Publications by Dr Ian Wilson - ePrints

Browsing publications by Dr Ian Wilson.

Newcastle Authors	Title	Year
Dr Eric Olinger Dr Ian Wilson Professor John Sayer	UMOD Genotype and Determinants of Urinary Uromodulin in African Populations	2024
Dr Eric Olinger Dr Ian Wilson Sarah Orr Miguel Barroso Gil Ruxandra Neatu et al.	Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene for autosomal recessive retinopathy	2024
Dr Eric Olinger Sotia Iosifidou Miguel Barroso Gil Ruxandra Neatu Dr Katrina Wood et al.	Molecular genetic diagnosis of kidney ciliopathies: Lessons from interpreting genomic sequencing data and the requirement for accurate phenotypic data	2024
Dr Yuko Takeda Dr Louise Hyslop Dr Meenakshi Choudhary Dr Fiona Robertson Dr Angela Pyle et al.	Feasibility and impact of haplogroup matching for mitochondrial replacement treatment.	2023
Dr Ursula Moore Esther Fernández-Simón Dr Marianela Schiava Daniel Cox Meredith James et al.	Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy	2023
Dr Rob Geraghty Dr Ian Wilson Dr Eric Olinger Alistair Rogers Professor John Sayer et al.	Routine Urinary Biochemistry Does Not Accurately Predict Stone Type Nor Recurrence in Kidney Stone Formers: A Multicentre, Multimodel, Externally Validated Machine-Learning Study	2023
Laura Devlin Miguel Barroso Gil Ruxandra Neatu Laura Powell Dr Emanuela Molinari et al.	Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome	2022
Dr Eric Olinger Dr Ian Wilson Professor John Sayer	Kidney traits on repeat—the role of MUC1 VNTR	2022
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 mutations	2022
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 dysferlinopathy	2022
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 dysferlinopathy	2022
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 families	2021
Sidharth Maheshwari Venkateshwarlu Gudur Professor Rishad Shafik Dr Ian Wilson Professor Alex Yakovlev et al.	CORAL: Verification-aware OpenCL based Read Mapper for Heterogeneous Systems	2021
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 technique	2020
Dr Ian Wilson Professor Boguslaw Obara Professor David Steel	Macular hole morphology and measurement using an automated three-dimensional image segmentation algorithm	2020
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 myopathy	2019
Dr Peter Kullar Dr Ian Wilson Professor Johannes Attems Dr Christopher Morris	Frequency and signature of somatic variants in 1461 human brain exomes	2019
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 brain	2018
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 brains	2018
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 factors	2018
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 leukaemia	2017
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 Resource	2017
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 brains	2017
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 review	2017
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 bottleneck	2016
Dr Brian Wilson Professor Judith Goodship Dr Ian Wilson	The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care	2016
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 Fallot	2015
Dr Angela Pyle Professor 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 Humans	2015
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 Disease	2015
Dr Helen Griffin Dr Angela Pyle Dr Charlotte Alston Dr Jennifer Duff Professor Gavin Hudson et al.	Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations	2014
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 Imaging	2014
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 maintenance	2014
Professor 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 Diseases	2014
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 failure	2014
Dr Gerald Pfeffer Dr Ian Wilson Professor Patrick Chinnery	Titinopathy in a Canadian Family Sharing the British Founder Haplotype	2014
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 failure	2013
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 tumours	2013
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 Fallot	2013
Professor 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 controls	2013
Dr Luca Ermini Dr Ian Wilson Professor Tim Goodship Professor Neil Sheerin	Complement polymorphisms: Geographical distribution and relevance to disease	2012
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 Disease	2012
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 controls	2012
Professor Gavin Hudson Dr Ian Wilson Dr Brendan Payne Dr Joanna Elson Professor David Samuels et al.	Unique mitochondrial DNA in highly inbred feral cattle	2012
Dr Brendan Payne Dr Ian Wilson Dr Patrick Yu Wai Man Dr Jonathan Coxhead Professor David Deehan et al.	Universal heteroplasmy of human mitochondrial DNA	2012
Dr Ian Wilson Darren Houniet Dr Mauro Santibanez Koref	Finding genes that influence quantitative traits with tree-based clustering	2011
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 mutations	2011
Professor Hing Leung Dr Ian Wilson	A Predominantly Neolithic Origin for European Paternal Lineages	2010
Dr Ian Wilson	Demography, Ascertainment and the Genealogy of haplotype blocks	2008
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 study	2008
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 study	2008
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 selfing	2007
Dr Ian Wilson	A worldwide phylogeography for the human X chromosome	2007
Dr Ian Wilson	Molecular and evolutionary epidemiology of Schistosoma mansoni in human hosts	2007
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 Females	2006
Dr Ian Wilson	Slow fiber cluster pattern in pig longissimus thoracis muscle: Implications for myogenesis	2005
Dr Ian Wilson	A model for bacterial conjugal gene transfer on solid surfaces	2003
Dr Ian Wilson	Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities	2003
Dr Ian Wilson	Assessment of mechanism of acquired skewed X inactivation by analysis of twins	2001
Dr Ian Wilson Lesley Noble	Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid	2001
Dr Ian Wilson	Inferring population history from microsatellite and enzyme data in serially introduced cane toads, Bufo marinus	2001
Dr Ian Wilson	Discussion of Stephens M, Donnelly P. Inference in molecular population genetics	2000