Parimal Das

5PUBLICATIONS
8CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Cancer geneticsEnvironmental epidemiologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|Aug 27, 2024
Computational exploration of protein structure dynamics and RNA structural consequences of PKD1 missense variants: implications in ADPKD pathogenesis.

Chandra Devi, Prashant Ranjan, Sonam Raj

|Mar 07, 2024
Genetic and in silico analysis of Indian sporadic young onset patient with amyotrophic lateral sclerosis.

Saileyee Roychowdhury, Deepika Joshi, Vinay Kumar Singh

|Nov 14, 2022
An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis.

Tanmoy Sarkar, Prashant Ranjan, Smitha Kanathur

|Nov 24, 2021
Understanding the impact of missense mutations on the structure and function of the EDA gene in X-linked hypohidrotic ectodermal dysplasia: A bioinformatics approach.

Prashant Ranjan, Parimal Das

|Oct 19, 2018
Novel splicing in IGFN1 intron 15 and role of stable G-quadruplex in the regulation of splicing in renal cell carcinoma.

Shiv Prakash Verma, Parimal Das

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Frequent Collaborators

2 joint publications

Prashant Ranjan

1 joint publications

Tanmoy Sarkar

1 joint publications

Smitha Kanathur

1 joint publications

Ankush Gupta