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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Dr Eric Olinger Dr Ian Wilson Professor John Sayer
| Kidney traits on repeat—the role of MUC1 VNTR | 2022 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Dr Ian Wilson Professor Boguslaw Obara Professor David Steel
| Macular hole morphology and measurement using an automated three-dimensional image segmentation algorithm | 2020 |
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Dr Rob Geraghty Dr Ian Wilson Professor John Sayer
| Regarding “Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis” | 2020 |
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Dr Oksana Pogoryelova Dr Ian Wilson Professor Hanns Lochmuller
| GNE genotype explains 20% of phenotypic variability in GNE myopathy | 2019 |
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Dr Peter Kullar Dr Ian Wilson Professor Johannes Attems Dr Christopher Morris
| Frequency and signature of somatic variants in 1461 human brain exomes | 2019 |
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Dr Sarah Pickett Dr Alasdair Blain Dr Yi Ng Dr Ian Wilson Professor Robert Taylor et al. | Mitochondrial donation - Which women could benefit? | 2019 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Dr Gerald Pfeffer Dr Ian Wilson Professor Patrick Chinnery
| Titinopathy in a Canadian Family Sharing the British Founder Haplotype | 2014 |
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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 |
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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 |
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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 |
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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 |
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Dr Luca Ermini Dr Ian Wilson Professor Tim Goodship Professor Neil Sheerin
| Complement polymorphisms: Geographical distribution and relevance to disease | 2012 |
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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 |
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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 |
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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 |
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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 |
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Dr Ian Wilson Darren Houniet Dr Mauro Santibanez Koref
| Finding genes that influence quantitative traits with tree-based clustering | 2011 |
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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 |
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Professor Hing Leung Dr Ian Wilson
| A Predominantly Neolithic Origin for European Paternal Lineages | 2010 |
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Dr Ian Wilson
| Demography, Ascertainment and the Genealogy of haplotype blocks | 2008 |
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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 |
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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 |
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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 |
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Dr Ian Wilson
| A worldwide phylogeography for the human X chromosome | 2007 |
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Dr Ian Wilson
| Molecular and evolutionary epidemiology of Schistosoma mansoni in human hosts | 2007 |
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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 |
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Dr Ian Wilson
| Slow fiber cluster pattern in pig longissimus thoracis muscle: Implications for myogenesis | 2005 |
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Dr Ian Wilson
| A model for bacterial conjugal gene transfer on solid surfaces | 2003 |
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Dr Ian Wilson
| Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities | 2003 |
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Dr Ian Wilson
| Assessment of mechanism of acquired skewed X inactivation by analysis of twins | 2001 |
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Dr Ian Wilson Lesley Noble
| Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid | 2001 |
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Dr Ian Wilson
| Inferring population history from microsatellite and enzyme data in serially introduced cane toads, Bufo marinus | 2001 |
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Dr Ian Wilson
| Discussion of Stephens M, Donnelly P. Inference in molecular population genetics | 2000 |
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