Patrick F Chinnery

53PUBLICATIONS
235CO-AUTHORS
Medical devicesNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Speciation and extinction
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (53)

|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

Pageof 9

Frequent Collaborators

8 joint publications

Rita Horvath

7 joint publications

Wei Wei

6 joint publications

Katherine Schon

5 joint publications

Stephen P Burr