Published in Am J Hum Genet on June 16, 2004
A predominantly neolithic origin for European paternal lineages. PLoS Biol (2010) 4.39
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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
Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean. Am J Hum Genet (2008) 1.50
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The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20
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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
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The dawn of human matrilineal diversity. Am J Hum Genet (2008) 3.60
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
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Where west meets east: the complex mtDNA landscape of the southwest and Central Asian corridor. Am J Hum Genet (2004) 3.05
Spread of an inactive form of caspase-12 in humans is due to recent positive selection. Am J Hum Genet (2006) 3.00
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
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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
Male demography in East Asia: a north-south contrast in human population expansion times. Genetics (2006) 2.30
A genetic landscape reshaped by recent events: Y-chromosomal insights into central Asia. Am J Hum Genet (2002) 2.21
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A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. Am J Hum Genet (2003) 1.85
A calibrated human Y-chromosomal phylogeny based on resequencing. Genome Res (2012) 1.83
Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy. Eur J Hum Genet (2007) 1.78
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet (2004) 1.76
Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of Africa. Am J Hum Genet (2004) 1.76
Y-chromosomal diversity in Lebanon is structured by recent historical events. Am J Hum Genet (2008) 1.75
Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12. Mol Biol Evol (2007) 1.69
State of the art in forensic investigation of sudden cardiac death. Am J Forensic Med Pathol (2011) 1.61
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Am J Hum Genet (2012) 1.60
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
Signature of recent historical events in the European Y-chromosomal STR haplotype distribution. Hum Genet (2005) 1.54
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Toward male individualization with rapidly mutating y-chromosomal short tandem repeats. Hum Mutat (2014) 1.53
Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean. Am J Hum Genet (2008) 1.50
Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans. Nat Commun (2013) 1.50
Parallel evolution of genes and languages in the Caucasus region. Mol Biol Evol (2011) 1.48
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Recent spread of a Y-chromosomal lineage in northern China and Mongolia. Am J Hum Genet (2005) 1.46
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Dev Med Child Neurol (2013) 1.44
Genetic basis of Y-linked hearing impairment. Am J Hum Genet (2013) 1.42
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Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency. Hum Mutat (2003) 1.42
Focussing on hard science in forensic medicine: genetics of sudden cardiac death (SCD). Forensic Sci Int (2007) 1.39
Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan. Eur J Hum Genet (2006) 1.37
Distinct variants at LIN28B influence growth in height from birth to adulthood. Am J Hum Genet (2010) 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
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Am J Hum Genet (2009) 1.34
Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry. Nucleic Acids Res (2002) 1.34
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DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry (2011) 1.29
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy. Am J Hum Genet (2002) 1.28
Variation of 52 new Y-STR loci in the Y Chromosome Consortium worldwide panel of 76 diverse individuals. Int J Legal Med (2006) 1.26
Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans. Hum Genet (2003) 1.24
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A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. Hum Mutat (2011) 1.21
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A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS Genet (2009) 1.20
HI: haplotype improver using paired-end short reads. Bioinformatics (2009) 1.20
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Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics (2004) 1.19
Y-chromosomal insights into the genetic impact of the caste system in India. Hum Genet (2006) 1.19
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