Published in Am J Hum Genet on September 01, 1995
Inference of population structure using multilocus genotype data. Genetics (2000) 147.76
Use of unlinked genetic markers to detect population stratification in association studies. Am J Hum Genet (1999) 23.67
Association mapping in structured populations. Am J Hum Genet (2000) 16.79
Archaic African and Asian lineages in the genetic ancestry of modern humans. Am J Hum Genet (1997) 8.63
Mapping genes that underlie ethnic differences in disease risk: methods for detecting linkage in admixed populations, by conditioning on parental admixture. Am J Hum Genet (1998) 7.96
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
Ethnic-affiliation estimation by use of population-specific DNA markers. Am J Hum Genet (1997) 6.72
Signatures of population expansion in microsatellite repeat data. Genetics (1998) 5.76
Detecting population expansion and decline using microsatellites. Genetics (1999) 5.72
Genetic traces of ancient demography. Proc Natl Acad Sci U S A (1998) 5.48
Microsatellite diversity and the demographic history of modern humans. Proc Natl Acad Sci U S A (1997) 4.96
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Genetic distances and reconstruction of phylogenetic trees from microsatellite DNA. Genetics (1996) 4.55
mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe. Am J Hum Genet (1998) 3.94
Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Res (1997) 3.73
Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome Res (2004) 3.34
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Genetic evidence on the origins of Indian caste populations. Genome Res (2001) 3.25
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Genetic evidence for a Paleolithic human population expansion in Africa. Proc Natl Acad Sci U S A (1998) 3.02
The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data. Am J Hum Genet (2000) 2.91
Ethnic India: a genomic view, with special reference to peopling and structure. Genome Res (2003) 2.88
Genetic relationship of populations in China. Proc Natl Acad Sci U S A (1998) 2.65
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Genetic variation among world populations: inferences from 100 Alu insertion polymorphisms. Genome Res (2003) 2.47
Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations. Am J Hum Genet (2000) 2.25
Geographic patterns of mtDNA diversity in Europe. Am J Hum Genet (2000) 2.18
Clines of nuclear DNA markers suggest a largely neolithic ancestry of the European gene pool. Proc Natl Acad Sci U S A (1998) 2.16
Compilation of human mtDNA control region sequences. Nucleic Acids Res (1998) 2.00
Ascertainment bias in estimates of average heterozygosity. Am J Hum Genet (1996) 1.94
Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms. Am J Hum Genet (2001) 1.91
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. Am J Hum Genet (2000) 1.85
Marker selection for the transmission/disequilibrium test, in recently admixed populations. Am J Hum Genet (1998) 1.66
Mobile element scanning (ME-Scan) identifies thousands of novel Alu insertions in diverse human populations. Genome Res (2013) 1.66
Paleolithic and Neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet (1997) 1.64
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Mobile element scanning (ME-Scan) by targeted high-throughput sequencing. BMC Genomics (2010) 1.54
Fine-scaled human genetic structure revealed by SNP microarrays. Genome Res (2009) 1.48
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Microsatellite mutations and inferences about human demography. Genetics (2000) 1.37
Mitochondrial and nuclear genetic relationships among Pacific Island and Asian populations. Am J Hum Genet (1998) 1.36
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy. Genetics (1999) 1.21
A genomic portrait of human microsatellite variation. Mol Biol Evol (2010) 1.21
Effects of worldwide population subdivision on ALDH2 linkage disequilibrium. Genome Res (1999) 1.13
Differential structuring of human populations for homologous X and Y microsatellite loci. Am J Hum Genet (1997) 1.12
Mitochondrial DNA analysis: polymorphisms and pathogenicity. J Med Genet (1999) 1.12
Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms. BMC Genet (2008) 1.11
The Chinese human genome diversity project. Proc Natl Acad Sci U S A (1998) 1.07
Population structure in a comprehensive genomic data set on human microsatellite variation. G3 (Bethesda) (2013) 1.05
Crohn's disease and genetic hitchhiking at IBD5. Mol Biol Evol (2011) 1.03
EWS/FLI-responsive GGAA microsatellites exhibit polymorphic differences between European and African populations. Cancer Genet (2012) 0.94
A panel of ancestry informative markers for the complex five-way admixed South African coloured population. PLoS One (2013) 0.85
Genotyping of PCR-based polymorphisms and linkage-disequilibrium analysis at the NF1 locus. Am J Hum Genet (1996) 0.85
Influence of language and ancestry on genetic structure of contiguous populations: a microsatellite based study on populations of Orissa. BMC Genet (2005) 0.83
Structural analysis of insulin minisatellite alleles reveals unusually large differences in diversity between Africans and non-Africans. Am J Hum Genet (2002) 0.82
How do SNP ascertainment schemes and population demographics affect inferences about population history? BMC Genomics (2015) 0.81
Mitochondrial lineages in Ladin-speaking communities of the eastern Alps. Proc Biol Sci (1998) 0.81
Genomes, populations and diseases: ethnic genomics and personalized medicine. Acta Naturae (2010) 0.77
A consensus tree approach for reconstructing human evolutionary history and detecting population substructure. IEEE/ACM Trans Comput Biol Bioinform (2011) 0.77
Phylogenetic estimation in humans and neck riddles. Am J Hum Genet (1997) 0.76
A discordance between mtDNA diversity and blood-protein heterozygosity in northern Siberian populations. Am J Hum Genet (1996) 0.75
APOL1 risk alleles among individuals with CKD in Northern Tanzania: A pilot study. PLoS One (2017) 0.75
Discovery of rare, diagnostic AluYb8/9 elements in diverse human populations. Mob DNA (2017) 0.75
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High resolution of human evolutionary trees with polymorphic microsatellites. Nature (1994) 28.48
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African populations and the evolution of human mitochondrial DNA. Science (1991) 18.08
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Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. Am J Hum Genet (1995) 3.12
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Craniometric variation, genetic theory, and modern human origins. Am J Phys Anthropol (1994) 2.35
Studies of three Amerindian populations using nuclear DNA polymorphisms. Hum Biol (1991) 2.09
Genetic relationships of Europeans, Asians and Africans and the origin of modern Homo sapiens. Hum Hered (1989) 2.00
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Genetic structure of the Utah Mormons: comparison of results based on RFLPs, blood groups, migration matrices, isonymy, and pedigrees. Hum Biol (1994) 1.35
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Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
Signatures of population expansion in microsatellite repeat data. Genetics (1998) 5.76
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Mismatch distributions of mtDNA reveal recent human population expansions. Hum Biol (1994) 4.39
Out of Africa and back again: nested cladistic analysis of human Y chromosome variation. Mol Biol Evol (1998) 4.35
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nat Genet (1997) 3.91
Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Res (1997) 3.73
Genetic evidence on the origins of Indian caste populations. Genome Res (2001) 3.25
Lactase haplotype diversity in the Old World. Am J Hum Genet (2000) 3.19
The geographic distribution of human Y chromosome variation. Genetics (1997) 3.18
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Hierarchical patterns of global human Y-chromosome diversity. Mol Biol Evol (2001) 3.04
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mtDNA control-region sequence variation suggests multiple independent origins of an "Asian-specific" 9-bp deletion in sub-Saharan Africans. Am J Hum Genet (1996) 2.79
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Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1. Mol Biol Evol (2001) 2.64
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Hum Genet (1998) 2.44
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations. Am J Hum Genet (1998) 2.23
Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity. J Mol Biol (2001) 2.16
Using mitochondrial and nuclear DNA markers to reconstruct human evolution. Bioessays (1998) 2.09
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Mitochondrial mutation rate revisited: hot spots and polymorphism. Nat Genet (1998) 1.94
High polymorphism at the human melanocortin 1 receptor locus. Genetics (1999) 1.94
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Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. Am J Hum Genet (2000) 1.85
Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping. Am J Hum Genet (1993) 1.83
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Y chromosome probe p49a detects complex PvuII haplotypes and many new TaqI haplotypes in southern African populations. Am J Hum Genet (1992) 1.53
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mtDNA variation in caste populations of Andhra Pradesh, India. Hum Biol (1996) 1.50
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet (1996) 1.49
Population genomics: a bridge from evolutionary history to genetic medicine. Hum Mol Genet (2001) 1.49
The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12. Am J Hum Genet (1992) 1.45
Human population genetic structure and diversity inferred from polymorphic L1(LINE-1) and Alu insertions. Hum Hered (2006) 1.44
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome. Am J Hum Genet (1999) 1.41
Genetic similarities within and between human populations. Genetics (2007) 1.38
Mitochondrial mismatch analysis is insensitive to the mutational process. Mol Biol Evol (1996) 1.37
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The origins of the Lemba "Black Jews" of southern Africa: evidence from p12F2 and other Y-chromosome markers. Am J Hum Genet (1996) 1.36
Genetic structure of the Utah Mormons: comparison of results based on RFLPs, blood groups, migration matrices, isonymy, and pedigrees. Hum Biol (1994) 1.35
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene. Am J Hum Genet (1999) 1.35
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A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter. Am J Hum Genet (1997) 1.26
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A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9. Am J Hum Genet (1994) 1.24
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Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene. Am J Hum Genet (1997) 1.23
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Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families. Am J Med Genet (2000) 1.11
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