Published in Genome Res on October 01, 1997
A nomenclature system for the tree of human Y-chromosomal binary haplogroups. Genome Res (2002) 7.56
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet (2001) 5.61
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Ancestral Asian source(s) of new world Y-chromosome founder haplotypes. Am J Hum Genet (1999) 2.89
The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations. Am J Hum Genet (2003) 2.82
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Population genetic implications from sequence variation in four Y chromosome genes. Proc Natl Acad Sci U S A (2000) 2.62
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High-resolution analysis of human Y-chromosome variation shows a sharp discontinuity and limited gene flow between northwestern Africa and the Iberian Peninsula. Am J Hum Genet (2001) 2.32
Genetic restriction of HIV-1 pathogenesis to AIDS by promoter alleles of IL10. Proc Natl Acad Sci U S A (2000) 2.24
Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland. Am J Hum Genet (2000) 2.22
The central Siberian origin for native American Y chromosomes. Am J Hum Genet (1999) 2.03
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Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Hum Genet (2000) 1.95
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Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci U S A (2002) 1.92
European Y-chromosomal lineages in Polynesians: a contrast to the population structure revealed by mtDNA. Am J Hum Genet (1998) 1.87
Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea. Am J Hum Genet (2002) 1.86
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Y chromosomal evidence for the origins of oceanic-speaking peoples. Genetics (2002) 1.81
Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations. Am J Hum Genet (1999) 1.81
Global analysis of ATM polymorphism reveals significant functional constraint. Am J Hum Genet (2001) 1.80
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Polynesian origins: insights from the Y chromosome. Proc Natl Acad Sci U S A (2000) 1.79
A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania. Am J Hum Genet (2001) 1.76
Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C. Am J Hum Genet (2000) 1.76
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations. Am J Hum Genet (2001) 1.70
Effective population size and population subdivision in demographically structured populations. Genetics (2002) 1.70
High levels of Y-chromosome nucleotide diversity in the genus Pan. Proc Natl Acad Sci U S A (2001) 1.70
Distribution of haplotypes from a chromosome 21 region distinguishes multiple prehistoric human migrations. Proc Natl Acad Sci U S A (1999) 1.68
Messages through bottlenecks: on the combined use of slow and fast evolving polymorphic markers on the human Y chromosome. Am J Hum Genet (2000) 1.65
The dual origin and Siberian affinities of Native American Y chromosomes. Am J Hum Genet (2001) 1.65
DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates. Am J Hum Genet (1999) 1.64
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula. Am J Hum Genet (2008) 1.64
Quantitative trait symmetry independent of Hsp90 buffering: distinct modes of genetic canalization and developmental stability. Proc Natl Acad Sci U S A (2003) 1.64
Single nucleotide polymorphism markers for genetic mapping in Drosophila melanogaster. Genome Res (2001) 1.63
Sex-specific migration patterns in Central Asian populations, revealed by analysis of Y-chromosome short tandem repeats and mtDNA. Am J Hum Genet (1999) 1.61
High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews. Hum Genet (2000) 1.61
Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet (2000) 1.58
A short tandem repeat-based phylogeny for the human Y chromosome. Am J Hum Genet (2000) 1.58
Origins and divergence of the Roma (gypsies). Am J Hum Genet (2001) 1.53
Human Y chromosome haplogroup R-V88: a paternal genetic record of early mid Holocene trans-Saharan connections and the spread of Chadic languages. Eur J Hum Genet (2010) 1.47
A view of modern human origins from Y chromosome microsatellite variation. Genome Res (1999) 1.45
Variation in short tandem repeats is deeply structured by genetic background on the human Y chromosome. Am J Hum Genet (1999) 1.42
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility. J Med Genet (2004) 1.40
Human population structure and its effects on sampling Y chromosome sequence variation. Genetics (2003) 1.38
Y-chromosome based evidence for pre-neolithic origin of the genetically homogeneous but diverse Sardinian population: inference for association scans. PLoS One (2008) 1.35
Toward integration of comparative genetic, physical, diversity, and cytomolecular maps for grasses and grains, using the sorghum genome as a foundation. Plant Physiol (2001) 1.34
Single nucleotide polymorphism seeking long term association with complex disease. Nucleic Acids Res (2002) 1.33
Microsatellites provide evidence for Y chromosome diversity among the founders of the New World. Proc Natl Acad Sci U S A (1999) 1.33
Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans. Hum Genet (2003) 1.24
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 rapid method to map mutations in Drosophila. Genome Biol (2001) 1.20
Genetic studies of human diversity in East Asia. Philos Trans R Soc Lond B Biol Sci (2007) 1.19
Sequence variability of a human pseudogene. Genome Res (2001) 1.18
Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays. Genome Res (2001) 1.18
A recent shift from polygyny to monogamy in humans is suggested by the analysis of worldwide Y-chromosome diversity. J Mol Evol (2003) 1.16
A cSNP map and database for human chromosome 21. Genome Res (2001) 1.15
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography. Nucleic Acids Res (2000) 1.12
A highly variable segment of human subterminal 16p reveals a history of population growth for modern humans outstide Africa. Proc Natl Acad Sci U S A (2001) 1.05
Molecular genetic evidence for the human settlement of the Pacific: analysis of mitochondrial DNA, Y chromosome and HLA markers. Philos Trans R Soc Lond B Biol Sci (1999) 1.04
Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians. PLoS One (2012) 1.03
Y-chromosome short tandem repeat DYS458.2 non-consensus alleles occur independently in both binary haplogroups J1-M267 and R1b3-M405. Croat Med J (2007) 1.01
Rapid and simple detection of hot spot point mutations of epidermal growth factor receptor, BRAF, and NRAS in cancers using the loop-hybrid mobility shift assay. J Mol Diagn (2006) 0.99
Pasture names with Romance and Slavic roots facilitate dissection of Y chromosome variation in an exclusively German-speaking alpine region. PLoS One (2012) 0.98
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi Levites. Nat Commun (2013) 0.96
Molecular epidemiological analysis of the changing nature of a meningococcal outbreak following a vaccination campaign. J Clin Microbiol (2002) 0.96
Y-chromosome short tandem repeat intermediate variant alleles DYS392.2, DYS449.2, and DYS385.2 delineate new phylogenetic substructure in human Y-chromosome haplogroup tree. Croat Med J (2009) 0.96
Evidence from Y-chromosome analysis for a late exclusively eastern expansion of the Bantu-speaking people. Eur J Hum Genet (2012) 0.95
Three single-nucleotide polymorphisms in LPA account for most of the increase in lipoprotein(a) level elevation in African Americans compared with European Americans. J Med Genet (2006) 0.93
Uniparental genetic markers in South Amerindians. Genet Mol Biol (2012) 0.92
The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers. Hum Genet (2004) 0.90
Order emerging from chaos in human evolutionary genetics. Proc Natl Acad Sci U S A (2001) 0.88
Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: introduction. Can J Cardiol (2010) 0.88
Analysis of single nucleotide polymorphisms in the promoter region of interleukin-10 by denaturing high-performance liquid chromatography. J Biomol Tech (2005) 0.86
Lack of association between Y-chromosomal haplogroups and prostate cancer in the Korean population. PLoS One (2007) 0.85
Molecular diagnostics in preimplantation genetic diagnosis. J Mol Diagn (2002) 0.85
DNA diagnostics by surface-bound melt-curve reactions. J Mol Diagn (2007) 0.84
Choosing and using introns in molecular phylogenetics. Evol Bioinform Online (2007) 0.84
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information. Eur J Hum Genet (2009) 0.83
Candidate-gene testing for orphan limb-girdle muscular dystrophies. Acta Myol (2008) 0.83
Micro-processing events in mRNAs identified by DHPLC analysis. Nucleic Acids Res (2002) 0.83
Assay validation for identification of hereditary nonpolyposis colon cancer-causing mutations in mismatch repair genes MLH1, MSH2, and MSH6. J Mol Diagn (2005) 0.82
Development of a denaturing high-performance liquid chromatography method for detection of protist parasites of metazoans. Appl Environ Microbiol (2008) 0.81
Automated mutation analysis. J Inherit Metab Dis (1999) 0.81
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Archaic African and Asian lineages in the genetic ancestry of modern humans. Am J Hum Genet (1997) 8.63
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