Published in Am J Hum Genet on August 28, 2008
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Genome-wide association study link novel loci to endometriosis. PLoS One (2013) 1.05
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. PLoS One (2013) 1.04
Indian Siddis: African descendants with Indian admixture. Am J Hum Genet (2011) 1.03
Analysis of the genetic basis of disease in the context of worldwide human relationships and migration. PLoS Genet (2013) 1.01
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Visualizing spatial population structure with estimated effective migration surfaces. Nat Genet (2015) 0.96
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Impact of genetic similarity on imputation accuracy. BMC Genet (2015) 0.78
SCN9A Variants May be Implicated in Neuropathic Pain Associated With Diabetic Peripheral Neuropathy and Pain Severity. Clin J Pain (2015) 0.78
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies. Am J Hum Genet (2016) 0.78
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-wide Association Study. Gastroenterology (2016) 0.77
Across language families: Genome diversity mirrors linguistic variation within Europe. Am J Phys Anthropol (2015) 0.77
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Genetic contribution to multiple sclerosis risk among Ashkenazi Jews. BMC Med Genet (2015) 0.77
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Genomic analysis of the blood attributed to Louis XVI (1754-1793), king of France. Sci Rep (2014) 0.76
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Convex clustering: an attractive alternative to hierarchical clustering. PLoS Comput Biol (2015) 0.75
Connecting the Human Variome Project to nutrigenomics. Genes Nutr (2010) 0.75
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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science (2007) 43.16
Population structure and eigenanalysis. PLoS Genet (2006) 37.21
Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet (2008) 30.94
Genetic structure of human populations. Science (2002) 30.91
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Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet (2007) 24.68
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A unified mixed-model method for association mapping that accounts for multiple levels of relatedness. Nat Genet (2005) 20.97
The NCBI dbGaP database of genotypes and phenotypes. Nat Genet (2007) 17.93
Genes mirror geography within Europe. Nature (2008) 14.23
New models of collaboration in genome-wide association studies: the Genetic Association Information Network. Nat Genet (2007) 13.76
Genotype, haplotype and copy-number variation in worldwide human populations. Nature (2008) 12.40
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Interpreting principal component analyses of spatial population genetic variation. Nat Genet (2008) 8.49
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Proportionally more deleterious genetic variation in European than in African populations. Nature (2008) 6.61
Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet (2008) 6.42
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Nat Genet (2008) 6.06
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Measuring European population stratification with microarray genotype data. Am J Hum Genet (2007) 4.03
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. Am J Hum Genet (2008) 3.95
Matching strategies for genetic association studies in structured populations. Am J Hum Genet (2004) 3.13
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. Am J Hum Genet (2003) 2.71
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Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions. Pharmacogenomics J (2008) 1.48
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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
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
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science (2012) 17.12
Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med (2007) 17.06
Genome-wide association analysis identifies 20 loci that influence adult height. Nat Genet (2008) 16.92
Evolutionary and biomedical insights from the rhesus macaque genome. Science (2007) 16.21
Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet (2008) 15.94
Fast model-based estimation of ancestry in unrelated individuals. Genome Res (2009) 15.63
Genes mirror geography within Europe. Nature (2008) 14.23
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet (2011) 13.25
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature (2011) 13.23
Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet (2009) 12.44
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
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Variants in MTNR1B influence fasting glucose levels. Nat Genet (2008) 10.85
Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data. PLoS Genet (2009) 9.16
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