Dr Gavin HudsonResearch Associate
Email: gavin.hudson@ncl.ac.uk Telephone: +44 (0) 191 241 8818 Address: Institute of Human Genetics
Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL. Epigenetics, epidemiology and mitochondrial DNA diseases .
International Journal of Epidemiology 2012, 41 (1), 177-187.
Winder-Rhodes SE, Garcia-Reitbock P, Ban M, Evans JR, Jacques TS, Kemppinen A, Foltynie T, Williams-Gray CH, Chinnery PF, Hudson G, Burn DJ, Allcock LM, Sawcer SJ, Barker RA, Spillantini MG. Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome .
Movement Disorders 2012, 27 (2), 312-315.
Sitarz KS, Yu-Wai-Man P, Hudson G, Jacob A, Boggild M, Horvath R, Chinnery PF. Genetic variations within the OPA1 gene are not associated with neuromyelitis optica .
Multiple Sclerosis 2012, 18 (2), 240-243.
Lythgow KT, Hudson G, Andras P, Chinnery PF. A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization .
Mitochondrion 2011, 11 (3), 444-449.
Hicks D, Sarkozy A, Muelas N, Koehler K, Huebner A, Hudson G, Chinnery PF, Barresi R, Eagle M, Polvikoski T, Bailey G, Miller J, Radunovic A, Hughes PJ, Roberts R, Krause S, Walter MC, Laval SH, Straub V, Lochmuller H, Bushby K. A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy .
In: Neuromuscular Disorders: United Kingdom Neuromuscular Translational Research Conference . 2011, London, UK: Elsevier Ltd.
de Alwis N, Aithal G, Bugianesi E, Leathart J, Hudson G, Pyle A, Mowbray C, Henderson E, Burt AD, Chinnery PF, Day CP. Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver disease .
Mitochondrion 2011, 11 (1), 234-235.
Hudson G, Faini D, Stutt A, Eccles M, Robinson L, Burn DJ, Chinnery PF. No evidence of substantia nigra telomere shortening in Parkinson's disease .
Neurobiology of Aging 2011, 32 (11), 2107.e3.
Hudson G, Yu-Wai-Man P, Griffiths PG, Horvath R, Carelli V, Zeviani M, Chinnery PF. Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON .
Mitochondrion 2011, 11 (4), 620-622.
Hudson G, Yu Wai Man P, Chinnery P. Leber hereditary optic neuropathy .
Expert Opinion on Medical Diagnostics 2008, 2 (7), 789-799.
