Genome-wide association studies in diverse populations.

paper Cited Public

Authors: Rosenberg, Noah A; Huang, Lucy; Jewett, Ethan M; Szpiech, Zachary A; Jankovic, Ivana; Boehnke, Michael
Year: 2010
Journal: Nature reviews. Genetics
PMID: 20395969
DOI: 10.1038/nrg2760
PMCID: PMC3079573

#	Section	Preview
40	Highlighted references	50 This simulation study argues that fine mapping of causal variants is improved by joint analysis…
41	Highlighted references	69 This article and the article that precedes it provide detailed analyses of genotype imputation in…

Name	Type
1000 Genomes Project	cohort
admixed population	cohort
African	cohort
Alzheimer’s disease	phenotype
ancestral African populations local	cohort
apoE	gene
APOE-ε4	gene
Australia	cohort
Canada	cohort
cardiomyopathy	phenotype
causal variants	cohort
CEPH European collection local	cohort
common variants	cohort
disease	phenotype
disease-allele local	variant
Disease-risk variation local	variant
disease variation local	phenotype
diverse populations	cohort
European ancestry	cohort
European population	cohort
Europeans	cohort
Finland	cohort
genetically intermediate populations local	cohort
Genetically intermediate populations local	cohort
Genetic resource local	cohort
GWA discoveries local	phenotype
GWA study	cohort
HapMap	cohort
HapMap CEU	cohort
HapMap reference panels local	cohort
Iceland	cohort
imputation accuracy	drug
Indian subcontinent local	cohort
indigenous populations local	cohort
intermediate-LD indigenous populations local	cohort
intermediate population local	cohort
International Haplotype Map project	cohort
Kcnq1	gene
Known variants local	variant
low-LD populations local	cohort
marker ascertainment local	drug
mixture panels local	cohort
mixture strategy local	drug
multiple populations local	cohort
MYBPC3	gene
MYBPC3 risk variant local	variant
non-European ancestry	cohort
Other European populations local	cohort
parental populations	cohort
phenotype	phenotype
phenotypic variation	phenotype
population	cohort
population-genetic data local	cohort
population-genetic modeling local	cohort
population structure local	drug
rare disease-risk variant local	variant
rare risk alleles local	variant
rare variant	cohort
reference groups local	cohort
reference panel	cohort
reference population	cohort
risk allele	cohort
Risk-variant local	variant
Sardinia	cohort
separate association study local	cohort
small population local	cohort
SNP	cohort
study cohort	cohort
sub-Saharan African populations local	cohort
tag-SNP portability local	drug
tag-SNP portability local	phenotype
tag SNPs	cohort
target population	cohort
TCF7L2	gene
type 2 diabetes	phenotype
United States	cohort

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Genetic parameters and single-step genome-wide association analysis for trematode (Fasciola hepatica and Calicophoron/Paramphistomum spp.) infections in German dairy cows.	May K et al.	—	2025	→
GenomicSEM Modelling of Diverse Executive Function GWAS Improves Gene Discovery.	Perry LC et al.	—	2025	→
Improving Cardiovascular Health Through the Consideration of Social Factors in Genetics and Genomics Research: A Scientific Statement From the American Heart Association.	Suglia SF et al.	—	2025	→
Multi-population GWAS detects robust marker associations in a newly established six-rowed winter barley breeding program.	Skovbjerg CK et al.	—	2025	→
QTL detection in multi-breed cattle populations including crossbred animals: a simulation study.	Guillenea A et al.	—	2025	→
Sparse multitask group Lasso for genome-wide association studies.	Nouira A et al.	—	2025	→
The causal relationship between obstructive sleep apnea and otitis media: a bidirectional Mendelian randomization study.	Guo R et al.	—	2025	→
The Impact of Ancestry on Genome-Wide Association Studies.	Jones SC et al.	—	2025	→
The value-ladenness of ancestry.	Haddad Y	—	2025	→
Accounting for heterogeneity due to environmental sources in meta-analysis of genome-wide association studies.	Wang S et al.	—	2024	→
A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations.	Fu S et al.	—	2024	→
Bowel Habits, Obesity, Intestinal Microbiota and Their Influence on Hemorrhoidal Disease: a Mendelian Randomization Study.	Yu M et al.	—	2024	→
Cross-ancestry genetic architecture and prediction for cholesterol traits.	Momin MM et al.	—	2024	→
Development of a novel GWAS method to detect QTL effects interacting with the discrete and continuous population structure	Hamazaki K et al.	—	2024	—
Epigenome-wide association study of DNA methylation in maternal blood leukocytes with BMI in pregnancy and gestational weight gain.	Opsahl JO et al.	—	2024	→
Extreme-Phenotype Genome-Wide Association Analysis for Growth Traits in Spotted Sea Bass (<i>Lateolabrax maculatus</i>) Using Whole-Genome Resequencing.	Zhou Z et al.	—	2024	→
Gene-environment interactions in the influence of maternal education on adolescent neurodevelopment using ABCD study.	Shi R et al.	—	2024	→
Novel risk loci for COVID-19 hospitalization among admixed American populations.	Diz-de Almeida S et al.	—	2024	→
Shaping immunity: The influence of natural selection on population immune diversity.	Randolph HE et al.	—	2024	→
The Inclusion of Underrepresented Populations in Cardiovascular Genetics and Epidemiology.	Chappell E et al.	—	2024	→
A genome-wide association study identifies a possible role for cannabinoid signalling in the pathogenesis of diabetic kidney disease.	Osman W et al.	—	2023	→
Alcohol use polygenic risk score, social support, and alcohol use among European American and African American adults.	Su J et al.	—	2023	→
Animal-SNPAtlas: a comprehensive SNP database for multiple animals.	Gao Y et al.	—	2023	→
A Polygenic Risk Score for Predicting Racial and Genetic Susceptibility to Prurigo Nodularis.	Vasavda C et al.	—	2023	→
Assessment of NLRP3 Gene Polymorphisms with Periodontitis as Compared with Healthy Periodontium in Iraqi Arabs Patients.	Mahmood AA et al.	—	2023	→
Biobank-scale methods and projections for sparse polygenic prediction from machine learning.	Raben TG et al.	—	2023	→
Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study.	Long Y et al.	—	2023	→
Childhood trajectories of internalising and externalising problems associated with a polygenic risk score for neuroticism in a UK birth cohort study.	Costantini I et al.	—	2023	→
Evaluating significance of European-associated index SNPs in the East Asian population for 31 complex phenotypes.	Qiao J et al.	—	2023	→
Future prospects for human genetics and genomics in drug discovery.	Ghoussaini M et al.	—	2023	→
Genes of Predisposition to Childhood Beta-Cell Acute Lymphoblastic Leukemia in the Kazakh Population.	Svyatova G et al.	—	2023	→
Genetic Liability, Exposure Severity, and Post-Traumatic Stress Disorder Predict Cognitive Impairment in World Trade Center Responders.	Mann FD et al.	—	2023	→
Impact of cross-ancestry genetic architecture on GWASs in admixed populations.	Mester R et al.	—	2023	→
Limitations of principal components in quantitative genetic association models for human studies.	Yao Y et al.	—	2023	→
Proteome and genome integration analysis of obesity.	Zhao Q et al.	—	2023	→
Similarity and diversity of genetic architecture for complex traits between East Asian and European populations.	Zhang J et al.	—	2023	→
Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals.	Juárez-Luis J et al.	—	2023	→
Strategies for the Genomic Analysis of Admixed Populations.	Tan T et al.	—	2023	→
The Recombination Hotspot Paradox: Co-evolution between PRDM9 and its target sites.	Úbeda F et al.	—	2023	→
Characterization of Genetic Risk of End-Stage Knee Osteoarthritis Treated with Total Knee Arthroplasty: A Genome-Wide Association Study.	Kulm S et al.	—	2022	→
Cohort Profile: The Alliance for Maternal and Newborn Health Improvement (AMANHI) biobanking study.	Aftab F et al.	—	2022	→
Coronavirus Host Genomics Study: South Africa (COVIGen-SA).	May AK et al.	—	2022	→
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.	Byun J et al.	—	2022	→
Detecting associated genes for complex traits shared across East Asian and European populations under the framework of composite null hypothesis testing.	Qiao J et al.	—	2022	→
Dissection of Maize Drought Tolerance at the Flowering Stage Using Genome-Wide Association Studies.	Khan SU et al.	—	2022	→
Genetic diversity of the LILRB1 and LILRB2 coding regions in an admixed Brazilian population sample.	Oliveira MLG et al.	—	2022	→
Genetics of Alzheimer Disease.	Jayadev S	—	2022	→
Genome-Wide Association Study of Adhesive Capsulitis Suggests Significant Genetic Risk Factors.	Kulm S et al.	—	2022	→
Including diverse and admixed populations in genetic epidemiology research.	Caliebe A et al.	—	2022	→
LmTag: functional-enrichment and imputation-aware tag SNP selection for population-specific genotyping arrays.	Thanh Nguyen D et al.	—	2022	→
No person left behind: Mapping the health policy landscape for genomics research in the Caribbean.	Bolleddula J et al.	—	2022	→
Optimizing sampling design and sequencing strategy for the genomic analysis of quantitative traits in natural populations.	Paril JF et al.	—	2022	→
Polygenic Risk Score in African populations: progress and challenges.	Adam Y et al.	—	2022	→
Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.	O'Sullivan JW et al.	—	2022	→
Prevalence and correlates of joint pain among Chinese breast cancer survivors receiving aromatase inhibitor treatment.	Wang T et al.	—	2022	→
Promoting Inclusive Recruitment: a Qualitative Study of Black Adults' Decision to Participate in Genetic Research.	Connor J et al.	—	2022	→
The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force.	Wang QS et al.	—	2022	→
VEGF-A, VEGFR1 and VEGFR2 single nucleotide polymorphisms and outcomes from the AGITG MAX trial of capecitabine, bevacizumab and mitomycin C in metastatic colorectal cancer.	Chionh F et al.	—	2022	→
Admixed Populations Improve Power for Variant Discovery and Portability in Genome-Wide Association Studies.	Lin M et al.	—	2021	→
Advances in multiplex PCR for Alzheimer's disease diagnostics targeting CDK genes.	Lim KH et al.	—	2021	→
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages.	Park JY et al.	—	2021	→
Association of Genetic Risk Score With NAFLD in An Ethnically Diverse Cohort.	Wang J et al.	—	2021	→
Benefits of Cohort Studies in a Consortia-Dominated Landscape.	Zenebe-Gete S et al.	—	2021	→
Evaluating marginal genetic correlation of associated loci for complex diseases and traits between European and East Asian populations.	Lu H et al.	—	2021	→
False discovery rate control in genome-wide association studies with population structure.	Sesia M et al.	—	2021	→
Genetic Susceptibility to Acute Kidney Injury.	Ortega-Loubon C et al.	—	2021	→
Genome-wide association study of signature genetic alterations among pseudomonas aeruginosa cystic fibrosis isolates.	Hwang W et al.	—	2021	→
Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension.	Kolifarhood G et al.	—	2021	→
GenoPheno: cataloging large-scale phenotypic and next-generation sequencing data within human datasets.	Gutiérrez-Sacristán A et al.	—	2021	→
Gout prevalence in the Hmong: a prime example of health disparity and the role of community-based genetic research.	Roman YM et al.	—	2021	→
JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation.	Sarnowski C et al.	—	2021	→
Non-communicable diseases pandemic and precision medicine: Is Africa ready?	Chikowore T et al.	—	2021	→
Osteopontin Gene Polymorphisms Are Associated with Cardiovascular Risk Factors in Patients with Premature Coronary Artery Disease.	Pérez-Hernández N et al.	—	2021	→
Pygmalion in the Genes? On the potentially negative impacts of polygenic scores for educational attainment.	Matthews LJ et al.	—	2021	→
Quantifying genetic heterogeneity between continental populations for human height and body mass index.	Guo J et al.	—	2021	→
The impact of late-career job loss and genetic risk on body mass index: Evidence from variance polygenic scores.	Schmitz LL et al.	—	2021	→
Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.	Takei R et al.	—	2021	→
Association of the <i>NEGR1</i> rs2815752 with obesity and related traits in Pakistani females.	Rana S et al.	—	2020	→
Canalization and Robustness in Human Genetics and Disease.	Gibson G et al.	—	2020	→
Causal Inference between Rheumatoid Arthritis and Breast Cancer in East Asian and European Population: A Two-Sample Mendelian Randomization.	Ahn C et al.	—	2020	→
CUBAP: an interactive web portal for analyzing codon usage biases across populations.	Hodgman MW et al.	—	2020	→
Enabling Technologies for Personalized and Precision Medicine.	Ho D et al.	—	2020	→
Evolutionary perspectives on polygenic selection, missing heritability, and GWAS.	Uricchio LH	—	2020	→
Functional genomics, genetic risk profiling and cell phenotypes in neurodegenerative disease.	Finkbeiner S	—	2020	→
Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research.	Elsayed NA et al.	—	2020	→
Genome-wide association analyses of quantitative disease resistance in diverse sets of soybean [Glycine max (L.) Merr.] plant introductions.	Rolling W et al.	—	2020	→
Genome-wide association studies of fruit quality traits in jujube germplasm collections using genotyping-by-sequencing.	Hou L et al.	—	2020	→
Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway.	Manry J et al.	—	2020	→
Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx.	Gay NR et al.	—	2020	→
Influence of inflammasome NLRP3, and IL1B and IL2 gene polymorphisms in periodontitis susceptibility.	de Alencar JB et al.	—	2020	→
Informed consent for genetic testing in hematology.	Marron JM	—	2020	→
Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data.	Shi H et al.	—	2020	→
Obesity-related loci in TMEM18, CDKAL1 and FAIM2 are associated with obesity and type 2 diabetes in Chinese Han patients.	Kang J et al.	—	2020	→
p.Arg72Pro polymorphism of P53 and breast cancer risk: a meta-analysis of case-control studies.	Diakite B et al.	—	2020	→
Pinyin Is an Effective Proxy for Early Screening for Mandarin-Speaking Children at Risk of Reading Disorders.	Ma S et al.	—	2020	→
PRDM15 Is Associated with Risk of Chronic Obstructive Pulmonary Disease in a Rural Population in Chile.	Hosgood Iii HD et al.	—	2020	→
Preliminary study of structural magnetic resonance imaging phenotypes related to genetic variation in Interleukin-1β rs16944 in adolescents with Bipolar Disorder.	Shonibare DO et al.	—	2020	→
Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy.	Kerns SL et al.	—	2020	→
The Role of ARID5B in Acute Lymphoblastic Leukemia and Beyond.	Wang P et al.	—	2020	→
A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population.	Nudel R et al.	—	2019	→
An association study in PTPN22 suggests that is a risk factor to Takayasu's arteritis.	Soto ME et al.	—	2019	→
An Exome-Wide Association Study Identifies New Susceptibility Loci for Age of Smoking Initiation in African- and European-American Populations.	Jiang K et al.	—	2019	→
Benefits and limitations of genome-wide association studies.	Tam V et al.	—	2019	→
Clinical use of current polygenic risk scores may exacerbate health disparities.	Martin AR et al.	—	2019	→
Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry.	Mufford M et al.	—	2019	→
Cross-population analysis for functional characterization of type II diabetes variants.	Elmansy D et al.	—	2019	→
Dissecting <i>in silico</i> Mutation Prediction of Variants in African Genomes: Challenges and Perspectives.	Bope CD et al.	—	2019	→
Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese.	Liu L et al.	—	2019	→
Established and emerging strategies to crack the genetic code of obesity.	Tam V et al.	—	2019	→
Examining sex differences in pleiotropic effects for depression and smoking using polygenic and gene-region aggregation techniques.	Schmitz LL et al.	—	2019	→
First Genome-wide Association Analysis for Growth Traits in the Largest Coral Reef-Dwelling Bony Fishes, the Giant Grouper (Epinephelus lanceolatus).	Wu L et al.	—	2019	→
Generality of genomic findings on blood pressure traits and its usefulness in precision medicine in diverse populations: A systematic review.	Kolifarhood G et al.	—	2019	→
Genome-wide association studies of structural birth defects: A review and commentary.	Lupo PJ et al.	—	2019	→
Genome-Wide Characterization of Arabian Peninsula Populations: Shedding Light on the History of a Fundamental Bridge between Continents.	Fernandes V et al.	—	2019	→
Genomics of disease risk in globally diverse populations.	Gurdasani D et al.	—	2019	→
Heritability of blood pressure traits in diverse populations: a systematic review and meta-analysis.	Kolifarhood G et al.	—	2019	→
Modeling Heterogeneity in the Genetic Architecture of Ethnically Diverse Groups Using Random Effect Interaction Models.	Veturi Y et al.	—	2019	→
Population Levels Assessment of the Distribution of Disease-Associated Variants With Emphasis on Armenians - A Machine Learning Approach.	Nikoghosyan M et al.	—	2019	→
PRDM9 and the evolution of recombination hotspots.	Úbeda F et al.	—	2019	→
Spontaneous premature birth as a target of genomic research.	Hallman M et al.	—	2019	→
The AIRE Ser196Ser synonymous variant is a risk factor for systemic lupus erythematosus.	Montufar-Robles I et al.	—	2019	→
The paucity of genetic studies of alcohol phenotypes in diverse populations: what are the consequences and opportunities?	Chartier KG	—	2019	→
TRANSCULTURAL DIABETES CARE IN THE UNITED STATES - A POSITION STATEMENT BY THE AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS.	Mechanick JI et al.	—	2019	→
Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China.	Wei Q et al.	—	2019	→
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response.	Adeyemo AA et al.	—	2019	→
A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease.	Williams LM et al.	—	2018	→
A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations.	Duan Q et al.	—	2018	→
Association between inflammatory-response gene polymorphisms and risk of acute kidney injury in children.	He J et al.	—	2018	→
Association of CACNA1C with bipolar disorder among the Pakistani population.	Khalid M et al.	—	2018	→
Associations Between Dopamine D2 Receptor (DRD2) Gene, Maternal Positive Parenting and Trajectories of Depressive Symptoms from Early to Mid-Adolescence.	Cao C et al.	—	2018	→
Complex Haplotypes of <i>GSTM1</i> Gene Deletions Harbor Signatures of a Selective Sweep in East Asian Populations.	Saitou M et al.	—	2018	→
Copy Number Variation.	Macé A et al.	—	2018	→
Examining interactions between genetic risk for alcohol problems, peer deviance, and interpersonal traumatic events on trajectories of alcohol use disorder symptoms among African American college students.	Su J et al.	—	2018	→
Frequency and phenotype consequence of APOC3 rare variants in patients with very low triglyceride levels.	Crawford DC et al.	—	2018	→
Genetic Ancestry for Sleep Research: Leveraging Health Inequalities to Identify Causal Genetic Variants.	Prasad B et al.	—	2018	→
Genetic disease risks can be misestimated across global populations.	Kim MS et al.	—	2018	→
Genetics and Crime: Integrating New Genomic Discoveries Into Psychological Research About Antisocial Behavior.	Wertz J et al.	—	2018	→
Genome-wide and Phenome-wide Approaches to Understand Variable Drug Actions in Electronic Health Records.	Robinson JR et al.	—	2018	→
Genome-Wide Association Studies of Cancer in Diverse Populations.	Park SL et al.	—	2018	→
Genome-wide mapping of quantitative trait loci in admixed populations using mixed linear model and Bayesian multiple regression analysis.	Toosi A et al.	—	2018	→
Genotyping by Sequencing and Genome-Environment Associations in Wild Common Bean Predict Widespread Divergent Adaptation to Drought.	Cortés AJ et al.	—	2018	→
Global genetic variation of select opiate metabolism genes in self-reported healthy individuals.	Wendt FR et al.	—	2018	→
Identification of functional missense single-nucleotide polymorphisms in <i>TNFAIP3</i> in a predominantly Hispanic population.	Zhang B et al.	—	2018	→
Lessons from a natural experiment: Allopatric morphological divergence and sympatric diversification in the Midas cichlid species complex are largely influenced by ecology in a deterministic way.	Kautt AF et al.	—	2018	→
Prioritizing diversity in human genomics research.	Hindorff LA et al.	—	2018	→
Progress in defining the genetic contribution to type 2 diabetes susceptibility.	Morris AP	—	2018	→
Single Nucleotide Polymorphism (SNP) markers associated with high folate content in wild potato species.	Bali S et al.	—	2018	→
TG haplotype in the LRP8 is associated with myocardial infarction in south Indian population.	Asif M et al.	—	2018	→
The framework for population epigenetic study.	Zhao L et al.	—	2018	→
The VEGFA -1154G/A polymorphism is associated with reduced risk of rheumatoid arthritis but not with systemic lupus erythematosus in Mexican women.	Ramírez-Bello J et al.	—	2018	→
Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.	Gong J et al.	—	2018	→
Transethnic differences in GWAS signals: A simulation study.	Zanetti D et al.	—	2018	→
Validation of a genetic risk score for atrial fibrillation: A prospective multicenter cohort study.	Muse ED et al.	—	2018	→
Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.	Parra EJ et al.	—	2017	→
Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.	Tabb KL et al.	—	2017	→
An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry.	Meyers JL et al.	—	2017	→
Assessing the degree of stratification between closely related Holstein-Friesian populations.	Szyda J et al.	—	2017	→
Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans.	Gottlieb A et al.	—	2017	→
Complex Ancient Genetic Structure and Cultural Transitions in Southern African Populations.	Montinaro F et al.	—	2017	→
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease.	Takahashi S et al.	—	2017	→
Differential methylation between ethnic sub-groups reflects the effect of genetic ancestry and environmental exposures.	Galanter JM et al.	—	2017	→
Disentangling Timing of Admixture, Patterns of Introgression, and Phenotypic Indicators in a Hybridizing Wolf Population.	Galaverni M et al.	—	2017	→
Endotypes of difficult-to-control asthma in inner-city African American children.	Brown KR et al.	—	2017	→
Ethical considerations in genomic testing for hematologic disorders.	Marron JM et al.	—	2017	→
Ethical considerations surrounding germline next-generation sequencing of children with cancer.	Johnson LM et al.	—	2017	→
Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.	Archer NP et al.	—	2017	→
Genetic polymorphism at <i>BCL2</i> as a predictor for rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone efficacy in patients with diffuse large B-cell lymphoma.	Bashash M et al.	—	2017	→
Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index.	Chen G et al.	—	2017	→
Genome-Wide Association Mapping of Stem Rust Resistance in <i>Hordeum vulgare</i> subsp. <i>spontaneum</i>.	Sallam AH et al.	—	2017	→
Genome-Wide Association Study Identifies Loci Associated with Resistance to Viral Nervous Necrosis Disease in Asian Seabass.	Wang L et al.	—	2017	→
Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations.	Dajani R et al.	—	2017	→
Genome-wide two-locus interaction analysis identifies multiple epistatic SNP pairs that confer risk of prostate cancer: A cross-population study.	Shen J et al.	—	2017	→
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.	Martin AR et al.	—	2017	→
Microbial genome-wide association studies: lessons from human GWAS.	Power RA et al.	—	2017	→
Multiethnic polygenic risk scores improve risk prediction in diverse populations.	Márquez-Luna C et al.	—	2017	→
Polygenic hypercholesterolemia: examples of GWAS results and their replication in the Czech-Slavonic population.	Hubacek JA et al.	—	2017	→
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.	Sanderson SC et al.	—	2017	→
Racial disparity in metabolic regulation of cancer.	Attri KS et al.	—	2017	→
Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations.	Pulit SL et al.	—	2017	→
Review: Genetic research on alcohol use outcomes in African American populations: A review of the literature, associated challenges, and implications.	Dick DM et al.	—	2017	→
Self-reported race and ethnicity of US biobank participants compared to the US Census.	Cohn EG et al.	—	2017	→
The genetic underpinnings of body fat distribution.	Pulit SL et al.	—	2017	→
The genomic landscape of evolutionary convergence in mammals, birds and reptiles.	Levin L et al.	—	2017	→
The SDF1 A/G Gene Variant: A Susceptibility Variant for Myocardial Infarction.	Mansoori Y et al.	—	2017	→
The utility of empirically assigning ancestry groups in cross-population genetic studies of addiction.	Peterson RE et al.	—	2017	→
Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution.	Mägi R et al.	—	2017	→
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.	Mez J et al.	—	2017	→
Use of Natural Diversity and Biotechnology to Increase the Quality and Nutritional Content of Tomato and Grape.	Gascuel Q et al.	—	2017	→
Visualizing the geography of genetic variants.	Marcus JH et al.	—	2017	→
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.	Daneshjou R et al.	—	2017	→
Admixture in Latin America.	Adhikari K et al.	—	2016	→
Association between DPP4 gene polymorphism and serum lipid levels in Chinese type 2 diabetes individuals.	Xing X et al.	—	2016	→
Atopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.	Eaaswarkhanth M et al.	—	2016	→
Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.	Wang X et al.	—	2016	→
EWAS: epigenome-wide association studies software 1.0 - identifying the association between combinations of methylation levels and diseases.	Xu J et al.	—	2016	→
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.	Evans DS et al.	—	2016	→
Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans.	David SP et al.	—	2016	→
Genes involved in stress response and alcohol use among high-risk African American youth.	Goyal N et al.	—	2016	→
Genetics and genomic medicine in Mali: challenges and future perspectives.	Landouré G et al.	—	2016	→
Gene variants at FTO, 9p21, and 2q36.3 are age-independently associated with myocardial infarction in Czech men.	Hubacek JA et al.	—	2016	→
Genome-wide time-to-event analysis on smoking progression stages in a family-based study.	He L et al.	—	2016	→
Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).	Nelson SC et al.	—	2016	→
Increasing the power of genome wide association studies in natural populations using repeated measures - evaluation and implementation.	Rönnegård L et al.	—	2016	→
Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents.	Munung NS et al.	—	2016	→
Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans.	Daneshjou R et al.	—	2016	→
Protein tyrosine phosphatase nonreceptor type 22 (PTPN22) gene polymorphism in pulmonary tuberculosis in the Indian population.	Narasimha VR et al.	—	2016	→
Racial Disparities in Poverty Account for Mortality Differences in US Medicare Beneficiaries.	Kimmel PL et al.	—	2016	→
Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.	Gonzalez S et al.	—	2016	→
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).	Williams RC et al.	—	2016	→
Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants.	Uricchio LH et al.	—	2016	→
Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.	Bien SA et al.	—	2016	→
TESTING POPULATION-SPECIFIC QUANTITATIVE TRAIT ASSOCIATIONS FOR CLINICAL OUTCOME RELEVANCE IN A BIOREPOSITORY LINKED TO ELECTRONIC HEALTH RECORDS: LPA AND MYOCARDIAL INFARCTION IN AFRICAN AMERICANS.	Dumitrescu L et al.	—	2016	→
THE CHALLENGES IN USING ELECTRONIC HEALTH RECORDS FOR PHARMACOGENOMICS AND PRECISION MEDICINE RESEARCH.	Laper SM et al.	—	2016	→
The Columbian Exchange as a source of adaptive introgression in human populations.	Jordan IK	—	2016	→
The impact of personalized medicine of Type 2 diabetes mellitus in the global health context.	Thomas PPM et al.	—	2016	→
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.	Horikoshi M et al.	—	2016	→
Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach.	Zhu Q et al.	—	2016	→
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.	Liu CT et al.	—	2016	→
Transfer of genetic therapy across human populations: molecular targets for increasing patient coverage in repeat expansion diseases.	Varela MA et al.	—	2016	→
Unravelling the human genome-phenome relationship using phenome-wide association studies.	Bush WS et al.	—	2016	→
A call for global governance of biobanks.	Chen H et al.	—	2015	→
A General Model of the Relationship between the Apportionment of Human Genetic Diversity and the Apportionment of Human Phenotypic Diversity.	Edge MD et al.	—	2015	→
A Genome-Wide Association Study of Post-bronchodilator Lung Function in Children with Asthma.	Brehm JM et al.	—	2015	→
Ankyrin-B metabolic syndrome combines age-dependent adiposity with pancreatic β cell insufficiency.	Lorenzo DN et al.	—	2015	→
Association of GABAA receptor α2 subunit gene (GABRA2) with alcohol dependence-related aggressive behavior.	Strac DS et al.	—	2015	→
Common Variants Associated with Type 2 Diabetes in a Black South African Population of Setswana Descent: African Populations Diverge.	Chikowore T et al.	—	2015	→
Complex Genetics of Type 2 Diabetes and Effect Size: What have We Learned from Isolated Populations?	Nair AK et al.	—	2015	→
Connecting SNPs in Diabetes: A Spatial Analysis of Meta-GWAS Loci.	Schierding W et al.	—	2015	→
Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics.	Lehner T et al.	—	2015	→
Ethical, legal and social implications of incorporating personalized medicine into healthcare.	Brothers KB et al.	—	2015	→
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.	Tang CS et al.	—	2015	→
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease.	Tosto G et al.	—	2015	→
Genetic Diversity and Societally Important Disparities.	Rosenberg NA et al.	—	2015	→
Genetic identities and local inbreeding in pure diploid clones with homoplasic markers: SNPs may be misleading.	De Meeûs T	—	2015	→
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration.	Lanktree MB et al.	—	2015	→
Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL).	Bloomfield GS et al.	—	2015	→
Genetics and brain morphology.	Strike LT et al.	—	2015	→
Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.	Peprah E et al.	—	2015	→
Genome-wide association studies in pharmacogenomics of antidepressants.	Lin E et al.	—	2015	→
Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations.	Wei Z et al.	—	2015	→
Genomic approaches for understanding the genetics of complex disease.	Lowe WL et al.	—	2015	→
Identification and characterization of more than 4 million intervarietal SNPs across the group 7 chromosomes of bread wheat.	Lai K et al.	—	2015	→
Identification of possible pathogenic pathways in Behçet's disease using genome-wide association study data from two different populations.	Bakir-Gungor B et al.	—	2015	→
Joint genome-wide association study for milk fatty acid traits in Chinese and Danish Holstein populations.	Li X et al.	—	2015	→
Novel genetic matching methods for handling population stratification in genome-wide association studies.	Lacour A et al.	—	2015	→
Population Genetics and Reproductive Strategies of African Trypanosomes: Revisiting Available Published Data.	Koffi M et al.	—	2015	→
The H3Africa policy framework: negotiating fairness in genomics.	de Vries J et al.	—	2015	→
Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES).	Winnier DA et al.	—	2015	→
Admixture mapping identifies a locus at 15q21.2-22.3 associated with keloid formation in African Americans.	Velez Edwards DR et al.	—	2014	→
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.	Ko A et al.	—	2014	→
Beyond landraces: developing improved germplasm resources for underutilized species - a case for Bambara groundnut.	Aliyu S et al.	—	2014	→
eMERGEing progress in genomics-the first seven years.	Crawford DC et al.	—	2014	→
Ethnic background and genetic variation in the evaluation of cancer risk: a systematic review.	Jing L et al.	—	2014	→
Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project.	Tantoso E et al.	—	2014	→
Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval.	Seyerle AA et al.	—	2014	→
Fine mapping of type 2 diabetes susceptibility loci.	Morris AP	—	2014	→
Gene-carbohydrate and gene-fiber interactions and type 2 diabetes in diverse populations from the National Health and Nutrition Examination Surveys (NHANES) as part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study.	Villegas R et al.	—	2014	→
Genetic Variants in the FADS Gene: Implications for Dietary Recommendations for Fatty Acid Intake.	Mathias RA et al.	—	2014	→
Genome-wide association study and admixture mapping identify different asthma-associated loci in Latinos: the Genes-environments & Admixture in Latino Americans study.	Galanter JM et al.	—	2014	→
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.	Xie T et al.	—	2014	→
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium et al.	—	2014	→
GIMAP and Behçet disease: no association in the European population.	Ortiz-Fernández L et al.	—	2014	→
Knowing who to trust: exploring the role of 'ethical metadata' in mediating risk of harm in collaborative genomics research in Africa.	de Vries J et al.	—	2014	→
Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study.	Kocarnik JM et al.	—	2014	→
Multi-ethnic fine-mapping of 14 central adiposity loci.	Liu CT et al.	—	2014	→
Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.	Lubitz SA et al.	—	2014	→
Null allele, allelic dropouts or rare sex detection in clonal organisms: simulations and application to real data sets of pathogenic microbes.	Séré M et al.	—	2014	→
On the threshold from genome-wide association studies to whole-genome sequencing. Looking for signal in all the right places.	Hansel NN et al.	—	2014	→
PATH-SCAN: a reporting tool for identifying clinically actionable variants.	Daneshjou R et al.	—	2014	→
Personalized medicine, availability, and group disparity: an inquiry into how physicians perceive and rate the elements and barriers of personalized medicine.	Petersen KE et al.	—	2014	→
Pharmacogenomics, ancestry and clinical decision making for global populations.	Ramos E et al.	—	2014	→
Prevalence of adiposity and associated cardiometabolic risk factors in the Samoan genome-wide association study.	Hawley NL et al.	—	2014	→
Rare-variant association analysis: study designs and statistical tests.	Lee S et al.	—	2014	→
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.	SIGMA Type 2 Diabetes Consortium et al.	—	2014	→
Spatial localization of recent ancestors for admixed individuals.	Yang WY et al.	—	2014	→
The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings.	Abdullah N et al.	—	2014	→
Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant.	Xing C et al.	—	2014	→
Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI.	Bailey SD et al.	—	2014	→
Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa.	Alkan C et al.	—	2014	→
A century after Fisher: time for a new paradigm in quantitative genetics.	Nelson RM et al.	—	2013	→
Addressing human variability in next-generation human health risk assessments of environmental chemicals.	Zeise L et al.	—	2013	→
Characterization of the genetic variation present in CYP3A4 in three South African populations.	Drögemöller B et al.	—	2013	→
Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.	Deo R et al.	—	2013	→
Comparison of genetic variation of breast cancer susceptibility genes in Chinese and German populations.	Barzan D et al.	—	2013	→
Confounding and heterogeneity in genetic association studies with admixed populations.	Liu J et al.	—	2013	→
Dissecting genome-wide association signals for loss-of-function phenotypes in sorghum flavonoid pigmentation traits.	Morris GP et al.	—	2013	→
Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans.	Walsh KM et al.	—	2013	→
Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	Jeff JM et al.	—	2013	→
Genetic risk prediction: individualized variability in susceptibility to toxicants.	Nebert DW et al.	—	2013	→
Genetics of obesity and type 2 diabetes in African Americans.	McCormack S et al.	—	2013	→
Genetic variation in the extended major histocompatibility complex and susceptibility to childhood acute lymphoblastic leukemia: a review of the evidence.	Urayama KY et al.	—	2013	→
Genome-wide association analysis for nine agronomic traits in maize under well-watered and water-stressed conditions.	Xue Y et al.	—	2013	→
Genome-wide association study of age at menarche in African-American women.	Demerath EW et al.	—	2013	→
Genomic landscapes of Chinese hamster ovary cell lines as revealed by the Cricetulus griseus draft genome.	Lewis NE et al.	—	2013	→
Genomic markers of ovarian reserve.	Wood MA et al.	—	2013	→
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.	Weissglas-Volkov D et al.	—	2013	→
High trans-ethnic replicability of GWAS results implies common causal variants.	Marigorta UM et al.	—	2013	→
Human monogenic disease genes have frequently functionally redundant paralogs.	Chen WH et al.	—	2013	→
Impact of TCF7L2 single nucleotide polymorphisms on hydrochlorothiazide-induced diabetes.	Karnes JH et al.	—	2013	→
Integrating genetic and genomic information into effective cancer care in diverse populations.	Fashoyin-Aje L et al.	—	2013	→
Interaction between polygenic risk for cigarette use and environmental exposures in the Detroit Neighborhood Health Study.	Meyers JL et al.	—	2013	→
Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES).	Farook VS et al.	—	2013	→
Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).	Goodloe R et al.	—	2013	→
MaCH-admix: genotype imputation for admixed populations.	Liu EY et al.	—	2013	→
Mapping of immune-mediated disease genes.	Ricaño-Ponce I et al.	—	2013	→
Modeling human disease with pluripotent stem cells: from genome association to function.	Merkle FT et al.	—	2013	→
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.	Xu H et al.	—	2013	→
Pleiotropy in complex traits: challenges and strategies.	Solovieff N et al.	—	2013	→
Polymorphisms in LEPR, PPARG and APM1 genes: associations with energy intake and metabolic traits in young children.	Zandoná MR et al.	—	2013	→
Positive Emotion Regulation and Psychopathology: A Transdiagnostic Cultural Neuroscience Approach.	Hechtman LA et al.	—	2013	→
Response to "A closer look at FBXO41 as a Parkinson's disease risk factor".	Liang H et al.	—	2013	→
SNP genotyping reveals genetic diversity between cultivated landraces and contemporary varieties of tomato.	Corrado G et al.	—	2013	→
Stacks: an analysis tool set for population genomics.	Catchen J et al.	—	2013	→
Statins work around the world.	Postmus I et al.	—	2013	→
The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.	Valsesia A et al.	—	2013	→
The identification of pathway markers in intracranial aneurysm using genome-wide association data from two different populations.	Bakir-Gungor B et al.	—	2013	→
The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN.	de las Fuentes L et al.	—	2013	→
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.	Wu Y et al.	—	2013	→
2011 Presidential Address: from classroom to courtroom to clinic-closing the gaps in human genetics education.	Jorde LB	—	2012	→
Assessing gene-gene interactions in pharmacogenomics.	Lane HY et al.	—	2012	→
Association test based on SNP set: logistic kernel machine based test vs. principal component analysis.	Zhao Y et al.	—	2012	→
A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations.	Wang X et al.	—	2012	→
Bayesian genome-wide association analysis of growth and yearling ultrasound measures of carcass traits in Brangus heifers.	Peters SO et al.	—	2012	→
BDNF Val66Met and cognition: all, none, or some? A meta-analysis of the genetic association.	Mandelman SD et al.	—	2012	→
Breed-specific ancestry studies and genome-wide association analysis highlight an association between the MYH9 gene and heat tolerance in Alaskan sprint racing sled dogs.	Huson HJ et al.	—	2012	→
Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.	Delaney JT et al.	—	2012	→
Common roots: a contextual review of HIV epidemics in black men who have sex with men across the African diaspora.	Millett GA et al.	—	2012	→
Consistency of genome-wide associations across major ancestral groups.	Ntzani EE et al.	—	2012	→
Correction for population stratification in random forest analysis.	Zhao Y et al.	—	2012	→
C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans.	Doumatey AP et al.	—	2012	→
Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation.	Nakagome S et al.	—	2012	→
Efficiency of trans-ethnic genome-wide meta-analysis and fine-mapping.	Ong RT et al.	—	2012	→
Estimating ancestral proportions in a multi-ethnic US sample: implications for studies of admixed populations.	Levran O et al.	—	2012	→
European genetic variants associated with type 2 diabetes in North African Arabs.	Cauchi S et al.	—	2012	→
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study.	Buyske S et al.	—	2012	→
Evolution and medicine in undergraduate education: a prescription for all biology students.	Antolin MF et al.	—	2012	→
Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population.	Ram Murthy A et al.	—	2012	→
Genetic architecture in a marine hybrid zone: comparing outlier detection and genomic clines analysis in the bivalve Macoma balthica.	Luttikhuizen PC et al.	—	2012	→
Genetic variants at the ITPA locus protect against ribavirin-induced hemolytic anemia and dose reduction in an HCV G2/G3 cohort.	Eskesen AN et al.	—	2012	→
Genome-wide approaches in pharmacogenomics: heritability estimation and pharmacoethnicity as primary challenges.	Gamazon ER et al.	—	2012	→
Genome-wide association studies and prediction of normal tissue toxicity.	West CM et al.	—	2012	→
Genome-wide meta-analyses of smoking behaviors in African Americans.	David SP et al.	—	2012	→
Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative.	Liu EY et al.	—	2012	→
Health disparities in endocrine disorders: biological, clinical, and nonclinical factors--an Endocrine Society scientific statement.	Golden SH et al.	—	2012	→
Human genetic susceptibility to infectious disease.	Chapman SJ et al.	—	2012	→
Identification and association analysis of several hundred single nucleotide polymorphisms within candidate genes for back fat thickness in Italian Large White pigs using a selective genotyping approach.	Fontanesi L et al.	—	2012	→
Imputation reliability on DNA biallelic markers for drug metabolism studies.	Mijatovic V et al.	—	2012	→
Investigating the potential for ethnic group harm in collaborative genomics research in Africa: is ethnic stigmatisation likely?	de Vries J et al.	—	2012	→
New advances in the genetic basis of atrial fibrillation.	Mahida S et al.	—	2012	→
NGS technologies for analyzing germplasm diversity in genebanks.	Kilian B et al.	—	2012	→
Polymorphism of the serotonin transporter gene (5-HTTLPR) in major depressive disorder patients in Malaysia.	Mohamed Saini S et al.	—	2012	→
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation.	Kidd JM et al.	—	2012	→
Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation.	Chang D et al.	—	2012	→
Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study.	Chen CT et al.	—	2012	→
Sex differences in disease risk from reported genome-wide association study findings.	Liu LY et al.	—	2012	→
The influence of race and ethnicity on the biology of cancer.	Henderson BE et al.	—	2012	→
The matrix metalloproteinase 2-1575 gene polymorphism is associated with the risk of developing myocardial infarction in Mexican patients.	Pérez-Hernández N et al.	—	2012	→
Turkish population structure and genetic ancestry reveal relatedness among Eurasian populations.	Hodoğlugil U et al.	—	2012	→
Type 2 Diabetes Genetics: Beyond GWAS.	Sanghera DK et al.	—	2012	→
Why personalized medicine will fail if we stay the course.	Ramos E et al.	—	2012	→
A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese.	Cui B et al.	—	2011	→
A genome-wide perspective on the evolutionary history of enigmatic wolf-like canids.	vonHoldt BM et al.	—	2011	→
Cardiovascular diseases and genome-wide association studies.	Ndiaye NC et al.	—	2011	→
Developing biobanks in developing countries.	Rudan I et al.	—	2011	→
DNA amplification techniques in pharmacogenomics.	Morlighem JÉ et al.	—	2011	→
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium.	Pasaniuc B et al.	—	2011	→
Ethical issues in human genomics research in developing countries.	de Vries J et al.	—	2011	→
Evaluation of genetic susceptibility loci for chronic hepatitis B in Chinese: two independent case-control studies.	Wang L et al.	—	2011	→
Genetic architecture of cancer and other complex diseases: lessons learned and future directions.	Hindorff LA et al.	—	2011	→
Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.	Dumitrescu L et al.	—	2011	→
Genetic predictors for cardiovascular disease in hispanics.	Qi L et al.	—	2011	→
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families.	Arnett DK et al.	—	2011	→
Genome-wide association studies of asthma.	Tamari M et al.	—	2011	→
Genome-wide association studies of the PR interval in African Americans.	Smith JG et al.	—	2011	→
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).	Reiner AP et al.	—	2011	→
Genotype imputation with thousands of genomes.	Howie B et al.	—	2011	→
Haplotype variation and genotype imputation in African populations.	Huang L et al.	—	2011	→
Human genetics and genomics a decade after the release of the draft sequence of the human genome.	Naidoo N et al.	—	2011	→
Inclusion and exclusion in nutrigenetics clinical research: ethical and scientific challenges.	Hurlimann T et al.	—	2011	→
Invited commentary: dietary pattern analysis.	Imamura F et al.	—	2011	→
Mapping of disease-associated variants in admixed populations.	Shriner D et al.	—	2011	→
Mapping rare and common causal alleles for complex human diseases.	Raychaudhuri S	—	2011	→
Multi-ethnic studies in complex traits.	Fu J et al.	—	2011	→
New approaches to disease mapping in admixed populations.	Seldin MF et al.	—	2011	→
Pharmacogenomic Research in South Africa: Lessons Learned and Future Opportunities in the Rainbow Nation.	Warnich L et al.	—	2011	→
Recent findings in the genetics of blood pressure and hypertension traits.	Franceschini N et al.	—	2011	→
Six Degrees of Epistasis: Statistical Network Models for GWAS.	McKinney BA et al.	—	2011	→
Systematic review of birth cohort studies in Africa.	Campbell A et al.	—	2011	→
Systematic review of birth cohort studies in South East Asia and Eastern Mediterranean regions.	McKinnon R et al.	—	2011	→
The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study.	Matise TC et al.	—	2011	→
Transethnic meta-analysis of genomewide association studies.	Morris AP	—	2011	→
Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias.	van Oven M et al.	—	2011	→
Whole-genome resequencing in pharmacogenomics: moving away from past disparities to globally representative applications.	Drögemöller BI et al.	—	2011	→
A risky business--identifying susceptibility loci for lung cancer.	Gazdar AF et al.	—	2010	→
Chipping away the 'missing heritability': GIANT steps forward in the molecular elucidation of obesity - but still lots to go.	Hebebrand J et al.	—	2010	→
Fine-scale population structure and the era of next-generation sequencing.	Henn BM et al.	—	2010	→
Genetic control of host resistance to porcine reproductive and respiratory syndrome virus (PRRSV) infection.	Lunney JK et al.	—	2010	→
Genetic heterogeneity in colorectal cancer associations between African and European americans.	Kupfer SS et al.	—	2010	→
Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome.	Cockram J et al.	—	2010	→
Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study.	Engelman CD et al.	—	2010	→
Insights from GWAS into the quantitative genetics of transcription in humans.	Kim J et al.	—	2010	→
Multiethnic genetic association studies improve power for locus discovery.	Pulit SL et al.	—	2010	→
Pharmacogenomics of chronic hepatitis C therapy with genome-wide association studies.	Wang CH et al.	—	2010	→
Towards identifying genes underlying ecologically relevant traits in Arabidopsis thaliana.	Bergelson J et al.	—	2010	→
Whole-genome genetic diversity in a sample of Australians with deep Aboriginal ancestry.	McEvoy BP et al.	—	2010	→