Lista de obras - Ian Wilson - Dominio Público Uruguay

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

artículo científico publicado en 2007

A model for bacterial conjugal gene transfer on solid surfaces

artículo científico publicado en 2003

A predominantly neolithic origin for European paternal lineages

artículo científico publicado en 2010

A worldwide phylogeography for the human X chromosome

artículo científico publicado en 2007

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

artículo científico publicado en 2014

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

artículo científico publicado en 2001

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

artículo científico publicado en 2013

Complement polymorphisms: geographical distribution and relevance to disease.

artículo científico publicado en 2011

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2011

Genealogical Inference From Microsatellite Data ⬇️

artículo científico publicado el 1 de septiembre de 1998

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

artículo científico publicado en 1999

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Titinopathy in a Canadian family sharing the British founder haplotype.

artículo científico publicado en 2014

Universal heteroplasmy of human mitochondrial DNA.

artículo científico publicado en 2012

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

artículo científico publicado en 2006

Lista de obras de 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

Genealogical Inference From Microsatellite Data ⬇️

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