Author

Dhanya Lakshmi Narayanan

Manipal Academy of Higher EducationORCID 0000-0002-1627-3252Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:dimensionality reduction· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anju ShuklaiD· 2 shared Katta M. GirishaiD· 2 shared Afrah AlshammariiD· 1 shared Akhil Kanathay Ashokan· 1 shared Alaa A. Mohammed· 1 shared Alex Michael PagnozziiD· 1 shared Andreas MerkenschlageriD· 1 shared Andrew E. FryiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anju ShuklaORCID

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Author profile →

2 papers

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

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly

Chiara Klöckner, J. Pedro Fernández-Murray, Mahtab Tavasoli, Heinrich Sticht, Gisela Stoltenburg, Leila Motlagh Scholle, Somayeh Bakhtiari, Michael C. Kruer, Hossein Darvish, Saghar Ghasemi Firouzabadi, Alex Michael Pagnozzi, Anju Shukla, Katta M. Girisha, Dhanya Lakshmi Narayanan, Parneet Kaur, , Konrad Platzer

The paper identifies bi-allelic CHKA variants causing a neurodevelopmental disorder with epilepsy and microcephaly through functional analysis in yeast.

Brain · Feb 21, 2022Peer-reviewedGenetic & Genomic Medicine