Author

Ravi Prabhakar More

Tata Institute of Fundamental Research

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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Neuroscience· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:whole-exome sequencing· 3 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:database / resource· 1

Frequent Co-Authors

Biju ViswanathiD· 3 shared Sanjeev JainiD· 3 shared Bhupesh MehtaiD· 2 shared Husayn Ahmed PallikondaiD· 2 shared Mahendra S. Rao· 2 shared Odity MukherjeeiD· 2 shared Ravi Kumar NadellaiD· 2 shared A. Shyamsundar· 1 shared

Activity by Year

2018-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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3 shared papersNeuroscience

Biju ViswanathORCID

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Author profile →

3 papers

Recent·Most cited

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

INDEX-db: The Indian Exome Reference database (Phase-I)

Husayn Ahmed Pallikonda, V. Vidhya, Ravi Prabhakar More, Biju Viswanath, Sanjeev Jain, Mahendra S. Rao, Odity Mukherjee, Naren Prahalada Rao, Janardhanan C. Narayanaswamy, Palanimuthu Thangaraju Sivakumar, ArunKandaswamy, MuralidharanKesavan, Urvakhsh-Meherwan Mehta, GanesanVenkatasubramanian, John P. John, , MahendraRao

The paper develops a database of coding variations from the Indian population to aid in understanding genotype-phenotype correlations and disease mechanisms.

Journal of Computational Biology · Jan 7, 2019Peer-reviewedGenomics

Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes

Suhas Ganesh, Husayn Ahmed Pallikonda, Ravi Kumar Nadella, Ravi Prabhakar More, Manasa Seshadri, Biju Viswanath, Mahendra S. Rao, Sanjeev Jain, Odity Mukherjee

Psychiatry and Clinical Neurosciences · Oct 27, 2018Peer-reviewedNeuroscience