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 | 319 | 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 | 198 | 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 | 148 | 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 | 113 | 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 | 56 | 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 | 54 | 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 | 44 | 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 | 40 | 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 | 39 | 2012 |
SLC45A2 variations in Indian oculocutaneous albinism patients M Sengupta, M Chaki, N Arti, K Ray Mol Vis 13, 1406-11, 2007 | 33 | 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 | 32 | 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 | 26 | 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 | 22 | 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 | 18 | 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 | 17 | 2010 |
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 | 16 | 2018 |
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 (1), 673895, 2014 | 14 | 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 | 13 | 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 | 12 | 2015 |
Meta-analysis and prioritization of human skin pigmentation-associated GWAS-SNPs using ENCODE data-based web-tools K Ganguly, T Saha, A Saha, T Dutta, S Banerjee, D Sengupta, ... Archives of Dermatological Research 311, 163-171, 2019 | 11 | 2019 |