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Dr Moulinath Acharya

vidwan id: 594307
Male

Associate Professor,
National Institute Of Biomedical Genomics

Expertise

  • Genetics and Heredity

Publications

Total Articles 44
Books 0
Proceedings 0

Publications

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Scopus

Citations 137
h-index 2

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Citations 132
h-index 2
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Professional Recognition

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Community & Membership

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Indian Society of Developmental Biologists

2024
Life Member

Society for Biological Chemists

2012
Life Member

Calcutta Consortium of Human Genetics

2012
Life Member

Indian Society of Human Genetics

2007
Life Member

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
Ph.D
CSIR-Indian Institute of Chemical Biology 2007
Associate Professor Apr 2012 – Present
National Institute Of Biomedical Genomics

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Organisations (3+)

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Moulinath

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Co-Authors (11)

Arindam

Dr Arindam Mukherjee

Indian Institute of Science Education and Research(IISER), Kolkata

Jagmohan

Prof Jagmohan Singh

Amity University

Mitali

Prof Mitali Mukerji

Indian Institute of Technology Jodhpur

Rajdeep

Dr Rajdeep Chowdhury

Birla Institute of Technology and Science

Rajesh

Dr Rajesh Raju

Yenepoya (Deemed to be University), Mangalore

Saikat

Dr Saikat Chakrabarti

CSIR-Indian Institute of Chemical Biology

Saurabh

Prof Saurabh Ghosh (Late)

Indian Statistical Institute, Kolkata

Samir K

Prof Samir K Brahmachari

Academy of Scientific and Innovative Research ((AcSIR))

S K

Dr S K Rath

Chief Scientist

Tavpritesh

Dr Tavpritesh Sethi

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

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

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

Completed
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

Completed
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

Completed

Investigating Genomic Signatures Causal To Rare Congenital Muscle Disorders In Indian Population.

University National Institute of Biomedical Genomics/University of Calcutta
Year 2024

Genome-wide association study of primary angle closure glaucoma in the Indian Population

University National Institute of Biomedical Genomics/Regional Centre for Biotechnology
Year 2024
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Scholarly Publications

Role of myocilin in glaucoma: Molecular defects and possible functional aberrations leading to pathogenesis Bhattacharjee A

Open Access
article
Authors: ACHARYA, M. and Mookherjee, S. and Banerjee, S. and Mukhopadhyay, A. and Bandyopadhyay, A.K. and Thakur, S.K.D. and Sen, A. and Ray, K.

Primary role of CYP1B1 in Indian juvenile-onset POAG patients

Open Access
article
Authors: M, Mookherjee S. and A, Bhattacharjee and AK, Bandyopadhyay and SKD, Thakur and G, Bhaduri and A, Sen and K, Ray

Myocilin variants in Indian open angle glaucoma patients

Open Access
article
Authors: Bhattacharjee, A. and ACHARYA, M. and Mukhopadhyay, A. and Mookherjee, S. and Banerjee, D. and Bandyopadhyay, A.K. and Thakur, S.K.D. and Sen, A. and Ray, K.

Evaluation of the Opticin gene in primary open angle glaucoma: functional significance of a silent change

Open Access
article
Authors: M, Mookherjee S. and A, Bhattacharjee and SKD, Thakur and AK, Bandyopadhyay and A, Sen and S, Chakrabarti and K, Ray

Complex genetics of glaucoma: Defects in CYP1B1, and not MYOC, cause pathogenesis in an early-onset POAG patient with double variants at both loci

Open Access
article
Authors: M#, Mukhopadhyay A.# and A, Bhattacharjee and SKD, Thakur and AK, Bandyopadhyay and K, Ray

Analysis of mutations of the PITX2 transcription factor found in Axenfeld-Rieger Syndrome patients

Open Access
article
Authors: Footz, T. and Idrees, F. and ACHARYA, M. and Kozlowski, K. and Walter, M.A.

Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cells

Open Access
article
Authors: M, Lingenfelter D.J. and L, Huang and PJ, Gage and MA, Walter

A complex regulatory network of transcription factors critical for ocular development and disease

Open Access
article
Authors: M, Huang L. and VF, Fleisch and WT, Allison and MA, Walter