Published in BMC Genet on July 24, 2009
Functionally defective germline variants of sialic acid acetylesterase in autoimmunity. Nature (2010) 2.10
European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups. Mol Med (2009) 1.59
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
Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples. Investig Genet (2011) 1.22
The GenoChip: a new tool for genetic anthropology. Genome Biol Evol (2013) 1.12
Effect of NQO1 and CYP4F2 genotypes on warfarin dose requirements in Hispanic-Americans and African-Americans. Pharmacogenomics (2012) 1.09
Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing. PLoS One (2012) 1.08
Current genetic methodologies in the identification of disaster victims and in forensic analysis. J Appl Genet (2011) 1.07
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
An overview of STRUCTURE: applications, parameter settings, and supporting software. Front Genet (2013) 1.02
Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data. BMC Syst Biol (2012) 1.00
Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women. Diabetologia (2012) 0.99
Relationship between adiposity and admixture in African-American and Hispanic-American women. Int J Obes (Lond) (2011) 0.97
African ancestry protects against Alzheimer's disease-related neuropathology. Mol Psychiatry (2011) 0.93
The challenges of collecting data on race and ethnicity in a diverse, multiethnic state. Hawaii Med J (2011) 0.93
CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins. PLoS One (2010) 0.91
HAART-associated dyslipidemia varies by biogeographical ancestry in the multicenter AIDS cohort study. AIDS Res Hum Retroviruses (2013) 0.87
Human biosample authentication using the high-throughput, cost-effective SNPtrace(TM) system. PLoS One (2015) 0.87
Using ancestry-informative markers to identify fine structure across 15 populations of European origin. Eur J Hum Genet (2014) 0.87
The Genomic Revolution and Beliefs about Essential Racial Differences: A Backdoor to Eugenics? Am Sociol Rev (2013) 0.86
A panel of ancestry informative markers for the complex five-way admixed South African coloured population. PLoS One (2013) 0.85
ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation. J Lipid Res (2011) 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
Cigarette experimentation in Mexican origin youth: psychosocial and genetic determinants. Cancer Epidemiol Biomarkers Prev (2011) 0.82
Validation of a cost-efficient multi-purpose SNP panel for disease based research. PLoS One (2011) 0.82
Associations of Genetically Determined Continental Ancestry With CD4+ Count and Plasma HIV-1 RNA Beyond Self-Reported Race and Ethnicity. J Acquir Immune Defic Syndr (2016) 0.82
A single nucleotide polymorphism in the corticotropin receptor gene is associated with a blunted cortisol response during pediatric critical illness. Pediatr Crit Care Med (2014) 0.82
A small number of candidate gene SNPs reveal continental ancestry in African Americans. Ann Hum Genet (2013) 0.81
Race, Ethnicity and Ancestry in Unrelated Transplant Matching for the National Marrow Donor Program: A Comparison of Multiple Forms of Self-Identification with Genetics. PLoS One (2015) 0.81
Evaluating the accuracy of AIM panels at quantifying genome ancestry. BMC Genomics (2014) 0.80
Sensation-seeking genes and physical activity in youth. Genes Brain Behav (2012) 0.80
Integrative analysis of single nucleotide polymorphisms and gene expression efficiently distinguishes samples from closely related ethnic populations. BMC Genomics (2012) 0.80
What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research. AJOB Prim Res (2012) 0.79
Relationship between hysterectomy and admixture in African American women. Am J Obstet Gynecol (2013) 0.79
Selecting SNPs to identify ancestry. Ann Hum Genet (2011) 0.76
Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. PLoS One (2014) 0.76
ETHNOPRED: a novel machine learning method for accurate continental and sub-continental ancestry identification and population stratification correction. BMC Bioinformatics (2013) 0.76
Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study. Exp Ther Med (2016) 0.75
Relationship between glaucoma and admixture in postmenopausal African American women. Ethn Dis (2014) 0.75
Detecting a hierarchical genetic population structure via Multi-InDel markers on the X chromosome. Sci Rep (2016) 0.75
Genetic ancestry as an effect modifier of naltrexone in smoking cessation among African Americans: an analysis of a randomized controlled trial. Pharmacogenet Genomics (2015) 0.75
Applying genome-wide gene-based expression quantitative trait locus mapping to study population ancestry and pharmacogenetics. BMC Genomics (2014) 0.75
Genetic, psychosocial, and demographic factors associated with social disinhibition in Mexican-origin youth. Brain Behav (2014) 0.75
The influence of population stratification on genetic markers associated with type 1 diabetes. Sci Rep (2017) 0.75
Design, conduct, and analysis of a multicenter, pharmacogenomic, biomarker study in matched patients with severe sepsis treated with or without drotrecogin Alfa (activated). Ann Intensive Care (2012) 0.75
Interest in genomic SNP testing for prostate cancer risk: a pilot survey. Hered Cancer Clin Pract (2015) 0.75
Prediction of biogeographical ancestry from genotype: a comparison of classifiers. Int J Legal Med (2016) 0.75
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
The International HapMap Project. Nature (2003) 73.65
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
Worldwide human relationships inferred from genome-wide patterns of variation. Science (2008) 22.44
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
Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet (2008) 6.42
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
Human population genetic structure and inference of group membership. Am J Hum Genet (2003) 4.73
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. Hum Mutat (2009) 4.65
Measuring European population stratification with microarray genotype data. Am J Hum Genet (2007) 4.03
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
Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics. Genet Epidemiol (2005) 3.03
A panel of ancestry informative markers for estimating individual biogeographical ancestry and admixture from four continents: utility and applications. Hum Mutat (2008) 2.96
Implications of correlations between skin color and genetic ancestry for biomedical research. Nat Genet (2004) 2.46
Low levels of genetic divergence across geographically and linguistically diverse populations from India. PLoS Genet (2006) 2.26
Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs. Forensic Sci Int Genet (2007) 2.03
Application of ancestry informative markers to association studies in European Americans. PLoS Genet (2008) 1.90
Analysis of East Asia genetic substructure using genome-wide SNP arrays. PLoS One (2008) 1.65
Human population genetic structure and diversity inferred from polymorphic L1(LINE-1) and Alu insertions. Hum Hered (2006) 1.44
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
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. Hum Mutat (2009) 4.65
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