Published in Hum Genet on March 06, 2010
Y-chromosomal variation in sub-Saharan Africa: insights into the history of Niger-Congo groups. Mol Biol Evol (2010) 1.32
AMY-tree: an algorithm to use whole genome SNP calling for Y chromosomal phylogenetic applications. BMC Genomics (2013) 1.01
Afghanistan's ethnic groups share a Y-chromosomal heritage structured by historical events. PLoS One (2012) 0.93
Association between Y haplogroups and autosomal AIMs reveals intra-population substructure in Bolivian populations. Int J Legal Med (2014) 0.92
Phylogeographic Refinement and Large Scale Genotyping of Human Y Chromosome Haplogroup E Provide New Insights into the Dispersal of Early Pastoralists in the African Continent. Genome Biol Evol (2015) 0.84
Molecular dissection of the basal clades in the human Y chromosome phylogenetic tree. PLoS One (2012) 0.83
Understanding the Y chromosome variation in Korea--relevance of combined haplogroup and haplotype analyses. Int J Legal Med (2012) 0.82
Admixture and genetic diversity distribution patterns of non-recombining lineages of Native American ancestry in Colombian populations. PLoS One (2015) 0.81
Mosaic maternal ancestry in the Great Lakes region of East Africa. Hum Genet (2015) 0.79
Forensic use of Y-chromosome DNA: a general overview. Hum Genet (2017) 0.79
Male Lineages in Brazil: Intercontinental Admixture and Stratification of the European Background. PLoS One (2016) 0.77
Y-chromosome R-M343 African lineages and sickle cell disease reveal structured assimilation in Lebanon. J Hum Genet (2010) 0.76
The genetic landscape of Equatorial Guinea and the origin and migration routes of the Y chromosome haplogroup R-V88. Eur J Hum Genet (2012) 0.76
Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evol Bioinform Online (2007) 54.21
The genetic structure and history of Africans and African Americans. Science (2009) 10.65
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. Genome Res (2008) 6.45
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet (2001) 6.24
The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time. Am J Hum Genet (2003) 4.34
A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes. Am J Hum Genet (2002) 3.71
The making of the African mtDNA landscape. Am J Hum Genet (2002) 3.52
Y-chromosomal DNA variation in Pakistan. Am J Hum Genet (2002) 3.35
Origin, diffusion, and differentiation of Y-chromosome haplogroups E and J: inferences on the neolithization of Europe and later migratory events in the Mediterranean area. Am J Hum Genet (2004) 3.28
Hierarchical patterns of global human Y-chromosome diversity. Mol Biol Evol (2001) 3.04
Contrasting patterns of Y chromosome and mtDNA variation in Africa: evidence for sex-biased demographic processes. Eur J Hum Genet (2005) 2.51
Ethiopians and Khoisan share the deepest clades of the human Y-chromosome phylogeny. Am J Hum Genet (2001) 2.46
Y-chromosome variation among Sudanese: restricted gene flow, concordance with language, geography, and history. Am J Phys Anthropol (2008) 2.23
The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20
Statistical properties of the variation at linked microsatellite loci: implications for the history of human Y chromosomes. Mol Biol Evol (1996) 2.07
History of click-speaking populations of Africa inferred from mtDNA and Y chromosome genetic variation. Mol Biol Evol (2007) 2.00
Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers. Proc Natl Acad Sci U S A (2008) 1.96
Genetic and demographic implications of the Bantu expansion: insights from human paternal lineages. Mol Biol Evol (2009) 1.86
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
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
The genetic legacy of western Bantu migrations. Hum Genet (2005) 1.62
On the edge of Bantu expansions: mtDNA, Y chromosome and lactase persistence genetic variation in southwestern Angola. BMC Evol Biol (2009) 1.51
Mutation rates at Y chromosome specific microsatellites. Hum Mutat (2005) 1.48
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
Y-chromosomal evidence of a pastoralist migration through Tanzania to southern Africa. Proc Natl Acad Sci U S A (2008) 1.46
Insights into the western Bantu dispersal: mtDNA lineage analysis in Angola. Hum Genet (2004) 1.19
Hierarchical analysis of 30 Y-chromosome SNPs in European populations. Int J Legal Med (2004) 1.09
Micro-phylogeographic and demographic history of Portuguese male lineages. Ann Hum Genet (2006) 1.03
Thomas Jefferson's Y chromosome belongs to a rare European lineage. Am J Phys Anthropol (2007) 1.01
Bantu and European Y-lineages in Sub-Saharan Africa. Ann Hum Genet (2002) 0.96
Nilotes from Karamoja, Uganda: haplotype data defined by 17 Y-chromosome STRs. Forensic Sci Int Genet (2009) 0.78
Dissecting the genetic history of São Tomé e Príncipe: a new window from Y-chromosome biallelic markers. Ann Hum Genet (2007) 0.75
Common variants conferring risk of schizophrenia. Nature (2009) 10.37
Transcriptome and genome sequencing uncovers functional variation in humans. Nature (2013) 8.89
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet (2008) 6.26
Synaptic, transcriptional and chromatin genes disrupted in autism. Nature (2014) 5.30
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A (2010) 4.30
The making of the African mtDNA landscape. Am J Hum Genet (2002) 3.52
Reconstructing Native American population history. Nature (2012) 3.49
The African diaspora: mitochondrial DNA and the Atlantic slave trade. Am J Hum Genet (2004) 2.63
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nat Genet (2013) 2.62
A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis (2006) 2.59
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS Genet (2011) 2.47
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. Nat Genet (2010) 2.45
Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet (2011) 2.21
A critical reassessment of the role of mitochondria in tumorigenesis. PLoS Med (2005) 1.96
A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics. Biochem Biophys Res Commun (2005) 1.93
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Nat Genet (2013) 1.85
High-resolution mtDNA evidence for the late-glacial resettlement of Europe from an Iberian refugium. Genome Res (2005) 1.85
Assessing individual interethnic admixture and population substructure using a 48-insertion-deletion (INSEL) ancestry-informative marker (AIM) panel. Hum Mutat (2010) 1.74
SNPs in forensic genetics: a review on SNP typing methodologies. Forensic Sci Int (2005) 1.74
Development of a panel of genome-wide ancestry informative markers to study admixture throughout the Americas. PLoS Genet (2012) 1.74
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
The genetic legacy of western Bantu migrations. Hum Genet (2005) 1.62
Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity cases. Forensic Sci Int (2002) 1.59
Testing for kinship in a subdivided population. Forensic Sci Int (2003) 1.58
Risk of cancer in cases of suspected lynch syndrome without germline mutation. Gastroenterology (2013) 1.55
Genetic signatures of a Mediterranean influence in Iberian Peninsula sheep husbandry. Mol Biol Evol (2006) 1.55
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy. Neuromuscul Disord (2011) 1.55
Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects. Hum Mutat (2003) 1.54
The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269. Proc Biol Sci (2011) 1.52
The c.156_157insAlu BRCA2 rearrangement accounts for more than one-fourth of deleterious BRCA mutations in northern/central Portugal. Breast Cancer Res Treat (2008) 1.51
SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access. BMC Bioinformatics (2008) 1.51
TGFβ1 SNPs and radio-induced toxicity in prostate cancer patients. Radiother Oncol (2012) 1.49
New population and phylogenetic features of the internal variation within mitochondrial DNA macro-haplogroup R0. PLoS One (2009) 1.47
Charting the ancestry of African Americans. Am J Hum Genet (2005) 1.47
ISFG: Recommendations on biostatistics in paternity testing. Forensic Sci Int Genet (2007) 1.46
The human early-life exposome (HELIX): project rationale and design. Environ Health Perspect (2014) 1.44
mtDNA phylogeny and evolution of laboratory mouse strains. Genome Res (2007) 1.42
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. Hum Mol Genet (2008) 1.40
Shipwrecks and founder effects: divergent demographic histories reflected in Caribbean mtDNA. Am J Phys Anthropol (2005) 1.40
A new multiplex for human identification using insertion/deletion polymorphisms. Electrophoresis (2009) 1.38
A GEP-ISFG collaborative study on the optimization of an X-STR decaplex: data on 15 Iberian and Latin American populations. Int J Legal Med (2008) 1.38
Publication of population data for forensic purposes. Forensic Sci Int Genet (2010) 1.31
Highly polymorphic microsatellite for identification of Candida albicans strains. J Clin Microbiol (2003) 1.27
New microsatellite multiplex PCR for Candida albicans strain typing reveals microevolutionary changes. J Clin Microbiol (2005) 1.26
The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation, results and perspectives. Forensic Sci Int (2004) 1.26
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10). PLoS One (2009) 1.23
Predicting sampling saturation of mtDNA haplotypes: an application to an enlarged Portuguese database. Int J Legal Med (2004) 1.22
Association of PDCD1 with susceptibility to systemic lupus erythematosus: evidence of population-specific effects. Arthritis Rheum (2004) 1.22
Quantification of epigenetic and genetic 2nd hits in CDH1 during hereditary diffuse gastric cancer syndrome progression. Gastroenterology (2009) 1.21
Insights into the western Bantu dispersal: mtDNA lineage analysis in Angola. Hum Genet (2004) 1.19
Multiplex SNaPshot for detection of BRCA1/2 common mutations in Spanish and Spanish related breast/ovarian cancer families. BMC Med Genet (2007) 1.19
Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages. Electrophoresis (2005) 1.18
A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism. Hum Mol Genet (2009) 1.18
Is mitochondrial DNA variation associated with sporadic breast cancer risk? Cancer Res (2008) 1.18
J1-M267 Y lineage marks climate-driven pre-historical human displacements. Eur J Hum Genet (2009) 1.15
Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment. Am J Med Genet B Neuropsychiatr Genet (2009) 1.14
Inactivation status of PCDH11X: sexual dimorphisms in gene expression levels in brain. Hum Genet (2006) 1.14
Novel high-throughput SNP genotyping cosegregation analysis for genetic diagnosis of autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. Hum Mutat (2007) 1.14
Allele-specific CDH1 downregulation and hereditary diffuse gastric cancer. Hum Mol Genet (2009) 1.13
Signatures of the preagricultural peopling processes in sub-Saharan Africa as revealed by the phylogeography of early Y chromosome lineages. Mol Biol Evol (2011) 1.13
Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes. Hum Genet (2005) 1.13
Genetic analysis of three US population groups using an X-chromosomal STR decaplex. Int J Legal Med (2007) 1.13
Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype. Gastroenterology (2010) 1.11
Forensic validation of the SNPforID 52-plex assay. Forensic Sci Int Genet (2007) 1.11
Reconstructing ancient mitochondrial DNA links between Africa and Europe. Genome Res (2012) 1.10
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophr Bull (2014) 1.10
Identification of species with DNA-based technology: current progress and challenges. Recent Pat DNA Gene Seq (2008) 1.10
Genetic diversity of 10 X chromosome STRs in northern Portugal. Int J Legal Med (2007) 1.08
Dissection of mitochondrial superhaplogroup H using coding region SNPs. Electrophoresis (2006) 1.08
Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing. PLoS One (2012) 1.08
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. PLoS Genet (2013) 1.08
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Hum Mol Genet (2011) 1.07
mtDNA mutations in tumors of the central nervous system reflect the neutral evolution of mtDNA in populations. Oncogene (2004) 1.07
Tracing the history of goat pastoralism: new clues from mitochondrial and Y chromosome DNA in North Africa. Mol Biol Evol (2009) 1.07
Use of a comprehensive panel of biomarkers to predict response to a fluorouracil-oxaliplatin regimen in patients with metastatic colorectal cancer. Pharmacogenomics (2011) 1.06
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome. BMC Genomics (2010) 1.06
Analysis of 10 X-STRs in three African populations. Forensic Sci Int Genet (2007) 1.04