Patrick F Chinnery

53PUBLICATIONS

235CO-AUTHORS

Medical devicesNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Speciation and extinction

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Publications (53)

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|Jun 21, 2026

Mitochondrial DNA heteroplasmy drives cortical neuronal disturbances in human organoids harbouring the common m.3243A>G mutation.

|May 02, 2026

Genetic landscape of adult executive function reveals a cell-type-specific developmental origin.

|Apr 30, 2026

Nuclear genetic modulation of tissue-specific mitochondrial RNA processing contributes to common disease risk.

|Apr 01, 2026

MitoPerturb-Seq identifies gene-specific single-cell responses to mitochondrial DNA depletion and heteroplasmy.

Stephen P Burr, Kathryn Auckland, Angelos Glynos

|Nov 20, 2025

An inherited mitochondrial DNA mutation remodels inflammatory cytokine responses in macrophages and in vivo in mice.

Eloïse Marques, Stephen P Burr, Alva M Casey

|Nov 12, 2025

The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy.

Laura S Kremer, Zoe Golder, Tom Barton-Owen

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Frequent Collaborators

Rita Horvath

Wei Wei

Katherine Schon

Stephen P Burr

Henry Houlden

James B Stewart

Gerome Breen

John R Bradley

Kathy Stirrups

Julien Prudent

Frequent Collaborators

Rita Horvath

Wei Wei

Katherine Schon

Stephen P Burr