Browsing publications by Dr Ian Wilson

Newcastle AuthorsTitleYearFull text
Dr Helen Griffin
Dr Angela Pyle
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 Gerald Pfeffer
Dr 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
Dr 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
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