Patrick F Chinnery
Patrick F Chinnery
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Cited by
Cited by
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
RM Andrews, I Kubacka, PF Chinnery, RN Lightowlers, DM Turnbull, ...
Nature genetics 23 (2), 147-147, 1999
Mitochondrial diseases
GS Gorman, PF Chinnery, S DiMauro, M Hirano, Y Koga, R McFarland, ...
Nature reviews Disease primers 2 (1), 1-22, 2016
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
The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease
JB Stewart, PF Chinnery
Nature Reviews Genetics 16 (9), 530-542, 2015
The human phenotype ontology in 2017
S K÷hler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S AymÚ, ...
Nucleic acids research 45 (D1), D865-D876, 2017
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 Neurologicalá…, 2008
Disturbed mitochondrial dynamics and neurodegenerative disorders
F BurtÚ, V Carelli, PF Chinnery, P Yu-Wai-Man
Nature reviews neurology 11 (1), 11-24, 2015
Pathogenic mitochondrial DNA mutations are common in the general population
HR Elliott, DC Samuels, JA Eden, CL Relton, PF Chinnery
The American journal of human genetics 83 (2), 254-260, 2008
A unique gene regulatory network resets the human germline epigenome for development
WWC Tang, S Dietmann, N Irie, HG Leitch, VI Floros, CR Bradshaw, ...
Cell 161 (6), 1453-1467, 2015
Mitochondrial optic neuropathies–disease mechanisms and therapeutic strategies
P Yu-Wai-Man, PG Griffiths, PF Chinnery
Progress in retinal and eye research 30 (2), 81-114, 2011
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
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease
RN Lightowlers, PF Chinnery, DM Turnbull, N Howell
Trends in Genetics 13 (11), 450-455, 1997
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
ARJ Curtis, C Fey, CM Morris, LA Bindoff, PG Ince, PF Chinnery, ...
Nature genetics 28 (4), 350-354, 2001
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population
FLM Norwood, C Harling, PF Chinnery, M Eagle, K Bushby, V Straub
Brain 132 (11), 3175-3186, 2009
Leber hereditary optic neuropathy
PYW Man, DM Turnbull, PF Chinnery
Journal of medical genetics 39 (3), 162-169, 2002
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
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 Neurologicalá…, 2000
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
LM Cree, DC Samuels, SC de Sousa Lopes, HK Rajasimha, ...
Nature genetics 40 (2), 249-254, 2008
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
A randomized placebo-controlled trial of idebenone in Leber’s hereditary optic neuropathy
T Klopstock, P Yu-Wai-Man, K Dimitriadis, J Rouleau, S Heck, M Bailie, ...
Brain 134 (9), 2677-2686, 2011
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