Author

Alaa A. Mohammed

Birmingham Women’s and Children’s NHS Foundation Trust

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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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:dimensionality reduction· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Afrah AlshammariiD· 1 shared Akhil Kanathay Ashokan· 1 shared Andrew E. FryiD· 1 shared Anju ShuklaiD· 1 shared Ankur ChaurasiaiD· 1 shared Ataf Hussain SabiriD· 1 shared Christopher Mark WatsoniD· 1 shared Colin A. JohnsoniD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Afrah AlshammariORCID

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Author profile →

1 paper

Recent·Most cited

Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders

Ankur Chaurasia, Anju Shukla, Shruti Pande, Greeshma Purushothama, Akhil Kanathay Ashokan, Purvi Majethia, Namanpreet Kaur, Priyanka Upadhyai, Neha Quadri, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, Shalini S. Nayak, Sheela Nampoothiri, Ataf Hussain Sabir, Alaa A. Mohammed, , Katta M. Girisha

The paper systematically analyzes homozygous autosomal copy number losses in exomes to improve diagnostic yield and identify ultra-rare recessive disorders.

European Journal of Human Genetics · Jun 27, 2026Peer-reviewedGenetic & Genomic Medicine