Follow
Doug Turnbull
Doug Turnbull
Professor of Neurology, Newcastle University
Verified email at newcastle.ac.uk
Title
Cited by
Cited by
Year
Mitochondrial DNA mutations in human disease
RW Taylor, DM Turnbull
Nature Reviews Genetics 6 (5), 389-402, 2005
21622005
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
9832014
The epidemiology of Leber hereditary optic neuropathy in the North East of England
PYW Man, PG Griffiths, DT Brown, N Howell, DM Turnbull, PF Chinnery
The American Journal of Human Genetics 72 (2), 333-339, 2003
5522003
Mitochondrial genetics
PF Chinnery, G Hudson
British medical bulletin 106 (1), 135-159, 2013
4882013
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
4622017
What causes mitochondrial DNA deletions in human cells?
KJ Krishnan, AK Reeve, DC Samuels, PF Chinnery, JK Blackwood, ...
Nature genetics 40 (3), 275-279, 2008
4562008
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
4172011
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age
JL Elson, DC Samuels, DM Turnbull, PF Chinnery
The American Journal of Human Genetics 68 (3), 802-806, 2001
3802001
Mitochondrial DNA and disease
LC Greaves, AK Reeve, RW Taylor, DM Turnbull
The Journal of pathology 226 (2), 274-286, 2012
3722012
Mutations causing mitochondrial disease: What is new and what challenges remain?
RN Lightowlers, RW Taylor, DM Turnbull
Science 349 (6255), 1494-1499, 2015
3382015
An evaluation of the measurement of the activities of complexes I-IV in the respiratory chain of human skeletal muscle mitochondria
MA Birchmachin, HL Briggs, AA Saborido, LA BINDoFF, DM Turnbull
Biochemical medicine and metabolic biology 51 (1), 35-42, 1994
3291994
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
3222000
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
2972008
Mitochondrial diseases: hope for the future
OM Russell, GS Gorman, RN Lightowlers, DM Turnbull
Cell 181 (1), 168-188, 2020
2922020
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase γ mutations
S Winterthun, G Ferrari, L He, RW Taylor, M Zeviani, DM Turnbull, ...
Neurology 64 (7), 1204-1208, 2005
2762005
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
2642013
Recent advances in mitochondrial disease
L Craven, CL Alston, RW Taylor, DM Turnbull
Annual review of genomics and human genetics 18, 257-275, 2017
2442017
Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection
JL Elson, DM Turnbull, N Howell
The American Journal of Human Genetics 74 (2), 229-238, 2004
2402004
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
2322017
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
2262016
The system can't perform the operation now. Try again later.
Articles 1–20