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Amitabh Biswas
Amitabh Biswas
Scientist D, AIIMS New Delhi; Consultant (Genomics), CCMB
在 ccmb.res.in 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Genomics of rare genetic diseases—experiences from India
S Sivasubbu, ....... Scaria, Vinod, A Biswas, VR Rao
Human genomics 13 (1), 1-18, 2019
662019
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 Rao
Journal of affective disorders 151 (2), 673-678, 2013
312013
Next generation sequencing in cardiomyopathy: towards personalized genomics and medicine
A Biswas, VR Rao, S Seth, SK Maulik
Molecular biology reports 41, 4881-4888, 2014
272014
Dynamic nature of heavy metal toxicity in water and sediments of Ayad River with climatic change
MS Sankhla, R Kumar, A Biswas
Int J Hydro 3 (5), 339-343, 2019
212019
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, 2019
162019
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 Rao
Journal of Primary Care Specialties 1 (2), 143-149, 2015
152015
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, 2018
122018
Number needed to treat
A Biswas
Journal of Primary Care Specialties 3 (2), 106-108, 2017
112017
Epidemiology of cardiomyopathy-A clinical and genetic study of dilated cardiomyopathy: The EPOCH-D study
S Das, A Biswas, M Kapoor, S Seth, B Bhargava, VR Rao
Journal of the Practice of Cardiovascular Sciences 1 (1), 30-34, 2015
112015
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 Rao
Journal of Clinical & Experimental Cardiology 3 (12), Article ID 1000225, 2012
82012
Multiple tier detection of TNT using curcumin functionalized silver nanoparticles
A Raza, A Biswas, A Zehra, A Mengesha
Forensic science international: synergy 2, 240-247, 2020
52020
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 Bhargava
Journal of the Practice of Cardiovascular Sciences 3 (3), 143-149, 2017
42017
TNNT2 5 bp deletion, sedentary lifestyle & abdominal adiposity accentuate the phenotypic severity in hypertrophic cardiomyopathy patients
A Biswas, M Kapoor, S Das, S Seth, B Bhargava, VR Rao
Meta Gene 20, 100567, 2019
32019
Mutations in hotspot region of MYH7 gene exon 23 associated with restrictive cardiomyopathy
M Kapoor, S Das, A Biswas, S Seth, B Bhargava, VR Rao
Cardiogenetics 7 (1), 6358, 2017
32017
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 Rao
Molecular Cytogenetics 7 (1), 1-1, 2014
32014
Understanding Musculoskeletal Disorders Through Next-Generation Sequencing
B Garg, N Tomar, A Biswas, N Mehta, R Malhotra
JBJS Reviews 10 (4), e21.00165, 2022
22022
Story of Gene: Part II–Genetics and Genomics
P Sharma, S Das, A Biswas
Journal of the Practice of Cardiovascular Sciences 4 (3), 224-232, 2018
22018
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 Rao
Molecular Cytogenetics 7 (1), 1-1, 2014
12014
Gait analysis technologies for biomechanical assessment in knee osteoarthritis: Understanding variability and distinctions
A Biswas, M Gupta, B Garg
Gait & Posture 113, 25-26, 2024
2024
Decoding the Genetic Threads of Disc Degeneration
A Biswas, B Garg
Indian Spine Journal 7 (2), 148-158, 2024
2024
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