Published in PLoS Genet on March 05, 2010
Fine mapping of the association with obesity at the FTO locus in African-derived populations. Hum Mol Genet (2010) 2.48
Genome-wide association of anthropometric traits in African- and African-derived populations. Hum Mol Genet (2010) 1.90
Inference of relationships in population data using identity-by-descent and identity-by-state. PLoS Genet (2011) 1.43
High-density SNP genotyping detects homogeneity of Spanish and French Basques, and confirms their genomic distinctiveness from other European populations. Hum Genet (2010) 1.13
Genome wide allele frequency fingerprints (GWAFFs) of populations via genotyping by sequencing. PLoS One (2013) 1.11
Development of admixture mapping panels for African Americans from commercial high-density SNP arrays. BMC Genomics (2010) 1.05
Genetic risk variants in African Americans with multiple sclerosis. Neurology (2013) 0.99
Cost-effective genome-wide estimation of allele frequencies from pooled DNA in Atlantic salmon (Salmo salar L.). BMC Genomics (2013) 0.87
Finding markers that make a difference: DNA pooling and SNP-arrays identify population informative markers for genetic stock identification. PLoS One (2013) 0.81
The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA. Hum Genet (2011) 0.79
Comparison of genotyping using pooled DNA samples (allelotyping) and individual genotyping using the affymetrix genome-wide human SNP array 6.0. BMC Genomics (2013) 0.78
Study on the introgression of beef breeds in Canchim cattle using single nucleotide polymorphism markers. PLoS One (2017) 0.75
A variant reference data set for the Africanized honeybee, Apis mellifera. Sci Data (2016) 0.75
Different Evolutionary History for Basque Diaspora Populations in USA and Argentina Unveiled by Mitochondrial DNA Analysis. PLoS One (2015) 0.75
Identifying Potential Regions of Copy Number Variation for Bipolar Disorder. Microarrays (Basel) (2014) 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 second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Genomic control for association studies. Biometrics (1999) 64.39
Population structure and eigenanalysis. PLoS Genet (2006) 37.21
Genetic structure of human populations. Science (2002) 30.91
Estimating African American admixture proportions by use of population-specific alleles. Am J Hum Genet (1998) 22.90
Worldwide human relationships inferred from genome-wide patterns of variation. Science (2008) 22.44
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays. PLoS Genet (2008) 20.38
Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet (2008) 19.55
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet (2008) 15.89
A multiethnic cohort in Hawaii and Los Angeles: baseline characteristics. Am J Epidemiol (2000) 13.17
A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes. Am J Hum Genet (2006) 9.56
Demonstrating stratification in a European American population. Nat Genet (2005) 9.49
Discerning the ancestry of European Americans in genetic association studies. PLoS Genet (2007) 7.81
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. PLoS One (2008) 7.16
Admixture mapping for hypertension loci with genome-scan markers. Nat Genet (2005) 6.78
DNA Pooling: a tool for large-scale association studies. Nat Rev Genet (2002) 5.66
European population substructure: clustering of northern and southern populations. PLoS Genet (2006) 5.27
A genomewide admixture map for Latino populations. Am J Hum Genet (2007) 4.71
Mapping by admixture linkage disequilibrium: advances, limitations and guidelines. Nat Rev Genet (2005) 4.04
Association mapping, using a mixture model for complex traits. Genet Epidemiol (2002) 3.95
Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet (2008) 3.79
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. Am J Hum Genet (2006) 3.67
The genetic structure of Pacific Islanders. PLoS Genet (2008) 3.31
Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Res (2008) 3.08
A unified association analysis approach for family and unrelated samples correcting for stratification. Am J Hum Genet (2008) 3.00
What can genome-wide association studies tell us about the genetics of common disease? PLoS Genet (2008) 2.35
Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans. Nucleic Acids Res (2006) 2.33
Genetic ancestry and the search for personalized genetic histories. Nat Rev Genet (2004) 2.08
Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates. Nucleic Acids Res (2006) 1.88
Association studies of common variants in 10 hypogonadotropic hypogonadism genes with age at menarche. J Clin Endocrinol Metab (2008) 1.83
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays. Nucleic Acids Res (2005) 1.71
Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study. Diabetes (2007) 1.58
Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation. Hum Genet (2009) 1.37
Genome-wide association studies: past, present and future. Hum Mol Genet (2008) 1.31
Simple method to analyze SNP-based association studies using DNA pools. Genet Epidemiol (2003) 1.29
Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studies. BMC Genomics (2007) 1.22
Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies. Bioinformatics (2008) 1.21
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. Am J Hum Genet (2009) 1.11
MPDA: microarray pooled DNA analyzer. BMC Bioinformatics (2008) 1.11
Three novel mtDNA restriction site polymorphisms allow exploration of population affinities of African Americans. Hum Biol (2003) 1.02
PoooL: an efficient method for estimating haplotype frequencies from large DNA pools. Bioinformatics (2008) 0.95
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nat Genet (2003) 53.59
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science (2007) 51.70
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet (2008) 35.06
Integrating common and rare genetic variation in diverse human populations. Nature (2010) 32.30
Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet (2008) 30.94
Mapping and sequencing of structural variation from eight human genomes. Nature (2008) 30.28
Genome-wide association study identifies novel breast cancer susceptibility loci. Nature (2007) 29.23
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet (2008) 22.35
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet (2008) 20.73
Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet (2008) 20.66
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med (2008) 19.71
Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet (2008) 19.55
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
The mutational landscape of head and neck squamous cell carcinoma. Science (2011) 16.88
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet (2003) 16.51
Assessing the impact of population stratification on genetic association studies. Nat Genet (2004) 16.28
Identification of ten loci associated with height highlights new biological pathways in human growth. Nat Genet (2008) 16.25
Replicating genotype-phenotype associations. Nature (2007) 16.11
Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet (2008) 15.94
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet (2008) 15.89
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet (2007) 14.99
A common genetic variant is associated with adult and childhood obesity. Science (2006) 14.95
Multiple regions within 8q24 independently affect risk for prostate cancer. Nat Genet (2007) 14.37
Body-mass index and mortality among 1.46 million white adults. N Engl J Med (2010) 13.34
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet (2012) 12.10
Genetic signatures of strong recent positive selection at the lactase gene. Am J Hum Genet (2004) 11.90
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet (2007) 10.81
Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men. Proc Natl Acad Sci U S A (2006) 10.32
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer. Nat Genet (2012) 9.93
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet (2010) 9.90
Polymorphisms associated with cholesterol and risk of cardiovascular events. N Engl J Med (2008) 9.83
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science (2010) 9.61
Demonstrating stratification in a European American population. Nat Genet (2005) 9.49
The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health. Am J Cardiol (2004) 9.43
Hypertension prevalence and blood pressure levels in 6 European countries, Canada, and the United States. JAMA (2003) 9.06
Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet (2013) 8.24
Subclinical thyroid disease: scientific review and guidelines for diagnosis and management. JAMA (2004) 8.12
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet (2010) 7.94
A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol. Am J Hum Genet (2006) 7.89
Ethnic and racial differences in the smoking-related risk of lung cancer. N Engl J Med (2006) 7.82
Discerning the ancestry of European Americans in genetic association studies. PLoS Genet (2007) 7.81
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet (2008) 7.65
Genome-wide association studies: potential next steps on a genetic journey. Hum Mol Genet (2008) 7.54
Common variants in the GDF5-UQCC region are associated with variation in human height. Nat Genet (2008) 7.31
Punctuated evolution of prostate cancer genomes. Cell (2013) 7.23
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. PLoS One (2008) 7.16
A common genetic risk factor for colorectal and prostate cancer. Nat Genet (2007) 7.11
Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet (2008) 7.07
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer. Nat Genet (2009) 6.99
A common variant of HMGA2 is associated with adult and childhood height in the general population. Nat Genet (2007) 6.87
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia. N Engl J Med (2010) 6.84
Admixture mapping for hypertension loci with genome-scan markers. Nat Genet (2005) 6.78
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale. Nat Genet (2011) 6.67
Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science (2008) 6.66
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nat Genet (2008) 6.42
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet (2006) 6.39
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet (2008) 6.22