M
Mainak Sengupta
Researcher at Indian Institute of Engineering Science and Technology, Shibpur
Publications - Ā 129
Citations - Ā 1203
Mainak Sengupta is an academic researcher from Indian Institute of Engineering Science and Technology, Shibpur. The author has contributed to research in topics: Switched reluctance motor & Finite element method. The author has an hindex of 14, co-authored 107 publications receiving 1003 citations. Previous affiliations of Mainak Sengupta include Council of Scientific and Industrial Research & Indian Institutes of Technology.
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Genetic landscape of the people of India: A canvas for disease gene exploration
Samir K. Brahmachari,Partha P. Majumder,Mitali Mukerji,Saman Habib,Debasis Dash,Kunal Ray,Samira Bahl,Lalji Singh,Abhay Sharma,Susanta Roychoudhury,Giriraj R. Chandak,Kumarasamy Thangaraj,Devendra Parmar,Shantanu Sengupta,Dwaipayan Bharadwaj,Srikanta Kumar Rath,Jagmohan Singh,Ganga Nath Jha,Komal Virdi,V. R. Rao,Swapnil Sinha,Ashok K. Singh,Amit Kumar Mitra,Shrawan K. Mishra,Qadar Pasha,Sridhar Sivasubbu,Rajesh Pandey,Aradhita Baral,Prashant Singh,Amitabh Sharma,Jitender Kumar,Tsering Stobdan,Yasha Bhasin,Chitra Chauhan,Ashiq Hussain,Elyanambi Sundaramoorthy,Suchita Singh,Arun Bandyopadhyay,Krishanu Dasgupta,A. K. Reddy,Charles J. Spurgeon,M. Mohd Idris,Vinay K. Khanna,Alok Dhawan,Mohini Anand,Ravi Shankar,R. S. Bharti,Madhu Singh,Arvind P. Singh,Anwar J. Khan,Parag P. Shah,A. B. Pant,Rupinder Kaur,Kamlesh Bisht,Ashok Kumar,Victor Rajamanickam,Eugene Wilson,Antony Thangadurai,Pankaj Jha,Mahua Maulik,Neelam Makhija,Abdur Rahim,Sangeeta Sharma,Rupali Chopra,Pooja Rana,Manickam Chidambaram,Arindam Maitra,Ruchi Chawla,Suruchika Soni,Preeti Khurana,Mohamed Nadeem Khan,Sushanta Das Sutar,Amit Tuteja,K. Narayansamy,Rachna Shukla,S. Prakash,Swapna Mahurkar,K. Radha Mani,J. Hemavathi,Seema Bhaskar,Pankaj Khanna,G. S. Ramalakshmi,Shalini Mani Tripathi,Nikita Thakur,Balaram Ghosh,Ritushree Kukreti,Taruna Madan,Ranjana Verma,G. Sudheer,Anubha Mahajan,Sreenivas Chavali,Rubina Tabassum,Sandeep Grover,Meenal Gupta,Jyotsna Batra,Amrendra Kumar,Abdoulazim Nejatizadeh,Mudit Vaid,Swapan K Das,Shilpy Sharma,Mamta Sharma,Rajshekhar Chatterjee,Jinny A. Paul,Pragya Srivastava,Charu Rajput,Uma Mittal,Mridula Singh,Manoj Hariharan,S.K. Das,Keya Chaudhuri,Mainak Sengupta,Moulinath Acharya,Ashima Bhattacharyya,A Saha,Arindam Biswas,Moumita Chaki,Arnab Gupta,Saibal Mukherjee,Suddhasil Mookherjee,Ishita Chattopadhyay,Taraswi Banerjee,Meenakshi Chakravorty,Chaitali Misra,Gourish Monadal,Shiladitya Sengupta,Dipanjana Dutta De,Swati Bajaj,Ishani Deb,Arunava Banerjee,Rajdeep Chowdhury,Debalina Banerjee,Deepak Kumar,Sumit Ranjan Das,Shrish Tiwari,Anshu Bharadwaj,Ikhlak Ahmed,Sumera Parveen,Nivedita Singh,Dipayan Dasgupta,Siddharth Singh Bisht,Sangeeta Khanna,Rashmi Rajput,Biswaroop Ghosh,Naveen Kumar,Amit Kumar Chaurasia,James Kappukalayil Abraham,Amit Sinha,Vinod Scaria,Tavpritesh Sethi,A. Mandal,Arijit Mukhopadhyay +150 more
TL;DR: High levels of genetic divergence are observed between groups of populations that cluster largely on the basis of ethnicity and language in diverse populations of India.
Journal ArticleDOI
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water.
Pritha Ghosh,Anamika Basu,Julie Mahata,Sreemanti Basu,Mainak Sengupta,Jayanta Das,Angshuman Mukherjee,Ajoy K. Sarkar,Lakshmikanta Mondal,Kunal Ray,Ashok K. Giri +10 more
TL;DR: Results show a protective role of GSTM1 null in arsenic toxicity and indicate that asymptomatic individuals are sub clinically affected and are also significantly susceptible to arsenicāinduced genotoxicity.
Journal ArticleDOI
Tyrosinase and ocular diseases: Some novel thoughts on the molecular basis of oculocutaneous albinism type 1
TL;DR: Two additional possibilities are proposed, which on further investigations might shed light on the molecular basis of UCMs in TYR of OCA1 patients; partial deletion of the exons 4 and 5 region of TYR that is homologous with TYRL and variations in the polymorphic GA complex repeat located between distal and proximal elements of the human TYR promoter that can modulate the expression of the gene leading to disease pathogenesis.
Journal ArticleDOI
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients.
Moumita Chaki,Mainak Sengupta,Maitreyee Mondal,Abhisek Bhattacharya,Shampa Mallick,Ranjan Bhadra,Kunal Ray +6 more
Journal ArticleDOI
Genetic defects in Indian Wilson disease patients and genotype-phenotype correlation.
S Mukherjee,Shruti Dutta,Sulagna Majumdar,Tamoghna Biswas,Preeti Jaiswal,Mainak Sengupta,Abhisek Bhattacharya,P K Gangopadhyay,Ashish Bavdekar,Shyamal Kumar Das,Kunal Ray +10 more
TL;DR: The neurological involvement score was devised to capture the spectrum of neurological involvement in WD patients and generated a genotype-phenotype matrix that could be effectively used to depict the phenotypic spectra of WD affected individuals and serve as a platform to identify prospective "outliers" to be investigated for their remarkable phenotypesic divergence.