Author

A. A. M. Morris

Manchester University NHS Foundation TrustORCID 0000-0002-7854-4396Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:differential expression· 1 Research Focus:dimensionality reduction· 1 Assay:metabolomics· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Abeer DannouraiD· 1 shared Alain Fouilhoux· 1 shared Andrew Michael FreyiD· 1 shared Arunabha GhoshiD· 1 shared Belén González‐HerreroiD· 1 shared Cécile RouzieriD· 1 shared Charlotte L. AlstoniD· 1 shared Claire Hart· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abeer DannouraORCID

Mutual co-authors in cluster

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2 papers

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

Rare Cholesterol Related Disorders: A Sterolomic Library for Diagnosis and Monitoring of Diseases

Mohsen Ali Asgari, Eylan Yutuc, Jonas Abdel‐Khalik, Peter J. Crick, A. A. M. Morris, Simon Allan Jones, Arunabha Ghosh, Richard Curnock, Claire Hart, Ludger J. Schöls, Silke Matysik, Ιωάννα Λαϊνά, Evan Reid, Thomas T. Warner, Belén González‐Herrero, , Yuqin Wang

The paper introduces a mass spectrometry sterolomic library to aid in diagnosing cholesterol-related inherited disorders by analyzing sterol profiles from 13 autosomal recessive disorders and predicting data for 8 more.

medRxiv · Jun 23, 2025 · PreprintGenetic & Genomic Medicine