Published in Hum Mutat on January 01, 2009
Accounting for ancestry: population substructure and genome-wide association studies. Hum Mol Genet (2008) 3.39
The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. Am J Epidemiol (2011) 2.98
Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records. Am J Hum Genet (2011) 2.27
Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records. Genet Med (2010) 2.09
Tourette syndrome is associated with recurrent exonic copy number variants. Neurology (2010) 1.99
An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels. BMC Genet (2009) 1.80
Pharmacogenetic approach at the serotonin transporter gene as a method of reducing the severity of alcohol drinking. Am J Psychiatry (2011) 1.69
Analysis of East Asia genetic substructure using genome-wide SNP arrays. PLoS One (2008) 1.65
A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis. Cancer Res (2009) 1.64
High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. PLoS Genet (2009) 1.61
European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups. Mol Med (2009) 1.59
Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival. J Thorac Cardiovasc Surg (2015) 1.41
Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus. Ann Rheum Dis (2011) 1.41
Relationship of pain and ancestry in African American women. Eur J Pain (2015) 1.40
Validation of a small set of ancestral informative markers for control of population admixture in African Americans. Am J Epidemiol (2011) 1.36
Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) Consortium. Diabetes (2012) 1.31
Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study. Hum Genet (2010) 1.26
Differences in albuminuria between Hispanics and whites: an evaluation by genetic ancestry and country of origin: the multi-ethnic study of atherosclerosis. Circ Cardiovasc Genet (2010) 1.23
Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples. Investig Genet (2011) 1.22
Identification of novel genetic susceptibility loci in African American lupus patients in a candidate gene association study. Arthritis Rheum (2011) 1.19
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. Ann Neurol (2012) 1.19
ALFRED: an allele frequency resource for research and teaching. Nucleic Acids Res (2011) 1.12
The GenoChip: a new tool for genetic anthropology. Genome Biol Evol (2013) 1.12
Evaluating self-declared ancestry of U.S. Americans with autosomal, Y-chromosomal and mitochondrial DNA. Hum Mutat (2010) 1.12
Brazilian urban population genetic structure reveals a high degree of admixture. Eur J Hum Genet (2011) 1.10
Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies. Genet Epidemiol (2012) 1.10
Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. Clin Infect Dis (2011) 1.09
Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing. PLoS One (2012) 1.08
African ancestry is associated with asthma risk in African Americans. PLoS One (2012) 1.07
Race, ancestry, and development of food-allergen sensitization in early childhood. Pediatrics (2011) 1.06
Tracking crop varieties using genotyping-by-sequencing markers: a case study using cassava (Manihot esculenta Crantz). BMC Genet (2015) 1.05
Development of admixture mapping panels for African Americans from commercial high-density SNP arrays. BMC Genomics (2010) 1.05
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosus. Arthritis Rheum (2010) 1.04
Functional variants of the sphingosine-1-phosphate receptor 1 gene associate with asthma susceptibility. J Allergy Clin Immunol (2010) 1.04
Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. Investig Genet (2013) 1.04
The role of complementary bipartite visual analytical representations in the analysis of SNPs: a case study in ancestral informative markers. J Am Med Inform Assoc (2012) 1.04
Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study. Hum Reprod (2013) 1.03
European genetic ancestry is associated with a decreased risk of lupus nephritis. Arthritis Rheum (2012) 1.01
Impact of genetic ancestry and sociodemographic status on the clinical expression of systemic lupus erythematosus in American Indian-European populations. Arthritis Rheum (2012) 1.01
Revisiting the genetic ancestry of Brazilians using autosomal AIM-Indels. PLoS One (2013) 1.00
Evidence for gene-gene epistatic interactions among susceptibility loci for systemic lupus erythematosus. Arthritis Rheum (2012) 0.99
Genetic heterogeneity of self-reported ancestry groups in an admixed Brazilian population. J Epidemiol (2011) 0.99
Interethnic admixture and the evolution of Latin American populations. Genet Mol Biol (2014) 0.99
Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women. Diabetologia (2012) 0.99
Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21. Arthritis Rheum (2011) 0.98
Genetic variants of TSLP and asthma in an admixed urban population. PLoS One (2011) 0.98
Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico. Cancer (2014) 0.97
Relationship between adiposity and admixture in African-American and Hispanic-American women. Int J Obes (Lond) (2011) 0.97
Privacy-preserving genomic testing in the clinic: a model using HIV treatment. Genet Med (2016) 0.97
European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus. Arthritis Rheum (2009) 0.96
Replication of association of a novel insulin receptor gene polymorphism with polycystic ovary syndrome. Fertil Steril (2011) 0.94
Susceptibility locus in neurokinin-1 receptor gene associated with alcohol dependence. Neuropsychopharmacology (2009) 0.94
Underlying genetic structure impacts the association between CYP2B6 polymorphisms and response to efavirenz and nevirapine. AIDS (2012) 0.93
Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia. Carcinogenesis (2014) 0.93
Multiplex genotyping system for efficient inference of matrilineal genetic ancestry with continental resolution. Investig Genet (2011) 0.92
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia. Gut (2013) 0.92
CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins. PLoS One (2010) 0.91
PNPLA3 polymorphisms and liver aminotransferase levels in a Mexican American population. Clin Invest Med (2012) 0.91
Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis. Genes Immun (2012) 0.91
HLA class I, KIR, and genome-wide SNP diversity in the RV144 Thai phase 3 HIV vaccine clinical trial. Immunogenetics (2014) 0.90
Patient genotypes impact survival after surgery for isolated congenital heart disease. Ann Thorac Surg (2014) 0.90
Ancestral effect on HOMA-IR levels quantitated in an American population of Mexican origin. Diabetes Care (2012) 0.90
Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome. Blood (2013) 0.90
Estrogen-related genes and their contribution to racial differences in breast cancer risk. Cancer Causes Control (2012) 0.89
European population substructure correlates with systemic lupus erythematosus endophenotypes in North Americans of European descent. Genes Immun (2009) 0.88
Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium. PLoS One (2014) 0.88
African ancestry, early life exposures, and respiratory morbidity in early childhood. Clin Exp Allergy (2011) 0.88
HAART-associated dyslipidemia varies by biogeographical ancestry in the multicenter AIDS cohort study. AIDS Res Hum Retroviruses (2013) 0.87
Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate. Transl Psychiatry (2014) 0.87
Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, -DQB1, and -DPB1. BMC Genet (2014) 0.87
Genetic ancestry-smoking interactions and lung function in African Americans: a cohort study. PLoS One (2012) 0.87
Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. PLoS One (2015) 0.86
Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes. J Autoimmun (2015) 0.86
WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening. Age (Dordr) (2014) 0.86
Identifying genetic variation for alcohol dependence. Alcohol Res (2012) 0.86
Indigenous American ancestry is associated with arsenic methylation efficiency in an admixed population of northwest Mexico. J Toxicol Environ Health A (2012) 0.86
Socioeconomic status and lung cancer: unraveling the contribution of genetic admixture. Am J Public Health (2013) 0.86
A panel of ancestry informative markers for the complex five-way admixed South African coloured population. PLoS One (2013) 0.85
Mutational Landscape of Aggressive Prostate Tumors in African American Men. Cancer Res (2016) 0.85
Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study. PLoS One (2015) 0.85
Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia. J Natl Cancer Inst (2014) 0.85
Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis. Arthritis Rheum (2012) 0.85
Genetic risk factors for thrombosis in systemic lupus erythematosus. J Rheumatol (2012) 0.85
Associations between genetic variants in vitamin D metabolism and asthma characteristics in young African Americans: a pilot study. J Investig Med (2011) 0.84
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus. Genes Immun (2014) 0.84
Single nucleotide polymorphisms and haplotypes in Native American populations. Am J Phys Anthropol (2011) 0.84
Genetic analysis of ancestry, admixture and selection in Bolivian and Totonac populations of the New World. BMC Genet (2012) 0.84
Race as a social construct in head and neck cancer outcomes. Otolaryngol Head Neck Surg (2011) 0.84
Examination of ancestral informative markers and self-reported race with tumor characteristics of breast cancer among Black and White women. Breast Cancer Res Treat (2012) 0.84
The association between APOL1 risk alleles and longitudinal kidney function differs by HIV viral suppression status. Clin Infect Dis (2014) 0.84
Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. PLoS One (2013) 0.84
Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb. Investig Genet (2012) 0.83
Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis. Genes Immun (2010) 0.83
Genetic susceptibility to therapy-related leukemia after Hodgkin lymphoma or non-Hodgkin lymphoma: role of drug metabolism, apoptosis and DNA repair. Blood Cancer J (2012) 0.83
Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years. Am J Obstet Gynecol (2010) 0.83
The National DNA Data Bank of Canada: a Quebecer perspective. Front Genet (2013) 0.83
Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. Oncotarget (2012) 0.82
Genetic ancestry and risk of mortality among U.S. Latinas with breast cancer. Cancer Res (2013) 0.82
Racial and ethnic health disparities in reproductive medicine: an evidence-based overview. Semin Reprod Med (2013) 0.82
Ancestry informative markers for distinguishing between Thai populations based on genome-wide association datasets. Leg Med (Tokyo) (2015) 0.82
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Inference of population structure using multilocus genotype data. Genetics (2000) 147.76
Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet (2006) 115.71
A haplotype map of the human genome. Nature (2005) 105.70
Genomic control for association studies. Biometrics (1999) 64.39
Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. Genetics (2003) 53.11
Genetic structure of human populations. Science (2002) 30.91
A high-resolution recombination map of the human genome. Nat Genet (2002) 28.66
Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet (2005) 25.34
Association mapping in structured populations. Am J Hum Genet (2000) 16.79
Assessing the impact of population stratification on genetic association studies. Nat Genet (2004) 16.28
The effects of human population structure on large genetic association studies. Nat Genet (2004) 14.88
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science (2005) 12.02
Genetic signatures of strong recent positive selection at the lactase gene. Am J Hum Genet (2004) 11.90
A high-density admixture map for disease gene discovery in african americans. Am J Hum Genet (2004) 10.87
Demonstrating stratification in a European American population. Nat Genet (2005) 9.49
Convergent adaptation of human lactase persistence in Africa and Europe. Nat Genet (2006) 9.44
Control of confounding of genetic associations in stratified populations. Am J Hum Genet (2003) 7.99
Discerning the ancestry of European Americans in genetic association studies. PLoS Genet (2007) 7.81
Design and analysis of admixture mapping studies. Am J Hum Genet (2004) 7.20
Informativeness of genetic markers for inference of ancestry. Am J Hum Genet (2003) 6.90
Clines, clusters, and the effect of study design on the inference of human population structure. PLoS Genet (2005) 6.73
Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet (2008) 6.42
Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model. Am J Hum Genet (2001) 5.66
An Icelandic example of the impact of population structure on association studies. Nat Genet (2004) 5.53
European population substructure: clustering of northern and southern populations. PLoS Genet (2006) 5.27
The New York Cancer Project: rationale, organization, design, and baseline characteristics. J Urban Health (2004) 5.21
A genomewide admixture map for Latino populations. Am J Hum Genet (2007) 4.71
Detection of the signature of natural selection in humans: evidence from the Duffy blood group locus. Am J Hum Genet (2000) 4.39
A simple and improved correction for population stratification in case-control studies. Am J Hum Genet (2007) 4.29
Measuring European population stratification with microarray genotype data. Am J Hum Genet (2007) 4.03
A genomewide admixture mapping panel for Hispanic/Latino populations. Am J Hum Genet (2007) 3.85
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping. Am J Hum Genet (2006) 3.77
A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. Am J Hum Genet (2007) 3.39
Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics. Genet Epidemiol (2005) 3.03
Implications of correlations between skin color and genetic ancestry for biomedical research. Nat Genet (2004) 2.46
Evidence of positive selection on a class I ADH locus. Am J Hum Genet (2007) 1.48
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Strong association of de novo copy number mutations with autism. Science (2007) 27.84
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science (2006) 27.49
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding. Genome Res (2009) 15.15
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet (2006) 15.14
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet (2004) 13.71
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nat Genet (2008) 12.51
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. N Engl J Med (2007) 12.24
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science (2005) 12.02
Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus. Proc Natl Acad Sci U S A (2003) 11.65
A high-density admixture map for disease gene discovery in african americans. Am J Hum Genet (2004) 10.87
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet (2010) 9.90
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. N Engl J Med (2007) 9.80
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. N Engl J Med (2008) 9.61
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Nat Genet (2007) 8.74
Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet (2008) 7.07
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus. Nat Genet (2006) 6.98
Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circ Cardiovasc Genet (2010) 6.74
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4. Am J Hum Genet (2005) 6.61
Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet (2008) 6.42
Development of personalized tumor biomarkers using massively parallel sequencing. Sci Transl Med (2010) 6.08
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus. Nat Genet (2009) 5.75
European population substructure: clustering of northern and southern populations. PLoS Genet (2006) 5.27
The New York Cancer Project: rationale, organization, design, and baseline characteristics. J Urban Health (2004) 5.21
Refining the complex rheumatoid arthritis phenotype based on specificity of the HLA-DRB1 shared epitope for antibodies to citrullinated proteins. Arthritis Rheum (2005) 5.18
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis. Nat Genet (2012) 5.11
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. Am J Hum Genet (2005) 5.00
An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist. N Engl J Med (2009) 4.97
An Aboriginal Australian genome reveals separate human dispersals into Asia. Science (2011) 4.84
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus. Proc Natl Acad Sci U S A (2007) 4.71
Clan genomics and the complex architecture of human disease. Cell (2011) 4.53
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. Am J Hum Genet (2004) 4.46
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nat Genet (2012) 4.46
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat Genet (2012) 4.41
Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus. Nat Genet (2008) 4.33
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. Am J Hum Genet (2005) 3.95
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping. Am J Hum Genet (2006) 3.77
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. Arthritis Rheum (2003) 3.73
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. PLoS Genet (2011) 3.68
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. Nat Genet (2009) 3.65
Gene-gene and gene-environment interactions involving HLA-DRB1, PTPN22, and smoking in two subsets of rheumatoid arthritis. Am J Hum Genet (2007) 3.62
A second-generation combined linkage physical map of the human genome. Genome Res (2007) 3.60
Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy. Circulation (2003) 3.54
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. Nat Genet (2009) 3.52
Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research. Am J Public Health (2005) 3.50
Accounting for ancestry: population substructure and genome-wide association studies. Hum Mol Genet (2008) 3.39
A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. Am J Hum Genet (2007) 3.39
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. Nat Genet (2009) 3.36
Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. J Med Genet (2009) 3.33
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. Nat Genet (2010) 3.15
Regulation of anti-cyclic citrullinated peptide antibodies in rheumatoid arthritis: contrasting effects of HLA-DR3 and the shared epitope alleles. Arthritis Rheum (2005) 2.88
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. Nature (2010) 2.85
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome. Am J Hum Genet (2008) 2.71
The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping. J Biomol Tech (2005) 2.64
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Nat Genet (2010) 2.61
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy. Circulation (2005) 2.58
Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus. Nat Genet (2011) 2.54
Elevated serum levels of interferon-regulated chemokines are biomarkers for active human systemic lupus erythematosus. PLoS Med (2006) 2.53
Confirmation study of prostate cancer risk variants at 8q24 in African Americans identifies a novel risk locus. Genome Res (2007) 2.53
Genomics and the multifactorial nature of human autoimmune disease. N Engl J Med (2011) 2.52
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. Am J Hum Genet (2002) 2.47
Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis. Hum Mol Genet (2003) 2.33
Genetic ancestry is associated with subclinical cardiovascular disease in African-Americans and Hispanics from the multi-ethnic study of atherosclerosis. Circ Cardiovasc Genet (2009) 2.31
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Nat Genet (2012) 2.31
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases. Proc Natl Acad Sci U S A (2009) 2.31