Author

Husayn Ahmed Pallikonda

Tata Institute of Fundamental ResearchORCID 0000-0003-4472-2067Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Cancer Biology· 1 Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 3 Assay:whole-exome sequencing· 3 Research Focus:variant calling· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Biju ViswanathiD· 2 shared Mahendra S. Rao· 2 shared Odity MukherjeeiD· 2 shared Padinjat RaghuiD· 2 shared Ravi Prabhakar More· 2 shared Sanjeev JainiD· 2 shared A. Shyamsundar· 1 shared Aastha KumariiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersGenomics

Biju ViswanathORCID

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5 papers

Recent·Most cited

Cancer BiologybioRxivPreprintMay 3, 2026

Distinct functions of PBRM1 and BAP1 reconcile the course of kidney cancer evolution and disease progression

Daqi Deng, Hugang Feng, Annika Fendler…·Samra Turajlic

This study identifies distinct molecular programs in PBRM1- and BAP1-driven ccRCC, explaining their different evolutionary trajectories and clinical outcomes.

DOI 10.64898/2026.04.30.721837

humanbulk RNA-seq

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Molecular BiologybioRxivPreprintFeb 29, 2024

Conserved helical motifs in the Ikaros IDR mediate NuRD interaction and transcriptional repression

Tianyi Zhang, Yi-Fang Wang, Alex Montoya…·Matthias Merkenschlager

This study identifies conserved helical motifs in Ikaros that mediate NuRD interaction and transcriptional repression in pre-B cells and B-ALL.

1 citation

humanproteomics

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GenomicsbioRxivPreprintJun 22, 2021

Genomic sequencing of Lowe syndrome trios reveal a mechanism for the heterogeneity of neurodevelopmental phenotypes

Husayn Ahmed Pallikonda, Pramod Kumar Singh, Rajan S. Thakur…·Padinjat Raghu

The paper identifies genetic variants contributing to clinical heterogeneity in Lowe syndrome by analyzing genomic data from affected family members.

4 citations

humanwhole-exome sequencing

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GenomicsJournal of Computational BiologyPeer-reviewedJan 7, 2019

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

Husayn Ahmed Pallikonda, V. Vidhya, Ravi Prabhakar More…·MahendraRao

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

14 citations

humanwhole-exome sequencing

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NeurosciencePsychiatry and Clinical NeurosciencesPeer-reviewedOct 27, 2018

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…·Odity Mukherjee

39 citations

humanwhole-exome sequencing

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