Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A worldwide phylogeography for the human X chromosome.

PloS one - 27 Jun 2007

Santos-Lopes Simone S, Pereira Rinaldo W, Wilson Ian J, Pena Sérgio D J

Abstract excerpt

BACKGROUND: We reasoned that by identifying genetic markers on human X chromosome regions where recombination is rare or absent, we should be able to construct X chromosome genealogies analogous to those based on Y chromosome and mitochondrial DNA polymorphisms, with the advantage of providing information about both male and female components of the population. METHODOLOGY/PRINCIPAL FINDINGS: We identified a 47...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alu Elements
Share to Chromosomes, Human, X
Share to Chromosomes, Human, Y

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetics, Population

Share to Genome, Human

Share to Linkage Disequilibrium

Share to Microsatellite Repeats

Share to Physical Chromosome Mapping

Source

Open in PubMed Open full text

Identifiers

PMID: 17593958
DOI: 10.1371/journal.pone.0000557
PMCID: PMC1891433

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A worldwide phylogeography for the human X chromosome.PMID 17593958Read ↗

A novel polymorphic Alu insertion embedded in a LINE 1 retrotransposon in the human X chromosome (DXS225): identification and worldwide population study.Semantic proximity Read ↗

Divergent haplotypes and human history as revealed in a worldwide survey of X-linked DNA sequence variation.Semantic proximity Read ↗

DNA polymorphism in a worldwide sample of human X chromosomes.Semantic proximity Read ↗

DNA sequence variation in a non-coding region of low recombination on the human X chromosome.Semantic proximity Read ↗

An X-linked haplotype of Neandertal origin is present among all non-African populations.Semantic proximity Read ↗

Strong selective sweeps before 45,000BP displaced archaic admixture across the human X chromosomeSemantic proximity Read ↗

X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations.Semantic proximity Read ↗

Signatures of human European Palaeolithic expansion shown by resequencing of non-recombining X-chromosome segments.Semantic proximity Read ↗

Tracing genetic history of modern humans using X-chromosome lineages.Semantic proximity Read ↗

Recombination networks as genetic markers in a human variation study of the Old World.Semantic proximity Read ↗

Human population dispersal "Out of Africa" estimated from linkage disequilibrium and allele frequencies of SNPs.Semantic proximity Read ↗

A tale of two haplotypes: the EDA2R/AR Intergenic region is the most divergent genomic segment between Africans and East Asians in the human genome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.