檢索結果 - Kumaramanickavel, Govindasamy

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

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

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Genetic analysis of axial length genes in high grade myopia from Indian population() 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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