Published in Am J Hum Genet on April 01, 1997
Use of unlinked genetic markers to detect population stratification in association studies. Am J Hum Genet (1999) 23.67
Estimating African American admixture proportions by use of population-specific alleles. Am J Hum Genet (1998) 22.90
Multilocus genotypes, a tree of individuals, and human evolutionary history. Am J Hum Genet (1997) 14.46
Informativeness of genetic markers for inference of ancestry. Am J Hum Genet (2003) 6.90
Estimating local ancestry in admixed populations. Am J Hum Genet (2008) 5.90
Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model. Am J Hum Genet (2001) 5.66
Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am J Hum Genet (1998) 5.26
Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. Am J Hum Genet (2000) 4.74
Human population genetic structure and inference of group membership. Am J Hum Genet (2003) 4.73
Statistical tests for admixture mapping with case-control and cases-only data. Am J Hum Genet (2004) 4.52
Color and genomic ancestry in Brazilians. Proc Natl Acad Sci U S A (2002) 3.29
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes. Proc Natl Acad Sci U S A (2000) 3.10
Markers for mapping by admixture linkage disequilibrium in African American and Hispanic populations. Am J Hum Genet (2001) 3.04
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature (2004) 2.90
Genome screens using linkage disequilibrium tests: optimal marker characteristics and feasibility. Am J Hum Genet (1998) 2.86
The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations. Am J Hum Genet (2003) 2.82
Empirical evaluation of genetic clustering methods using multilocus genotypes from 20 chicken breeds. Genetics (2001) 2.52
Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans. Am J Hum Genet (2000) 2.32
Measuring and using admixture to study the genetics of complex diseases. Hum Genomics (2003) 2.31
Genetic ancestry is associated with subclinical cardiovascular disease in African-Americans and Hispanics from the multi-ethnic study of atherosclerosis. Circ Cardiovasc Genet (2009) 2.31
Analysis of genomic admixture in Uyghur and its implication in mapping strategy. Am J Hum Genet (2008) 2.30
Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. Am J Hum Genet (2002) 2.29
Genetic bio-ancestry and social construction of racial classification in social surveys in the contemporary United States. Demography (2014) 2.00
A genome-wide analysis of admixture in Uyghurs and a high-density admixture map for disease-gene discovery. Am J Hum Genet (2008) 1.92
Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population. Hum Genet (2003) 1.80
Consistent long-range linkage disequilibrium generated by admixture in a Bantu-Semitic hybrid population. Am J Hum Genet (2000) 1.65
Admixture mapping of male nuptial colour and body shape in a recently formed hybrid population of threespine stickleback. Mol Ecol (2012) 1.56
Systemic lupus erythematosus in a multiethnic cohort: LUMINA XXXV. Predictive factors of high disease activity over time. Ann Rheum Dis (2006) 1.47
Genetics. Toward a new vocabulary of human genetic variation. Science (2002) 1.44
Measurement of admixture proportions and description of admixture structure in different U.S. populations. Hum Mutat (2009) 1.33
Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study. Hum Genet (2007) 1.25
Putative ancestral origins of chromosomal segments in individual african americans: implications for admixture mapping. Genome Res (2004) 1.18
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program. Genome Res (2003) 1.13
Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals. PLoS One (2013) 1.11
Risk for rheumatic disease in relation to ethnicity and admixture. Arthritis Res (2000) 1.08
Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing. PLoS One (2012) 1.08
Comparison of measures of marker informativeness for ancestry and admixture mapping. BMC Genomics (2011) 1.07
Comparing genetic ancestry and self-reported race/ethnicity in a multiethnic population in New York City. J Genet (2010) 1.06
Mapping genes that predict treatment outcome in admixed populations. Pharmacogenomics J (2010) 1.05
Characterization of X-linked SNP genotypic variation in globally distributed human populations. Genome Biol (2010) 1.02
Demographic changes and marker properties affect detection of human population differentiation. BMC Genet (2007) 1.00
Reconciling apparent conflicts between mitochondrial and nuclear phylogenies in African elephants. PLoS One (2011) 1.00
Interethnic admixture and the evolution of Latin American populations. Genet Mol Biol (2014) 0.99
Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities. Hum Genomics (2015) 0.98
Genetic variants of TSLP and asthma in an admixed urban population. PLoS One (2011) 0.98
Evaluation of approaches for identifying population informative markers from high density SNP chips. BMC Genet (2011) 0.96
Difficulties in the estimation of ethnic affiliation. Am J Hum Genet (1998) 0.92
Developing a set of ancestry-sensitive DNA markers reflecting continental origins of humans. BMC Genet (2009) 0.92
Database mining for selection of SNP markers useful in admixture mapping. BioData Min (2009) 0.91
Shape based assignment tests suggest transgressive phenotypes in natural sculpin hybrids (Teleostei, Scorpaeniformes, Cottidae). Front Zool (2005) 0.89
Multilocus detection of wolf x dog hybridization in italy, and guidelines for marker selection. PLoS One (2014) 0.89
Body fat and racial genetic admixture are associated with aerobic fitness levels in a multiethnic pediatric population. Obesity (Silver Spring) (2011) 0.86
Design and analysis issues in gene and environment studies. Environ Health (2012) 0.86
Genetics and genomics in Brazil: a promising future. Mol Genet Genomic Med (2014) 0.85
Application of next-generation sequencing technology in forensic science. Genomics Proteomics Bioinformatics (2014) 0.81
A small number of candidate gene SNPs reveal continental ancestry in African Americans. Ann Hum Genet (2013) 0.81
Finding markers that make a difference: DNA pooling and SNP-arrays identify population informative markers for genetic stock identification. PLoS One (2013) 0.81
Inferring ethnicity from mitochondrial DNA sequence. BMC Proc (2011) 0.80
Development of a genetic tool for product regulation in the diverse British pig breed market. BMC Genomics (2012) 0.80
Hybridization hotspots at bat swarming sites. PLoS One (2012) 0.79
AncestrySNPminer: a bioinformatics tool to retrieve and develop ancestry informative SNP panels. Genomics (2012) 0.79
What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research. AJOB Prim Res (2012) 0.79
A single-tube 27-plex SNP assay for estimating individual ancestry and admixture from three continents. Int J Legal Med (2015) 0.79
Uncoupling protein 2 Ala55Val polymorphism is associated with a higher acute insulin response to glucose. Metabolism (2009) 0.78
Estimates of continental ancestry vary widely among individuals with the same mtDNA haplogroup. Am J Hum Genet (2015) 0.77
Polymorphisms in the maternal sex steroid pathway are associated with behavior problems in male offspring. Psychiatr Genet (2012) 0.77
Selecting SNPs to identify ancestry. Ann Hum Genet (2011) 0.76
Iranian human genome project: Overview of a research process among Iranian ethnicities. Indian J Hum Genet (2009) 0.76
African ancestry is associated with facial melasma in women: a cross-sectional study. BMC Med Genet (2017) 0.75
Genetic ancestry analysis in non-alcoholic fatty liver disease patients from Brazil and Portugal. World J Hepatol (2015) 0.75
Ancient and current gene flow between two distantly related Mediterranean oak species, Quercus suber and Q. ilex. Ann Bot (2009) 0.75
Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran. Iran J Public Health (2013) 0.75
Genetic structure and differentiation analysis of a Eurasian Uyghur population by use of 27 continental ancestry-informative SNPs. Int J Legal Med (2016) 0.75
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science (1988) 220.77
High resolution of human evolutionary trees with polymorphic microsatellites. Nature (1994) 28.48
Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic data. Am J Hum Genet (1995) 17.65
Slipped-strand mispairing: a major mechanism for DNA sequence evolution. Mol Biol Evol (1987) 15.79
Mutation of human short tandem repeats. Hum Mol Genet (1993) 14.03
Mutational processes of simple-sequence repeat loci in human populations. Proc Natl Acad Sci U S A (1994) 11.84
Allele frequencies at microsatellite loci: the stepwise mutation model revisited. Genetics (1993) 8.60
Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci. Proc Natl Acad Sci U S A (1988) 8.22
VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. Genetics (1993) 8.22
Mapping by admixture linkage disequilibrium in human populations: limits and guidelines. Am J Hum Genet (1994) 7.16
Study of 47 DNA markers in five populations from four continents. Gene Geogr (1987) 4.04
Caucasian genes in American blacks: new data. Am J Hum Genet (1992) 3.78
Linkage disequilibrium in admixed populations: applications in gene mapping. J Hered (1994) 3.46
Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. Am J Hum Genet (1995) 3.12
African origin of human-specific polymorphic Alu insertions. Proc Natl Acad Sci U S A (1994) 3.09
"Private" genetic variants and the frequency of mutation among South American Indians. Proc Natl Acad Sci U S A (1973) 2.64
Origins of U.S. Hispanics. Implications for diabetes. Diabetes Care (1991) 2.47
Polymorphic admixture typing in human ethnic populations. Am J Hum Genet (1994) 2.37
Studies of three Amerindian populations using nuclear DNA polymorphisms. Hum Biol (1991) 2.09
Study of an additional 58 DNA markers in five human populations from four continents. Gene Geogr (1991) 1.98
Assessment of race from the pelvis. Am J Phys Anthropol (1983) 1.13
Assessing ethnicity from human mitochondrial DNA types determined by hybridization with sequence-specific oligonucleotides. J Forensic Sci (1994) 1.08
Multiple discriminant function analysis of sex and race in the postcranial skeleton. Am J Phys Anthropol (1983) 1.03
Estimating African American admixture proportions by use of population-specific alleles. Am J Hum Genet (1998) 22.90
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science (2000) 8.64
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. Genetics (1993) 8.22
Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron (1996) 7.20
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics (1992) 6.40
A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. Genome Res (2001) 6.06
Haplotypes vs single marker linkage disequilibrium tests: what do we gain? Eur J Hum Genet (2001) 5.41
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. Am J Hum Genet (1998) 5.24
Localization of neuronal and glial glutamate transporters. Neuron (1994) 5.14
Kin selection, social structure, gene flow, and the evolution of chimpanzees. Science (1994) 5.08
Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays. Nat Genet (1999) 4.79
Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. Am J Hum Genet (2000) 4.74
A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history. Proc Natl Acad Sci U S A (1996) 4.52
Proteins induced by anaerobiosis in Escherichia coli. J Bacteriol (1983) 3.95
A unified approach to study hypervariable polymorphisms: statistical considerations of determining relatedness and population distances. EXS (1993) 3.86
Caucasian genes in American blacks: new data. Am J Hum Genet (1992) 3.78
Phytochrome regulation and differential expression of gibberellin 3beta-hydroxylase genes in germinating Arabidopsis seeds. Plant Cell (1998) 3.76
Ancestral proportions and admixture dynamics in geographically defined African Americans living in South Carolina. Am J Phys Anthropol (2001) 3.76
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema. Nat Genet (2000) 3.66
Genetic acceleration of AIDS progression by a promoter variant of CCR5. Science (1998) 3.60
Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. Am J Hum Genet (1999) 3.60
Individual admixture estimates: disease associations and individual risk of diabetes and gallbladder disease among Mexican-Americans in Starr County, Texas. Am J Phys Anthropol (1986) 3.52
The Eurasian heartland: a continental perspective on Y-chromosome diversity. Proc Natl Acad Sci U S A (2001) 3.38
Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. Proc Natl Acad Sci U S A (1997) 3.32
Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. Am J Hum Genet (1995) 3.12
Variances of the average numbers of nucleotide substitutions within and between populations. Mol Biol Evol (1989) 3.11
A population genetic study of six VNTR loci in three ethnically defined populations. Genomics (1991) 3.03
A model for gene therapy of human hereditary lymphedema. Proc Natl Acad Sci U S A (2001) 2.88
Identity of the B56.5 protein, the A-protein, and the groE gene product of Escherichia coli. J Bacteriol (1981) 2.82
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat Genet (1998) 2.82
A scan for linkage disequilibrium across the human genome. Genetics (1999) 2.79
Proteins induced by aerobiosis in Escherichia coli. J Bacteriol (1983) 2.77
Quality of diabetes care in community health centers. Am J Public Health (2000) 2.76
Measles vaccination and antibody response in autism spectrum disorders. Arch Dis Child (2008) 2.71
Relationship of prevalence of non-insulin-dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas. Genet Epidemiol (1986) 2.71
Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22. Proc Natl Acad Sci U S A (2000) 2.67
A novel measure of genetic distance for highly polymorphic tandem repeat loci. Mol Biol Evol (1995) 2.65
Genetic relationship of populations in China. Proc Natl Acad Sci U S A (1998) 2.65
p27kip1: a multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers. Am J Pathol (1999) 2.47
Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis. Neuron (1998) 2.45
The heritability of otitis media: a twin and triplet study. JAMA (1999) 2.34
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J Med Genet (2002) 2.33
Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans. Am J Hum Genet (2000) 2.32
Limited humoral immunity in hepatitis C virus infection. Gastroenterology (1999) 2.31
Distribution of the four founding lineage haplotypes in Native Americans suggests a single wave of migration for the New World. Am J Phys Anthropol (1995) 2.30
The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures. Am J Hum Genet (2001) 2.29
Genetic variation in components of dopamine neurotransmission impacts ventral striatal reactivity associated with impulsivity. Mol Psychiatry (2007) 2.29
Genetic restriction of HIV-1 pathogenesis to AIDS by promoter alleles of IL10. Proc Natl Acad Sci U S A (2000) 2.24
Determination of relatedness between individuals using DNA fingerprinting. Hum Biol (1993) 2.23
The dopamine D3-receptor: a postsynaptic receptor inhibitory on rat locomotor activity. J Neural Transm Gen Sect (1993) 2.20
Admixture in the Hispanics of the San Luis Valley, Colorado, and its implications for complex trait gene mapping. Ann Hum Genet (2004) 2.20
Evaluation of 13 short tandem repeat loci for use in personal identification applications. Am J Hum Genet (1994) 2.15
'Unique' alleles in admixed populations: a strategy for determining 'hereditary' population differences of disease frequencies. Ethn Dis (1991) 2.11
Feature (gene) selection in gene expression-based tumor classification. Mol Genet Metab (2001) 2.08
Heterozygote deficiency, population substructure and their implications in DNA fingerprinting. Hum Genet (1992) 2.06
Normal high density lipoprotein inhibits three steps in the formation of mildly oxidized low density lipoprotein: step 1. J Lipid Res (2000) 2.05
Medical and psychosocial services in drug abuse treatment: do stronger linkages promote client utilization? Health Serv Res (2000) 1.99
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics (1999) 1.97
A full genome scan for age-related maculopathy. Hum Mol Genet (2000) 1.96
Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Hum Genet (2000) 1.95
Bridging the NFAT and NF-kappaB families: NFAT5 dimerization regulates cytokine gene transcription in response to osmotic stress. Immunity (2001) 1.94
High polymorphism at the human melanocortin 1 receptor locus. Genetics (1999) 1.94
Model for lentivirus capsid core assembly based on crystal dimers of EIAV p26. J Mol Biol (1999) 1.93
Clinical characteristics and MR imaging features of nonalcoholic Wernicke encephalopathy. AJNR Am J Neuroradiol (2008) 1.92
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Diabetes among Mexican Americans in Starr County, Texas. Am J Epidemiol (1983) 1.91
Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions. Am J Ophthalmol (2001) 1.88
Measurement of the rate of nu(e) + d --> p + p + e(-) interactions produced by (8)B solar neutrinos at the Sudbury Neutrino Observatory. Phys Rev Lett (2001) 1.88
Molecular anatomy of an intracranial aneurysm: coordinated expression of genes involved in wound healing and tissue remodeling. Stroke (2001) 1.87
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. Am J Hum Genet (2000) 1.86
Biology, cytogenetics, and sensitivity to immunological effector cells of new head and neck squamous cell carcinoma lines. Cancer Res (1989) 1.84
Chronic inhibition of glutamate uptake produces a model of slow neurotoxicity. Proc Natl Acad Sci U S A (1993) 1.84
Paternity evaluation in cases lacking a mother and nondetectable alleles. Int J Legal Med (1994) 1.83
Body mass index as a predictor of outcome in total knee replacement. Int Orthop (2001) 1.81
Structure of the collagen-binding domain from a Staphylococcus aureus adhesin. Nat Struct Biol (1997) 1.80
Albumin Yanomama-2, a 'private' polymorphism of serum albumin. Ann Hum Genet (1974) 1.80
Polynesian origins: insights from the Y chromosome. Proc Natl Acad Sci U S A (2000) 1.79
Crystal structure of calcium bound domain VI of calpain at 1.9 A resolution and its role in enzyme assembly, regulation, and inhibitor binding. Nat Struct Biol (1997) 1.78
Signatures of differentially regulated interferon gene expression and vasculotrophism in the peripheral blood cells of systemic sclerosis patients. Rheumatology (Oxford) (2006) 1.77
UK measles outbreak in non-immune anthroposophic communities: the implications for the elimination of measles from Europe. Epidemiol Infect (2000) 1.77
Dynamics of repeat polymorphisms under a forward-backward mutation model: within- and between-population variability at microsatellite loci. Genetics (1996) 1.77
Comprehensive transcript analysis in small quantities of mRNA by SAGE-lite. Nucleic Acids Res (1999) 1.72
A disease-associated cellular immune response in type 1 diabetics to an immunodominant epitope of insulin. J Clin Invest (2001) 1.70
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. Science (1981) 1.70
Molecular epidemiology of vitamin D receptor gene variants. Epidemiol Rev (2000) 1.68
A mitochondrial-like chaperonin 60 gene in Giardia lamblia: evidence that diplomonads once harbored an endosymbiont related to the progenitor of mitochondria. Proc Natl Acad Sci U S A (1998) 1.68