Mainak Sengupta
Mainak Sengupta
Assistant Professor
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Genetic landscape of the people of India: a canvas for disease gene exploration
Indian Genome Variation Consortium
Journal of genetics 87 (1), 3-20, 2008
EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda
S Aggarwal, S Negi, P Jha, PK Singh, T Stobdan, MAQ Pasha, S Ghosh, ...
Proceedings of the National Academy of Sciences 107 (44), 18961-18966, 2010
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic‐induced cancer through drinking water
P Ghosh, A Basu, J Mahata, S Basu, M Sengupta, JK Das, A Mukherjee, ...
International journal of cancer 118 (10), 2470-2478, 2006
Tyrosinase and ocular diseases: some novel thoughts on the molecular basis of oculocutaneous albinism type 1
K Ray, M Chaki, M Sengupta
Progress in retinal and eye research 26 (4), 323-358, 2007
Genetic defects in Indian Wilson disease patients and genotype–phenotype correlation
S Mukherjee, S Dutta, S Majumdar, T Biswas, P Jaiswal, M Sengupta, ...
Parkinsonism & related disorders 20 (1), 75-81, 2014
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients.
M Chaki, M Sengupta, M Mondal, A Bhattacharya, S Mallick
differentiation 22, 2992-3003, 2011
Indian genetic disease database
S Pradhan, M Sengupta, A Dutta, K Bhattacharyya, SK Bag, C Dutta, ...
Nucleic acids research 39 (suppl_1), D933-D938, 2010
OCA1 in different ethnic groups of India is primarily due to founder mutations in the tyrosinase gene
M Chaki, M Sengupta, A Mukhopadhyay, I Subba Rao, PP Majumder, ...
Annals of human genetics 70 (5), 623-630, 2006
Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings
M Mondal, M Sengupta, S Samanta, A Sil, K Ray
Gene 511 (2), 470-474, 2012
SLC45A2 variations in Indian oculocutaneous albinism patients
M Sengupta, M Chaki, N Arti, K Ray
Mol Vis 13, 1406-11, 2007
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient
A Gupta, I Chattopadhyay, S Mukherjee, M Sengupta, SK Das, K Ray
Behavioral and Brain Functions 6, 1-5, 2010
In silico analyses of missense mutations in coagulation factor VIII: identification of severity determinants of haemophilia A
M Sengupta, D Sarkar, K Ganguly, D Sengupta, S Bhaskar, K Ray
Haemophilia 21 (5), 662-669, 2015
Meta-analysis of polymorphic variants conferring genetic risk to cervical cancer in Indian women supports CYP1A1 as an important associated locus
D Sengupta, U Guha, S Mitra, S Ghosh, S Bhattacharjee, M Sengupta
Asian Pacific journal of cancer prevention: APJCP 19 (8), 2071, 2018
Association of Interleukin‐1 beta and tumor necrosis factor‐alpha genetic polymorphisms with gastric cancer in India
Z Sultana, B Bankura, AK Pattanayak, D Sengupta, M Sengupta, ML Saha, ...
Environmental and molecular mutagenesis 59 (7), 653-667, 2018
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease
S Roy, K Ganguly, P Pal, S Ghosh, SK Das, PK Gangopadhyay, ...
Annals of Human Genetics 82 (2), 53-59, 2018
Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene
M Sengupta, M Mondal, P Jaiswal, S Sinha, M Chaki, S Samanta, K Ray
British Journal of Dermatology 163 (3), 487-494, 2010
Structure-function correlation analysis of connexin50 missense mutations causing congenital cataract: electrostatic potential alteration could determine intracellular …
D Sarkar, K Ray, M Sengupta
Biomed Research International 2014, 2014
Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos
M Sengupta, D Sarkar, M Mondal, S Samanta, A Sil, K Ray
Journal of Genetics 92, 305-308, 2013
Molecular phylogenetic studies based on rDNA ITS, cpDNA trnL intron sequence and cladode characteristics in nine Protasparagus taxa
PS Saha, S Ray, M Sengupta, S Jha
Protoplasma 252, 1121-1134, 2015
Association of 12 polymorphic variants conferring genetic risk to lung cancer in Indian population: An extensive meta‐analysis
D Sengupta, U Guha, S Bhattacharjee, M Sengupta
Environmental and Molecular Mutagenesis 58 (9), 688-700, 2017
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