I. Wilson

发表

Genealogical inference from microsatellite data.

D. Balding, I. Wilson, 1998, Genetics.

A Predominantly Neolithic Origin for European Paternal Lineages

Guido Barbujani, Chris Tyler-Smith, Ian J. Wilson, 2010, PLoS biology.

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

David C Samuels, Patrick F Chinnery, Rita Horvath, 2011, Nature Genetics.

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

Marc Gewillig, Rachel Soemedi, Koenraad Devriendt, 2012, American journal of human genetics.

Prevalence, incidence and carrier frequency of 5q–linked spinal muscular atrophy – a literature review

Hanns Lochmüller, I. Wilson, Suzanne F. Cook, 2017, Orphanet Journal of Rare Diseases.

Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases

P. Chinnery, I. Wilson, G. Hudson, 2014, PLoS genetics.

Finding genes that influence quantitative traits with tree-based clustering

M. Santibanez-Koref, I. Wilson, Darren T. Houniet, 2011, BMC proceedings.

High prevalence of focal and multi-focal somatic genetic variants in the human brain

S. Luo, C. Haudenschild, J. Attems, 2018, Nature Communications.

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

I. Wilson, M. Vickers, S. J. Canning, 2006, Stem cells.

Frequency and signature of somatic variants in 1461 human brain exomes

J. Attems, C. Troakes, Colin Smith, 2018, Genetics in Medicine.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance

Robert W. Taylor, D. Turnbull, J. Coxhead, 2014, Brain : a journal of neurology.

Atopic dermatitis and skin disease Filaggrin null mutations and childhood atopic eczema : A population-based case-control study

H. Cordell, C. Relton, I. Wilson, 2022 .

The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care

J. Goodship, I. Wilson, D. Pilz, 2015, Genetics in Medicine.

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism.

C. Tyler-Smith, M. Hurles, M. Jobling, 1999, American journal of human genetics.

Universal heteroplasmy of human mitochondrial DNA

David C. Samuels, Ian J. Wilson, Patrick F. Chinnery, 2012, Human molecular genetics.

Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains

J. Attems, C. Troakes, Colin Smith, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Mitochondrial Donation - Which Women Could Benefit?

Robert W. Taylor, D. Turnbull, I. Wilson, 2019, The New England journal of medicine.

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

Robert W. Taylor, H. Smeets, M. Zeviani, 2016, Human molecular genetics.

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors

Robert W. Taylor, D. Turnbull, H. Cordell, 2018, Annals of clinical and translational neurology.

Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations

M. Boerries, I. Wilson, T. Eisenberger, 2022, American journal of human genetics.

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

Robert W. Taylor, M. Santibanez-Koref, P. Chinnery, 2014, Genetics in Medicine.

Complement polymorphisms: geographical distribution and relevance to disease.

I. Wilson, L. Ermini, T. Goodship, 2012, Immunobiology.

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

Kevin Walters, John Burn, M. Santibanez-Koref, 2013, Journal of theoretical biology.

A Worldwide Phylogeography for the Human X Chromosome

I. Wilson, S. Pena, R. Pereira, 2007, PloS one.

A Worldwide Phylogeography for the Human X

I. Wilson, R. Pereira, D. J. Pena, 2007 .

Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities

David J. Balding, Michael E. Weale, Ian J. Wilson, 2003 .

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

James W Ironside, Olaf Ansorge, Patrick F Chinnery, 2017, Genome research.

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

M. Hurles, K. Devriendt, M. Lathrop, 2011, Human molecular genetics.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot

S. Heath, G. Lathrop, A. Moorman, 2013, Human molecular genetics.

High prevalence of focal and multi-focal somatic genetic variants in the human brain

S. Luo, J. Attems, N. Jones, 2018, Nature Communications.

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

M W Bruford, R A Nichols, P. Brakefield, 1999, Genetics.

A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families

E. Molinari, I. Wilson, E. Faqeih, 2021, Human mutation.

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

M. Herbert, J. Coxhead, M. Santibanez-Koref, 2015, PLoS genetics.

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

L. Noble, P. Boyle, I. Wilson, 2001, Molecular ecology.

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

T. Spector, I. Wilson, M. Vickers, 2001, Blood.

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.

K. Dawson, I. Wilson, 2007, Theoretical population biology.

Genetic differentiation in spatially structured populations with particular regard to the Atlantic salmon (Salmo salar L.)

I. Wilson, 1996 .

Genealogies and geography.

N. Barton, I. Wilson, N. H. Barton, 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

GNE genotype explains 20% of phenotypic variability in GNE myopathy

I. Nishino, Hanns Lochmüller, I. Wilson, 2019, Neurology: Genetics.

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

J. Attems, C. Morris, C. Troakes, 2017, Acta neuropathologica communications.

A model for bacterial conjugal gene transfer on solid surfaces.

I. Wilson, J. Prosser, L. A. Glover, 2003, FEMS microbiology ecology.

An intermediate-effect size variant in UMOD confers risk for chronic kidney disease

A. Köttgen, I. Wilson, K. Eckardt, 2021, medRxiv.

Inferring population history from microsatellite and enzyme data in serially introduced cane toads, Bufo marinus.

J. Cornuet, A. Estoup, C. Moritz, 2001, Genetics.

No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls

T. Spector, P. Deloukas, E. Zeggini, 2012, Annals of the rheumatic diseases.

Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

J. Attems, C. Morris, C. Troakes, 2017, Acta neuropathologica communications.

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

K. Bushby, P. Chinnery, Hanns Lochmüller, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Edinburgh Research Explorer Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

J. Attems, C. Morris, C. Troakes, 2022 .

Discussion on the Paper by Wilson, Weale and Balding

I. Wilson, 2003 .

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource

J. Attems, C. Troakes, S. Rollinson, 2017, Genome research.

Unique mitochondrial DNA in highly inbred feral cattle

P. Chinnery, I. Wilson, J. Elson, 2012, Mitochondrion.