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Browsing publications by Dr Ian Wilson.

Newcastle AuthorsTitleYearFull text
Dr Eric Olinger
Dr Ian Wilson
Professor John Sayer
Kidney traits on repeat—the role of MUC1 VNTR2022
Carina Oliva
Laura Powell
Dr Ian Wilson
Dr Sarah Rice
Dr Colin Miles
et al.
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations2022
Dr Fiona Smith
Dr Ian Wilson
Roberto Fernandez-Torron
Meredith James
Dr Ursula Moore
et al.
Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy2022
Dr ursula Moore
Dr Fiona Smith
Dr Ian Wilson
Meredith James
Dr Anna Mayhew
et al.
Water T2 could predict functional decline in patients with dysferlinopathy2022
Dr Eric Olinger
Dr Elisa Molinari
Miguel Barroso Gil
Laura Powell
Dr Colin Miles
et al.
A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families2021
Sidharth Maheshwari
Venkateshwarlu Gudur
Dr Rishad Shafik
Dr Ian Wilson
Professor Alex Yakovlev
et al.
CORAL: Verification-aware OpenCL based Read Mapper for Heterogeneous Systems2021
Dr William Manning
Dr Ian Wilson
Dr Geoff Hide
Lee Longstaff
Professor David Deehan
et al.
Improved mediolateral load distribution without adverse laxity pattern in robot-assisted knee arthroplasty compared to a standard manual measured resection technique2020
Dr Ian Wilson
Professor Boguslaw Obara
Professor David Steel
Macular hole morphology and measurement using an automated three-dimensional image segmentation algorithm2020
Dr Rob Geraghty
Dr Ian Wilson
Professor John Sayer
Regarding “Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis”2020
Dr Oksana Pogoryelova
Dr Ian Wilson
Professor Hanns Lochmuller
GNE genotype explains 20% of phenotypic variability in GNE myopathy2019
Dr Peter Kullar
Dr Ian Wilson
Professor Johannes Attems
Dr Christopher Morris
Frequency and signature of somatic variants in 1461 human brain exomes2019
Dr Sarah Pickett
Dr Alasdair Blain
Dr Yi Ng
Dr Ian Wilson
Professor Robert Taylor
et al.
Mitochondrial donation - Which women could benefit?2019
Dr Lauren Walker
Dr Jonathan Coxhead
Dr Ian Wilson
Dr Matthew Bashton
Dr Christopher Morris
et al.
High prevalence of focal and multi-focal somatic genetic variants in the human brain2018
Dr Michael Keogh
Dr Wei Wei
Dr Ian Wilson
Professor Johannes Attems
Dr Christopher Morris
et al.
Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains2018
Dr Sarah Pickett
Dr John Grady
Dr Yi Ng
Professor Grainne Gorman
Dr Andrew Schaefer
et al.
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors2018
Dr Kenneth Rankin
Jayasree Ramaskandhan
Michelle Bardgett
Dr Ian Wilson
Professor David Deehan
et al.
Synovectomy during total knee arthroplasty: a pilot single-centre randomised controlled trial.2018
Dr Alex Elder
Dr Simon Bomken
Dr Ian Wilson
Dr Helen Blair
Dr Simon Cockell
et al.
Abundant and equipotent founder cells establish and maintain acute lymphoblastic leukaemia2017
Dr Michael Keogh
Dr Wei Wei
Dr Ian Wilson
Dr Jonathan Coxhead
Dr Helen Griffin
et al.
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource2017
Dr Michael Keogh
Dr Ian Wilson
Dr Jonathan Coxhead
Dr Helen Griffin
Dr Marzena Kurzawa-Akanbi
et al.
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains2017
Dr Ingrid Verhaart
Agata Robertson
Dr Ian Wilson
Professor Annemieke Aartsma-Rus
Dr Shona Cameron
et al.
Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - A literature review2017
Dr Ian Wilson
Pip Carling
Dr Charlotte Alston
Vasileios Floros
Dr Angela Pyle
et al.
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck2016
Dr Brian Wilson
Professor Judith Goodship
Dr Ian Wilson
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care2016
Professor Judith Goodship
Matthieu Miossec
Dr Danielle Brown
Dr Ian Wilson
Dr Lou Sutcliffe
et al.
Analysis of rare variants and CNVs in non-syndromic tetralogy of Fallot2015
Dr Angela Pyle
Dr Gavin Hudson
Dr Ian Wilson
Dr Jonathan Coxhead
Tania Smertenko
et al.
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans2015
Dr Catherine Napier
Dr Anna Mitchell
Dr Earn Gan
Dr Ian Wilson
Professor Simon Pearce
et al.
Role of the X-Linked Gene GPR174 in Autoimmune Addison's Disease2015
Dr Helen Griffin
Dr Angela Pyle
Dr Charlotte Alston
Dr Jennifer Duff
Dr Gavin Hudson
et al.
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations2014
Dr Britta Vormoor
Henrike Knizia
Michael Batey
Dr Ian Wilson
Dr Petra Dildey
et al.
Development of a Preclinical Orthotopic Xenograft Model of Ewing Sarcoma and Other Human Malignant Bone Disease Using Advanced In Vivo Imaging2014
Dr Gerald Pfeffer
Professor Grainne Gorman
Dr Helen Griffin
Dr Marzena Kurzawa-Akanbi
Dr Ian Wilson
et al.
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance2014
Dr Gavin Hudson
Dr Aurora Gomez Duran
Dr Ian Wilson
Professor Patrick Chinnery
Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases2014
Dr Gerald Pfeffer
Dr Rita Barresi
Dr Ian Wilson
Dr Steven Hardy
Dr Helen Griffin
et al.
Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure2014
Dr Gerald Pfeffer
Dr Ian Wilson
Professor Patrick Chinnery
Titinopathy in a Canadian Family Sharing the British Founder Haplotype2014
Dr Gerald Pfeffer
Dr Rita Barresi
Dr Ian Wilson
Dr Helen Griffin
Dr Hannah Elliott
et al.
A founder mutation in the titin gene is a common cause of myofibrillar myopathy with early respiratory failure2013
Professor Sir John Burn
Dr Ian Wilson
Dr Mauro Santibanez Koref
Bayesian inference supports a location and neighbour-dependent model of DNA methylation propagation at the MGMT gene promoter in lung tumours2013
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Dr Rebecca Darlay
Rachel Soemedi
et al.
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot2013
Dr Gavin Hudson
Dr Ian Wilson
Professor Fraser Birrell
Professor Andrew McCaskie
Professor John Loughlin
et al.
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls2013
Dr Luca Ermini
Dr Ian Wilson
Professor Tim Goodship
Professor Neil Sheerin
Complement polymorphisms: Geographical distribution and relevance to disease2012
Rachel Soemedi
Dr Ian Wilson
Dr Rebecca Darlay
Dr Ana Topf
Dr Simon Zwolinski
et al.
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease2012
Rachel Soemedi
Dr Ana Topf
Dr Ian Wilson
Dr Rebecca Darlay
Dr Thahira Rahman
et al.
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls2012
Dr Gavin Hudson
Dr Ian Wilson
Dr Brendan Payne
Dr Joanna Elson
Professor David Samuels
et al.
Unique mitochondrial DNA in highly inbred feral cattle2012
Dr Brendan Payne
Dr Ian Wilson
Dr Patrick Yu Wai Man
Dr Jonathan Coxhead
Professor David Deehan
et al.
Universal heteroplasmy of human mitochondrial DNA2012
Dr Ian Wilson
Darren Houniet
Dr Mauro Santibanez Koref
Finding genes that influence quantitative traits with tree-based clustering2011
Dr Brendan Payne
Dr Ian Wilson
Professor Rita Horvath
Dr Mauro Santibanez Koref
Dr David Samuels
et al.
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations2011
Professor Hing Leung
Dr Ian Wilson
A Predominantly Neolithic Origin for European Paternal Lineages2010
Dr Ian Wilson
Demography, Ascertainment and the Genealogy of haplotype blocks2008
Adillah Binti Yusof
Professor Caroline Relton
Dr Ian Wilson
Professor Sir John Burn
Professor Nick Reynolds
et al.
Filaggrin null mutations and childhood atopic eczema: A population-based case-control study2008
Dr Sara Brown
Professor Caroline Relton
Dr Ian Wilson
Professor Sir John Burn
Professor Nick Reynolds
et al.
Filaggrin null mutations in mild-moderate atopic eczema: a population-based case-control study2008
Dr 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 selfing2007
Dr Ian Wilson
A worldwide phylogeography for the human X chromosome2007
Dr Ian Wilson
Molecular and evolutionary epidemiology of Schistosoma mansoni in human hosts2007
Wendy Craig
Dr Ian Wilson
X Inactivation Patterns of Closely, but Not Distantly, Related Cells Are Highly Correlated: Little Evidence for Stem Cell Plasticity in Normal Females2006
Dr Ian Wilson
Slow fiber cluster pattern in pig longissimus thoracis muscle: Implications for myogenesis2005
Dr Ian Wilson
A model for bacterial conjugal gene transfer on solid surfaces2003
Dr Ian Wilson
Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities2003
Dr Ian Wilson
Assessment of mechanism of acquired skewed X inactivation by analysis of twins2001
Dr Ian Wilson
Lesley Noble
Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid2001
Dr Ian Wilson
Inferring population history from microsatellite and enzyme data in serially introduced cane toads, Bufo marinus2001
Dr Ian Wilson
Discussion of Stephens M, Donnelly P. Inference in molecular population genetics2000