Gavin Hudson
Gavin Hudson
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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
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
Inherited mitochondrial optic neuropathies
P Yu-Wai-Man, PG Griffiths, G Hudson, PF Chinnery
Journal of medical genetics 46 (3), 145-158, 2009
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD study
AJ Yarnall, DP Breen, GW Duncan, TK Khoo, SY Coleman, MJ Firbank, ...
Neurology 82 (4), 308-316, 2014
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA–haplogroup background
G Hudson, V Carelli, L Spruijt, M Gerards, C Mowbray, A Achilli, A Pyle, ...
The American Journal of Human Genetics 81 (2), 228-233, 2007
Mitochondrial genetics
PF Chinnery, G Hudson
British medical bulletin 106 (1), 135-159, 2013
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
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
Mitochondrial DNA polymerase-γ and human disease
G Hudson, PF Chinnery
Human molecular genetics 15 (suppl_2), R244-R252, 2006
Mutant POLG2 disrupts DNA polymerase γ subunits and causes progressive external ophthalmoplegia
MJ Longley, S Clark, CYW Man, G Hudson, SE Durham, RW Taylor, ...
The American Journal of Human Genetics 78 (6), 1026-1034, 2006
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy
C Giordano, L Iommarini, L Giordano, A Maresca, A Pisano, ML Valentino, ...
Brain 137 (2), 335-353, 2014
A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy
D Hicks, A Sarkozy, N Muelas, K Köehler, A Huebner, G Hudson, ...
Brain 134 (1), 171-182, 2011
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Human molecular genetics 20 (2), 345-353, 2011
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder
G Hudson, S Keers, PYW Man, P Griffiths, K Huoponen, ML Savontaus, ...
The American Journal of Human Genetics 77 (6), 1086-1091, 2005
Epigenetics, epidemiology and mitochondrial DNA diseases
PF Chinnery, HR Elliott, G Hudson, DC Samuels, CL Relton
International journal of epidemiology 41 (1), 177-187, 2012
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations
P Yu-Wai-Man, PG Griffiths, A Burke, PW Sellar, MP Clarke, L Gnanaraj, ...
Ophthalmology 117 (8), 1538-1546. e1, 2010
Reduced mitochondrial DNA copy number is a biomarker of Parkinson's disease
A Pyle, H Anugrha, M Kurzawa-Akanbi, A Yarnall, D Burn, G Hudson
Neurobiology of Aging 38, 216. e7-216. e10, 2016
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases
G Hudson, A Gomez-Duran, IJ Wilson, PF Chinnery
PLoS Genet 10 (5), e1004369, 2014
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
G Hudson, M Nalls, JR Evans, DP Breen, S Winder-Rhodes, KE Morrison, ...
Neurology 80 (22), 2042-2048, 2013
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