Ankur Chaurasia

2PUBLICATIONS
21CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Genetic immunology
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Publications (2)

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|Jun 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.

|Dec 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.

Shruti Pande, Purvi Majethia, Karthik Nair

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Frequent Collaborators

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Shruti Pande

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Sheela Nampoothiri

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Shalini S Nayak

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Katta Mohan Girisha

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Anju Shukla

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Purvi Majethia

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Karthik Nair

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Jeevan Kumar

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Dhanya Lakshmi Narayanan

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Naveen Sankhyan

Frequent Collaborators

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Shruti Pande

2 joint publications

Sheela Nampoothiri

2 joint publications

Shalini S Nayak

2 joint publications

Katta Mohan Girisha

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