| Genetic landscape of the people of India: a canvas for disease gene exploration SK Brahmachari, PP Majumder, M Mukerji, S Habib, D Dash, K Ray, ... 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 |
| The Indian genome variation database (IGVdb): a project overview H Genet Hum Genet, 1-11, 2005 | 153 | 2005 |
| Primary role of CYP1B1 in Indian juvenile-onset POAG patients M Acharya, S Mookherjee, A Bhattacharjee, AK Bandyopadhyay, ... Mol Vis 12 (1), 399-404, 2006 | 131 | 2006 |
| Recent advances in molecular genetics of glaucoma K Ray, A Mukhopadhyay, M Acharya Molecular and cellular biochemistry 253, 223-231, 2003 | 101 | 2003 |
| Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma A Bhattacharjee, D Banerjee, S Mookherjee, M Acharya, A Banerjee, ... Molecular vision 14, 841, 2008 | 71 | 2008 |
| Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India S Chakrabarti, K Kaur, S Komatireddy, M Acharya, KR Devi, ... Molecular vision 11, 111-113, 2005 | 71 | 2005 |
| Molecular basis for involvement of CYP1B1 in MYOC upregulation and its potential implication in glaucoma pathogenesis S Mookherjee, M Acharya, D Banerjee, A Bhattacharjee, K Ray Public Library of Science 7 (9), e45077, 2012 | 67 | 2012 |
| Mutations in MYOC gene of Indian primary open angle glaucoma patients A Mukhopadhyay, M Acharya, S Mukherjee, J Ray, S Choudhury, M Khan, ... Mol Vis 8, 442-8, 2002 | 67 | 2002 |
| Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development DM Kaiser, M Acharya, PLA Leighton, H Wang, N Daude, S Wohlgemuth, ... PLoS one 7 (12), e51305, 2012 | 61 | 2012 |
| A complex regulatory network of transcription factors critical for ocular development and disease M Acharya, LJ Huang, VC Fleisch, WT Allison, MA Walter Human molecular genetics 20 (8), 1610-1624, 2011 | 57 | 2011 |
| Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndrome T Footz, F Idrees, M Acharya, K Kozlowski, MA Walter Investigative ophthalmology & visual science 50 (6), 2599-2606, 2009 | 53 | 2009 |
| Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma. A Mukhopadhyay, S Komatireddy, M Acharya, A Bhattacharjee, ... | 53 | 2005 |
| Distribution of p53 codon 72 polymorphism in Indian primary open angle glaucoma patients M Acharya, S Mitra, A Mukhopadhyay, M Khan, S Roychoudhury, K Ray Mol Vis 8, 367-71, 2002 | 53 | 2002 |
| Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change A Moulinath, M Suddhasil, B Ashima, T Sanjay, B Arun, S Abhijit, ... BMC Molecular Biology 8, 2007 | 34 | 2007 |
| Myocilin variants in Indian patients with open-angle glaucoma A Bhattacharjee, M Acharya, A Mukhopadhyay, S Mookherjee, ... Archives of ophthalmology 125 (6), 823-829, 2007 | 29 | 2007 |
| Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cells M Acharya, DJ Lingenfelter, LJ Huang, PJ Gage, MA Walter Journal of Biological Chemistry 284 (50), 34829-34838, 2009 | 25 | 2009 |
| Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations S Sanga, A Ghosh, K Kumar, K Polavarapu, V Preethish‐Kumar, ... European Journal of Neurology 28 (3), 992-1003, 2021 | 9 | 2021 |
| Complex genetics of glaucoma: defects in CYP1B1, and not MYOC, cause pathogenesis in an early-onset POAG patient with double variants at both loci M Acharya, A Mukhopadhyay, A Bhattacharjee, K Sanjay, D Thakur, ... Journal of genetics 87 (3), 265, 2008 | 8 | 2008 |
| Haplotype-based genomic analysis reveals novel association of CNTNAP5 genic region with primary angle closure glaucoma S Chakraborty, A Sharma, A Sharma, R Sihota, S Bhattacharjee, ... Journal of Biosciences 46, 1-9, 2021 | 7 | 2021 |
