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Patrick Chinnery
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British neurologist
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Works
14
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study
scientific article published on 04 November 2021
mtDNA point mutations are present at various levels of heteroplasmy in human oocytes
scientific article published on 26 January 2007
Somatic mtDNA variation is an important component of Parkinson's disease
scientific article published on 6 November 2015
The mitochondrial protein CHCHD2 primes the differentiation potential of human induced pluripotent stem cells to neuroectodermal lineages.
scientific article published on 17 October 2016
LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood
scientific article published in July 2010
A high frequency of mtDNA polymorphisms in HeLa cell sublines
scientific article published in April 2002
Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility
scientific article
Titinopathy in a Canadian family sharing the British founder haplotype
scientific article published in January 2014
Patients with neurological or psychiatric complications of COVID-19 have worse long-term functional outcomes: COVID-CNS—A multicentre case–control study
scientific article published on 27 January 2025
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
scientific article
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Patrick Francis Chinnery is a neurologist, clinician scientist, and Wellcome Trust Principal Research Fellow based in the Medical Research Council Mitochondrial Biology Unit and the University of Cambridge, where he is also professor of neurology and head of the department of clinical neurosciences.

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Human
Occupation
Researcher
Neurologist
Physician
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