Author

Sherifa Ahmed Hamed

Assiut UniversityORCID 0000-0002-1441-3530Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Albena JordanovaiD· 2 shared Camila Armirola-RicaurteiD· 2 shared Henry HouldeniD· 2 shared Liedewei Van de VondeliD· 2 shared Mary M. ReillyiD· 2 shared Michael G. HannaiD· 2 shared Stephan L. ZuchneriD· 2 shared Stéphanie EfthymiouiD· 2 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Albena JordanovaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy

Camila Armirola-Ricaurte, Laura Morant, Isabelle Adant, Sherifa Ahmed Hamed, Menelaos Pipis, Stéphanie Efthymiou, Silvia Amor‐Barris, Derek Atkinson, Liedewei Van de Vondel, Aleksandra Tomić, Els De Vriendt, Stephan L. Zuchner, Bart Ghesquière, Michael G. Hanna, Henry Houlden, , Albena Jordanova

This study identifies biallelic COX18 variants as a cause of autosomal recessive axonal CMT with peripheral neuropathy and potential central nervous system involvement.

medRxiv · Jul 3, 2024 · PreprintGenetic & Genomic Medicine

Biallelic variants in ARHGAP19 cause a motor-predominant neuropathy with asymmetry and conduction slowing

Natalia Dominik, Stéphanie Efthymiou, Christopher J. Record, Xinyu Miao, Renee Lin, J. Parmar, Annarita Scardamaglia, Reza Maroofian, Gabriel Aughey, Abigail D. Wilson, Simon A. Lowe, Riccardo Curró, Ricardo Parolin Schnekenberg, Shahryar Alavi, Leif Leclaire, , Henry Houlden

The paper identifies biallelic variants in ARHGAP19 as a cause of motor-predominant neuropathy with conduction slowing in multiple families.

medRxiv · May 10, 2024 · PreprintGenetic & Genomic Medicine