Dr Moulinath Acharya
vidwan id: 594307
Associate Professor,
National Institute Of Biomedical Genomics
Expertise
- Genetics and Heredity
Publications
Publications
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Scopus
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2
CrossRef
Citations
132
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2
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Professional Recognition
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Community & Membership
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Indian Society of Developmental Biologists
Society for Biological Chemists
Calcutta Consortium of Human Genetics
Indian Society of Human Genetics
Bio
Dr. Moulinath Acharya is trained in human genetics and molecular biology. He did MS in Zoology (Molecular and Applied Clinical Genetics) from the Banaras Hindu University and later PhD in Molecular and Human Genetics from the CSIR-IICB. Subsequently, he moved to the Dept. of Medical Genetics at the University of Alberta, Canada for his post-doctoral training. In 2012, he joined the National Institute of Biomedical Genomics, where he is currently working as an Associate Professor.
Personal Details
- Male
- Associate Professor , National Institute Of Biomedical Genomics
- Kalyani, West Bengal, India
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Dr Jyothi Alias Jyotsna Baragi
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Organisations (3+)
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Co-Authors (11)
Indian Institute of Science Education and Research(IISER), Kolkata
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Amity University
Indian Institute of Technology Jodhpur
Birla Institute of Technology and Science
Yenepoya (Deemed to be University), Mangalore
CSIR-Indian Institute of Chemical Biology
Indian Statistical Institute, Kolkata
Academy of Scientific and Innovative Research ((AcSIR))
Chief Scientist
Indraprastha Institute of Information Technology Delhi (IIIT Delhi)
Scholarly Work
Integrative-genomics approach to identify and functionalize regulatory variants from GWAS data with applications to type-2 diabetes and coronary artery disease
Funding Agency: Department of Biotechnology
Co Investigator
5,600,000
2025 - Ongoing
Investigating the role of PTPRM gene in lens thickness, identified from quantitative trait genome-wide association study
Funding Agency: ANRF-Science and Engineering Research Board
Principal Investigator
5,068,840
2024 - Ongoing
A Multi-centric Effort Towards Understanding a High-Resolution Genomic Architecture of Congenital Non-Syndromic Deafness in India
Funding Agency: Department of Biotechnology
Principal Investigator
5,398,000
2019 - 2023
Dissecting the functional genomic basis of rare eye diseases in children
Funding Agency: Science and Engineering Research Board
Co Investigator
6,265,000
2018 - 2022
Genome-wide association study of phenotypic extremes in primary angle closure glaucoma
Funding Agency: Department of Biotechnology
Principal Investigator and Program Coordinator
5,484,000
2016 - 2019
Investigating Genomic Signatures Causal To Rare Congenital Muscle Disorders In Indian Population.
Genome-wide association study of primary angle closure glaucoma in the Indian Population
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