| Mitochondrial DNA mutations in human disease RW Taylor, DM Turnbull Nature Reviews Genetics 6 (5), 389-402, 2005 | 2177 | 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 | 994 | 2014 |
| 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 | 555 | 2003 |
| Mitochondrial genetics PF Chinnery, G Hudson British medical bulletin 106 (1), 135-159, 2013 | 489 | 2013 |
| 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 | 466 | 2017 |
| 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 | 457 | 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 | 420 | 2011 |
| 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 | 383 | 2001 |
| Mitochondrial DNA and disease LC Greaves, AK Reeve, RW Taylor, DM Turnbull The Journal of pathology 226 (2), 274-286, 2012 | 374 | 2012 |
| Mutations causing mitochondrial disease: What is new and what challenges remain? RN Lightowlers, RW Taylor, DM Turnbull Science 349 (6255), 1494-1499, 2015 | 339 | 2015 |
| 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 | 329 | 1994 |
| 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 | 325 | 2000 |
| 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 | 298 | 2008 |
| Mitochondrial diseases: hope for the future OM Russell, GS Gorman, RN Lightowlers, DM Turnbull Cell 181 (1), 168-188, 2020 | 295 | 2020 |
| 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 | 277 | 2005 |
| 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 | 265 | 2013 |
| Recent advances in mitochondrial disease L Craven, CL Alston, RW Taylor, DM Turnbull Annual review of genomics and human genetics 18, 257-275, 2017 | 246 | 2017 |
| 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 | 240 | 2004 |
| 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 | 233 | 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 | 229 | 2016 |
