Author

Ahmed Aly Ibrahim

Hospital Sant Joan de Déu BarcelonaORCID 0000-0002-2103-1995Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:imaging· 1 Organism:mouse· 1

Frequent Co-Authors

Alain VerloèsiD· 1 shared Albena Todorova· 1 shared Alekh ParanjapyeiD· 1 shared Allan Micheil InnesiD· 1 shared Amelle ShillingtoniD· 1 shared Annastelle CoheniD· 1 shared Anne‐Marie GuerrotiD· 1 shared Ashish R. DeshwariD· 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 paperGenetic & Genomic Medicine

Alain VerloèsORCID

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1 paper

Recent·Most cited

Loss of DOT1L disrupts neuronal transcription, behavior, and leads to a neurodevelopmental disorder

Marissa J. Maroni, Melissa Barton, Katherine Lynch, Ashish R. Deshwar, Philip D. Campbell, Josephine Millard, Rachel Lee, Annastelle Cohen, Rili Ahmad, Alekh Paranjapye, Víctor Faùndes, Gabriela M. Repetto, Caoimhe S. McKenna, Amelle Shillington, Chanika Phornphutkul, , Erica Korb

This study shows that partial loss of DOT1L causes transcriptional, morphological, and behavioral defects in neurons across multiple models.

medRxiv · Oct 31, 2024 · PreprintGenetic & Genomic Medicine