Author

Jamie K. Leighton

Newcastle University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

A. A. M. MorrisiD· 1 shared Abeer DannouraiD· 1 shared Alain Fouilhoux· 1 shared Andrew Michael FreyiD· 1 shared Cécile RouzieriD· 1 shared Charlotte L. AlstoniD· 1 shared Emma L. BlakelyiD· 1 shared Emmanuelle C. Genin· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. A. M. MorrisORCID

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1 paper

Recent·Most cited

Bi-allelic UQCC1 variants impair mitochondrial complex III assembly causing early-onset mitochondrial disease

Sarah J. Smith, Samira Ait-El-Mkadem Saadi, Jamie K. Leighton, Lucie S Taylor, Andrew Michael Frey, Michael G. Nelson, Paulina Castañeda-Támez, Emmanuelle C. Genin, Richard C. Caswell, Abeer Dannoura, Hanan E. Shamsheldin, Konstantina Fragaki, Cécile Rouzier, Langping He, Mahmoud R. Fassad, , Robert William Taylor

This study identifies biallelic UQCC1 variants as a cause of early-onset mitochondrial disease by impairing complex III assembly and function.

medRxiv · Oct 19, 2026 · PreprintGenetic & Genomic Medicine