List of works - Ian Wilson

A 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

scientific article published on 12 March 2007

A model for bacterial conjugal gene transfer on solid surfaces.

scientific article

A predominantly neolithic origin for European paternal lineages

scientific article published in January 2010

A worldwide phylogeography for the human X chromosome

scientific article

Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations

scientific article

Assessment of mechanism of acquired skewed X inactivation by analysis of twins

article

Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid.

scientific article published in May 2001

Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumours

scientific article published on 30 July 2013

Complement polymorphisms: geographical distribution and relevance to disease.

scientific article published on 26 July 2011

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

scientific article

Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans

scientific article published on 14 May 2015

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

article

Finding genes that influence quantitative traits with tree-based clustering

scientific article

Inbreeding of bottlenecked butterfly populations. Estimation using the likelihood of changes in marker allele frequencies.

scientific article

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

scientific article published on 5 January 2016

Mitochondrial ageing and antiretroviral therapy exposure

scholarly article by Brendan Payne et al published 2010 in Journal of the International AIDS Society

Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations

scientific article published on 26 June 2011

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

scientific article

Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases

scientific article

Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure

scientific article published on 13 March 2013

Titinopathy in a Canadian family sharing the British founder haplotype.

scientific article published in January 2014

Universal heteroplasmy of human mitochondrial DNA.

scientific article

X Inactivation Patterns of Closely, but Not Distantly, Related Cells Are Highly Correlated: Little Evidence for Stem Cell Plasticity in Normal Females

scientific article published on 06 July 2006

List of works by Ian Wilson

A 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

A model for bacterial conjugal gene transfer on solid surfaces.

A predominantly neolithic origin for European paternal lineages

A worldwide phylogeography for the human X chromosome

Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations

Assessment of mechanism of acquired skewed X inactivation by analysis of twins

Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid.

Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumours

Complement polymorphisms: geographical distribution and relevance to disease.

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

Finding genes that influence quantitative traits with tree-based clustering

Inbreeding of bottlenecked butterfly populations. Estimation using the likelihood of changes in marker allele frequencies.

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

Mitochondrial ageing and antiretroviral therapy exposure

Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases

Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure

Titinopathy in a Canadian family sharing the British founder haplotype.

Universal heteroplasmy of human mitochondrial DNA.

X Inactivation Patterns of Closely, but Not Distantly, Related Cells Are Highly Correlated: Little Evidence for Stem Cell Plasticity in Normal Females