The distribution and most recent common ancestor of the 17q21 inversion in humans
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The microcephalin ancestral allele in a Neanderthal individualThe genomic landscape underlying phenotypic integrity in the face of gene flow in crowsHunter-gatherer genomic diversity suggests a southern African origin for modern humansAn alignment-free method to find and visualise rearrangements between pairs of DNA sequencesExome sequencing identifies recurrent somatic RAC1 mutations in melanomaFluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research ApplicationsDissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.The 8p23 inversion polymorphism determines local recombination heterogeneity across human populationsGenome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism.Human inversions and their functional consequencesStructural and functional characterization of H2 haplotype MAPT promoter: unique neurospecific domains and a hypoxia-inducible element would enhance rationally targeted tauopathy research for Alzheimer's disease.Structural diversity and African origin of the 17q21.31 inversion polymorphism.A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci.Mini-haplotypes as lineage informative SNPs and ancestry inference SNPsOn the structural plasticity of the human genome: chromosomal inversions revisited.Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism.Common variants at 6q22 and 17q21 are associated with intracranial volume.Widespread Impact of Chromosomal Inversions on Gene Expression Uncovers Robustness via Phenotypic Buffering.Characterizing polymorphic inversions in human genomes by single-cell sequencing.GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.Parkinson's disease: from genetics to clinical practice.Tau deletion promotes brain insulin resistanceSNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians.Tau pathology: predictive diagnostics, targeted preventive and personalized medicine and application of advanced research in medical practice.Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country.
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P2860
The distribution and most recent common ancestor of the 17q21 inversion in humans
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The distribution and most recent common ancestor of the 17q21 inversion in humans
@ast
The distribution and most recent common ancestor of the 17q21 inversion in humans
@en
The distribution and most recent common ancestor of the 17q21 inversion in humans
@nl
type
label
The distribution and most recent common ancestor of the 17q21 inversion in humans
@ast
The distribution and most recent common ancestor of the 17q21 inversion in humans
@en
The distribution and most recent common ancestor of the 17q21 inversion in humans
@nl
prefLabel
The distribution and most recent common ancestor of the 17q21 inversion in humans
@ast
The distribution and most recent common ancestor of the 17q21 inversion in humans
@en
The distribution and most recent common ancestor of the 17q21 inversion in humans
@nl
P2093
P2860
P3181
P1476
The distribution and most recent common ancestor of the 17q21 inversion in humans
@en
P2093
Andrew J Pakstis
Csaba Barta
David Comas
David Gurwitz
Haseena Rajeevan
Jong-Jin Kim
Judith R Kidd
Kenneth K Kidd
Marcello Siniscalco
P2860
P304
P3181
P356
10.1016/J.AJHG.2010.01.007
P407
P577
2010-01-28T00:00:00Z