Doug Turnbull
Doug Turnbull
Professor of Neurology, Newcastle University
Verified email at
Cited by
Cited by
Mitochondrial DNA mutations in human disease
RW Taylor, DM Turnbull
Nature Reviews Genetics 6 (5), 389-402, 2005
Ageing and Parkinson's disease: why is advancing age the biggest risk factor?
A Reeve, E Simcox, D Turnbull
Ageing research reviews 14, 19-30, 2014
What causes mitochondrial DNA deletions in human cells?
KJ Krishnan, AK Reeve, DC Samuels, PF Chinnery, JK Blackwood, ...
Nature genetics 40 (3), 275, 2008
Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis
GR Campbell, I Ziabreva, AK Reeve, KJ Krishnan, R Reynolds, O Howell, ...
Annals of neurology 69 (3), 481-492, 2011
Mitochondrial DNA and disease
LC Greaves, AK Reeve, RW Taylor, DM Turnbull
The Journal of pathology 226 (2), 274-286, 2012
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
PF Chinnery, DR Thorburn, DC Samuels, SL White, HHM Dahl, ...
Trends in Genetics 16 (11), 500-505, 2000
The genetics and pathology of mitochondrial disease
CL Alston, MC Rocha, NZ Lax, DM Turnbull, RW Taylor
The Journal of pathology 241 (2), 236-250, 2017
Mutations causing mitochondrial disease: What is new and what challenges remain?
RN Lightowlers, RW Taylor, DM Turnbull
Science 349 (6255), 1494-1499, 2015
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A> G mitochondrial point mutation
R Murphy, DM Turnbull, M Walker, AT Hattersley
Diabetic Medicine 25 (4), 383-399, 2008
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m. 3243A> G mutation—implications for diagnosis and management
V Nesbitt, RDS Pitceathly, DM Turnbull, RW Taylor, MG Sweeney, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (8), 936-938, 2013
Mitochondria and disease progression in multiple sclerosis
D Mahad, H Lassmann, D Turnbull
Neuropathology and applied neurobiology 34 (6), 577-589, 2008
Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement
J Betts, E Jaros, RH Perry, AM Schaefer, RW Taylor, Z Abdel‐All, ...
Neuropathology and applied neurobiology 32 (4), 359-373, 2006
Mitochondrial DNA mutations in disease, aging, and neurodegeneration
AK Reeve, KJ Krishnan, D Turnbull
Annals of the New York Academy of Sciences 1147 (1), 21-29, 2008
Increased mitochondrial content in remyelinated axons: implications for multiple sclerosis
JL Zambonin, C Zhao, N Ohno, GR Campbell, S Engeham, I Ziabreva, ...
Brain 134 (7), 1901-1913, 2011
Fatty acid oxidation is required for the respiration and proliferation of malignant glioma cells
H Lin, S Patel, VS Affleck, I Wilson, DM Turnbull, AR Joshi, R Maxwell, ...
Neuro-oncology 19 (1), 43-54, 2017
Mitochondrial DNA Depletion in Respiratory Chain–Deficient P arkinson Disease Neurons
A Grünewald, KA Rygiel, PD Hepplewhite, CM Morris, M Picard, ...
Annals of neurology 79 (3), 366-378, 2016
Variation in the calpain-10 gene affects blood glucose levels in the British population
S Lynn, JC Evans, C White, TM Frayling, AT Hattersley, DM Turnbull, ...
Diabetes 51 (1), 247-250, 2002
Recent advances in mitochondrial disease
L Craven, CL Alston, RW Taylor, DM Turnbull
Annual review of genomics and human genetics 18, 257-275, 2017
Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies
PF Chinnery, GA Taylor, N Howell, RM Andrews, CM Morris, RW Taylor, ...
Neurology 55 (2), 302-304, 2000
The ageing mitochondrial genome
KJ Krishnan, LC Greaves, AK Reeve, D Turnbull
Nucleic acids research 35 (22), 7399-7405, 2007
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