Author

M. Shahrour

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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Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:wet-lab / biochemical assay· 1

Frequent Co-Authors

A. Kusnierczyk· 1 shared A. Lang· 1 shared B. Abu-Libdeh· 1 shared B. Van Loon· 1 shared E. Kristiansen· 1 shared F. Jacob· 1 shared G. J. Sullivan· 1 shared G. Slupphaug· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperPathology

A. Kusnierczyk

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Author profile →

1 paper

Recent·Most cited

Loss-of-function mutation in human Oxidation Resistance gene 1 disrupts the spatial-temporal regulation of histone arginine methylation in early brain development

X. Lin, W. Wang, M. Yang, N. Damseh, M. M. L. d. Sousa, F. Jacob, A. Lang, E. Kristiansen, M. Pannone, M. Kissova, R. Almaas, A. Kusnierczyk, R. Siller, M. Shahrour, M. Al-Ashhab, , M. Bjoras

This study identifies a loss-of-function mutation in OXR1 causing neurodevelopmental disorders and shows its role in regulating histone arginine methylation in brain organoids.

bioRxiv · May 24, 2022 · PreprintPathology