Author

Aisha Al Shamsi

Tawam HospitalORCID 0000-0001-8757-7782Unclaimed 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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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Abdulaziz Al Saman· 1 shared Ahmad N. Abou TayouniD· 1 shared Aida Maria Bertoli‐AvellaiD· 1 shared Alan TayloriD· 1 shared Alawi A.A. Alsheikh-AliiD· 1 shared Almundher A. Al-MaawaliiD· 1 shared Amna Mohammed Al-FutaisiiD· 1 shared Anju JacobiD· 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

Abdulaziz Al Saman

Mutual co-authors in cluster

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 28, 2024

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

Navin B. Ramakrishna, Yoshikazu Johmura, Nur Ain Ali…·Ahmad N. Abou Tayoun

This study identifies FBXO22 deficiency as a cause of a pleiotropic syndrome with growth restriction and neurodevelopmental delay, linked to an epigenetic signature involving histone demethylase KDM4B.

1 citation

humanDNA methylation

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