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Staff Profile

Professor Gavin Hudson

Professor of Mitochondrial Genomics

  • Telephone: +44 (0) 191 241 8650
  • Address: Biosciences Institute
    Wellcome Centre for Mitochondrial Research
    缅北禁地
    4th Floor Cookson Building
    Medical School
    Framlington Place
    缅北禁地 upon Tyne
    NE2 4HH
    UK
Research

Research Area:

Mitochondrial DNA (mtDNA) is highly variable, with individuals easily classified by characteristic clades of inherited variation. My research to date has solidified the role of inherited mtDNA variation in several complex traits. However, we know little of how this inherited mtDNA variation exerts its effect in these complex diseases. Mitochondrial function is dependent on the continued cooperation of both the mitochondrial and nuclear genomes (mtDNA/nDNA communication), raising the possibility that the associations between inherited mtDNA variation and disease are a manifestation of a break in the tightly controlled communication that exists between mtDNA and nDNA.

 

My current research is aimed at improving our understanding of this interaction in human disease and development by:

  1. Directly assessing the role that inherited mtDNA variation plays in these contexts.
  2. Assessing the effect of combinations of mtDNA/nDNA variants in the population on disease.
  3. Assessing the role that inherited mtDNA variation plays is shaping cellular transcriptomics in disease and development.

 

Current Research Projects:

Investigating mitochondrial homeostasis during early development

PhD Student; Jordan Marley

Co-Investigator: Prof Mary Herbert

 

Mitochondrial donation offers the potential to prevent transmission of mtDNA disease. Our work indicates that expansion of mtDNA carried over during pronuclear transfer (PNT) is unpredictable, with highly similar sequences (effectively clones) reverting back to “maternal” type in ~20% of embryonic stem cell lines derived from PNT blastocysts. Among the possible explanations are (i) Preferential replication of mitochondrial genomes located in the peri-nuclear region (ii) Replicative advantage associated with certain mitochondrial genomes (iii) A founder cell effect due to unequal distribution of variant mitochondrial genomes during the early embryonic divisions. The principle aim of this project is to improve our understanding of the roles that mitochondrial function and mitochondrial DNA play in developing embryos. Jordan's PhD will investigate the effects of several key components of mitochondrial function, including mitophagy, mitochondrial DNA variation and transcriptomics on the safety of future MRT experiments. This cross-disciplinary PhD will utilise expertise from the 缅北禁地 Fertility Centre, Institute of Genetic Medicine and Wellcome Centre for Mitochondrial Research.

 

Investigating the role of inherited and acquired mitochondrial DNA variation in neurodegeneration.

Collaborators: Dr Mauro Santibanez-Koref

/igm/staff/profile/maurosantibanez-koref.html#research

 

The aim of this research project is to investigate the role of mitochondrial DNA (mtDNA) variation in neurodegenerative diseases. Previous research during my PDUK senior fellowship (F-1202) has shown that particular mtDNA variants (haplogroups) can protect from or increase the risk of developing PD. I will explore this by investigating the effect of inherited mtDNA variation on cellular transcriptomics in different brain regions from PD patients, comparing RNA abundance to asymptomatic controls.

 

The role of cell-free mtDNA in neurodegenerative disease.

Post-Doctoral Scientist: Dr Hannah Lowes.

 

mtDNA has been found to exist cell-free within human body fluids, coined circulating cell-free mtDNA (ccf-mtDNA). Ccf-mtDNA copy number has been found to be depleted in both Parkinson’s disease (PD) and Alzheimer’s disease (AD) cerebrospinal fluid (CSF), raising the hypothesis that it could be used as a biomarker for neurodegenerative disease. This project utilises a broad clinical spectrum including PD, AD, dementia with Lewy bodies and Multiple Sclerosis, where we will assess the function and integrity of ccf-mtDNA within the CSF to better understand how it contributes to the development and progression of neurodegeneration. This project utilises samples and data from the Parkinson’s Progression Markers Initiative (PPMI).

 

Is circular RNA a biomarker of Parkinson’s Disease?

Co-investigators: Dr Mike Jackson & Dr Mauro Santibanez-Koref

/igm/staff/profile/michaeljackson.html#research

/igm/staff/profile/maurosantibanez-koref.html#research

 

Circular RNAs (circRNAs) are rapidly gaining attention in studies of human disease due to their possible use as clinical biomarkers and their potential to affect gene expression. It is likely that circRNAs play an important role in Parkinson’s disease (PD), possibly correlating to disease pathoetiology or potentially acting as biomarkers which predict PD or the transition to Parkinson’s disease dementia (PDD). However, existing circRNA investigations in PD are very limited.

In this Michael J Fox Foundation funded study, we will characterise and measure the abundance of circRNAs in human tissues (Serum/Blood/Brain), under the hypothesis that specific circRNAs will be significantly different between PD patients and controls and will correlate to clinical and neuropathological hallmarks of PD and PDD. Our ultimate aim is to identify circRNAs that may be viable biomarkers of disease onset and progression. Project URL:

 

Longitudinal study of mitochondrial DNA variant selection enabled by single-cell nanobiopsy

PhD Student; Alex Bury

Co-investigators: Dr Paolo Actis (Leeds), Dr Amy Vincent and Prof Doug Turnbull

 

In postmitotic cells, mtDNA is replicated and destroyed continuously. If a heteroplasmic variant occurs then changes in heteroplasmy level are believed to be dictated by chance (where ‘relaxed replication’ of the mtDNA replicates the mutant mtDNA faster than the wild-type mtDNA). However, traditional approaches to investigating this phenomenon rely on single time-point assessments in laser microdissected tissues, which are unable to assess the changes in heteroplasmy over time and provide little information of the selection of the variant in vivo.

The aim of this MRC-DTP funded PhD is to improve our understanding of mtDNA variant selection in human tissues and live cells by combining novel “nanobiopsy” techniques with next generation sequencing technology. The nanobiopsy technique relies on ultra-sharp quartz nanopipette that can be positioned with nm resolution within the cytoplasm of a living cell to extract intracellular contents without affecting its viability. The nanobiopsy has been validated as a tool for investigating mtDNA heteroplasmy in live cells and within this PhD project it will be employed to measure heteroplasmy segregation and selection during cellular proliferation. By using live cells harbouring different mtDNA heteroplasmic mutations, heteroplasmy levels can be measured serially to investigate both segregation and selectivity of different mtDNA mutations. Cellular heteroplasmy levels will be correlated to cardinal measurements of mitochondrial function to assess selectivity. In addition, the techniques would be expanded and optimised on fresh frozen tissue samples such as human brain, where a cell specific accumulation of mtDNA variation contributes age related phenotypes such as Parkinson’s disease.


Current Funding:

2017, Wellcome Trust Centre for Mitochondrial Research. Genomics Core Theme lead. (As CoI, 5 yrs, awarded £5.9m, with Prof D Turnbull).

 

2018, Michael J Fox Foundation, Project Grant, “The role of circular RNA in Parkinson’s disease and dementia” (As PI, 2 yrs, awarded $185,451).

 

2018, MRC-DTP PhD studentship, “The application of ‘nano-biopsying’ as a tool for NGS and transcriptomics in mitochondria” (AS PI, 3 yrs, awarded £~120,000).

 

2018, Michael J Fox Foundation, Project Grant (As CoI, 2 yrs, awarded £187,000, with Dr Mary Doherty).


Collaborators:

  • Dr Paolo Actis (School of Electronic and Electrical Engineering, Leeds University, UK)
  • Prof David Burn and Dr Alison Yarnall (ICICLE-PD, 缅北禁地, UK)
  • Dr Valerio Carelli (Department of Biomedical and Neuromotor Sciences, Bologna, IT).
  • Prof Patrick Chinnery (Department of Clinical Neurosciences, Cambridge University, UK)
  • Dr Mary Doherty (Centre for Health Science, University of the Highlands and Islands, UK)
  • Dr Aldi Kraja (Charge , Division of Statistical Genetics Washington University , USA)
  • Dr Neil Rajan (Institute of Genetic Medicine, 缅北禁地, UK)
  • Prof Adam Eyre-Walker (School of Life Sciences, Sussex University, UK)

 


Current PhD Students:

  • Jordan Marley (with Prof Mary Herbert, 缅北禁地, UK).
  • Alex Bury (with Dr Paolo Actis, Leeds University, UK).
  • Lauren Phillips (with Drs Simon Bamforth and Helen Phillips, Cardiac Research Centre, 缅北禁地, UK).

 


Previous PhD students

  • Dr Hannah Lowes, “: Cell-free mitochondrial DNA variation in Neurodegenerative disease.”, graduated 2018.
  • Dr Rebecca Brennan, “Genetic factors modulating mitochondrial DNA copy number.”, graduated 2017.
  • Dr Emily Mcilwaine, “Investigating the potential role of recombination regulator PRDM9 in mitochondria.”, graduated 2017.

 


External Committees/Panels:

  • Genomics England GeCIP membership, Neurology and Population Genetics.
  • Multiple Sclerosis and Parkinson's Tissue Bank Review Panel Member (Imperial University, UK).
  • Frontiers in Genetics, editorial board member.
  • Parkinson’s UK 2018 Meeting organising committee.


Publications

  • Articles

    • Hipps D, Pyle A, Porter ALR, Dobson PF, Tuppen H, Lawless C, Russell OM, Turnbull DM, Deehan DJ, Hudson G. . Scientific Reports 2024, 14(1), 20989.
    • Gojanovich GS, Marsit CJ, Kacanek D, Russell J, Hudson G, Van Dyke RB, Naini AB, Gerschenson M. . Mitochondrion 2024, 79, 101949.
    • Bury A, Pyle A, Vincent AE, Actis P, Hudson G. . Scientific Reports 2024, 14(1), 13789.
    • Whittle BJ, Izuogu OG, Lowes H, Deen D, Pyle A, Coxhead J, Lawson RA, Yarnall AJ, Jackson MS, Santibanez-Koref M, Hudson G. . npj Parkinson's Disease 2024, 10, 25.
    • Dobolyi A, Cservenak M, Bago AG, Chen C, Stepanova A, Paal K, Lee J, Palkovits M, Hudson G, Chinopoulos C. . Communications Biology 2024, 7(1), 1045.
    • Xia C, Pickett SJ, Liewald DCM, Weiss A, Hudson G, Hill WD. . Nature Communications 2023, 14(1), 3146.
    • Chen C, McDonald D, Blain A, Mossman E, Atkin K, Marusich MF, Capaldi R, Bone L, Smith A, Filby A, Erskine D, Russell O, Hudson G, Vincent AE, Reeve AK. . npj Parkinson's Disease 2023, 9, 120.
    • Takeda Y, Hyslop L, Choudhary M, Robertson F, Pyle A, Wilson I, Santibanez-Koref M, Turnbull D, Herbert M, Hudson G. . EMBO Reports 2023, 24(10), e54540.
    • Pickett SJ, Deen D, Pyle A, Santibanez-Koref M, Hudson G. . Mitochondrion 2022, 63, 85-88.
    • Calabrese C, Pyle A, Griffin H, Coxhead J, Hussain R, Braund PS, Li L, Burgess A, Munroe PB, Little L, Warren HR, Cabrera C, Hall A, Caulfield MJ, Rothwell PM, Samani NJ, Hudson G, Chinnery PF. . PLoS Genetics 2022, 18(4), e1010068.
    • Szwedo AA, Dalen I, Pedersen KF, Camacho M, Bäckström D, Forsgren L, Tzoulis C, Winder-Rhodes S, Hudson G, Liu G, Scherzer C, Lawson RA, Yarnall AJ, Williams-Gray CH, Macleod AD, Counsell CE, Tysnes OB, Alves G, Maple-Grødem J. . Movement Disorders 2022, 37(5), 1016-1027.
    • Chen C, Mossman E, Malko P, McDonald D, Blain AP, Bone L, Erskine D, Filby A, Vincent AE, Hudson G, Reeve AK. . Movement Disorders 2022, 37(2), 302-314.
    • Kurzawa-Akanbi M, Keogh M, Tsefou E, Ramsay L, Johnson M, Keers S, Ochieng LW, McNair A, Singh P, Khan A, Pyle A, Hudson G, Ince PG, Attems J, Burn J, Chinnery PF, Morris CM. . Neuropathology and Applied Neurobiology 2021, 47(1), 26-42.
    • Roca-Bayerri C, Robertson F, Pyle A, Hudson G, Payne BAI. . Clinical Infectious Diseases 2021, 73(2), e466-e473.
    • Chen C, McDonald D, Blain A, Sachdeva A, Bone L, Smith ALM, Warren C, Pickett SJ, Hudson G, Filby A, Vincent AE, Turnbull DM, Reeve AK. . npj Parkinson's Disease 2021, 7(1), 39.
    • Turro E, Astle WJ, Graf S, Greene D, Allen HL, Frontini M, Stephens J, Downes K, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Caulfield MJ, Chinnery PF, Dixon PH, James R, Laffan MA, Levine AP, Maher ER, Markus HS, Morales J, Morrell NW, Mumford AD, Rankin S, Rendon A, Richardson S, Roberts I, Roy NBA, Saleem MA, Smith KGC, Tan RYY, Thrasher AJ, Watkins H, Webster AR, Wilkins MR, Williamson C, Whitworth J, Humphray S, Abbs S, Abulhoul L, Adlard J, Ahmed M, Aitman TJ, Alachkar H, Allsup DJ, Almeida-King J, Ancliff P, Antrobus R, Armstrong R, Arno G, Ashford S, Astle WJ, Attwood A, Aurora P, Babbs C, Bacchelli C, Bakchoul T, Banka S, Bariana T, Barwell J, Batista J, Baxendale HE, Beales PL, Bennett DL, Bentley DR, Bentley DR, Bierzynska A, Biss T, Bitner-Glindzicz MAK, Black GC, Bleda M, Blesneac I, Bockenhauer D, Bogaard H, Bourne CJ, Boyce S, Bradley JR, Bragin E, Breen G, Brennan P, Brewer C, Brown M, Browning AC, Browning MJ, Buchan RJ, Buckland MS, Bueser T, Diz CB, Burn J, Burns SO, Burren OS, Burren OS, Burrows N, Calleja P, Campbell C, Carr-White G, Carss K, Carss K, Casey R, Caulfield MJ, Chambers J, Chambers J, Chan MMY, Cheah C, Cheng F, Chinnery PF, Chitre M, Christian MT, Church C, Clayton-Smith J, Cleary M, Brod NC, Coghlan G, Colby E, Cole TRP, Collins J, Collins PW, Colombo C, Compton CJ, Condliffe R, Cook S, Cook HT, Cooper N, Corris PA, Furnell A, Cunningham F, Curry NS, Cutler AJ, Daniels MJ, Dattani M, Daugherty LC, Davis J, De Soyza A, Deevi SVV, Dent T, Deshpande C, Dewhurst EF, Dixon PH, Douzgou S, Downes K, Drazyk AM, Drewe E, Duarte D, Dutt T, Edgar JDM, Edwards K, Egner W, Ekani MN, Elliott P, Erber WN, Erwood M, Estiu MC, Evans DG, Evans G, Everington T, Eyries M, Fassihi H, Favier R, Findhammer J, Fletcher D, Flinter FA, Floto RA, Fowler T, Fox J, Frary AJ, French CE, Freson K, Frontini M, Gale DP, Gale DP, Gall H, Ganesan V, Gattens M, Geoghegan C, Gerighty TSA, Gharavi AG, Ghio S, Ghofrani H-A, Gibbs JSR, Gibson K, Gilmour KC, Girerd B, Gleadall NS, Goddard S, Goldstein DB, Gomez K, Gordins P, Gosal D, Graf S, Graham J, Grassi L, Greene D, Greenhalgh L, Greinacher A, Gresele P, Griffiths P, Grigoriadou S, Grocock RJ, Grozeva D, Gurnell M, Hackett S, Hadinnapola C, Hague WM, Hague R, Haimel M, Haimel M, Hall M, Hanson HL, Haque E, Harkness K, Harper AR, Harris CL, Hart D, Hassan A, Hayman G, Henderson A, Herwadkar A, Hoffman J, Holden S, Horvath R, Houlden H, Houweling AC, Howard LS, Hu F, Hudson G, Hughes J, Huissoon AP, Humbert M, Humphray S, Hunter S, Hurles M, Irving M, Izatt L, James R, Johnson SA, Jolles S, Jolley J, Josifova D, Jurkute N, Karten T, Karten J, Kasanicki MA, Kazkaz H, Kazmi R, Kelleher P, Kelly AM, Kelsall W, Kempster C, Kiely DG, Kingston N, Klima R, Koelling N, Kostadima M, Kovacs G, Koziell A, Koziell A, Kreuzhuber R, Kuijpers TW, Kumar A, Kumararatne D, Kurian MA, Laffan MA, Lalloo F, Lambert M, Allen HL, Lawrie A, Layton DM, Lench N, Lentaigne C, Lester T, Levine AP, Linger R, Longhurst H, Lorenzo LE, Louka E, Lyons PA, Machado RD, MacKenzie Ross RV, Madan B, Maher ER, Maimaris J, Malka S, Mangles S, Mapeta R, Mapeta R, Marchbank KJ, Marks S, Markus HS, Marschall H-U, Marshall A, Martin J, Mathias M, Matthews E, Maxwell H, McAlinden P, McCarthy MI, McKinney H, McMahon A, Meacham S, Mead AJ, Castello IM, Megy K, Megy K, Mehta SG, Michaelides M, Millar C, Mohammed SN, Moledina S, Montani D, Moore AT, Morales J, Morrell NW, Mozere M, Muir KW, Mumford AD, Nemeth AH, Newman WG, Newnham M, Noorani S, Nurden P, O'Sullivan J, Obaji S, Odhams C, Okoli S, Olschewski A, Olschewski H, Ong KR, Oram SH, Ormondroyd E, Ormondroyd E, Ouwehand WH, Palles C, Papadia S, Park S-M, Parry D, Patel S, Paterson J, Peacock A, Pearce SH, Peden J, Peerlinck K, Pepke-Zaba J, Petersen R, Pilkington C, Poole KES, Prathalingam R, Psaila B, Pyle A, Quinton R, Rahman S, Rankin S, Rao A, Raymond FL, Rayner-Matthews PJ, Rees C, Rendon A, Renton T, Rhodes CJ, Rice ASC, Richardson S, Richter A, Robert L, Roberts I, Rogers A, Rose SJ, Ross-Russell R, Roughley C, Roy NBA, Ruddy DM, Sadeghi-Alavijeh O, Saleem MA, Samani N, Samarghitean C, Sanchis-Juan A, Sanchis-Juan A, Sargur RB, Sarkany RN, Satchell S, Savic S, Sayer JA, Sayer G, Scelsi L, Schaefer AM, Schulman S, Scott R, Scully M, Searle C, Seeger W, Sen A, Sewell WAC, Seyres D, Shah N, Shamardina O, Shamardina O, Shapiro SE, Shaw AC, Short PJ, Sibson K, Side L, Simeoni I, Simpson MA, Sims MC, Sivapalaratnam S, Smedley D, Smith KR, Smith KGC, Snape K, Soranzo N, Soubrier F, Southgate L, Spasic-Boskovic O, Staines S, Staples E, Stark H, Stark H, Stephens J, Steward C, Stirrups KE, Stuckey A, Suntharalingam J, Swietlik EM, Syrris P, Tait RC, Talks K, Tan RYY, Tate K, Taylor JM, Taylor JC, Thaventhiran JE, Themistocleous AC, Themistocleous AC, Thomas E, Thomas D, Thomas MJ, Thomas P, Thomson K, Thrasher AJ, Threadgold G, Thys C, Thys C, Tilly T, Tischkowitz M, Titterton C, Todd JA, Toh C-H, Tolhuis B, Tomlinson IP, Toshner M, Traylor M, Treacy C, Treadaway P, Trembath R, Tuna S, Turek W, Turro E, Twiss P, Vale T, Geet CV, Zuydam N, Vandekuilen M, Vandersteen AM, Vazquez-Lopez M, von Ziegenweidt J, Noordegraaf AV, Wagner A, Waisfisz Q, Walker SM, Walker N, Walter K, Ware JS, Watkins H, Watt C, Webster AR, Wedderburn L, Wei W, Welch SB, Wessels J, Westbury SK, Westwood J-P, Wharton J, Whitehorn D, Whitworth J, Wilkie AOM, Wilkins MR, Williamson C, Wilson BT, Wong EKS, Wood N, Wood Y, Woods CG, Woodward ER, Wort SJ, Worth A, Wright M, Yates K, Yong PFK, Young T, Yu P, Yu-Wai-Man P, Zlamalova E, Kingston N, Walker N, Bradley JR, Ashford S, Penkett CJ, Penkett CJ, Freson K, Stirrups KE, Raymond FL, Ouwehand WH. . Nature 2020, 583, 96-102.
    • Lowes H, Kurzawa-Akanbi M, Pyle A, Hudson G. . Scientific Reports 2020, 10, 15253.
    • Bury A, Vincent AE, Turnbull DM, Actis P, Hudson G. . Wellcome Open Research 2020, 5, 226.
    • Lowes H, Pyle A, Santibanez-Koref M, Hudson G. . Molecular Neurodegeneration 2020, 15(1).
    • Smith ALM, Whitehall JC, Bradshaw C, Gay D, Robertson F, Blain AP, Hudson G, Pyle A, Houghton D, Hunt M, Sampson JN, Stamp C, Mallett G, Amarnath S, Leslie J, Oakley F, Wilson L, Baker A, Russell OM, Johnson R, Richardson CA, Gupta B, McCallum I, McDonald SAC, Kelly S, Mathers JC, Heer R, Taylor RW, Perkins ND, Turnbull DM, Sansom OJ, Greaves LC. . Nature Cancer 2020, 1, 976-989.
    • Kanagasundaram NS, Baudouin SV, Rowling S, Prabhu M, Dark JH, Goodship THJ, Chinnery PF, Hudson G. . Scientific Reports 2019, 9, 2279.
    • Lowes H, Pyle A, Duddy M, Hudson G. . Mitochondrion 2019, 46, 307-312.
    • Kraja AT, Liu C, Fetterman JL, Graff M, Have CT, Gu C, Yanek LR, Feitosa MF, Arking DE, Chasman DI, Young K, Ligthart S, Hill WD, Weiss S, Luan J, Giulianini F, Li-Gao R, Hartwig FP, Lin SJ, Wang L, Richardson TG, Yao J, Fernandez EP, Ghanbari M, Wojczynski MK, Lee W-J, Argos M, Armasu SM, Barve RA, Ryan KA, An P, Baranski TJ, Bielinski SJ, Bowden DW, Broeckel U, Christensen K, Chu AY, Corley J, Cox SR, Uitterlinden AG, Rivadeneira F, Cropp CD, Daw EW, van Heemst D, de las Fuentes L, Gao H, Tzoulaki I, Ahluwalia TS, de Mutsert R, Emery LS, Erzurumluoglu AM, Perry JA, Fu M, Forouhi NG, Gu Z, Hai Y, Harris SE, Hemani G, Hunt SC, Irvin MR, Jonsson AE, Justice AE, Kerrison ND, Larson NB, Lin K-H, Love-Gregory LD, Mathias RA, Lee JH, Nauck M, Noordam R, Ong KK, Pankow J, Patki A, Pattie A, Petersmann A, Qi Q, Ribel-Madsen R, Rohde R, Sandow K, Schnurr TM, Sofer T, Starr JM, Taylor AM, Teumer A, Timpson NJ, de Haan HG, Wang Y, Weeke PE, Williams C, Wu H, Yang W, Zeng D, Witte DR, Weir BS, Wareham NJ, Vestergaard H, Turner ST, Torp-Pedersen C, Stergiakouli E, Sheu WH-H, Rosendaal FR, Ikram MA, Franco OH, Ridker PM, Perls TT, Pedersen O, Nohr EA, Newman AB, Linneberg A, Langenberg C, Kilpelainen TO, Kardia SLR, Jorgensen ME, Jorgensen T, Sorensen TIA, Homuth G, Hansen T, Goodarzi MO, Deary IJ, Christensen C, Chen Y-DI, Chakravarti A, Brandslund I, Bonnelykke K, Taylor KD, Wilson JG, Rodriguez S, Davies G, Horta BL, Thyagarajan B, Rao DC, Grarup N, Davila-Roman VG, Hudson G, Guo X, Arnett DK, Hayward C, Vaidya D, Mook-Kanamori DO, Tiwari HK, Levy D, Loos RJF, Dehghan A, Elliott P, Malik AN, Scott RA, Becker DM, de Andrade M, Province MA, Meigs JB, Rotter JI, North KE. . American Journal of Human Genetics 2019, 104(1), 112-138.
    • Santibanez-Koref M, Griffin H, Turnbull DM, Chinnery PF, Herbert M, Hudson G. . Mitochondrion 2019, 46, 302-306.
    • Guyatt AL, Brennan RR, Burrows K, Guthrie PAI, Ascione R, Ring SM, Gaunt TR, Pyle A, Cordell HJ, Lawlor DA, Chinnery PF, Hudson G, Rodriguez S. . Human Genomics 2019, 13, 6.
    • Burns DT, Donkervoort S, Muller JS, Knierim E, Bharucha-Goebel D, Faqeih EA, Bell SK, AlFaifi AY, Monies D, Millan F, Retterer K, Dyack S, MacKay S, Morales-Gonzalez S, Giunta M, Munro B, Hudson G, Scavina M, Baker L, Massini TC, Lek M, Hu Y, Ezzo D, AlKuraya FS, Kang PB, Griffin H, Foley AR, Schuelke M, Horvath R, Bonnemann CG. . American Journal of Human Genetics 2018, 102(5), 858-873.
    • Floros VI, Pyle A, Dietmann S, Wei W, Tang WWC, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF. . Nature Cell Biology 2018, 20, 144-151.
    • Connor TM, Hoer S, Mallett A, Gale DP, Gomez-Duran A, Posse V, Antrobus R, Moreno P, Sciacovelli M, Frezza C, Duff J, Sheerin NS, Sayer JA, Ashcroft M, Wiesener MS, Hudson G, Gustafsson CM, Chinnery PF, Maxwell PH. . PLoS Genetics 2017, 13(3), e1006620.
    • Bury AG, Pyle A, Elson JL, Greaves L, Morris CM, Hudson G, Pienaar IS. . Annals of Neurology 2017, 82(6), 1016-1021.
    • Burte F, Houghton D, Lowes H, Pyle A, Nesbitt S, Yarnall A, Yu-Wai-Man P, Burn DJ, Santibanez-Koref M, Hudson G. . Movement Disorders 2017, 32(6), 927–932.
    • Witoelar A, Jansen IE, Wang Y, Desikan RS, Gibbs JR, Blauwendraat C, Thompson WK, Hernandez DG, Djurovic S, Schork AJ, Bettella F, Ellinghaus D, Franke A, Lie BA, McEvoy LK, Karlsen TH, Lesage S, Morris HR, Brice A, Wood NW, Heutink P, Hardy J, Singleton AB, Dale AM, Gasser T, Andreassen OA, Sharma M, Nalls MA, Plagnol V, Sheerin U-M, Saad M, Simon-Sanchez J, Schulte C, Sveinbjornsdottir S, Arepalli S, Barker R, Ben-Shlomo Y, Berendse HW, Berg D, Bhatia K, De Bie RMA, Biffi A, Bloem B, Bochdanovits Z, Bonin M, Bras JM, Brockmann K, Brooks J, Burn DJ, Majounie E, Charlesworth G, Lungu C, Chen H, Chinnery PF, Chong S, Clarke CE, Cookson MR, Cooper JM, Corvol JC, Counsell C, Damier P, Dartigues J-F, Deloukas P, Deuschl G, Dexter DT, Van Dijk KD, Dillman A, Durif F, Durr A, Edkins S, Evans JR, Foltynie T, Dong J, Gardner M, Goate A, Gray E, Guerreiro R, Harris C, Van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang X, Wurster I, Matzler W, Hudson G, Hunt SE, Huttenlocher J, Illig T, Jonsson PV, Lambert J-C, Langford C, Lees A, Lichtner P, Limousin P, Lopez G, Lorenz D, McNeill A, Moorby C, Moore M, Morrison KE, Escott-Price V, Mudanohwo E, O'Sullivan SS, Pearson J, Perlmutter JS, Petursson H, Pollak P, Post B, Potter S, Ravina B, Revesz T, Riess O, Rivadeneira F, Rizzu P, Ryten M, Sawcer S, Schapira A, Scheffer H, Shaw K, Shoulson I, Shulman J, Sidransky E, Smith C, Spencer CCA, Stefansson H, Stockton JD, Strange A, Talbot K, Tanner CM, Tashakkori-Ghanbaria A, Tison F, Trabzuni D, Traynor BJ, Uitterlinden AG, Velseboer D, Vidailhet M, Walker R, Van De Warrenburg B, Wickremaratchi M, Williams N, Williams-Gray CH, Winder-Rhodes S, Stefansson K, Martinez M, Ferrucci L, Johnson R, Longo DL, Nalls MA, O'Brien R, Troncoso J, Van Der Brug M, Zielke HR, Zonderman A, Hardy JA, Weale M. . JAMA Neurology 2017, 74(7), 780-792.
    • Jansen IE, Ye H, Heetveld S, Lechler MC, Michels H, Seinstra RI, Lubbe SJ, Drouet V, Lesage S, Majounie E, Gibbs JR, Nalls MA, Ryten M, Botia JA, Vandrovcova J, Simon-Sanchez J, Castillo-Lizardo M, Rizzu P, Blauwendraat C, Chouhan AK, Li Y, Yogi P, Amin N, van Duijn CM, Morris HR, Brice A, Singleton AB, David DC, Nollen EA, Jain S, Shulman JM, Heutink P, Hernandez DG, Arepalli S, Brooks J, Price R, Nicolas A, Chong S, Cookson MR, Dillman A, Moore M, Traynor BJ, Singleton, Plagnol V, Wood NW, Sheerin U-M, Bras JM, Charlesworth G, Gardner M, Guerreiro R, Trabzuni D, Hardy J, Sharma M, Saad M, Simon-Sanchez J, Schulte C, Corvol JC, Durr A, Vidailhet M, Sveinbjornsdottir S, Barker R, Williams-Gray CH, Ben-Shlomo Y, Berendse HW, van Dijk KD, Berg D, Brockmann K, Wurster I, Matzler W, Gasser T, Martinez M, de Bie RMA, Biffi A, Velseboer D, Bloem B, Post B, Wickremaratchi M, van de Warrenburg B, Bochdanovits Z, Bonin M, Petursson H, Riess O, Burn DJ, Lubbe S, Cooper JM, McNeill A, Schapira A, Lungu C, Chen H, Dong J, Chinnery PF, Hudson G, Clarke CE, Moorby C, Counsell C, Damier P, Dartigues J-F, Deloukas P, Gray E, Edkins S, Hunt SE, Potter S, Tashakkori-Ghanbaria A, Deuschl G, Lorenz D, Dexter DT, Durif F, Evans JR, Langford C, Foltynie T, Goate A, Harris C, van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang X, Illig T, Jonsson PV, Lambert J-C, O'Sullivan SS, Revesz T, Shaw K, Lees A, Lichtner P, Limousin P, Lopez G, Escott-Price V, Pearson J, Williams N, Mudanohwo E, Perlmutter JS, Pollak P, Rivadeneira F, Uitterlinden AG, Sawcer S, Scheffer H, Shoulson I, Shulman J, Smith C, Walker R, Spencer CCA, Strange A, Stefansson H, Bettella F, Stefansson K, Stockton JD, Talbot K, Tanner CM, Tison F, Winder-Rhodes S, Bhatia K. . Genome Biology 2017, 18, 22.
    • Wei W, Gomez-Duran A, Hudson G, Chinnery PF. . PLoS Genetics 2017, 13(12), e1007126.
    • Coxhead J, Kurzawa-Akanbi M, Hussain R, Pyle A, Chinnery P, Hudson G. . Neurobiology of Aging 2016, 38, 217.e1-217.e6.
    • Pyle A, Anugrha H, Kurzawa-Akanbi M, Yarnall A, Burn D, Hudson G. . Neurobiology of Aging 2016, 38, 216.e7–216.e10.
    • Wilson IJ, Carling PJ, Alston CL, Floros VI, Pyle A, Hudson G, Sallevelt SCEH, Lamperti C, Carelli V, Bindoff LA, Samuels DC, Wonnapinij P, Zeviani M, Taylor RW, Smeets HJM, Horvath R, Chinnery PF. . Human Molecular Genetics 2016, 25(5), 1031-1041.
    • Keogh MJ, Kurzawa-Akanbi M, Griffin H, Douroudis K, Ayers KL, Hussein RI, Hudson G, Pyle A, Cordell HJ, Attems J, McKeith IG, O'Brien JT, Burn DJ, Morris CM, Thomas AJ, Chinnery PF. . Translational Psychiatry 2016, 6, e728.
    • Carbutt S, Duff J, Yarnall A, Burn DJ, Hudson G. . Neuroscience Letters 2015, 594, 66-69.
    • Pyle A, Brennan R, Kurzawa-Akanbi M, Yarnall A, Thouin A, Mollenhauer B, Burn D, Chinnery PF, Hudson G. . Annals of Neurology 2015, 78(6), 1000-1004.
    • Hudson G, Uphill J, Hummerich H, Blevins J, Gambetti P, Zerr I, Collinge J, Mead S, Chinnery PF. . Neurobiology of Aging 2015, 36(10), 2908.e1-2908.e3.
    • Pyle A, Hudson G, Wilson IJ, Coxhead J, Smertenko T, Herbert M, Santibanez-Koref M, Chinnery PF. . PLoS Genetics 2015, 11(5), e1005040.
    • Hudson G, Gomez-Duran A, Wilson IJ, Chinnery PF. . PLoS Genetics 2014, 10(5), e1004369.
    • Bulstrode H, Nicoll JAR, Hudson G, Chinnery PF, Di Pietro V, Belli A. . Annals of Neurology 2014, 75(2), 186-195.
    • Giordano C, Iommarini L, Giordano L, Maresca A, Pisano A, Valentino ML, Caporali L, Liguori R, Deceglie S, Roberti M, Fanelli F, Fracasso F, Ross-Cisneros FN, D'Adamo P, Hudson G, Pyle A, Yu-Wai-Man P, Chinnery PF, Zeviani M, Salomao SR, Berezovsky A, Belfort R, Ventura DF, Moraes M, Moraes M, Barboni P, Sadun F, De Negri A, Sadun AA, Tancredi A, Mancini M, d'Amati G, Polosa PL, Cantatore P, Carelli V. . Brain 2014, 137(2), 335-353.
    • Yarnall AJ, Breen DP, Duncan GW, Khoo TK, Coleman SY, Firbank MJ, Nombela C, Winder-Rhodes S, Evans JR, Rowe JB, Mollenhauer B, Kruse N, Hudson G, Chinnery PF, O'Brien JT, Robbins TW, Wesnes K, Brooks DJ, Barker RA, Burn DJ, ICICLE-PD Study Group. . Neurology 2014, 82(4), 308-316.
    • Griffin HR, Pyle A, Blakely EL, Alston CL, Duff J, Hudson G, Horvath R, Wilson IJ, Santibanez-Koref M, Taylor RW, Chinnery PF. . Genetics in Medicine 2014, 16(12), 962-971.
    • Hudson G, Nalls M, Evans JR, Breen DP, Winder-Rhodes S, Morrision KE, Morris HR, Williams-Gray CH, Barker RA, Singleton AB, Hardy J, Wood NE, Burn DJ, Chinnery PF. . Neurology 2013, 80(22), 2042-2048.
    • Thouin A, Griffiths PG, Hudson G, Chinnery PF, Yu-Wai-Man P. . PLoS One 2013, 8(5), e63446.
    • Hudson G, Panoutsopoulou K, Wilson I, Southam L, Rayner NW, Arden N, Birrell F, Carluke I, Carr A, Chapman K, Deloukas P, Doherty M, McCaskie A, Ollier WE, Ralston SH, Reed MR, Spector TD, Valdes AM, Wallis GA, Wilkinson JM, Zeggini E, Samuels DC, Loughlin J, Chinnery PF. . Annals of Rheumatic Diseases 2013, 72(1), 136-139.
    • Chinnery PF, Hudson G. . British Medical Bulletin 2013, 106(1), 135-159.
    • Collerton J, Ashok D, Martin-Ruiz C, Pyle A, Hudson G, Yadegarfar M, Davies K, Jagger C, von Zglinicki T, Kirkwood T, Chinnery P. . Neurobiology of Aging 2013, 34(12), 2889.e1-2889.e4.
    • Neeve VCM, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombes A, Jardel C, Hirano M, DiMauro S, De Vries M, Smeitink J, Smits BW, de Coo IFM, Saft C, Klopstock T, Keiling BC, Czermin B, Abicht A, Lochmuller H, Hudson G, Gorman GG, Turnbull DM, Taylor RW, Holinski-Feder E, Chinnery PF, Horvath R. . Brain 2012, 135(12), 3614-3626.
    • Hudson G, Wilson I, Payne BI, Elson J, Samuels DC, Santibanez-Korev M, Hall SJ, Chinnery PF. . Mitochondrion 2012, 12(4), 438-440.
    • Hudson G, Sims R, Harold D, Chapman J, Hollingworth P, Gerrish A, Russo G, Hamshere M, Moskvina V, Jones N, Thomas C, Stretton A, Holmans PA, O'Donovan MC, Owen MJ, Williams J, Chinnery PF, GERAD1 Consortium. . Neurology 2012, 78(14), 1038-1042.
    • Sitarz KS, Yu-Wai-Man P, Hudson G, Jacob A, Boggild M, Horvath R, Chinnery PF. . Multiple Sclerosis 2012, 18(2), 240-243.
    • 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. . Movement Disorders 2012, 27(2), 312-315.
    • Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL. . International Journal of Epidemiology 2012, 41(1), 177-187.
    • Horvath R, Holinski Feder E, Neeve VC, Pyle A, Griffin H, Ashok D, Foley C, Hudson G, Rautenstrauss B, Nürnberg G, Nürnberg P, Kortler J, Neitzel B, Bäßmann I, Rahman T, Keavney B, Loughlin J, Hambleton S, Schoser B, Lochmüller H, Santibanez Koref M, Chinnery PF. . Movement Disorders 2012, 76(6), 789-793.
    • Hudson G, Yu-Wai-Man P, Griffiths PG, Horvath R, Carelli V, Zeviani M, Chinnery PF. . Mitochondrion 2011, 11(4), 620-622.
    • Hudson G, Faini D, Stutt A, Eccles M, Robinson L, Burn DJ, Chinnery PF. . Neurobiology of Aging 2011, 32(11), 2107.e3-2107.e5.
    • de Alwis N, Aithal G, Bugianesi E, Leathart J, Hudson G, Pyle A, Mowbray C, Henderson E, Burt AD, Chinnery PF, Day CP. . Mitochondrion 2011, 11(1), 234-235.
    • Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simon-Sanchez J, Schulte C, Lesage S, Sveinbjornsdottir S, Arepalli S, Barker R, Ben-Shlomo Y, Berendse HW, Berg D, Bhatia K, de Bie RMA, Biffi A, Bloem B, Bochdanovits Z, Bonin M, Bras JM, Brockmann K, Brooks J, Burn DJ, Charlesworth G, Chen HL, Chinnery PF, Chong S, Clarke CE, Cookson MR, Cooper JM, Corvol JC, Counsell C, Damier P, Dartigues JF, Deloukas P, Deuschl G, Dexter DT, van Dijk KD, Dillman A, Durif F, Durr A, Edkins S, Evans JR, Foltynie T, Gao JJ, Gardner M, Gibbs JR, Goate A, Gray E, Guerreiro R, Gustafsson O, Harris C, van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang XM, Huber H, Hudson G, Hunt SE, Huttenlocher J, Illig T, Jonsson PV, Lambert JC, Langford C, Lees A, Lichtner P, Limousin P, Lopez G, Lorenz D, McNeill A, Moorby C, Moore M, Morris HR, Morrison KE, Mudanohwo E, O'Sullivan SS, Pearson J, Perlmutter JS, Petursson H, Pollak P, Post B, Potter S, Ravina B, Revesz T, Riess O, Rivadeneira F, Rizzu P, Ryten M, Sawcer S, Schapira A, Scheffer H, Shaw K, Shoulson I, Sidransky E, Smith C, Spencer CCA, Stefansson H, Stockton JD, Strange A, Talbot K, Tanner CM, Tashakkori-Ghanbaria A, Tison F, Trabzuni D, Traynor BJ, Uitterlinden AG, Velseboer D, Vidailhet M, Walker R, van de Warrenburg B, Wickremaratchi M, Williams N, Williams-Gray CH, Winder-Rhodes S, Stefansson K, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW, Int Parkinson Dis Genomics Consort, Wellcome Trust Case-Control Consor. . Lancet 2011, 377(9766), 641-649.
    • Spencer CCA, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, Markus HS, Mathew CG, McCarthy MI, Morrison KE, Palmer CNA, Pearson JP, Peltonen L, Pirinen M, Plomin R, Potter S, Rautanen A, Sawcer SJ, Su Z, Trembath RC, Viswanathan AC, Williams NW, Morris HR, Donnelly P, Wood NW, UK Parkinson's Dis Consortium, Wellcome Trust Case Control Consor. . Human Molecular Genetics 2011, 20(2), 345-353.
    • 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. . Brain 2011, 134(1), 171-182.
    • Lythgow KT, Hudson G, Andras P, Chinnery PF. . Mitochondrion 2011, 11(3), 444-449.
    • Hudson G, Yu-Wai-Man P, Griffiths PG, Caporali L, Salomao SS, Berezovsky A, Carelli V, Zeviani M, Chinnery PF. . Molecular Vision 2010, 16, 2760-2764.
    • Yu-Wai-Man P, Griffiths PG, Burke A, Sellar PW, Clarke MP, Gnanaraj L, Ah-Kine D, Hudson G, Czermin B, Taylor RW, Horvath R, Chinnery PF. . Ophthalmology 2010, 117(8), 1538-1546.
    • Yu Wai Man P, Stewart JD, Hudson G, Andrews RM, Griffiths PG, Birch MK, Chinnery PF. . Journal of Medical Genetics 2010, 47(2), 120-125.
    • Yu Wai Man P, Griffiths PG, Gorman GS, Lourenco CM, Wright AF, Auer-Grumbach M, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, Baker MR, Jackson MJ, Clarke MP, Dhillon B, Czermin B, Stewart JD, Hudson G, Reynier P, Bonneau D, Marques W, Lenaers G, McFarland R, Taylor RW, Turnbull DM, Votruba M, Zeviani M, Carelli V, Bindoff LA, Horvath R, Amati-Bonneau P, Chinnery PF. . Brain 2010, 133(3), 771-786.
    • Walter MC, Czemin B, Muller-Ziermann S, Bulst S, Stewart JD, Hudson G, Schneiderat P, Abicht A, Holinski-Feder E, Lochmuller H, Chinnery PF, Klopstock T, Horvath R. . Journal of Neurology 2010, 257(9), 1517-1523.
    • Hudson G, Stutt A, Eccles M, Robinson L, Allcock LM, Wesnes KA, Chinnery PF, Burn DJ. . Neuroscience Letters 2010, 479(2), 123-125.
    • Elstner M, Morris C, Heim K, Lichtner P, Bender A, Mehta D, Schulte C, Sharma M, Hudson G, Goldwurm S, Giovanetti A, Zeviani M, Burn D, McKeith I, Perry R, Jaros E, Krüger R, Wichmann H, Schreiber S, Campbell H, Wilson J, Wright A, Dunlop M, Pistis G, Toniolo D, Chinnery P, Gasser T, Klopstock T, Meitinger T, Prokisch H, Turnbull D. . Annals of Neurology 2009, 66(6), 792-798.
    • Kirkman MA, Korsten A, Leonhardt M, Dimitriadis K, De Coo IF, Klopstock T, Griffiths PG, Hudson G, Chinnery PF, Yu Wai Man P. . Investigative Ophthalmology and Visual Science 2009, 50(7), 3112-3115.
    • Horvath R, Kemp JP, Tuppen HAL, Hudson G, Oldfors A, Marie SKN, Moslemi AR, Servidei S, Holme E, Shanske S, Kollberg G, Jayakar P, Pyle A, Marks HM, Holinski-Feder E, Scavina M, Walter MC, Coku J, Gunther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZMA, Lightowlers RN, Hirano M, Lochmuller H, Taylor RW, Chinnery PF, Tulinius M, DiMauro S. . Brain 2009, 132(11), 3165-3174.
    • Hudson G, Yu Wai Man P, Zeviani M, Chinnery PF. . Molecular Vision 2009, 15, 870-875.
    • McFarland R, Hudson G, Taylor RW, Green SH, Hodges S, McKiernan PJ, Chinnery PF, Ramesh V. . Archives of Disease in Childhood 2008, 93(2), 151-153.
    • Harrower T, Stewart JD, Hudson G, Houlden H, Warner G, O'Donovan DG, Findlay LJ, Taylor RW, De Silva R, Chinnery PF. . Archives of Neurology 2008, 65(1), 133-136.
    • Stewart JD, Tennant S, Powell H, Pyle A, Blakeley EL, He L, Hudson G, Roberts M, du Plessis D, Gow D, Mewasingh LD, Hanna MG, Omer S, Morris AAM, Roxburgh R, Livingston J, McFarland R, Turnbull DM, Chinnery PF, Taylor RW. . Journal of Medical Genetics 2008, 46(3), 209-214.
    • Blakely E, He L, Gardner JL, Hudson G, Walter J, Hughes I, Turnbull DM, Taylor RW. . Neuromuscular Disorders 2008, 18(7), 557-560.
    • Harrower T, Stewart JD, Hudson G, Houlden H, Warner G, Donovan OD, Findlay F, Taylor RW, De Silva R, Chinnery PF. . Archives of Neurology 2008, 65(1), 133-136.
    • Hudson G, Amati-Bonneau P, Blakely E, Stewart J, He L, Schaefer A, Griffiths P, Ahlqvist K, Suomalainen A, Reynier P, McFarland R, Turnbull D, Chinnery P, Taylor R. . Brain 2008, 131(2), 329-337.
    • Stewart JD, Hudson G, Yu Wai Man P, Blakeley EL, He L, Horvath R, Maddison P, Wright A, Griffiths PG, Turnbull DM, Taylor RW, Chinnery PF. . Neurology 2008, 71(22), 1829-1831.
    • Hudson G, Carelli V, Horvath R, Zeviani M, Smeets HJ, Chinnery PF. . Molecular Vision 2007, 13, 2339-2343.
    • Jaros E, Mahad D, Hudson G, Birchall D, Sawcer S, Griffiths P, Sunter J, Compston D, Perry R, Chinnery P. . Neurology 2007, 69(2), 214-216.
    • Hudson G, Schaefer AM, Taylor RW, Tiangyou W, Gibson A, Venables G, Griffiths P, Burn DJ, Turnbull DM, Chinnery PF. . Archives of Neurology 2007, 64(4), 553-557.
    • Hudson G, Schaefer AM, Taylor RW, Tiangyou W, Gibson A, Venables G, Griffiths P, Burn DJ, Turnbull DM, Chinnery PF. . Archives of Neurology 2007, 64(4), 553-557.
    • Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A, Pyle A, Elson J, Howell N, La Morgia C, Valentino ML, Huoponen K, Savontaus ML, Nikoskelainen E, Sadun AA, Salomao SR, Belfort Jr R, Griffiths P, Yu Wai Man P, de Coo RFM, Horvath R, Zeviani M, Smeets HJT, Torroni A, Chinnery PF. . American Journal of Human Genetics 2007, 81(2), 228-233.
    • Hudson G, Deschauer M, Taylor RW, Hanna MG, Fialho D, Schaefer AM, He L-P, Blakely E, Turnbull DM, Chinnery PF. . Neurology 2006, 66(9), 1439-1441.
    • Tiangyou W, Hudson G, Ghezzi D, Ferrari G, Zeviani M, Burn DJ, Chinnery PF. . Neurology 2006, 67(9), 1698-1700.
    • Horvath R, Hudson G, Ferrari G, Futterer N, Ahola S, Lamantea E, Prokisch H, Lochmuller H, McFarland R, Ramesh V, Klopstock T, Freisinger P, Salvi F, Mayr JA, Santer R, Tesarova M, Zeman J, Udd B, Taylor RW, Turnbull D, Hanna M, Fialho D, Suomalainen A, Zeviani M, Chinnery PF. . Brain 2006, 129(7), 1674-1684.
    • Hudson G, Deschauer M, Busse K, Zierz S, Chinnery PF. . Neurology 2005, 64(2), 371-373.
    • Hudson G, Keers SM, Yu Wai Man P, Griffiths P, Huoponen K, Savontaus M-L, Nikoskelainen E, Zeviani M, Carrara F, Horvath R, Karcagi V, Spruijt L, de Coo IMF, Smeets HJM, Chinnery PF. . American Journal of Human Genetics 2005, 77(6), 1086-1091.
    • Deschauer M, Hudson G, Muller T, Taylor RW, Chinnery PF, Zierz S. . Neuromuscular Disorders 2005, 15(4), 311-315.

  • Book Chapters

    • Deen D, Alston CL, Hudson G, Taylor RW, Pyle A. . In: Nicholls TJ; Uhler JP; Falkenberg M, ed. Mitochondrial DNA. New York: Humana Press, Inc, 2023, pp.397-425.
    • Bury AG, Robertson FM, Pyle A, Payne BAI, Hudson G. . In: Methods in Molecular Biology. Humana, New York: Humana Press Inc, 2021, pp.433-447.
    • Hudson G. . In: Reeve A; Simcox E; Duchen M; Turnbull D, ed. Mitochondrial Dysfunction in Neurodegenerative Disorders: Second Edition. Cham: Springer International Publishing, 2016, pp.59-80.

  • Conference Proceedings (inc. Abstracts)

    • Hill L, Bulstrode H, Nicholl J, Hudson G, Chinnery P, Di Pietro V, Belli A. . In: The 12th Symposium of the International Neurotrauma Society. 2016, Cape Town, South Africa: Mary Ann Liebert, Inc. Publishers.
    • Neeve VCM, Pyle A, Holinski-Feder E, Griffin H, Ashok D, Foley C, Hudson G, Rautensstrauss B, Lochmuller H, Santibanez-Koref M, Chinnery PF, Horvath R. . In: United Kingdom Neuromuscular Translational Research Conference. 2012, 缅北禁地 upon Tyne, UK: Elsevier Ltd.
    • Neeve VCM, Van den Bosch B, Van Goethem G, Bindoff L, Smeets B, Lombes A, Hirano M, DiMauro S, De Vries M, Smeitink J, Czermin B, Holinski-Feder E, Hudson G, Turnbull DM, Taylor RW, Chinnery PF, Horvath R. . In: United Kingdom Neuromuscular Translational Research Conference. 2010, Oxford: Neuromuscular Disorders, Elsevier.
    • Horvath R, Kemp JP, Tuppen HAL, Hudson G, Pyle A, Holinski-Feder E, Abicht A, Czermin B, Walter MC, Gunther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZMA, Lightowlers RN, Lochmuller H, Taylor RW, Chinnery PF. . In: United Kingdom Neuromuscular Translational Research Conference. 2010, Oxford, UK: Neuromuscular Disorders, Elsevier.
    • Taylor R, Stewart JD, Hudson G, Chevrollier A, Amati-Bonneau P, Yu Wai Man P, Horvath R, McFarland R, Maddison P, Wright A, Turnbull DM, Chinnery PF. . In: British Human Genetics Conference. 2008, University of York, York, England: Journal of Medical Genetics: BMJ Publishing Group.
    • Chinnery PF, Hudson G, Stewart J, Craig K, Taylor RW, Turnbull DM, Ramesh V, McFarland R, Burn DJ, Hanna MG, Horvath R, Lochmueller H, Zeviani M. . In: Journal of Neurology, Neurosurgery and Psychiatry: Spring Scientific Meeting of the Association of British Neurologists. 2007, Cambridge, UK: BMJ Group.
    • Stewart J, Harrower T, Taylor RW, Hudson G, Houlden H, Warner G, De Silva R, O'Donovan D, Findlay L, Chinnery PF. . In: Journal of Medical Genetics: British Human Genetics Conference. 2007, York, UK: BMJ Group.
    • Hudson G, Schaefer A, Taylor R, Deschauer M, Turnbull D, Chinnery P. . In: Biochimica et Biophysica Acta: Bioenergetics. 6th European Meeting on Mitochondrial Pathology (Euromit 6). 2004, Nijmegen, Netherlands: Elsevier BV.
    • Deschauer M, Hudson G, Taylor R, Muller T, Chinnery P, Zierz S. . In: BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS. 2004, Nijmegen, The Netherlands: Biochimica et Biophysica Acta - Bioenergetics: Elsevier BV.

  • Letters

    • Lowes H, Robertson F, Pyle A, Hussain R, Coxhead J, Yarnall AJ, Burn D, Payne BAI, Santibanez-Koref M, Hudson G. . Movement Disorders 2020, 35(12), 2134-2136.
    • Hudson G, Takeda Y, Herbert M. . Nature 2019, 574(7778), E8-E11.
    • Yu-Wai-Man P, Hudson G, Klopstock T, Chinnery PF. . Brain 2016, 139, e18-e18.
    • Pyle A, Lowes H, Brennan R, Kurzawa-Akanbi M, Yarnall A, Burn D, Hudson G. . Movement Disorders 2016, 31(12), 1923-1924.
    • Hudson G, Tiangyou W, Stutt A, Eccles M, Robinson L, Burn DJ, Chinnery PF. . Movement Disorders 2009, 24(7), 1092-1094.
    • De Alwis N, Hudson G, Burt AD, Day CP, Chinnery PF. . Hepatology 2009, 50(3), 992-993.
    • Yu Wai Man P, Bateman DE, Hudson G, Griffiths PG, Chinnery PF. . Journal of Neuro-Ophthalmology 2008, 28(2), 155-155.
    • Hudson G, Mowbray C, Elson J, Jacob A, Boggild M, Torroni A, Chinnery PF. . Brain 2008, 131(4), e93.
    • Craig K, Ferrari G, Tiangyou W, Hudson G, Gellera C, Zeviani M, Chinnery PF. . Brain 2007, 130(4), E69.

  • Note

    • Floros VI, Pyle A, Dietmann S, Wei W, Tang WWC, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF. . Nature Cell Biology 2023, 25, 194.

  • Reviews

    • Alston CL, Stenton SL, Hudson G, Prokisch H, Taylor RW. . Journal of Pathology 2021, 254(4), 430-442.
    • Blyth U, Craciunas L, Hudson G, Choudhary M. . Human Reproduction Update 2021, 27(5), 866-884.
    • Yu Wai Man P, Griffiths PG, Hudson G, Chinnery PF. . Journal of Medical Genetics 2009, 46(3), 145-158.
    • Hudson G, Yu Wai Man P, Chinnery P. . Expert Opinion on Medical Diagnostics 2008, 2(7), 789-799.
    • Hudson G, Chinnery PF. . Human Molecular Genetics 2006, 15(Review Issue 2), R244-R252.