Patrick Chinnery

Newcastle University

United Kingdom

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Articles (20)

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2025

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Collaborators (16)

Claire-Sophie Davoine

Institut du Cerveau et de la Moelle Épinière

FRANCE

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Katherine Schon

NIHR Academic Clinical Lecturer

University of Cambridge

UNITED KINGDOM

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Ludger Schöls

Section head

Eberhard Karls Universität Tübingen

GERMANY

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Nils-Göran Larsson

Karolinska Institutet

SWEDEN

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Richarda M de Voer

Assistant professor

Radboudumc

NETHERLANDS

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Guillermo Rodriguez-Bey

Research Assistant Professor

University of Pittsburgh

UNITED STATES

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Marc Tischkowitz

University of Cambridge

UNITED KINGDOM

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Timothy Nicholson

King’s College London

UNITED KINGDOM

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Mark J. Caulfield

Queen Mary University of London

UNITED KINGDOM

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Laura Kremer

University Medical Center Göttingen

GERMANY

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Thomas Pollak

King’s College London

UNITED KINGDOM

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Florian Rosenberger

Karolinska Institutet

SWEDEN

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Marek Turnovec

University Hospital in Motol

CZECH REPUBLIC

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Fredrik Levander

Associate Professor

Lund University

SWEDEN

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Ian Galea

Professor

University of Southampton

UNITED KINGDOM

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Alexander Murley

Clinical Lecturer in Neurology

University of Cambridge

UNITED KINGDOM

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Patrick Chinnery

Research Interests

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Articles (20)

Patients with neurological or psychiatric complications of COVID-19 have worse long-term functional outcomes: COVID-CNS-A multicentre case-control study.

Origin and cell-type specificity of mitochondrial DNA mutations in C9ORF72 ALS-FTLD human brain organoids

Cryptic mitochondrial DNA mutations coincide with mid-late life and are pathophysiologically informative in single cells across tissues and species

An oligodendrocyte silencer element underlies the pathogenic impact of lamin B1 structural variants.

Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation

Preventing excessive autophagy protects from the pathology of mtDNA mutations in Drosophila melanogaster.

The Feasibility of Omega-3 Supplementation Compared to Placebo in the Management of Long COVID Symptoms Among Healthcare Workers: A Randomized Controlled Trial.

Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses.

Retraction Note: 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.

Whole-genome sequencing for mitochondrial disorders identifies unexpected mimics

A role for BCL2L13 and autophagy in germline purifying selection of mtDNA

Precision mitochondrial medicine

Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes

Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degeneration

Implications of mitochondrial DNA mutations in human induced pluripotent stem cells

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data.

Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint.

Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues

Cell reprogramming shapes the mitochondrial DNA landscape.

Collaborators (16)

Claire-Sophie Davoine

Katherine Schon

Ludger Schöls

Nils-Göran Larsson

Richarda M de Voer

Guillermo Rodriguez-Bey

Marc Tischkowitz

Timothy Nicholson

Mark J. Caulfield

Laura Kremer

Thomas Pollak

Florian Rosenberger

Marek Turnovec

Fredrik Levander

Ian Galea

Alexander Murley

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