Author

Ola Abdelhadi

University of Manchester

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 Research Focus:dimensionality reduction· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam JacksoniD· 1 shared Alessandra RenieriiD· 1 shared Alexander J. M. BlakesiD· 1 shared Alison Milhench· 1 shared Amitav Parida· 1 shared Andrew Paul FennelliD· 1 shared Angela F. Brady· 1 shared Angelica Maria Delgado-VegaiD· 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

Adam JacksonORCID

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1 paper

Recent·Most cited

Biallelic variants in RNU2-2 cause a remarkably frequent developmental epileptic encephalopathy

Adam Jackson, Alexander J. M. Blakes, Bader Alhaddad, Olivia J. Henry, Angelica Maria Delgado-Vega, Elizabeth Wall, Ola Abdelhadi, Shakti Agrawal, Khadijah Bakur, Edward Blair, Angela F. Brady, Helen K. Brittain, Kate Chandler, Natasha Clarke, Miriana Danelli, , Siddharth Banka

The paper identifies biallelic variants in RNU2-2 as a frequent cause of a severe developmental epileptic encephalopathy, distinct from a dominant disorder, and links them to reduced U2-2 abundance.

Nature Genetics · Mar 30, 2026Peer-reviewedGenetic & Genomic Medicine