Published in PLoS One on November 07, 2012
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An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res (2006) 4.51
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Breast cancer in a multiethnic cohort in Hawaii and Los Angeles: risk factor-adjusted incidence in Japanese equals and in Hawaiians exceeds that in whites. Cancer Epidemiol Biomarkers Prev (2002) 2.45
A three-stage colonization model for the peopling of the Americas. PLoS One (2008) 2.40
Polynesian mitochondrial DNAs reveal three deep maternal lineage clusters. Hum Biol (1994) 2.38
Sex-biased evolutionary forces shape genomic patterns of human diversity. PLoS Genet (2008) 2.33
Comparing genetic ancestry and self-described race in african americans born in the United States and in Africa. Cancer Epidemiol Biomarkers Prev (2008) 2.29
Melanesian origin of Polynesian Y chromosomes. Curr Biol (2000) 2.27
Taiwan's gift to the world. Nature (2000) 2.21
Traces of archaic mitochondrial lineages persist in Austronesian-speaking Formosan populations. PLoS Biol (2005) 2.20
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Population genetics models of local ancestry. Genetics (2012) 2.10
Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians. Am J Hum Genet (2008) 2.02
Rapid, global demographic expansions after the origins of agriculture. Proc Natl Acad Sci U S A (2011) 1.96
Demographic history of Oceania inferred from genome-wide data. Curr Biol (2010) 1.93
Diabetes prevalence and body mass index differ by ethnicity: the Multiethnic Cohort. Ethn Dis (2009) 1.88
Y chromosomal evidence for the origins of oceanic-speaking peoples. Genetics (2002) 1.81
A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania. Am J Hum Genet (2001) 1.76
Development of a panel of genome-wide ancestry informative markers to study admixture throughout the Americas. PLoS Genet (2012) 1.74
Mutation patterns at dinucleotide microsatellite loci in humans. Am J Hum Genet (2002) 1.71
Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes. Hum Mutat (2009) 1.57
High-throughput sequencing of complete human mtDNA genomes from the Philippines. Genome Res (2010) 1.56
Melanesian mtDNA complexity. PLoS One (2007) 1.54
Characterizing the time dependency of human mitochondrial DNA mutation rate estimates. Mol Biol Evol (2008) 1.53
Health indicators of Native Hawaiian and Pacific Islanders in the United States. J Community Health (2010) 1.50
Ancient mitochondrial M haplogroups identified in the Southwest Pacific. Proc Natl Acad Sci U S A (2005) 1.29
Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study. Hum Genet (2010) 1.26
Maori origins, Y-chromosome haplotypes and implications for human history in the Pacific. Hum Mutat (2001) 1.19
Stability selection for genome-wide association. Genet Epidemiol (2011) 1.18
Established risk factors account for most of the racial differences in cardiovascular disease mortality. PLoS One (2007) 1.12
Correcting population stratification in genetic association studies using a phylogenetic approach. Bioinformatics (2010) 1.08
Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. Am J Hum Genet (2010) 1.02
Mitochondrial DNA diversity in Southeast Asian populations. Hum Biol (2002) 0.94
Explaining the imperfection of the molecular clock of hominid mitochondria. PLoS One (2009) 0.93
African and non-African admixture components in African Americans and an African Caribbean population. Genet Epidemiol (2010) 0.93
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
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
Genome-wide association study identifies novel breast cancer susceptibility loci. Nature (2007) 29.23
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Assessing the impact of population stratification on genetic association studies. Nat Genet (2004) 16.28
Multiple regions within 8q24 independently affect risk for prostate cancer. Nat Genet (2007) 14.37
Variants in MTNR1B influence fasting glucose levels. Nat Genet (2008) 10.85
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
The pattern of polymorphism in Arabidopsis thaliana. PLoS Biol (2005) 10.13
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome. Nat Genet (2006) 8.46
Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet (2013) 8.24
Ethnic and racial differences in the smoking-related risk of lung cancer. N Engl J Med (2006) 7.82
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet (2008) 7.65
A common genetic risk factor for colorectal and prostate cancer. Nat Genet (2007) 7.11
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
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet (2008) 6.22
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet (2012) 6.15
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Nat Genet (2009) 6.04
Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study. Hum Hered (2003) 5.78
Exploiting gene-environment interaction to detect genetic associations. Hum Hered (2007) 5.63
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Nat Genet (2013) 5.58
Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines. PLoS Genet (2008) 5.08
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nat Genet (2008) 4.84
Transferability of tag SNPs in genetic association studies in multiple populations. Nat Genet (2006) 4.78
A genomewide admixture map for Latino populations. Am J Hum Genet (2007) 4.71
Merging and emerging cohorts: not worth the wait. Nature (2007) 4.66
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies. J Natl Cancer Inst (2010) 4.54
Common variants at 19p13 are associated with susceptibility to ovarian cancer. Nat Genet (2010) 4.51
Fast and flexible simulation of DNA sequence data. Genome Res (2008) 4.45
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nat Genet (2009) 4.38
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat Genet (2012) 4.37
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nat Genet (2013) 4.35
Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals. Hum Hered (2003) 4.34
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations. Diabetes (2008) 4.20
The signature of positive selection on standing genetic variation. Evolution (2005) 4.17
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes (2010) 4.07
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Nat Genet (2010) 3.86
Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat Genet (2013) 3.81
Identification of a new prostate cancer susceptibility locus on chromosome 8q24. Nat Genet (2009) 3.76
Detectable clonal mosaicism and its relationship to aging and cancer. Nat Genet (2012) 3.69
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet (2011) 3.68
Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68
Functional enhancers at the gene-poor 8q24 cancer-linked locus. PLoS Genet (2009) 3.59