Хайлтын үр дүнгүүд - Kumaramanickavel, Govindasamy

Gene therapy in ophthalmology -н Uthra, Satagopan, Kumaramanickavel, Govindasamy

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах

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

Бүрэн текст авах Бүрэн текст авах

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 -н 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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Retinoblastoma genetics screening and clinical management -н 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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Ophthatome™: an integrated knowledgebase of ophthalmic diseases for translating vision research into the clinic -н 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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa -н 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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism -н 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

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration -н 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.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах

Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration -н 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.

Бүрэн текст авах Бүрэн текст авах Бүрэн текст авах