Author

Noha Elsakrmy

University of TorontoORCID 0000-0003-3450-5253Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Brian D. FreibaumiD· 1 shared Chloe Lauder· 1 shared Haissi CuiiD· 1 shared Hong Joo KimiD· 1 shared Hui PengiD· 1 shared J. Paul TayloriD· 1 shared Jolie M. MilleriD· 1 shared Qingyu Shi· 1 shared

Activity by Year

2025-2025 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperMolecular Biology

Brian D. FreibaumORCID

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1 paper

Recent·Most cited

Molecular BiologybioRxivPreprintSep 11, 2025

A point mutation in the nuclear speckle protein and splicing factor SRRM2 is associated with amyotrophic lateral sclerosis and causes dysregulation of synapse-associated genes

Qingyu Shi, Chloe Lauder, Jolie M. Miller…·Haissi Cui

This study identifies a point mutation in SRRM2 as a risk factor for ALS, showing it disrupts protein interactions and dysregulates synapse-related genes.

DOI 10.1101/2025.09.11.675713

humanbulk RNA-seq

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