Author

Srividya Shetty

National Institute of Mental Health and Neurosciences

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Developmental Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ramakrishnan KannaniD· 2 shared Anand G. SubramaniamiD· 1 shared Andrew J. SauriniD· 1 shared Anirudh S. Chellappa· 1 shared Bhupesh MehtaiD· 1 shared Biju ViswanathiD· 1 shared Bruno HudryiD· 1 shared David ForondaiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersDevelopmental Biology

Ramakrishnan KannanORCID

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2 papers

Recent·Most cited

Ambivalent partnership of the Drosophila posterior class Hox protein Abdominal-B with the Extradenticle and Homothorax cofactors

Jesús Rodríguez Curt, Paloma Martín, David Foronda, Bruno Hudry, Ramakrishnan Kannan, Srividya Shetty, Samir Merabet, Andrew J. Saurin, Yacine Graba, Ernesto Sánchez‐Herrero

The paper investigates how the Drosophila posterior Hox protein Abd-B interacts with Exd and Hth cofactors in different developmental contexts, revealing context-dependent synergistic or antagonistic functional relationships.

PLoS Genetics · Jan 13, 2025Peer-reviewedDevelopmental Biology

Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance

Ravi Kumar Nadella, Anirudh S. Chellappa, Anand G. Subramaniam, Ravi Prabhakar More, Srividya Shetty, Suriya Prakash, Nikhil Ratna, V.P. Vandana, Meera Purushottam, Jitender S. Saini, Biju Viswanath, Parayil Sankaran Bindu, Madhu Nagappa, Bhupesh Mehta, Sanjeev Jain, Ramakrishnan Kannan

The paper identifies two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome patients and shows their functional impact on Kir4.1 channel activity.

Human Genomics · Oct 22, 2019Peer-reviewedNeuroscience