Author

Kezia Mathew

National Institute of Mental Health and NeurosciencesORCID 0000-0002-5185-5434Unclaimed 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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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. Shyamsundar· 1 shared Alekhya VemulaiD· 1 shared Arun KandasamyiD· 1 shared B. Binukumar· 1 shared Bangalore N. GangadhariD· 1 shared Bharath HollaiD· 1 shared Bhupesh MehtaiD· 1 shared Biju ViswanathiD· 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 paperGenetic & Genomic Medicine

A. Shyamsundar

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1 paper

Recent·Most cited

Genetic & Genomic MedicineScientific ReportsPeer-reviewedDec 7, 2022

Whole Exome Sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes

Suhas Ganesh, Alekhya Vemula, Samsiddhi Bhattacharjee…·Meera Purushottam

This study uses whole exome sequencing in families with multiple affected individuals to identify rare variants in genes associated with both Mendelian and complex neuropsychiatric syndromes.

6 citations

humanwhole-exome sequencing

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