Published in Int J Legal Med on June 14, 2008
Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR Yfiler PCR amplification kit. Int J Legal Med (2009) 1.50
Mitochondrial DNA and Y chromosome variation provides evidence for a recent common ancestry between Native Americans and Indigenous Altaians. Am J Hum Genet (2012) 1.31
The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades. Mol Biol Evol (2014) 1.11
Kinship and Y-chromosome analysis of 7th century human remains: novel DNA extraction and typing procedure for ancient material. Croat Med J (2009) 0.90
Y chromosome interstitial deletion induced Y-STR allele dropout in AMELY-negative individuals. Int J Legal Med (2012) 0.86
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Copy number variation in the human Y chromosome in the UK population. Hum Genet (2015) 0.77
Genetic sub-structure in western Mediterranean populations revealed by 12 Y-chromosome STR loci. Int J Legal Med (2008) 0.75
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The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature (2003) 12.44
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A nomenclature system for the tree of human Y-chromosomal binary haplogroups. Genome Res (2002) 7.56
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Cross-cultural estimation of the human generation interval for use in genetics-based population divergence studies. Am J Phys Anthropol (2005) 4.48
Abundant gene conversion between arms of palindromes in human and ape Y chromosomes. Nature (2003) 4.31
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nat Genet (2001) 4.24
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nat Genet (2003) 3.97
The genetic legacy of the Mongols. Am J Hum Genet (2003) 3.84
High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nat Genet (2006) 3.46
Y-chromosomal DNA variation in Pakistan. Am J Hum Genet (2002) 3.35
Excavating Y-chromosome haplotype strata in Anatolia. Hum Genet (2003) 3.15
Y chromosome haplotype reference database (YHRD): update. Forensic Sci Int Genet (2007) 3.00
Male demography in East Asia: a north-south contrast in human population expansion times. Genetics (2006) 2.30
The dual origin of the Malagasy in Island Southeast Asia and East Africa: evidence from maternal and paternal lineages. Am J Hum Genet (2005) 2.27
The Y chromosome in forensic analysis and paternity testing. Int J Legal Med (1997) 2.27
DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis. Forensic Sci Int (2006) 2.22
A genetic landscape reshaped by recent events: Y-chromosomal insights into central Asia. Am J Hum Genet (2002) 2.21
A comprehensive survey of human Y-chromosomal microsatellites. Am J Hum Genet (2004) 1.97
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum Genet (1992) 1.94
Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas II. Nat Genet (1996) 1.92
Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure. Am J Hum Genet (2002) 1.81
Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism. J Med Genet (2000) 1.73
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males. Hum Mol Genet (1996) 1.68
A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N. Am J Hum Genet (2003) 1.62
A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics (2004) 1.56
Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19. Hum Genet (1996) 1.52
A novel multiplex for simultaneous amplification of 20 Y chromosome STR markers. Forensic Sci Int (2002) 1.50
Mutation rates at Y chromosome specific microsatellites. Hum Mutat (2005) 1.48
Recent spread of a Y-chromosomal lineage in northern China and Mongolia. Am J Hum Genet (2005) 1.46
Paternal and maternal lineages in the Balkans show a homogeneous landscape over linguistic barriers, except for the isolated Aromuns. Ann Hum Genet (2006) 1.44
Dynamics of a human interparalog gene conversion hotspot. Genome Res (2004) 1.40
High resolution Y chromosome typing: 19 STRs amplified in three multiplex reactions. Forensic Sci Int (2002) 1.40
Duplications of the AZFa region of the human Y chromosome are mediated by homologous recombination between HERVs and are compatible with male fertility. Hum Mol Genet (2003) 1.37
Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y. Hum Mol Genet (2006) 1.36
Paternity testing using Y-STR haplotypes: assigning a probability for paternity in cases of mutations. Int J Legal Med (2001) 1.33
Suppression of intrachromosomal gene conversion in mammalian cells by small degrees of sequence divergence. Genetics (1999) 1.24
26-Locus Y-STR typing in a Bhutanese population sample. Forensic Sci Int (2005) 1.13
Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis. Hum Mutat (2008) 1.10
Chromosomal duplications along the Y-chromosome and their potential impact on Y-STR interpretation. J Forensic Sci (2005) 1.06
Diversity of 26-locus Y-STR haplotypes in a Nepalese population sample: isolation and drift in the Himalayas. Forensic Sci Int (2006) 1.05
New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines. Hum Mutat (1994) 0.95
Y-chromosomal STR haplotypes in Kalmyk population samples. Forensic Sci Int (2007) 0.88
Rapid and sensitive typing of forensic stains by PCR amplification of polymorphic simple repeat sequences in case work. Forensic Sci Int (1992) 0.87
Constitutional duplication of a region of chromosome Yp encoding AMELY, PRKY, and TBL1Y: implications for sex chromosome analysis and bone marrow engraftment analysis. J Mol Diagn (2007) 0.86
Duplication of DYS19 flanking regions in other parts of the Y chromosome. Int J Legal Med (2004) 0.80
Phylogenetic evidence for multiple independent duplication events at the DYS19 locus. Forensic Sci Int Genet (2007) 0.79
Testing deficiency paternity cases with a Y-linked tetranucleotide repeat polymorphism. EXS (1993) 0.78
Global variation in copy number in the human genome. Nature (2006) 57.50
Origins and functional impact of copy number variation in the human genome. Nature (2009) 23.63
Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science (2007) 23.38
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27
A systematic survey of loss-of-function variants in human protein-coding genes. Science (2012) 12.25
Genetic history of an archaic hominin group from Denisova Cave in Siberia. Nature (2010) 8.99
Copy number variation: new insights in genome diversity. Genome Res (2006) 8.66
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. Nat Genet (2009) 8.30
The human Y chromosome: an evolutionary marker comes of age. Nat Rev Genet (2003) 6.73
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat Genet (2009) 6.31
Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree. Curr Biol (2009) 5.70
Global diversity in the human salivary microbiome. Genome Res (2009) 5.16
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome. Lancet (2012) 5.16
An Aboriginal Australian genome reveals separate human dispersals into Asia. Science (2011) 4.84
IFITM3 restricts the morbidity and mortality associated with influenza. Nature (2012) 4.66
The role of selection in the evolution of human mitochondrial genomes. Genetics (2005) 4.56
The functional spectrum of low-frequency coding variation. Genome Biol (2011) 4.42
A predominantly neolithic origin for European paternal lineages. PLoS Biol (2010) 4.39
Insights into hominid evolution from the gorilla genome sequence. Nature (2012) 4.12
The genetic legacy of the Mongols. Am J Hum Genet (2003) 3.84
A new approach for using genome scans to detect recent positive selection in the human genome. PLoS Biol (2007) 3.71
Hotspots for copy number variation in chimpanzees and humans. Proc Natl Acad Sci U S A (2006) 3.68
The dawn of human matrilineal diversity. Am J Hum Genet (2008) 3.60
Denisova admixture and the first modern human dispersals into Southeast Asia and Oceania. Am J Hum Genet (2011) 3.53
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing. Nat Genet (2010) 3.49
Y-chromosomal DNA variation in Pakistan. Am J Hum Genet (2002) 3.35
Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing. Am J Hum Genet (2012) 3.30
Where west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor. Am J Hum Genet (2004) 3.05
Y chromosome haplotype reference database (YHRD): update. Forensic Sci Int Genet (2007) 3.00
Spread of an inactive form of caspase-12 in humans is due to recent positive selection. Am J Hum Genet (2006) 3.00
Melanesian and Asian origins of Polynesians: mtDNA and Y chromosome gradients across the Pacific. Mol Biol Evol (2006) 2.98
Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes. Am J Hum Genet (2010) 2.98
Publication of population data of linearly inherited DNA markers in the International Journal of Legal Medicine. Int J Legal Med (2010) 2.97
Copy number variation and evolution in humans and chimpanzees. Genome Res (2008) 2.69
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia. Nat Genet (2009) 2.67
A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs. Am J Hum Genet (2009) 2.62
Adaptive evolution of UGT2B17 copy-number variation. Am J Hum Genet (2008) 2.58
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy. Am J Hum Genet (2007) 2.54
Loss-of-function variants in the genomes of healthy humans. Hum Mol Genet (2010) 2.45
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease. Hum Genet (2013) 2.44
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Lancet Oncol (2010) 2.42
Mitochondrial DNA and human evolution. Annu Rev Genomics Hum Genet (2005) 2.36
Worldwide population differentiation at disease-associated SNPs. BMC Med Genomics (2008) 2.32
Mannose binding lectin gene polymorphisms confer a major risk for severe infections after liver transplantation. Gastroenterology (2005) 2.30
A genome scan to detect candidate regions influenced by local natural selection in human populations. Mol Biol Evol (2003) 2.30
Male demography in East Asia: a north-south contrast in human population expansion times. Genetics (2006) 2.30
The dual origin of the Malagasy in Island Southeast Asia and East Africa: evidence from maternal and paternal lineages. Am J Hum Genet (2005) 2.27
A genetic landscape reshaped by recent events: Y-chromosomal insights into central Asia. Am J Hum Genet (2002) 2.21
Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes. J Hum Genet (2005) 2.19
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study. J Am Coll Cardiol (2013) 2.18
A melanocortin 1 receptor allele suggests varying pigmentation among Neanderthals. Science (2007) 2.15
Comprehensive comparison of three commercial human whole-exome capture platforms. Genome Biol (2011) 2.15
Molecular evolution of Pediculus humanus and the origin of clothing. Curr Biol (2003) 2.09
The functional impact of structural variation in humans. Trends Genet (2008) 2.03
A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa. Am J Hum Genet (2004) 2.02
Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians. Am J Hum Genet (2008) 2.02
Inferring human population sizes, divergence times and rates of gene flow from mitochondrial, X and Y chromosome resequencing data. Genetics (2007) 2.00
A comprehensive survey of human Y-chromosomal microsatellites. Am J Hum Genet (2004) 1.97
Demographic history of Oceania inferred from genome-wide data. Curr Biol (2010) 1.93
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications. Am J Hum Genet (2010) 1.88
The Genographic Project public participation mitochondrial DNA database. PLoS Genet (2007) 1.86
Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea. Am J Hum Genet (2002) 1.86
Molecular analysis reveals tighter social regulation of immigration in patrilocal populations than in matrilocal populations. Proc Natl Acad Sci U S A (2005) 1.83
A calibrated human Y-chromosomal phylogeny based on resequencing. Genome Res (2012) 1.83
Y chromosomal evidence for the origins of oceanic-speaking peoples. Genetics (2002) 1.81
Evaluation of saliva as a source of human DNA for population and association studies. Anal Biochem (2006) 1.81
High-throughput sequencing of complete human mtDNA genomes from the Caucasus and West Asia: high diversity and demographic inferences. Eur J Hum Genet (2011) 1.80
Ancient west Eurasian ancestry in southern and eastern Africa. Proc Natl Acad Sci U S A (2014) 1.79
Genome-wide data substantiate Holocene gene flow from India to Australia. Proc Natl Acad Sci U S A (2013) 1.78
Improving human forensics through advances in genetics, genomics and molecular biology. Nat Rev Genet (2011) 1.78
The genetic prehistory of southern Africa. Nat Commun (2012) 1.78
Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy. Eur J Hum Genet (2007) 1.78
Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms. Genome Res (2002) 1.78
Proportioning whole-genome single-nucleotide-polymorphism diversity for the identification of geographic population structure and genetic ancestry. Am J Hum Genet (2006) 1.76
Recent origin and cultural reversion of a hunter-gatherer group. PLoS Biol (2005) 1.75
Y-chromosomal diversity in Lebanon is structured by recent historical events. Am J Hum Genet (2008) 1.75
Founders, drift, and infidelity: the relationship between Y chromosome diversity and patrilineal surnames. Mol Biol Evol (2009) 1.68
Dating the age of admixture via wavelet transform analysis of genome-wide data. Genome Biol (2011) 1.65
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
Forensic value of 14 novel STRs on the human Y chromosome. Forensic Sci Int (2002) 1.64
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Am J Hum Genet (2012) 1.60
Insight into the early spread of chloroquine-resistant Plasmodium falciparum infections in Papua New Guinea. J Infect Dis (2005) 1.60
Independent origins of Indian caste and tribal paternal lineages. Curr Biol (2004) 1.58
Mitochondrial DNA analysis reveals diverse histories of tribal populations from India. Eur J Hum Genet (2003) 1.58
Clonal genetic variation in a Wolbachia-infected asexual wasp: horizontal transmission or historical sex? Mol Ecol (2011) 1.58
High-throughput sequencing of complete human mtDNA genomes from the Philippines. Genome Res (2010) 1.56
A worldwide survey of human male demographic history based on Y-SNP and Y-STR data from the HGDP-CEPH populations. Mol Biol Evol (2009) 1.56
Recent radiation within Y-chromosomal haplogroup R-M269 resulted in high Y-STR haplotype resemblance. Ann Hum Genet (2014) 1.55