Published in Ann Hum Genet on March 01, 2006
Africans in Yorkshire? The deepest-rooting clade of the Y phylogeny within an English genealogy. Eur J Hum Genet (2007) 1.78
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
Genetic diversity of 10 X chromosome STRs in northern Portugal. Int J Legal Med (2007) 1.08
Continent-wide decoupling of Y-chromosomal genetic variation from language and geography in native South Americans. PLoS Genet (2013) 1.04
Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe. Eur J Hum Genet (2009) 0.98
Digging deeper into East African human Y chromosome lineages. Hum Genet (2010) 0.93
Uniparental markers of contemporary Italian population reveals details on its pre-Roman heritage. PLoS One (2012) 0.89
Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers. BMC Genomics (2007) 0.88
Genetic signatures of parental contribution in black and white populations in Brazil. Genet Mol Biol (2009) 0.86
Analysis of 8 X-chromosomal markers in the population of central Croatia. Croat Med J (2013) 0.82
Portuguese crypto-Jews: the genetic heritage of a complex history. Front Genet (2015) 0.81
The admixture structure and genetic variation of the archipelago of Cape Verde and its implications for admixture mapping studies. PLoS One (2012) 0.79
Male Lineages in Brazil: Intercontinental Admixture and Stratification of the European Background. PLoS One (2016) 0.77
Assessing the genetic influence of ancient sociopolitical structure: micro-differentiation patterns in the population of Asturias (Northern Spain). PLoS One (2012) 0.76
Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula. PLoS One (2016) 0.75
Study of Modern Human Evolution via Comparative Analysis with the Neanderthal Genome. Genomics Inform (2013) 0.75
Reconstruction of major maternal and paternal lineages of the Cape Muslim population. Genet Mol Biol (2013) 0.75
Analysis of the R1b-DF27 haplogroup shows that a large fraction of Iberian Y-chromosome lineages originated recently in situ. Sci Rep (2017) 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
The portability of tagSNPs across populations: a worldwide survey. Genome Res (2006) 1.99
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
Genetic and demographic implications of the Bantu expansion: insights from human paternal lineages. Mol Biol Evol (2009) 1.86
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
Mitochondrial DNA of an Iberian Neandertal suggests a population affinity with other European Neandertals. Curr Biol (2006) 1.69
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
Balancing selection is the main force shaping the evolution of innate immunity genes. J Immunol (2008) 1.63
The genetic legacy of western Bantu migrations. Hum Genet (2005) 1.62
A highly divergent mtDNA sequence in a Neandertal individual from Italy. Curr Biol (2006) 1.59
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
Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages. Eur J Hum Genet (2004) 1.55
On the origins and admixture of Malagasy: new evidence from high-resolution analyses of paternal and maternal lineages. Mol Biol Evol (2009) 1.54
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
Statistical power analysis of neutrality tests under demographic expansions, contractions and bottlenecks with recombination. Genetics (2008) 1.49
A natural history of FUT2 polymorphism in humans. Mol Biol Evol (2009) 1.49
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
Genetic comparison of the head of Henri IV and the presumptive blood from Louis XVI (both Kings of France). Forensic Sci Int (2012) 1.44
The human early-life exposome (HELIX): project rationale and design. Environ Health Perspect (2014) 1.44
Insights into the demographic history of African Pygmies from complete mitochondrial genomes. Mol Biol Evol (2010) 1.43
mtDNA phylogeny and evolution of laboratory mouse strains. Genome Res (2007) 1.42
Accelerated evolution of Protocadherin11X/Y: a candidate gene-pair for cerebral asymmetry and language. Am J Med Genet B Neuropsychiatr Genet (2006) 1.41
Molecular and genotypic characterization of human thyroid follicular cell carcinoma-derived cell lines. Thyroid (2007) 1.41
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
Neandertal evolutionary genetics: mitochondrial DNA data from the iberian peninsula. Mol Biol Evol (2005) 1.40
High resolution Y chromosome typing: 19 STRs amplified in three multiplex reactions. Forensic Sci Int (2002) 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
The analysis of variation of mtDNA hypervariable region 1 suggests that Eastern and Western Pygmies diverged before the Bantu expansion. Am Nat (2004) 1.37
Publication of population data for forensic purposes. Forensic Sci Int Genet (2010) 1.31
Phylogeography of the human mitochondrial L1c haplogroup: genetic signatures of the prehistory of Central Africa. Mol Phylogenet Evol (2006) 1.30
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
Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba. BMC Evol Biol (2008) 1.26
SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data. Bioinformatics (2008) 1.24
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
Estimating the ancestral recombinations graph (ARG) as compatible networks of SNP patterns. J Comput Biol (2008) 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
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
Fragmentation of contaminant and endogenous DNA in ancient samples determined by shotgun sequencing; prospects for human palaeogenomics. PLoS One (2011) 1.16
A genomic analysis identifies a novel component in the genetic structure of sub-Saharan African populations. Eur J Hum Genet (2010) 1.15
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