| Genomics of rare genetic diseases—experiences from India S Sivasubbu, ....... Scaria, Vinod, A Biswas, VR Rao Human genomics 13 (1), 1-18, 2019 | 53 | 2019 |
| 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 | 29 | 2013 |
| 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 | 27 | 2014 |
| 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 | 17 | 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, 2019 | 16 | 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 Rao Journal of Primary Care Specialties 1 (2), 143-149, 2015 | 15 | 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, 2018 | 12 | 2018 |
| Number needed to treat A Biswas Journal of Primary Care Specialties 3 (2), 106-108, 2017 | 11 | 2017 |
| 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 | 11 | 2015 |
| 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 | 8 | 2012 |
| 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 | 5 | 2020 |
| 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 | 3 | 2019 |
| 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 | 3 | 2017 |
| 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 | 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 Rao Molecular Cytogenetics 7 (1), 1-1, 2014 | 3 | 2014 |
| Understanding Musculoskeletal Disorders Through Next-Generation Sequencing B Garg, N Tomar, A Biswas, N Mehta, R Malhotra JBJS Reviews 10 (4), e21.00165, 2022 | 1 | 2022 |
| 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 | 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 Rao Molecular Cytogenetics 7 (1), 1-1, 2014 | 1 | 2014 |
| D190Y mutation in C-terminal tail region of TNNI3 gene causing severe form of restrictive cardiomyopathy with mild hypertrophy in an Indian patient M Kapoor, S Das, A Biswas, PB Malgulwar, NK Devi, S Seth, B Bhargava, ... Meta Gene 26, 100777, 2020 | | 2020 |
| Ectodermal dysplasia-skin fragility syndrome–identification of a novel plakophilin1 (PKP1) gene variant through whole exome sequencing SC Konda, A Biswas, A Konda, VR Rao, V Adepu Indian Journal of Dermatology, Venereology and Leprology, 1-5, 0 | | |
DR SANDEEP SETHAll India Institute of Medical Sciences Delhi IndiaVerified email at J-PCS.ORG
