| Periodontitis and diabetes: a two-way relationship PM Preshaw, AL Alba, D Herrera, S Jepsen, A Konstantinidis, ... Diabetologia 55, 21-31, 2012 | 2338 | 2012 |
| Mitochondrial DNA mutations in human disease RW Taylor, DM Turnbull Nature Reviews Genetics 6 (5), 389-402, 2005 | 2293 | 2005 |
| High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease A Bender, KJ Krishnan, CM Morris, GA Taylor, AK Reeve, RH Perry, ... Nature genetics 38 (5), 515-517, 2006 | 1836 | 2006 |
| Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease GS Gorman, AM Schaefer, Y Ng, N Gomez, EL Blakely, CL Alston, ... Annals of neurology 77 (5), 753-759, 2015 | 1033 | 2015 |
| Mitochondrial DNA mutations and human disease HAL Tuppen, EL Blakely, DM Turnbull, RW Taylor Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (2), 113-128, 2010 | 860 | 2010 |
| Prevalence of mitochondrial DNA disease in adults AM Schaefer, R McFarland, EL Blakely, L He, RG Whittaker, RW Taylor, ... Annals of Neurology: Official Journal of the American Neurological …, 2008 | 733 | 2008 |
| Mitochondrial DNA mutations in human colonic crypt stem cells RW Taylor, MJ Barron, GM Borthwick, A Gospel, PF Chinnery, ... The Journal of clinical investigation 112 (9), 1351-1360, 2003 | 633 | 2003 |
| Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study COVIDSurg Collaborative Anaesthesia 76 (6), 748-758, 2021 | 598* | 2021 |
| Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease L Craven, HA Tuppen, GD Greggains, SJ Harbottle, JL Murphy, LM Cree, ... Nature 465 (7294), 82-85, 2010 | 577 | 2010 |
| Genetic diagnosis of Mendelian disorders via RNA sequencing LS Kremer, DM Bader, C Mertes, R Kopajtich, G Pichler, A Iuso, TB Haack, ... Nature communications 8 (1), 15824, 2017 | 571 | 2017 |
| The epidemiology of pathogenic mitochondrial DNA mutations PF Chinnery, MA Johnson, TM Wardell, R Singh‐Kler, C Hayes, ... Annals of Neurology: Official Journal of the American Neurological …, 2000 | 567 | 2000 |
| The epidemiology of mitochondrial disorders—past, present and future AM Schaefer, RW Taylor, DM Turnbull, PF Chinnery Biochimica et Biophysica Acta (BBA)-Bioenergetics 1659 (2-3), 115-120, 2004 | 533 | 2004 |
| 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 | 524 | 2017 |
| Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of … G Hudson, P Amati-Bonneau, EL Blakely, JD Stewart, L He, AM Schaefer, ... Brain 131 (2), 329-337, 2008 | 508 | 2008 |
| 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 | 469 | 2008 |
| Multi-system neurological disease is common in patients with OPA1 mutations P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ... Brain 133 (3), 771-786, 2010 | 465 | 2010 |
| Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ... Brain 129 (7), 1674-1684, 2006 | 461 | 2006 |
| Universal heteroplasmy of human mitochondrial DNA BAI Payne, IJ Wilson, P Yu-Wai-Man, J Coxhead, D Deehan, R Horvath, ... Human molecular genetics 22 (2), 384-390, 2013 | 440 | 2013 |
| Biochemical assays of respiratory chain complex activity DM Kirby, DR Thorburn, DM Turnbull, RW Taylor Methods in cell biology 80, 93-119, 2007 | 427 | 2007 |
| Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies RW Taylor, A Pyle, H Griffin, EL Blakely, J Duff, L He, T Smertenko, ... Jama 312 (1), 68-77, 2014 | 400 | 2014 |
Robert McFarlandNewcastle UniversityVerified email at ncl.ac.uk