Author

Oniz Suleyman

Queen Mary University of London

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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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:experimental assay· 3 Organism:zebrafish· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Charlotte Louise HalliD· 3 shared Márta KorbonitsiD· 3 shared Sayka BarryiD· 3 shared Anne DebeeriD· 2 shared Artem O. BorovikoviD· 2 shared Caroline H. BrennaniD· 2 shared Chih Yao Chung· 2 shared Chung Thong Lim· 2 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Charlotte Louise HallORCID

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Author profile →

4 papers

Recent·Most cited

Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation

Donato Iacovazzo, Federica Begalli, Oniz Suleyman, Márton Doleschall, Maria Alevizaki, Kevin E. Ashelford, Sherine Awad Mahmoud, Anne Barlier, Sayka Barry, Caroline E Brain, Claudia Cabrera, Frédéric Castinetti, Sabrina Chiloiro, Kevin Colclough, Alexandra Csábi, , Márta Korbonits

The paper identifies an SLC30A9 deletion causing familial medullary thyroid carcinoma through translation reinitiation and shows its oncogenic effects.

medRxiv · Feb 27, 2026 · PreprintGenetic & Genomic Medicine

Chaperone AIP Couples mTORC1 Activation and Catabolic Metabolism During Neonatal Development

Márta Korbonits, Xian Wang, Sayka Barry, Chung Thong Lim, Oniz Suleyman, Stefano De Tito, Nazia Uddin, Maria Lillina Vignola, Charlotte Louise Hall, Laura Perna, J. Paul Chapple, Gábor Czibik, Siân M. Henson, Valle Morales, Katiuscia Bianchi, , Oliver Haworth

The paper identifies AIP as a regulator that links mTORC1 activation with catabolic metabolism during neonatal development, ensuring metabolic adaptation and survival.

bioRxiv · Sep 18, 2025 · PreprintDevelopmental Biology

A cleaved cytosolic FOXG1 promotes excitatory neurogenesis by enhancing mitochondrial translation.

Hannah Bruce, Kathryn Adamson, Gessica Goncalves, Marnie E. Halpern, Clinton A. L. Monfries, Oniz Suleyman, Lourdes Osuna Almagro, Fursham Hamid, Katherine R. Long, Corinne Houart

The paper shows that a cleaved cytosolic FOXG1 enhances mitochondrial translation and promotes excitatory neurogenesis, offering a new therapeutic target for mitochondrial disorders.

bioRxiv · Aug 13, 2024 · PreprintNeuroscience

Biallelic Loss of Molecular Chaperone Molecule AIP Results in a Novel Severe Multisystem Disease Defined by Defective Proteostasis

Márta Korbonits, Xian Wang, Sayka Barry, Chung Thong Lim, Oniz Suleyman, Stefano De Tito, Nazia Uddin, Maria Lillina Vignola, Charlotte Louise Hall, Laura Perna, J. Paul Chapple, Gabor Czbik, Siân M. Henson, Valle Morales, Katiuscia Bianchi, , Oliver Haworth

This study shows that biallelic AIP loss causes a severe pediatric disease with proteostasis defects, observed in human and zebrafish models.

bioRxiv · Aug 8, 2024 · PreprintMolecular Biology