Browsing publications by Dr Ian Wilson

Newcastle AuthorsTitleYearFull text
Dr Ian Wilson
Pip Carling
Charlotte Alston
Vasileios Floros
Dr Angela Pyle
et al.
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck2016
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 Brian Wilson
Professor Judith Goodship
Dr Ian Wilson
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care2015
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
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