Author

Ahlam A. Hamed

University of Khartoum

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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Neuroscience· 1

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Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Binnaz YalciniD· 1 shared Bruno RinaldiiD· 1 shared Carlos M. A. GuardiaiD· 1 shared Efil BayamiD· 1 shared Elena BrivioiD· 1 shared Fabíola Paoli MonteiroiD· 1 shared Fernando KokiD· 1 shared Fowzan Sami AlkurayaiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Binnaz YalcinORCID

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1 paper

Recent·Most cited

Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans.

Efil Bayam, Peggy Tilly, Stephan C. Collins, José Rivera Alvarez, Meghna Kannan, Lucile Tonneau, Elena Brivio, Bruno Rinaldi, Romain Lecat, Noémie Schwaller, Ludovica Cotellessa, Sateesh Maddirevula, Fabíola Paoli Monteiro, Carlos M. A. Guardia, João Paulo Kitajima, , Juliette D. Godin

The paper identifies bi-allelic WDR47 variants as a cause of a neurodevelopmental syndrome with corpus callosum dysgenesis and associated neuroanatomical abnormalities.

EMBO Molecular Medicine · Nov 28, 2024Peer-reviewedNeuroscience