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职业迁徙
个人简介
I began my research studying the relationship of mitochondrial DNA and human disease in 1995 and became interested in the mechanisms of mitochondrial inheritance. My research has involved the identification of mitochondrial and nuclear gene defects responsible for mitochondrial disorders, dissecting out the downstream disease mechanisms, and studying the molecular and cellular basis of mitochondrial DNA inheritance - most recently through the UK 100,000 Genomes Project. I have an active clinical translational research programme studying the natural history of mitochondrial diseases linked to the development of new treatments, and an interest in the role of mitochondrial mechanisms in common diseases, and particularly neurodegenerative disorders.
研究兴趣
论文共 897 篇作者统计合作学者相似作者
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Thomas Paß,Konrad M Ricke, Pierre Hofmann,Roy S Chowdhury, Yu Nie,Patrick Chinnery,Heike Endepols,Bernd Neumaier, André Carvalho, Lionel Rigoux,Sophie M Steculorum,Julien Prudent,
Brain : a journal of neurology (2024)
Alexander G Murley,Catarina Rua,Heather Biggs, Christopher T Rodgers,Tomasz Matys,Jelle van den Ameele,Rita Horvath,Patrick F Chinnery
Annals of clinical and translational neurology (2024)
Patrick Chinnery, Kerry Dresser
http://isrctn.com/ (2024)
Sonia Boscenco, Jaqueline Tait-Mulder, Minsoo Kim, Cerise Tang, Mark Zucker, Tricia Park,Wei Wei,Patrick F. Chinnery,Payam A. Gammage, Ed Reznik
Cancer Researchno. 6_Supplement (2024): 4341-4341
CELL METABOLISMno. 1 (2024): 5-7
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 420-421
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Handbook of Clinical Neurologypp.xi-xi, (2023)
Natureno. 7975 (2023): 839-848
Science Advancesno. 43 (2023)
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A. Corvó, L. Matalonga,C. Hernandez-Ferrer, R. Thompson, L. Carmody,D. Piscia, A. Macaya, A. Lochmuller, A. Manta, B. Fontaine, S. Vicart,J. Desaphy,
HAL (Le Centre pour la Communication Scientifique Directe) (2023)
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