomic landscape of acute myeloid leukaemia. | Tyner JW et al. | β | 2018 | β |
| FUT2 genotype and secretory status are not associated with fecal microbial composition and inferred function in healthy subjects. | Turpin W et al. | β | 2018 | β |
| GABRA2, alcohol, and illicit drug use: An event-level model of genetic risk for polysubstance use. | Mallard TT et al. | β | 2018 | β |
| Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma. | Gamazon ER et al. | β | 2018 | β |
| Gene-Gene and Gene-Environment Interactions. | DeWan AT | β | 2018 | β |
| Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis. | Suzuki A et al. | β | 2018 | β |
| Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of <i>ERAP2</i> transcripts under balancing selection. | Ye CJ et al. | β | 2018 | β |
| Genetic association of the cytochrome c oxidase-related genes with Alzheimer's disease in Han Chinese. | Bi R et al. | β | 2018 | β |
| Genetics in the prevention and management of coronary artery disease. | Roberts R | β | 2018 | β |
| Genetics of male infertility. | Krausz C et al. | β | 2018 | β |
| Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations. | Wang Y et al. | β | 2018 | β |
| Genetic variants related to urate and risk of Parkinson's disease. | Hughes KC et al. | β | 2018 | β |
| Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences. | Manzoni C et al. | β | 2018 | β |
| Genome-Wide Association Studies and Risk Scores for Coronary Artery Disease: Sex Biases. | Byars SG et al. | β | 2018 | β |
| Genotype Imputation from Large Reference Panels. | Das S et al. | β | 2018 | β |
| Global analysis of population stratification using a smart panel of 27 continental ancestry-informative SNPs. | Jiang L et al. | β | 2018 | β |
| Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability. | Sokol J et al. | β | 2018 | β |
| Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland. | Martin AR et al. | β | 2018 | β |
| HD-Marker: a highly multiplexed and flexible approach for targeted genotyping of more than 10,000 genes in a single-tube assay. | Lv J et al. | β | 2018 | β |
| High-Quality Overlapping Paired-End Reads for the Detection of A-to-I Editing on Small RNA. | Galipon J et al. | β | 2018 | β |
| Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification. | Smieszek S et al. | β | 2018 | β |
| HLA-DQΞ²1 amino acid position 87 and DQB1*0301 are associated with Chinese Han SLE. | Sun J et al. | β | 2018 | β |
| HUMA: A platform for the analysis of genetic variation in humans. | Brown DK et al. | β | 2018 | β |
| Human genome-wide measurement of drug-responsive regulatory activity. | Johnson GD et al. | β | 2018 | β |
| Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach. | Kotnik P et al. | β | 2018 | β |
| Impact of histamine receptors H1 and H3 polymorphisms on antipsychotic-induced weight gain. | Tiwari AK et al. | β | 2018 | β |
| Improving imputation in disease-relevant regions: lessons from cystic fibrosis. | Panjwani N et al. | β | 2018 | β |
| Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. | Wojcik GL et al. | β | 2018 | β |
| Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patients. | Macauda A et al. | β | 2018 | β |
| Insights into respiratory disease through bioinformatics. | Hurgobin B et al. | β | 2018 | β |
| Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. | Abdulkadir M et al. | β | 2018 | β |
| Is evolutionary loss our gain? The role of ACTN3 p.Arg577Ter (R577X) genotype in athletic performance, ageing, and disease. | Houweling PJ 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 |
| KoVariome: Korean National Standard Reference Variome database of whole genomes with comprehensive SNV, indel, CNV, and SV analyses. | Kim J 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 |
| Letter: predicting azathioprine-associated pancreatitis in IBD-phenotype or genotype? | Teich N et al. | β | 2018 | β |
| Meat and fiber intake and interaction with pattern recognition receptors (TLR1, TLR2, TLR4, and TLR10) in relation to colorectal cancer in a Danish prospective, case-cohort study. | Kopp TI et al. | β | 2018 | β |
| Medical genetics and genomic medicine in Nigeria. | Adeyemo AA et al. | β | 2018 | β |
| Mendelian Randomization Studies Promise to Shorten the Journey to FDAΒ Approval. | Roberts R | β | 2018 | β |
| Model framework for governance of genomic research and biobanking in Africa - a content description. | Yakubu A et al. | β | 2018 | β |
| Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference. | Quinto-CortΓ©s CD et al. | β | 2018 | β |
| Molecular Basis for Dysregulated Activation of NKX2-5 in the Vascular Remodeling of Systemic Sclerosis. | Dritsoula A et al. | β | 2018 | β |
| Neurogenomics - towards a more rigorous science. | Mitchell KJ | β | 2018 | β |
| Neurotransmitter Pathway Genes in Cognitive Decline During Aging: Evidence for GNG4 and KCNQ2 Genes. | Bonham LW et al. | β | 2018 | β |
| New Risk Allele for Intracranial Aneurysm in French-Canadians. | Starke RM et al. | β | 2018 | β |
| Notch polymorphisms associated with sensitivity of noise induced hearing loss among Chinese textile factory workers. | Ding E et al. | β | 2018 | β |
| Novel disease syndromes unveiled by integrative multiscale network analysis of diseases sharing molecular effectors and comorbidities. | Li H et al. | β | 2018 | β |
| Nutrigenomics: Opportunities & challenges for public health nutrition. | Reddy VS et al. | β | 2018 | β |
| "Omics" data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy. | Campbell NV et al. | β | 2018 | β |
| On Estimation of Genome Composition in Genetically Admixed Individuals Using Constrained Genomic Regression. | Boerner V et al. | β | 2018 | β |
| Ovarian cancer risk, ALDH2 polymorphism and alcohol drinking: Asian data from the Ovarian Cancer Association Consortium. | Ugai T et al. | β | 2018 | β |
| Personalised Medicine: The Odyssey from Hope to Practice. | Visvikis-Siest S et al. | β | 2018 | β |
| Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data. | Hariprakash JM et al. | β | 2018 | β |
| Pharmacogenetics of Antiretroviral Drug Response and Pharmacokinetic Variations in Indigenous South African Populations. | O'Connell KS 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 |
| Pharmacogenomic Variability of Oral Baclofen Clearance and Clinical Response in Children With Cerebral Palsy. | McLaughlin MJ et al. | β | 2018 | β |
| Physiologic Interpretation of GWAS Signals for Type 2 Diabetes. | Watanabe RM | β | 2018 | β |
| Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission. | Carter TC et al. | β | 2018 | β |
| Polymorphisms in cytochrome P450 are associated with extensive efavirenz pharmacokinetics and CNS toxicities in an HIV cohort in Botswana. | Vujkovic M et al. | β | 2018 | β |
| Population-based dose-response analysis of liver transcriptional response to trichloroethylene in mouse. | Venkatratnam A et al. | β | 2018 | β |
| Powerful Inference with the D-Statistic on Low-Coverage Whole-Genome Data. | Soraggi S et al. | β | 2018 | β |
| Prostate Cancer in Southern Africa: Does Africa Hold Untapped Potential to Add Value to the Current Understanding of a Common Disease? | Hayes VM et al. | β | 2018 | β |
| Quantitative Relationship Between Cumulative Risk Alleles Based on Genome-Wide Association Studies and Type 2 Diabetes Mellitus: A Systematic Review and Meta-analysis. | Kodama S et al. | β | 2018 | β |
| Racial Disparities in Lung Cancer Survival: The Contribution of Stage, Treatment, and Ancestry. | Jones CC et al. | β | 2018 | β |
| Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease. | Gaare JJ et al. | β | 2018 | β |
| Rare <i>ABCA7</i> variants in 2 German families with Alzheimer disease. | May P et al. | β | 2018 | β |
| Realizing the significance of noncoding functionality in clinical genomics. | Gloss BS et al. | β | 2018 | β |
| Reconstructing an African haploid genome from the 18th century. | Jagadeesan A et al. | β | 2018 | β |
| Relationship of vitamin D receptor gene polymorphisms in <i>Helicobacter pylori</i> gastric patients. | Martins DJ et al. | β | 2018 | β |
| Sequence Analysis of <i>APOA5</i> Among the Kuwaiti Population Identifies Association of rs2072560, rs2266788, and rs662799 With TG and VLDL Levels. | Jasim AA et al. | β | 2018 | β |
| Sequence diversity of the Rh blood group system in Basques. | Flores-Bello A et al. | β | 2018 | β |
| Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. | Perez-Ortiz AC et al. | β | 2018 | β |
| Sparse Tensor Decomposition for Haplotype Assembly of Diploids and Polyploids. | Hashemi A et al. | β | 2018 | β |
| STAT3-enhancing germline mutations contribute to tumor-extrinsic immune evasion. | Kogan D et al. | β | 2018 | β |
| Strategies for processing and quality control of Illumina genotyping arrays. | Zhao S et al. | β | 2018 | β |
| Study of Deiodinase Type 2 Polymorphisms in Graves' Disease and Ophthalmopathy in a Swedish Population. | Shahida B et al. | β | 2018 | β |
| Sustainable data and metadata management at the BD2K-LINCS Data Coordination and Integration Center. | Stathias V et al. | β | 2018 | β |
| Tests of fit of historically-informed models of African American Admixture. | Gross JM | β | 2018 | β |
| The Arc Gene Confers Genetic Susceptibility to Alzheimer's Disease in Han Chinese. | Bi R et al. | β | 2018 | β |
| The Bermuda Triangle: The Pragmatics, Policies, and Principles for Data Sharing in the History of the Human Genome Project. | Maxson Jones K et al. | β | 2018 | β |
| The genetic assimilation in language borrowing inferred from Jing People. | Huang X et al. | β | 2018 | β |
| The Genomic Commons. | Contreras JL et al. | β | 2018 | β |
| The influence of Neanderthal alleles on cytotoxic response. | Akhtari FS et al. | β | 2018 | β |
| The Relationship between Single Nucleotide Polymorphisms in Taste Receptor Genes, Taste Function and Dietary Intake in Preschool-Aged Children and Adults in the Guelph Family Health Study. | Chamoun E et al. | β | 2018 | β |
| TIA: algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing. | Farris MH et al. | β | 2018 | β |
| TTN genotype is associated with fascicle length and marathon running performance. | Stebbings GK et al. | β | 2018 | β |
| Type I Interferon Receptor Variants in Gene Regulatory Regions are Associated with Susceptibility to Cerebral Malaria in Malawi. | Feintuch CM et al. | β | 2018 | β |
| Using Y-Chromosomal Haplogroups in Genetic Association Studies and Suggested Implications. | Erzurumluoglu AM et al. | β | 2018 | β |
| Vitamin D metabolic loci and preeclampsia risk in multi-ethnic pregnant women. | Baca KM et al. | β | 2018 | β |
| Vitamin D metabolic loci and vitamin D status in Black and White pregnant women. | Baca KM et al. | β | 2018 | β |
| A Bayesian group sparse multi-task regression model for imaging genetics. | Greenlaw K et al. | β | 2017 | β |
| Activated TAFI Promotes the Development of Chronic Thromboembolic Pulmonary Hypertension: A Possible Novel Therapeutic Target. | Satoh T et al. | β | 2017 | β |
| Addressing Beacon re-identification attacks: quantification and mitigation of privacy risks. | Raisaro JL et al. | β | 2017 | β |
| A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity. | Somers M et al. | β | 2017 | β |
| A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. | Noordam R et al. | β | 2017 | β |
| Analysis of Complement <i>C3</i> Gene Reveals Susceptibility to Severe Preeclampsia. | Lokki AI et al. | β | 2017 | β |
| Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. | Polushina T et al. | β | 2017 | β |
| Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach. | Falola O et al. | β | 2017 | β |
| A novel homozygous complex deletion in CFTR caused cystic fibrosis in a Chinese patient. | Liu K et al. | β | 2017 | β |
| A perspective on chronic kidney disease progression. | Zhong J et al. | β | 2017 | β |
| A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases. | Wang M et al. | β | 2017 | β |
| Association between polymorphisms in pre-miRNA genes and risk of oral squamous cell cancer in a Chinese population. | Zhang E et al. | β | 2017 | β |
| Association of genetic variations in FOXO3 gene with susceptibility to noise induced hearing loss in a Chinese population. | Guo H et al. | β | 2017 | β |
| Between Lake Baikal and the Baltic Sea: genomic history of the gateway to Europe. | Triska P et al. | β | 2017 | β |
| [Big Data Revolution or Data Hubris? : On the Data Positivism of Molecular Biology]. | Gramelsberger G | β | 2017 | β |
| Biological networks in Parkinson's disease: an insight into the epigenetic mechanisms associated with this disease. | Chatterjee P et al. | β | 2017 | β |
| BLOOM: BLoom filter based oblivious outsourced matchings. | Ziegeldorf JH et al. | β | 2017 | β |
| Cancer Stem Cell Gene Variants Predict Disease Recurrence in Patients Treated with Radical Prostatectomy for Prostate Cancer. | Lin VC et al. | β | 2017 | β |
| Can learning health systems help organisations deliver personalised care? | Nwaru BI et al. | β | 2017 | β |
| Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration. | Powis Z et al. | β | 2017 | β |
| Combined Genetic Biomarkers Confer Susceptibility to Risk of Urothelial Bladder Carcinoma in a Saudi Population. | Elhawary NA et al. | β | 2017 | β |
| Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. | de Vries PS et al. | β | 2017 | β |
| Compound heterozygous <i>SLC19A3</i> mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease. | Whitford W et al. | β | 2017 | β |
| Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. | Haraksingh RR et al. | β | 2017 | β |
| Concise Review: Induced Pluripotent Stem Cell Research in the Era of Precision Medicine. | Hamazaki T et al. | β | 2017 | β |
| Copy-number variants and candidate gene mutations in isolated split hand/foot malformation. | Carter TC et al. | β | 2017 | β |
| Cytochrome P450 Genetic Variations Can Predict mRNA Expression, Cyclophosphamide 4-Hydroxylation, and Treatment Outcomes in Chinese Patients With Non-Hodgkin's Lymphoma. | Shu W et al. | β | 2017 | β |
| Developmentally Specific Associations Between CNR1 Genotype and Cannabis Use Across Emerging Adulthood. | Ashenhurst JR et al. | β | 2017 | β |
| Differential expression analysis for RNAseq using Poisson mixed models. | Sun S et al. | β | 2017 | β |
| Downregulation of PKCΞΆ/Pard3/Pard6b is responsible for lung adenocarcinoma cell EMT and invasion. | Zhou Q et al. | β | 2017 | β |
| Effects of FCGRIIIa-158V/F polymorphism on antibody-dependent cellular cytotoxicity activity of adalimumab. | Kimura K et al. | β | 2017 | β |
| Emerging therapeutic targets in cancer induced bone disease: A focus on the peripheral type 2 cannabinoid receptor. | Marino S et al. | β | 2017 | β |
| Establishing a reliable framework for harnessing the creative power of the scientific crowd. | Carter AJ et al. | β | 2017 | β |
| Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study. | Saw WY et al. | β | 2017 | β |
| Evaluating the Neolithic Expansion at Both Shores of the Mediterranean Sea. | Pimenta J et al. | β | 2017 | β |
| Evaluation of a Panel of Single-Nucleotide Polymorphisms in miR-146a and miR-196a2 Genomic Regions in Patients with Chronic Periodontitis. | Venugopal P et al. | β | 2017 | β |
| Extremely low-coverage whole genome sequencing in South Asians captures population genomics information. | Rustagi N et al. | β | 2017 | β |
| Familial Analysis of Epistatic and Sex-Dependent Association of Genes of the Renin-Angiotensin-Aldosterone System and Blood Pressure. | Scurrah KJ et al. | β | 2017 | β |
| Fine-mapping inflammatory bowel disease loci to single-variant resolution. | Huang H et al. | β | 2017 | β |
| Fine-mapping of antipsychotic response genome-wide association studies reveals novel regulatory mechanisms. | Ovenden ES et al. | β | 2017 | β |
| Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations. | Olafsson S et al. | β | 2017 | β |
| Gene co-opening network deciphers gene functional relationships. | Li W et al. | β | 2017 | β |
| Genetic- and Lifestyle-dependent Dental Caries Defined by the Acidic Proline-rich Protein Genes PRH1 and PRH2. | StrΓΆmberg N et al. | β | 2017 | β |
| Genetic Association of Hematopoietic Stem Cell Transplantation Outcome beyond Histocompatibility Genes. | Gam R et al. | β | 2017 | β |
| Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA). | Wang Z et al. | β | 2017 | β |
| Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. | Hobbs BD et al. | β | 2017 | β |
| Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play. | Capone VP et al. | β | 2017 | β |
| Genetics of neurodegenerative diseases: an overview. | PihlstrΓΈm L et al. | β | 2017 | β |
| Genetic Variants Contributing to Colistin Cytotoxicity: Identification of TGIF1 and HOXD10 Using a Population Genomics Approach. | Eadon MT et al. | β | 2017 | β |
| Genetic variants of TRAF6 modulate peritoneal immunity and the risk of spontaneous bacterial peritonitis in cirrhosis: A combined prospective-retrospective study. | Mai M et al. | β | 2017 | β |
| Genetic Variation in Kruppel like Factor 15 Is Associated with Left Ventricular Hypertrophy in Patients with Type 2 Diabetes: Discovery and Replication Cohorts. | Patel SK et al. | β | 2017 | β |
| Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. | Agopian AJ 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 meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence. | Yin X et al. | β | 2017 | β |
| Germline Mutations in the Kallikrein 6 Region and Predisposition for Aggressive Prostate Cancer. | Briollais L et al. | β | 2017 | β |
| Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort. | PoniΕska JK et al. | β | 2017 | β |
| Haplotype Inference. | Song S et al. | β | 2017 | β |
| Haplotypes of the Ovine Adiponectin Gene and Their Association with Growth and Carcass Traits in New Zealand Romney Lambs. | An Q et al. | β | 2017 | β |
| Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders. | Lai MC et al. | β | 2017 | β |
| High frequency of the DRD2/ANKK1 A1 allele in Mexican Native Amerindians and Mestizos and its association with alcohol consumption. | Panduro A 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 genetics contributes to the understanding of disease pathophysiology and drug discovery. | Sakaue S et al. | β | 2017 | β |
| Human Y chromosome copy number variation in the next generation sequencing era and beyond. | Massaia A et al. | β | 2017 | β |
| <i>CPT1A</i> Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders. | Skotte L et al. | β | 2017 | β |
| Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder. | Sharp SI et al. | β | 2017 | β |
| Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach. | Suresh RV et al. | β | 2017 | β |
| IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry. | Sanabria-Salas MC et al. | β | 2017 | β |
| Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. | Murthy MN et al. | β | 2017 | β |
| Influence of common and rare genetic variation on warfarin dose among African-Americans and European-Americans using the exome array. | Liu N et al. | β | 2017 | β |
| Influence of <i>CFH</i> gene on symptom severity of schizophrenia. | Zhang C et al. | β | 2017 | β |
| Informatics and Data Analytics to Support Exposome-Based Discovery for Public Health. | Manrai AK et al. | β | 2017 | β |
| Integrative analysis of genome-wide gene copy number changes and gene expression in non-small cell lung cancer. | Jabs V et al. | β | 2017 | β |
| Integrative clustering reveals a novel split in the luminal A subtype of breast cancer with impact on outcome. | Aure MR et al. | β | 2017 | β |
| Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization. | Gage SH et al. | β | 2017 | β |
| Iron and thiol redox signaling in cancer: An exquisite balance to escape ferroptosis. | Toyokuni S et al. | β | 2017 | β |
| Lactase persistence in Tunisia as a result of admixture with other Mediterranean populations. | Ben Halima Y et al. | β | 2017 | β |
| LAIT: a local ancestry inference toolkit. | Hui D et al. | β | 2017 | β |
| Laying in silico pipelines for drug repositioning: a paradigm in ensemble analysis for neurodegenerative diseases. | Dovrolis N et al. | β | 2017 | β |
| Limited influence of germline genetic variation on all-cause mortality in women with early onset breast cancer: evidence from gene-based tests, single-marker regression, and whole-genome prediction. | Scannell Bryan M et al. | β | 2017 | β |
| Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits. | Shi H et al. | β | 2017 | β |
| Low cost, low tech SNP genotyping tools for resource-limited areas: Plague in Madagascar as a model. | Mitchell CL et al. | β | 2017 | β |
| <i>Trans</i>-ancestry Fine Mapping and Molecular Assays Identify Regulatory Variants at the <i>ANGPTL8</i> HDL-C GWAS Locus. | Cannon ME et al. | β | 2017 | β |
| Mapping of microRNAs related to cervical cancer in Latin American human genomic variants. | Guerrero FlΓ³rez M et al. | β | 2017 | β |
| Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges. | Cai B et al. | β | 2017 | β |
| Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer. | Rodriguez-Broadbent H et al. | β | 2017 | β |
| MergeReference: A Tool for Merging Reference Panels for HLA Imputation. | Cook S et al. | β | 2017 | β |
| Metabolomics in Sepsis and Its Impact on Public Health. | Evangelatos N et al. | β | 2017 | β |
| Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study. | Nolte IM et al. | β | 2017 | β |
| Moving beyond Bermuda: sharing data to build a medical information commons. | Cook-Deegan R et al. | β | 2017 | β |
| Multiauthored International Publications: Something Lost in Translation? | Roberts R | β | 2017 | β |
| Multiple single nucleotide polymorphism analysis and association of specific genotypes in FHIT, SAMD4A, and ANKRD17 in Indian patients with oral cancer. | D'Souza W et al. | β | 2017 | β |
| New multilocus linkage disequilibrium measure for tag SNP selection. | Liao B et al. | β | 2017 | β |
| NLRC5 polymorphism is associated with susceptibility to chronic periodontitis. | Zupin L et al. | β | 2017 | β |
| Novel Genetic Variants in Carboxylesterase 1 Predict Severe Early-Onset Capecitabine-Related Toxicity. | Hamzic S et al. | β | 2017 | β |
| Obstacles to Translating Genotype-Phenotype Correlates in Metabolic Disease. | Sharma A et al. | β | 2017 | β |
| Paclitaxel-induced sensory peripheral neuropathy is associated with an ABCB1 single nucleotide polymorphism and older age in Japanese. | Tanabe Y et al. | β | 2017 | β |
| Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls. | Buckley AR et al. | β | 2017 | β |
| Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies. | Friedrichs S et al. | β | 2017 | β |
| Perceived cognitive function for breast cancer survivors: association of genetic and behaviorally related variables for inflammation. | Myers JS et al. | β | 2017 | β |
| Personalised Medicine and the Economy of Biotechnological Promise. | Sturdy S | β | 2017 | β |
| P-glycoprotein gene MDR1 polymorphisms and susceptibility to systemic lupus erythematosus in Guangxi population: a case-control study. | Wang J et al. | β | 2017 | β |
| Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer. | Perez-Ortiz AC et al. | β | 2017 | β |
| Phenotype-Specific Association of Single-Nucleotide Polymorphisms with Heart Failure and Preserved Ejection Fraction: a Genome-Wide Association Analysis of the Cardiovascular Health Study. | Kao DP et al. | β | 2017 | β |
| Pitfalls of exome sequencing: a case study of the attribution of HABP2 rs7080536 in familial non-medullary thyroid cancer. | Gerhard GS et al. | β | 2017 | β |
| Polymorphisms in FFAR4 (GPR120) Gene Modulate Insulin Levels and Sensitivity after Fish Oil Supplementation. | VallΓ©e Marcotte B et al. | β | 2017 | β |
| PopNet: A Markov Clustering Approach to Study Population Genetic Structure. | Zhang J et al. | β | 2017 | β |
| Prediction for Intravenous Immunoglobulin Resistance by Using Weighted Genetic Risk Score Identified From Genome-Wide Association Study in Kawasaki Disease. | Kuo HC et al. | β | 2017 | β |
| Prediction of genome-wide DNA methylation in repetitive elements. | Zheng Y et al. | β | 2017 | β |
| Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease. | Cheema AN et al. | β | 2017 | β |
| Proteogenomics approaches for studying cancer biology and their potential in the identification of acute myeloid leukemia biomarkers. | Hernandez-Valladares M et al. | β | 2017 | β |
| QnAs with Pardis Sabeti. | Ravindran S | β | 2017 | β |
| Race/Ethnicity and the Pharmacogenetics of Reported Suicidality With Efavirenz Among Clinical Trials Participants. | Mollan KR et al. | β | 2017 | β |
| Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes. | Modi BP et al. | β | 2017 | β |
| Recent Historical Migrations Have Shaped the Gene Pool of Arabs and Berbers in North Africa. | Arauna LR et al. | β | 2017 | β |
| Refining the ideas of "ethnic" skin. | Torres V et al. | β | 2017 | β |
| Regulatory network changes between cell lines and their tissues of origin. | Lopes-Ramos CM 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 |
| Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes. | Rhead B et al. | β | 2017 | β |
| Role of DNA methylation in expression control of the IKZF3-GSDMA region in human epithelial cells. | Moussette S et al. | β | 2017 | β |
| Role of Structural Bioinformatics in Drug Discovery by Computational SNP Analysis: Analyzing Variation at the Protein Level. | Brown DK et al. | β | 2017 | β |
| Securing the use of existing sample collections for future human genetic research. | Kanoungi G et al. | β | 2017 | β |
| Semiparametric analysis of complex polygenic gene-environment interactions in case-control studies. | Stalder O et al. | β | 2017 | β |
| Sharing Data to Build a Medical Information Commons: From Bermuda to the Global Alliance. | Cook-Deegan R et al. | β | 2017 | β |
| Signatures of human European Palaeolithic expansion shown by resequencing of non-recombining X-chromosome segments. | Maisano Delser P et al. | β | 2017 | β |
| Single Nucleotide Variants of Candidate Genes in Aggrecan Metabolic Pathway Are Associated with Lumbar Disc Degeneration and Modic Changes. | Perera RS et al. | β | 2017 | β |
| SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations. | Wolin A et al. | β | 2017 | β |
| StrandScript: evaluation of Illumina genotyping array design and strand correction. | Wang J et al. | β | 2017 | β |
| Structured mating: Patterns and implications. | Sebro R et al. | β | 2017 | β |
| The Association of Estrogen Receptor-Ξ² Gene Variation With Salt-Sensitive Blood Pressure. | Manosroi W et al. | β | 2017 | β |
| The companion dog as a unique translational model for aging. | Mazzatenta A et al. | β | 2017 | β |
| The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation. | Velkova A et al. | β | 2017 | β |
| The genetic admixture in Tibetan-Yi Corridor. | Yao HB et al. | β | 2017 | β |
| The Genetics of Ischemic Heart Disease: From Current Knowledge to Clinical Implications. | Elosua R et al. | β | 2017 | β |
| The genetics revolution in rheumatology: large scale genomic arrays and genetic mapping. | Eyre S et al. | β | 2017 | β |
| The historical spread of Arabian Pastoralists to the eastern African Sahel evidenced by the lactase persistence -13,915*G allele and mitochondrial DNA. | PriehodovΓ‘ E 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 SNP-set based association study identifies ITGA1 as a susceptibility gene of attention-deficit/hyperactivity disorder in Han Chinese. | Liu L et al. | β | 2017 | β |
| TwoPaCo: an efficient algorithm to build the compacted de Bruijn graph from many complete genomes. | Minkin I et al. | β | 2017 | β |
| Unique Allelic eQTL Clusters in Human MHC Haplotypes. | Lam TH et al. | β | 2017 | β |
| Using omics approaches to understand pulmonary diseases. | Kan M et al. | β | 2017 | β |
| Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries. | Eckert S et al. | β | 2017 | β |
| Vermont: a multi-perspective visual interactive platform for mutational analysis. | Fassio AV et al. | β | 2017 | β |
| Vulnerability or Sensitivity to the Environment? Methodological Issues, Trends, and Recommendations in Gene-Environment Interactions Research in Human Behavior. | Leighton C et al. | β | 2017 | β |
| Warfarin Anticoagulation Therapy in Caribbean Hispanics of Puerto Rico: A Candidate Gene Association Study. | Claudio-Campos K et al. | β | 2017 | β |
| Whole-Genome Sequence of the Metastatic PC3 and LNCaP Human Prostate Cancer Cell Lines. | Seim I et al. | β | 2017 | β |
| Whole genome sequencing predicts novel human disease models in rhesus macaques. | Bimber BN et al. | β | 2017 | β |
| YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. | Gabriele M et al. | β | 2017 | β |
| A combined reference panel from the 1000βGenomes and UK10K projects improved rare variant imputation in European and Chinese samples. | Chou WC et al. | β | 2016 | β |
| Exploring the Underlying Genetics of Craniofacial Morphology through Various Sources of Knowledge. | Roosenboom J et al. | β | 2016 | β |
| Genetics-Current and Future Role in the Prevention and Management of Coronary Artery Disease. | Roberts R | β | 2016 | β |
| Genetics: Implications for Prevention and Management of Coronary Artery Disease. | Assimes TL et al. | β | 2016 | β |
| The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European Individuals. | Akhdar H et al. | β | 2016 | β |
| Transcriptomic Signature of Atherosclerosis in the Peripheral Blood: Fact or Fiction? | Chen HH et al. | β | 2016 | β |