Shalini Sanjeeva Nayak

8PUBLICATIONS
29CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyGene mappingNephrology and urologyAnthropological genetics
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Publications (8)

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

|Oct 14, 2025
The transient external granular layer in human foetal cerebellum: insights into neurogenesis, genetic regulation, and developmental disorders.

Aamna Kausar, Shalini Sanjeeva Nayak, Sapna Marpalli

|Apr 12, 2025
Biallelic Variant, c.644-13_644-9del in UNC50 Is Associated With Congenital Myasthenia Syndrome.

Mangalore S Shravya, Greeshma Purushothama, Periyasamy Radhakrishnan

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

Shruti Pande, Purvi Majethia, Karthik Nair

|May 09, 2023
Early and severe tricuspid valve dysplasia in a fetus with cardiospondylocarpofacial syndrome due to a variant c.616T>G p.(Tyr206Asp) in MAP3K7.

Subrahmanya Vasishta, Akkatai S Teli, Akhila Vasudeva

|Dec 08, 2022
Clinically diverse and perinatally lethal syndromes with urorectal septum malformation sequence.

Shalini S Nayak, Robert Harkness, Anju Shukla

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Frequent Collaborators

7 joint publications

Katta Mohan Girisha

5 joint publications

Anju Shukla

2 joint publications

William G Newman

2 joint publications

Shruti Pande