Moulinath Acharya

5PUBLICATIONS
10CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Gene mappingCancer diagnosis
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Publications (5)

|Jun 05, 2026
Novel truncating Desmin mutation Arg150Stop disrupts structural integrity and cellular homeostasis by formation of persistent aggregate-like structure.

|Dec 05, 2024
Functional investigation suggests CNTNAP5 involvement in glaucomatous neurodegeneration obtained from a GWAS in primary angle closure glaucoma.

Sudipta Chakraborty, Jyotishman Sarma, Shantanu Saha Roy

|Jun 21, 2024
Post-GWAS functional analyses of CNTNAP5 suggests its role in glaucomatous neurodegeneration.

Sudipta Chakraborty, Jyotishman Sarma, Shantanu Saha Roy

|Mar 17, 2023
A quantitative trait GWAS on lens thickness identifies novel risk loci on PTPRM in the narrow angle individuals susceptible to PACG.

Sudipta Chakraborty, Anshul Sharma, Soumen Pal

|Oct 30, 2020
Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Shamita Sanga, Arnab Ghosh, Krishna Kumar

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Frequent Collaborators

3 joint publications

Sudipta Chakraborty

2 joint publications

Arundhati Sharma

1 joint publications

Shamita Sanga

1 joint publications

Veeramani Preethish-Kumar