| 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 | 324* | 2008 |
| Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy K Nikopoulos, C Gilissen, A Hoischen, CE van Nouhuys, FN Boonstra, ... The American Journal of Human Genetics 86 (2), 240-247, 2010 | 248 | 2010 |
| L1 retrotransposition can occur early in human embryonic development JAJM van den Hurk, IC Meij, M del Carmen Seleme, H Kano, ... Human molecular genetics 16 (13), 1587-1592, 2007 | 232 | 2007 |
| Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP K Nikopoulos, H Venselaar, RWJ Collin, R Riveiro‐Alvarez, FN Boonstra, ... Human mutation 31 (6), 656-666, 2010 | 173 | 2010 |
| The Indian genome variation database (IGVdb): a project overview H Genet Hum Genet, 1-11, 2005 | 146 | 2005 |
| Myocilin gene implicated in primary congenital glaucoma K Kaur, ABM Reddy, A Mukhopadhyay, AK Mandal, SE Hasnain, K Ray, ... Clinical genetics 67 (4), 335-340, 2005 | 124 | 2005 |
| Recent advances in molecular genetics of glaucoma K Ray, A Mukhopadhyay, M Acharya Molecular and cellular biochemistry 253, 223-231, 2003 | 100 | 2003 |
| Exosome-enclosed microRNAs in exhaled breath hold potential for biomarker discovery in patients with pulmonary diseases A Sinha, AK Yadav, S Chakraborty, SK Kabra, R Lodha, M Kumar, ... Journal of allergy and clinical immunology 132 (1), 219-222. e7, 2013 | 92 | 2013 |
| Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy FN Boonstra, CE van Nouhuys, J Schuil, IJ de Wijs, KP van der Donk, ... Investigative ophthalmology & visual science 50 (9), 4379-4385, 2009 | 92 | 2009 |
| Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants A Mukhopadhyay, K Nikopoulos, A Maugeri, APM De Brouwer, ... Investigative ophthalmology & visual science 47 (8), 3565-3572, 2006 | 87 | 2006 |
| Genome-wide analysis reveals downregulation of miR-379/miR-656 cluster in human cancers SV Laddha, S Nayak, D Paul, R Reddy, C Sharma, P Jha, M Hariharan, ... Biology direct 8, 1-14, 2013 | 83 | 2013 |
| CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation A Mukhopadhyay, JM Kramer, G Merkx, D Lugtenberg, DF Smeets, ... Human genetics 128, 281-291, 2010 | 82 | 2010 |
| A-to-I editing in human miRNAs is enriched in seed sequence, influenced by sequence contexts and significantly hypoedited in glioblastoma multiforme D Paul, AN Sinha, A Ray, M Lal, S Nayak, A Sharma, B Mehani, ... Scientific reports 7 (1), 2466, 2017 | 76 | 2017 |
| Gene delivery to the retina: focus on non-viral approaches R Naik, A Mukhopadhyay, M Ganguli Drug discovery today 14 (5-6), 306-315, 2009 | 73 | 2009 |
| 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 | 69 | 2005 |
| 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 | 66 | 2002 |
| Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients S Mukherjee, A Mukhopadhyay, D Banerjee, GR Chandak, K Ray Haemophilia 10 (3), 259-263, 2004 | 59 | 2004 |
| Altered expression and editing of miRNA-100 regulates iTreg differentiation V Negi, D Paul, S Das, P Bajpai, S Singh, A Mukhopadhyay, A Agrawal, ... Nucleic Acids Research 43 (16), 8057-8065, 2015 | 55 | 2015 |
| Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma. A Mukhopadhyay, S Komatireddy, M Acharya, A Bhattacharjee, ... | 52 | 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 | 52 | 2002 |
Kunal RayProfessor, Ramakrishna Mission Vivekananda Educational and Research Institute, WB, IndiaVerified email at gm.rkmvu.ac.in
