Author

Ankur Chaurasia

Manipal Academy of Higher EducationORCID 0000-0002-7890-4590Unclaimed 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 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 Alaa A. Mohammed· 1 shared Andrew E. FryiD· 1 shared Anju ShuklaiD· 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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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