Published in Sci Rep on January 19, 2016
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Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos. Lipids Health Dis (2017) 0.75
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A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet (2007) 52.68
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Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Heart disease and stroke statistics--2014 update: a report from the American Heart Association. Circulation (2013) 28.02
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Genotype imputation for genome-wide association studies. Nat Rev Genet (2010) 14.59
LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics (2010) 13.54
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature (2010) 12.07
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet (2012) 11.29
PAGE: parametric analysis of gene set enrichment. BMC Bioinformatics (2005) 8.41
A linear complexity phasing method for thousands of genomes. Nat Methods (2011) 8.30
Discovery and refinement of loci associated with lipid levels. Nat Genet (2013) 7.86
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A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. BMC Med Genet (2007) 5.64
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GATES: a rapid and powerful gene-based association test using extended Simes procedure. Am J Hum Genet (2011) 3.34
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. PLoS Genet (2011) 2.68
Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. PLoS Genet (2011) 2.13
GSA-SNP: a general approach for gene set analysis of polymorphisms. Nucleic Acids Res (2010) 2.09
Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. PLoS Biol (2013) 2.08
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet (2012) 1.96
Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas. Diabetologia (2011) 1.60
Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia (2011) 1.59
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. PLoS One (2012) 1.56
HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis. Am J Hum Genet (2012) 1.41
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Circ Cardiovasc Genet (2012) 1.35
Prevalence of dyslipidemias in the Mexican National Health and Nutrition Survey 2006. Salud Publica Mex (2010) 1.27
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. Am J Hum Genet (2013) 1.27
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Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. J Med Genet (2013) 1.26
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Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. Nat Commun (2014) 1.02
Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. PLoS One (2011) 0.95
Integrative genomics: quantifying significance of phenotype-genotype relationships from multiple sources of high-throughput data. Front Genet (2013) 0.85
Structural architecture of SNP effects on complex traits. Am J Hum Genet (2014) 0.85
Steatosis and steatohepatitis: complex disorders. Int J Mol Sci (2014) 0.83
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet (2015) 2.84
Exploring the distribution of genetic markers of pharmacogenomics relevance in Brazilian and Mexican populations. PLoS One (2014) 1.51
Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat Genet (2014) 1.07
Cuba: exploring the history of admixture and the genetic basis of pigmentation using autosomal and uniparental markers. PLoS Genet (2014) 1.02
Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk. Nat Genet (2015) 1.00
Leveraging population admixture to characterize the heritability of complex traits. Nat Genet (2014) 0.95
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nat Genet (2015) 0.91
A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases. Nat Genet (2016) 0.85
HLA-DPB1*04:01 Protects Genetically Susceptible Children from Celiac Disease Autoimmunity in the TEDDY Study. Am J Gastroenterol (2015) 0.81
Association study confirms the role of two OCA2 polymorphisms in normal skin pigmentation variation in East Asian populations. Am J Hum Biol (2015) 0.81
Rapid evaluation of phenotypes, SNPs and results through the dbGaP CHARGE Summary Results site. Nat Genet (2016) 0.78
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. Nat Genet (2017) 0.76
Evaluation of fall Sun Exposure Score in predicting vitamin D status in young Canadian adults, and the influence of ancestry. J Photochem Photobiol B (2015) 0.76
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins. J Med Genet (2016) 0.75
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. PLoS Genet (2017) 0.75
Rationale, design and baseline characteristics of the Microbiome and Insulin Longitudinal Evaluation Study (MILES). Diabetes Obes Metab (2020) 0.75
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology. Nat Genet (2017) 0.75
Exome-wide association study of plasma lipids in >300,000 individuals. Nat Genet (2017) 0.75
Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. Sci Rep (2017) 0.75