نتائج البحث - Kumaramanickavel, Govindasamy

Gene therapy in ophthalmology حسب Uthra, Satagopan, Kumaramanickavel, Govindasamy

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Current concepts and molecular mechanisms in pharmacogenetics of essential hypertension حسب Rahman, Farhana, Muthaiah, Nagasundaram, Kumaramanickavel, Govindasamy

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Genetic analysis of axial length genes in high grade myopia from Indian population() حسب Sharmila, Ferdinamarie, Abinayapriya, Ramprabhu, Karthikeyan, Kumaramanickavel, Govindasamy, R.R.Sudhir, Sripriya, Sarangapani

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Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India حسب Ramprasad, Vedam Lakshmi, George, Ronnie, Soumittra, Nagasamy, Sharmila, Ferdinamarie, Vijaya, Lingam, Kumaramanickavel, Govindasamy

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Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus حسب Jeyabalan, Nallathambi, Shetty, Rohit, Ghosh, Anuprita, Anandula, Venkata Ramana, Ghosh, Arka Subhra, Kumaramanickavel, Govindasamy

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KIF14 and E2F3 mRNA expression in human retinoblastoma and its phenotype association حسب Madhavan, Jagadeesan, Mitra, Moutushy, Mallikarjuna, Kandalam, Pranav, Oberoi, Srinivasan, Ramalingam, Nagpal, Amit, Venkatesan, Perumal, Kumaramanickavel, Govindasamy

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Emerging trends in childhood blindness and ocular morbidity in India: the Pavagada Pediatric Eye Disease Study 2 حسب Kemmanu, Vasudha, Giliyar, Subramanya K., Shetty, Bhujanga K., Singh, Arvind Kumar, Kumaramanickavel, Govindasamy, McCarty, Catherine A

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Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2 حسب Kemmanu, Vasudha, Giliyar, Subramanya K., Rao, Harsha L., Shetty, Bhujanga K., Kumaramanickavel, Govindasamy, McCarty, Catherine A.

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Analysis of a comprehensive diabetic retinopathy screening model for rural and urban diabetics in developing countries حسب Rani, Padmaja Kumari, Raman, Rajiv, Sharma, Vikranth, Mahuli, Sachin Vasant, Tarigopala, Arokiasamy, Sudhir, RR, Kumaramanickavel, Govindasamy, Sharma, Tarun

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Association of PEDF polymorphisms with age-related macular degeneration and polypoidal choroidal vasculopathy: a systematic review and meta-analysis حسب Ma, Li, Tang, Shu Min, Rong, Shi Song, Chen, Haoyu, Young, Alvin L., Kumaramanickavel, Govindasamy, Pang, Chi Pui, Chen, Li Jia

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Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease حسب Battu, Rajani, Verma, Anshuman, Hariharan, Ramesh, Krishna, Shuba, Kiran, Ravi, Jacob, Jemima, Ganapathy, Aparna, Ramprasad, Vedam L., Kumaramanickavel, Govindasamy, Jeyabalan, Nallathambi, Ghosh, Arkasubhra

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Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis حسب Ramprasad, Vedam Lakshmi, Soumittra, Nagasamy, Nancarrow, Derek, Sen, Parveen, McKibbin, Martin, Williams, Grange A, Arokiasamy, Tharigopala, Lakshmipathy, Praveena, Inglehearn, Chris F, Kumaramanickavel, Govindasamy

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A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration حسب Ali, Manir, Ramprasad, Vedam Lakshmi, Soumittra, Nagasamy, Mohamed, Moin D., Jafri, Hussain, Rashid, Yasmin, Danciger, Michael, McKibbin, Martin, Kumaramanickavel, Govindasamy, Inglehearn, Chris F.

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ICAM-1 K469E polymorphism is a genetic determinant for the clinical risk factors of T2D subjects with retinopathy in Indians: a population-based case–control study حسب Vinita, Kumari, Sripriya, Sarangapani, Prathiba, Krishnamurthy, Vaitheeswaran, Kulothungan, Sathyabaarathi, Ravichandran, Rajesh, Mahendran, Amali, John, Umashankar, Vetrivel, Kumaramanickavel, Govindasamy, Pal, Swakshyar Saumya, Raman, Rajiv, Sharma, Tarun

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Retinoblastoma genetics screening and clinical management حسب Gupta, Himika, Malaichamy, Sivasankar, Mallipatna, Ashwin, Murugan, Sakthivel, Jeyabalan, Nallathambi, Suresh Babu, Vishnu, Ghosh, Anuprita, Ghosh, Arkasubhra, Santhosh, Sam, Seshagiri, Somasekar, Ramprasad, Vedam L., Kumaramanickavel, Govindasamy

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Ophthatome™: an integrated knowledgebase of ophthalmic diseases for translating vision research into the clinic حسب Raj, Praveen, Tejwani, Sushma, Sudha, Dandayudhapani, Muthu Narayanan, B., Thangapandi, Chandrasekar, Das, Sankar, Somasekar, J., Mangalapudi, Susmithasane, Kumar, Durgesh, Pindipappanahalli, Narendra, Shetty, Rohit, Ghosh, Arkasubhra, Kumaramanickavel, Govindasamy, Chaudhuri, Amitabha, Soumittra, Nagasamy

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Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa حسب Langmann, Thomas, Di Gioia, Silvio Alessandro, Rau, Isabella, Stöhr, Heidi, Maksimovic, Nela S., Corbo, Joseph C., Renner, Agnes B., Zrenner, Eberhart, Kumaramanickavel, Govindasamy, Karlstetter, Marcus, Arsenijevic, Yvan, Weber, Bernhard H.F., Gal, Andreas, Rivolta, Carlo

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Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism حسب Poulter, James A., Al-Araimi, Musallam, Conte, Ivan, van Genderen, Maria M., Sheridan, Eamonn, Carr, Ian M., Parry, David A., Shires, Mike, Carrella, Sabrina, Bradbury, John, Khan, Kamron, Lakeman, Phillis, Sergouniotis, Panagiotis I., Webster, Andrew R., Moore, Anthony T., Pal, Bishwanath, Mohamed, Moin D., Venkataramana, Anandula, Ramprasad, Vedam, Shetty, Rohit, Saktivel, Murugan, Kumaramanickavel, Govindasamy, Tan, Alex, Mackey, David A., Hewitt, Alex W., Banfi, Sandro, Ali, Manir, Inglehearn, Chris F., Toomes, Carmel

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A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration حسب Sivakumaran, Theru A., Igo, Robert P., Kidd, Jeffrey M., Itsara, Andy, Kopplin, Laura J., Chen, Wei, Hagstrom, Stephanie A., Peachey, Neal S., Francis, Peter J., Klein, Michael L., Chew, Emily Y., Ramprasad, Vedam L., Tay, Wan-Ting, Mitchell, Paul, Seielstad, Mark, Stambolian, Dwight E., Edwards, Albert O., Lee, Kristine E., Leontiev, Dmitry V., Jun, Gyungah, Wang, Yang, Tian, Liping, Qiu, Feiyou, Henning, Alice K., LaFramboise, Thomas, Sen, Parveen, Aarthi, Manoharan, George, Ronnie, Raman, Rajiv, Das, Manmath Kumar, Vijaya, Lingam, Kumaramanickavel, Govindasamy, Wong, Tien Y., Swaroop, Anand, Abecasis, Goncalo R., Klein, Ronald, Klein, Barbara E. K., Nickerson, Deborah A., Eichler, Evan E., Iyengar, Sudha K.

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Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration حسب Sivakumaran, Theru A., Igo, Robert P., Kidd, Jeffrey M., Itsara, Andy, Kopplin, Laura J., Chen, Wei, Hagstrom, Stephanie A., Peachey, Neal S., Francis, Peter J., Klein, Michael L., Chew, Emily Y., Ramprasad, Vedam L., Tay, Wan-Ting, Mitchell, Paul, Seielstad, Mark, Stambolian, Dwight E., Edwards, Albert O., Lee, Kristine E., Leontiev, Dmitry V., Jun, Gyungah, Wang, Yang, Tian, Liping, Qiu, Feiyou, Henning, Alice K., LaFramboise, Thomas, Sen, Parveen, Aarthi, Manoharan, George, Ronnie, Raman, Rajiv, Das, Manmath Kumar, Vijaya, Lingam, Kumaramanickavel, Govindasamy, Wong, Tien Y., Swaroop, Anand, Abecasis, Goncalo R., Klein, Ronald, Klein, Barbara E. K., Nickerson, Deborah A., Eichler, Evan E., Iyengar, Sudha K.

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