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Patrick F. Chinnery

Newcastle University
University of Cambridge
MRC Mitochondrial Biology Unit

583

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31697

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Biparental inheritance of mitochondrial DNA revisited.

2021 Nature Reviews Genetics
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An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank.

2021 Nature Genetics
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Primary Mitochondrial Disorders Overview

2021
- Patrick F. Chinnery
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Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

2021 medRxiv
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Editorial: Mitochondrial medicine special issue.

2021 Journal of Inherited Metabolic Disease
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Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.

2021 BMJ
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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.

2021 Brain
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Cell reprogramming shapes the mitochondrial DNA landscape.

2021
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1465 Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (MELAS) syndrome: the highly variable diagnostic journey

2021 Archives of Disease in Childhood
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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1).

2021 European Journal of Human Genetics
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Citations (4)