Robert W Taylor

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Robert McFarlandNewcastle UniversityEmail verificata su ncl.ac.uk
Doug TurnbullProfessor of Neurology, Newcastle UniversityEmail verificata su newcastle.ac.uk
Patrick F ChinneryUniversity of CambridgeEmail verificata su medschl.cam.ac.uk
Dr Charlotte L AlstonWellcome Centre for Mitochondrial ResearchEmail verificata su ncl.ac.uk
Grainne S GormanWellcome Trust Centre for Mitochondrial Research, ION, Newcastle UniversityEmail verificata su ncl.ac.uk
Rita HorvathUniversity of CambridgeEmail verificata su medschl.cam.ac.uk
Yi Shiau NgNewcastle upon Tyne Hospitals NHS Foundation TrustEmail verificata su ncl.ac.uk
Laura GreavesResearch Fellow, Newcastle UniversityEmail verificata su ncl.ac.uk
Amy K ReeveNewcastle UniversityEmail verificata su ncl.ac.uk
Gavin HudsonNewcastle UniversityEmail verificata su ncl.ac.uk
Prokisch HInstitute of Human Genetics TU-MunichEmail verificata su helmholtz-munich.de
david thorburnmurdoch children's research instituteEmail verificata su mcri.edu.au
Laurence BindoffUnversity of Bergen & Haukeland University HospitalEmail verificata su uib.no
Dr John Patrick GradyGarvan InstituteEmail verificata su garvan.org.au
Hanna MichaelUCL Institute of NeurologyEmail verificata su ucl.ac.uk
Joanna PoultonProfessor of Mitochondrial Genetics, University of Oxford, UKEmail verificata su wrh.ox.ac.uk
Mariana RochaEmail verificata su newcastle.ac.uk
Roger WhittakerEmail verificata su ncl.ac.uk
Kieren Grant HollingsworthTranslational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle UniversityEmail verificata su newcastle.ac.uk
Amy VincentNUAcT Fellow, Newcastle University, UKEmail verificata su ncl.ac.uk

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Robert W Taylor

Newcastle University

Email verificata su ncl.ac.uk

mitochondrial genetics and disease


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Periodontitis and diabetes: a two-way relationship PM Preshaw, AL Alba, D Herrera, S Jepsen, A Konstantinidis, ... Diabetologia 55, 21-31, 2012	2326	2012
Mitochondrial DNA mutations in human disease RW Taylor, DM Turnbull Nature Reviews Genetics 6 (5), 389-402, 2005	2316	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	1842	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	1046	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	867	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	737	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	639	2003
Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study D Lobo, JM Devys Anaesthesia 77 (1), 110, 2021	589*	2021
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	578	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	577	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	559	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	530	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	473	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	427	2007
Mitochondrial DNA and disease LC Greaves, AK Reeve, RW Taylor, DM Turnbull The Journal of pathology 226 (2), 274-286, 2012	404	2012

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