Browsing publications by Dr Ian Wilson

Newcastle AuthorsTitleYear
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 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
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
Rachel Soemedi
Dr Ian Wilson
Dr Rebecca Darlay
Dr Ana Topf
Dr Simon Zwolinksi
et al.
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease2012
Dr Umar Burki
Dr Alison Blain
Dr Ian Wilson
Dr Guillaume Launay
Dr Ross Maxwell
et al.
Development of in vivo imaging techniques to determine the biodistribution of antisense oligonucleotides in dystrophin deficient muscular dystrophy2012
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
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