about
A predominantly neolithic origin for European paternal lineagesPhenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsA worldwide phylogeography for the human X chromosome.Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.Finding genes that influence quantitative traits with tree-based clusteringInbreeding of bottlenecked butterfly populations. Estimation using the likelihood of changes in marker allele frequencies.Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations.Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutationsExtreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansContribution of global rare copy-number variants to the risk of sporadic congenital heart diseaseUniversal heteroplasmy of human mitochondrial DNA.Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckA Markov chain Monte Carlo strategy for sampling from the joint posterior distribution of pedigrees and population parameters under a Fisher-Wright model with partial selfing.Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.Complement polymorphisms: geographical distribution and relevance to disease.Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumours.A model for bacterial conjugal gene transfer on solid surfaces.Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid.Titinopathy in a Canadian family sharing the British founder haplotype.Filaggrin null mutations and childhood atopic eczema: A population-based case-control studyMitochondrial ageing and antiretroviral therapy exposureX Inactivation Patterns of Closely, but Not Distantly, Related Cells Are Highly Correlated: Little Evidence for Stem Cell Plasticity in Normal FemalesAssessment of mechanism of acquired skewed X inactivation by analysis of twins
P50
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P50
description
British researcher
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hulumtues
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wetenschapper
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հետազոտող
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name
Ian Wilson
@af
Ian Wilson
@an
Ian Wilson
@ast
Ian Wilson
@bar
Ian Wilson
@bm
Ian Wilson
@br
Ian Wilson
@ca
Ian Wilson
@co
Ian Wilson
@cs
Ian Wilson
@cy
type
label
Ian Wilson
@af
Ian Wilson
@an
Ian Wilson
@ast
Ian Wilson
@bar
Ian Wilson
@bm
Ian Wilson
@br
Ian Wilson
@ca
Ian Wilson
@co
Ian Wilson
@cs
Ian Wilson
@cy
prefLabel
Ian Wilson
@af
Ian Wilson
@an
Ian Wilson
@ast
Ian Wilson
@bar
Ian Wilson
@bm
Ian Wilson
@br
Ian Wilson
@ca
Ian Wilson
@co
Ian Wilson
@cs
Ian Wilson
@cy
P106
P21
P31
P496
0000-0001-6893-2873