Robert W Taylor

48PUBLICATIONS
262CO-AUTHORS
Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)Metabolic medicineNeurology and neuromuscular diseases
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Publications (48)

|Aug 25, 2026
Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

|Aug 13, 2026
A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

|Aug 06, 2026
The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

|Jul 17, 2026
Pathogenic DRP1 variants reveal a role for biomolecular condensation in mitochondrial fission.

|Jun 17, 2026
Activation of AMPK as a therapeutic strategy for FBXL4-related mitochondrial DNA depletion syndrome.

|May 30, 2026
COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathy.

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Frequent Collaborators

6 joint publications

Robert McFarland

5 joint publications

Holger Prokisch

5 joint publications

Monika Oláhová

4 joint publications

Charlotte L Alston