Author

Amitabh Biswas

Scientist D, AIIMS New Delhi; Consultant (Genomics), CCMB - Cited by 181 - Human Genetics - Molecular Biology - Forensic Genetics

Biography

Dr. Amitabh Biswas is from All-India Institute of Medical Sciences, Arba Minch University, CSIR-CCMB, Galgotias University, Lok Nayak Jayaprakash Narayan National Institute of Criminology and Forensic Science, University Grants Commission, University of Delhi, Delhi, located in India. His study is about Role of Modifying Genes on the Severity of Rare Mutation of MYH7 Gene in Hypertrophic Obstructive Cardiomyopathy. He is also specialized in PCR, Genetics, Genomics, Heart Failure, Gene Expression, Molecular Biology and DNA. He published 18 articles in good  journal and the articles are informative and got good citations.
Title
Cited by
Year
Genomics of rare genetic diseases—experiences from India
S Sivasubbu, ....... Scaria, Vinod, ..... Biswas, A, Rao V, RHuman genomics 13 (1), 1-18, 2019201
32
2019
Next generation sequencing in cardiomyopathy: towards personalized genomics and medicine
A Biswas, VR Rao, S Seth, SK MaulikMolecular biology reports 41, 4881-4888, 2014201
25
2014
High rate of suicide attempt and associated psychological traits in an isolated tribal population of North-East India
PK Singh, RK Singh, A Biswas, VR RaoJournal of affective disorders 151 (2), 673-678, 2013201
24
2013
Dynamic nature of heavy metal toxicity in water and sediments of Ayad River with climatic change
MS Sankhla, R Kumar, A BiswasInt J Hydro 3 (5), 339-343, 2019201
16
2019
Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy
A Biswas, A Raza, S Das, M Kapoor, R Jayarajan, A Verma, ...Purinergic signalling 15, 205-210, 2019201
14
2019
Epidemiology of cardiomyopathy-A clinical and genetic study of hypertrophic cardiomyopathy: The EPOCH-H study
A Biswas, S Das, M Kapoor, S Seth, B Bhargava, VR RaoJournal of the Practice of Cardiovascular Sciences 1 (2), 143-149, 2015201
13
2015
Familial Hypertrophic Cardiomyopathy-Identification of cause and risk stratification through exome sequencing
A Biswas, S Das, M Kapoor, KV Shamsudheen, R Jayarajan, A Verma, ...Gene 660, 151-156, 2018201
12
2018
Epidemiology of cardiomyopathy-A clinical and genetic study of dilated cardiomyopathy: The EPOCH-D study
S Das, A Biswas, M Kapoor, B Bhargava, S Seth, VR RaoJournal of the Practice of Cardiovascular Sciences 1 (1), 30-34, 2015201
12
2015
Number needed to treat
A BiswasJournal of the Practice of Cardiovascular Sciences 3 (2), 6, 2017201
10
2017
Role of modifying genes on the severity of rare mutation of MYH7 gene in hypertrophic obstructive cardiomyopathy
A Biswas, S Das, S Seth, SK Maulik, B Bhargava, VR RaoJournal of Clinical & Experimental Cardiology 3 (12), Article ID 1000225, 2012201
6
2012
Multiple tier detection of TNT using curcumin functionalized silver nanoparticles
A Raza, A Biswas, A Zehra, A MengeshaForensic science international: Synergy 2, 20-27, 2020202
4
2020
Epidemiology of cardiomyopathy – A Clinical and Genetic Study of Restrictive Cardiomyopathy: The EPOCH-R Study
VRR Mitali Kapoor, Soumi Das, Amitabh Biswas, Sandeep Seth, Balram BhargavaJournal of the Practice of Cardiovascular Sciences (), 14-149, 2017201
3
2017
Mutations in hotspot region of MYH7 gene exon 23 associated with restrictive cardiomyopathy
Mutations in hotspot region of MYH7 gene exon 2 associated with restrictive cardiomyopathyM Kapoor, S Das, A Biswas, S Seth, B Bhargava, VR RaoCardiogenetics 7 (1), 658, 2017201
3
2017
Clinical characterization of Idiopathic Restrictive Cardiomyopathy having rare variant (E949K) in β-cardiac myosin heavy chain gene
M Kapoor, A Biswas, S Das, S Seth, B Bhargava, V RaoMolecular Cytogenetics 7 (1), 1-1, 2014201
3
2014
Story of gene: Part II–Genetics and genomics
P Sharma, S Das, A BiswasJournal of the Practice of Cardiovascular Sciences 4 (3), 224, 20820
1
2018
A novel donor site mutation in LMNA gene leading to severe form of Dilated Cardiomyopathy in a proband of a family from Bihar, India
S Das, A Biswas, M Kapoor, S Seth, B Bhargava, V RaoMolecular Cytogenetics 7 (), -, 20420
1
2014
Understanding Musculoskeletal Disorders Through Next-Generation Sequencing
B Garg, N Tomar, A Biswas, N Mehta, R MalhotraJBJS Reviews 0 (4), e2.0065, 2022202
1
2022