| Systematic review and meta-analysis of the association between complement component 3 and age-related macular degeneration: a HuGE review and meta-analysis A Thakkinstian, GJ McKay, M McEvoy, U Chakravarthy, S Chakrabarti, ... American journal of epidemiology 173 (12), 1365-1379, 2011 | 146 | 2011 |
| The molecular genetic basis of age-related macular degeneration: an overview S Katta, I Kaur, S Chakrabarti Journal of genetics 88, 425-449, 2009 | 141 | 2009 |
| 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 | 128 | 2005 |
| Analysis of CFH, TLR4, and APOE polymorphism in India suggests the Tyr402His variant of CFH to be a global marker for age-related macular degeneration I Kaur, A Hussain, N Hussain, T Das, A Pathangay, A Mathai, A Hussain, ... Investigative ophthalmology & visual science 47 (9), 3729-3735, 2006 | 97 | 2006 |
| Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients ABM Reddy, K Kaur, AK Mandal, SG Panicker, R Thomas, SE Hasnain, ... Molecular vision 10, 696-702, 2004 | 86 | 2004 |
| LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population DN Azmanov, S Dimitrova, L Florez, S Cherninkova, D Draganov, B Morar, ... European journal of human genetics 19 (3), 326-333, 2011 | 83 | 2011 |
| Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients I Kaur, S Katta, A Hussain, N Hussain, A Mathai, R Narayanan, A Hussain, ... Investigative ophthalmology & visual science 49 (5), 1771-1776, 2008 | 83 | 2008 |
| Complex genetic mechanisms in glaucoma: an overview KN Rao, S Nagireddy, S Chakrabarti Indian journal of ophthalmology 59 (Suppl1), S31-S42, 2011 | 81 | 2011 |
| Cataract, visual impairment and long-term mortality in a rural cohort in India: the Andhra Pradesh Eye Disease Study RC Khanna, GVS Murthy, P Giridhar, S Krishnaiah, HB Pant, ... PLoS One 8 (10), e78002, 2013 | 76 | 2013 |
| The association between complement component 2/complement factor B polymorphisms and age-related macular degeneration: a HuGE review and meta-analysis A Thakkinstian, M McEvoy, U Chakravarthy, S Chakrabarti, GJ McKay, ... American journal of epidemiology 176 (5), 361-372, 2012 | 76 | 2012 |
| Glaucoma-associated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes S Chakrabarti, KR Devi, S Komatireddy, K Kaur, RS Parikh, AK Mandal, ... Investigative ophthalmology & visual science 48 (12), 5439-5444, 2007 | 75 | 2007 |
| Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds S Chakrabarti, K Kaur, I Kaur, AK Mandal, RS Parikh, R Thomas, ... Investigative ophthalmology & visual science 47 (1), 43-47, 2006 | 75 | 2006 |
| Primary congenital glaucoma and the involvement of CYP1B1 K Kaur, AK Mandal, S Chakrabarti Middle East African journal of ophthalmology 18 (1), 7-16, 2011 | 74 | 2011 |
| The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma S Chakrabarti, K Kaur, KN Rao, AK Mandal, I Kaur, RS Parikh, R Thomas Investigative ophthalmology & visual science 50 (1), 75-83, 2009 | 74 | 2009 |
| A systematic investigation on complement pathway activation in diabetic retinopathy S Shahulhameed, S Vishwakarma, J Chhablani, M Tyagi, RR Pappuru, ... Frontiers in Immunology 11, 154, 2020 | 73 | 2020 |
| 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 |
| Abnormal complement activation and inflammation in the pathogenesis of retinopathy of prematurity S Rathi, S Jalali, S Patnaik, S Shahulhameed, GR Musada, ... Frontiers in immunology 8, 1868, 2017 | 65 | 2017 |
| Complement factor H polymorphism in age-related macular degeneration R Narayanan, V Butani, DS Boyer, SR Atilano, GP Resende, DS Kim, ... Ophthalmology 114 (7), 1327-1331, 2007 | 63 | 2007 |
| Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India S Komatireddy, S Chakrabarti, AK Mandal, AB Reddy, S Sampath, ... Mol Vis 9, 43-48, 2003 | 63 | 2003 |
| The involvement of complement factor B and complement component C2 in an Indian cohort with age-related macular degeneration I Kaur, S Katta, RK Reddy, R Narayanan, A Mathai, AB Majji, ... Investigative ophthalmology & visual science 51 (1), 59-63, 2010 | 60 | 2010 |
Inderjeet KaurL V Prasad Eye Institute, Hyderabad India在 lvpei.org 的电子邮件经过验证
