Robert W Taylor

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Robert McFarlandNewcastle UniversityAdresse e-mail validée de ncl.ac.uk
Doug TurnbullProfessor of Neurology, Newcastle UniversityAdresse e-mail validée de newcastle.ac.uk
Patrick F ChinneryUniversity of CambridgeAdresse e-mail validée de medschl.cam.ac.uk
Dr Charlotte L AlstonWellcome Centre for Mitochondrial ResearchAdresse e-mail validée de ncl.ac.uk
Grainne S GormanWellcome Trust Centre for Mitochondrial Research, ION, Newcastle UniversityAdresse e-mail validée de ncl.ac.uk
Rita HorvathUniversity of CambridgeAdresse e-mail validée de medschl.cam.ac.uk
Yi Shiau NgNewcastle upon Tyne Hospitals NHS Foundation TrustAdresse e-mail validée de ncl.ac.uk
Laura GreavesResearch Fellow, Newcastle UniversityAdresse e-mail validée de ncl.ac.uk
Amy K ReeveNewcastle UniversityAdresse e-mail validée de ncl.ac.uk
Gavin HudsonNewcastle UniversityAdresse e-mail validée de ncl.ac.uk
Prokisch HInstitute of Human Genetics TU-MunichAdresse e-mail validée de helmholtz-munich.de
david thorburnmurdoch children's research instituteAdresse e-mail validée de mcri.edu.au
Laurence BindoffUnversity of Bergen & Haukeland University HospitalAdresse e-mail validée de uib.no
Dr John Patrick GradyGarvan InstituteAdresse e-mail validée de garvan.org.au
Hanna MichaelUCL Institute of NeurologyAdresse e-mail validée de ucl.ac.uk
Joanna PoultonProfessor of Mitochondrial Genetics, University of Oxford, UKAdresse e-mail validée de wrh.ox.ac.uk
Roger WhittakerAdresse e-mail validée de ncl.ac.uk
Mariana RochaAdresse e-mail validée de newcastle.ac.uk
Kieren Grant HollingsworthTranslational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle UniversityAdresse e-mail validée de newcastle.ac.uk
Amy VincentNUAcT Fellow, Newcastle University, UKAdresse e-mail validée de ncl.ac.uk

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Robert W Taylor

Newcastle University

Adresse e-mail validée de ncl.ac.uk

mitochondrial genetics and disease


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Periodontitis and diabetes: a two-way relationship PM Preshaw, AL Alba, D Herrera, S Jepsen, A Konstantinidis, ... Diabetologia 55, 21-31, 2012	2309	2012
Mitochondrial DNA mutations in human disease RW Taylor, DM Turnbull Nature Reviews Genetics 6 (5), 389-402, 2005	2308	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	1837	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	1039	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	865	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	736	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	637	2003
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	577	2017
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	575	2010
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	558	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	532	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	527	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
Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study D Lobo, JM Devys Anaesthesia 77 (1), 110, 2021	473*	2021
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	472	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	470	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	436	2013
Biochemical assays of respiratory chain complex activity DM Kirby, DR Thorburn, DM Turnbull, RW Taylor Methods in cell biology 80, 93-119, 2007	425	2007
Mitochondrial DNA and disease LC Greaves, AK Reeve, RW Taylor, DM Turnbull The Journal of pathology 226 (2), 274-286, 2012	403	2012

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