SLC4A11 mutations in Fuchs endothelial corneal dystrophy
Vithana, Eranga N., Morgan, Patricio E., Ramprasad, Vedam, Tan, Donald T.H., Yong, Victor H.K, Venkataraman, Divya, Venkatraman, Anandalakshmi, Yam, Gary H.F., Nagasamy, Soumittra, Law, Ricky W.K., Rajagopal, Rama, Pang, Chi P., Kumaramanickevel, Govindsamy, Casey, Joseph R., Aung, Tin
Published in Human molecular genetics (01.03.2008)
Published in Human molecular genetics (01.03.2008)
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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
Vithana, Eranga N, Morgan, Patricio, Sundaresan, Periasamy, Ebenezer, Neil D, Tan, Donald T H, Mohamed, Moin D, Anand, Seema, Khine, Khin O, Venkataraman, Divya, Yong, Victor H K, Salto-Tellez, Manuel, Venkatraman, Anandalakshmi, Guo, Ke, Hemadevi, Boomiraj, Srinivasan, Muthiah, Prajna, Venkatesh, Khine, Myint, Casey, Joseph R, Inglehearn, Chris F, Aung, Tin
Published in Nature genetics (01.07.2006)
Published in Nature genetics (01.07.2006)
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Analysis of the Posterior Polymorphous Corneal Dystrophy 3 Gene, TCF8, in Late-Onset Fuchs Endothelial Corneal Dystrophy
Mehta, Jodhbir S, Vithana, Eranga N, Tan, Donald T. H, Yong, Victor H. K, Yam, Gary H. F, Law, Ricky W. K, Chong, Wesley G. W, Pang, Calvin P, Aung, Tin
Published in Investigative ophthalmology & visual science (01.01.2008)
Published in Investigative ophthalmology & visual science (01.01.2008)
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Journal Article
Lack of Association between Interleukin-1 Gene Cluster Polymorphisms and Glaucoma in Chinese Subjects
How, Alicia C. S, Aung, Tin, Chew, Xinyi, Yong, Victor H. K, Lim, Marcus C. C, Lee, Kelvin Y. C, Toh, Ju-Yuan, Li, Yuqing, Liu, Jianjun, Vithana, Eranga N
Published in Investigative ophthalmology & visual science (01.05.2007)
Published in Investigative ophthalmology & visual science (01.05.2007)
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Molecular Analysis of the Myocilin Gene in Chinese Subjects with Chronic Primary-Angle Closure Glaucoma
Aung, Tin, Yong, Victor H. K, Chew, Paul T. K, Seah, Steve K. L, Gazzard, Gus, Foster, Paul J, Vithana, Eranga N
Published in Investigative ophthalmology & visual science (01.04.2005)
Published in Investigative ophthalmology & visual science (01.04.2005)
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Association of LOXL1 Gene Polymorphisms with Pseudoexfoliation in the Japanese
Ozaki, Mineo, Lee, Kelvin Y. C, Vithana, Eranga N, Yong, Victor H, Thalamuthu, Anbupalam, Mizoguchi, Takanori, Venkatraman, Anandalakshmi, Aung, Tin
Published in Investigative ophthalmology & visual science (01.09.2008)
Published in Investigative ophthalmology & visual science (01.09.2008)
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Association Analysis of CFH, C2, BF, and HTRA1 Gene Polymorphisms in Chinese Patients with Polypoidal Choroidal Vasculopathy
Lee, Kelvin Y, Vithana, Eranga N, Mathur, Ranjana, Yong, Victor H, Yeo, Ian Y, Thalamuthu, Anbupalam, Lee, Mun-Wai, Koh, Adrian H, Lim, Marcus C, How, Alicia C, Wong, Doric W, Aung, Tin
Published in Investigative ophthalmology & visual science (01.06.2008)
Published in Investigative ophthalmology & visual science (01.06.2008)
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CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients
Do, Tan, Shei, William, Chau, Pham Thi Minh, Trang, Doan Le, Yong, Victor H K, Ng, Xiao Yu, Chen, Yue Ming, Aung, Tin, Vithana, Eranga N
Published in Journal of glaucoma (01.05.2016)
Published in Journal of glaucoma (01.05.2016)
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Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in Singaporean subjects
Aung, Tin, Yong, Victor H K, Lim, Marcus C C, Venkataraman, Divya, Toh, Ju-Yuan, Chew, Paul T K, Vithana, Eranga N
Published in Journal of glaucoma (01.06.2008)
Published in Journal of glaucoma (01.06.2008)
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Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes
Aung, Tin, Lim, Marcus C C, Wong, Tina T L, Thalamuthu, Anbupalam, Yong, Victor H K, Venkataraman, Divya, Venkatraman, Anandalakshmi, Chew, Paul T K, Vithana, Eranga N
Published in Molecular vision (17.07.2008)
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Published in Molecular vision (17.07.2008)
Journal Article
Bradyopsia in an Asian man
Cheng, Jacob Y C, Luu, Chi D, Yong, Victor H K, Mathur, Ranjana, Aung, Tin, Vithana, Eranga N
Published in Archives of ophthalmology (1960) (01.08.2007)
Published in Archives of ophthalmology (1960) (01.08.2007)
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Rates of posterior capsule rupture during cataract surgery among different races in Singapore
Chan, Fiona M, Mathur, Ranjana, Ku, Jack J K, Chen, Ching, Chan, Siew Pang, Yong, Victor S H, Au Eong, Kah Guan
Published in Annals of the Academy of Medicine, Singapore (01.10.2006)
Published in Annals of the Academy of Medicine, Singapore (01.10.2006)
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Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Do, Tan, Nakano, Masakazu, George, Ronnie, Abu-Amero, Khaled, Duvesh, Roopam, Chen, Li Jia, Perera, Shamira A, Qiao, Chunyan, Wong, Hon-Tym, Dao, Thi Lam Huong, Ikeda, Yoko, Perez-Grossmann, Rodolfo A, Zarnowski, Tomasz, Tam, Pancy O S, Ayub, Humaira, Akhtar, Farah, Micheal, Shazia, Chew, Paul T K, Luu, Tam Thi, Wanichwecharungruang, Boonsong, Husain, Rahat, Jap, Aliza, Goh, David, Su, Daniel H, Wang, Huaizhou, Yip, Leonard W, Makornwattana, Manchima, Leuenberger, Edgar U, Tello, Celso, Kurimoto, Yasuo, Thapa, Suman S, Salmon, John F, Sohn, Yong Ho, Ozaki, Mineo, Lai, Jimmy S M, Nakano, Satoko, Tang, Guangxian, Wu, Renyi, Martinez, Jose Maria, Aung, Yin Mon, Fang, Seng Kheong, Chen, Xiao Yin, Foo, Jia Nee, Sim, Kar Seng, Wong, Tina T, Kavitha, Srinivasan, Krishnadas, Subbiah R, Shantha, Balekudaru, Lim, Boon-Ang, Ogle, Jeanne, de Souza, Bruno B, Aquino, Maria C, Fong, Guillermo Barreto, Fujita, Ricardo, Waseem, Naushin, Low, Sancy, Pham, Huan Nguyen, Al-Shahwan, Sami, Mohanty, Kuldeep, Faiq, Muneeb A, Hewitt, Alex W, Catacutan, Mary Ann T, Felarca, Irene R, Consolandi, Giulia, Pignata, Giulia, Mangkornkanokpong, Lerprat, Chansangpetch, Sunee, Choy, Bonnie N K, Than, Hlaing May, Hibberd, Martin L, Png, Eileen, Bei, Jinxin, Zeng, Yi Xin, Karkey, Abhilasha, Frezzotti, Paolo, Allingham, R Rand, Hauser, Michael A, Lim, Soon Thye, Chew, Soo Hong, Sakuntabhai, Anavaj, Snippe, Harm, Stead, Richard, Zaw, Su Nyunt, Shetty, Rohit, Zahari, Mimiwati, Kubota, Toshiaki, Hwang, Young Hoon, Jeoung, Jin Wook, Srisamran, Nuttamon, Sandragasu, Thayanithi, Lozano-Giral, David, Cheng, Ching-Yu, Yonahara, Michiko, Xu, Liang, Do, Nhu Hon, Sundaresan, Periasamy, Foster, Paul J, Vijaya, Lingam, Tashiro, Kei, Aung, Tin
Published in Nature genetics (01.05.2016)
Published in Nature genetics (01.05.2016)
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Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma
Vithana, Eranga N, Khor, Chiea-Chuen, Qiao, Chunyan, Nongpiur, Monisha E, George, Ronnie, Chen, Li-Jia, Do, Tan, Abu-Amero, Khaled, Huang, Chor Kai, Low, Sancy, Tajudin, Liza-Sharmini A, Perera, Shamira A, Cheng, Ching-Yu, Xu, Liang, Jia, Hongyan, Ho, Ching-Lin, Sim, Kar Seng, Wu, Ren-Yi, Tham, Clement C Y, Chew, Paul T K, Su, Daniel H, Oen, Francis T, Sarangapani, Sripriya, Soumittra, Nagaswamy, Osman, Essam A, Wong, Hon-Tym, Tang, Guangxian, Fan, Sujie, Meng, Hailin, Huong, Dao T L, Wang, Hua, Feng, Bo, Baskaran, Mani, Shantha, Balekudaru, Ramprasad, Vedam L, Kumaramanickavel, Govindasamy, Iyengar, Sudha K, How, Alicia C, Lee, Kelvin Y, Sivakumaran, Theru A, Yong, Victor H K, Ting, Serena M L, Li, Yang, Wang, Ya-Xing, Tay, Wan-Ting, Sim, Xueling, Lavanya, Raghavan, Cornes, Belinda K, Zheng, Ying-Feng, Wong, Tina T, Loon, Seng-Chee, Yong, Vernon K Y, Waseem, Naushin, Yaakub, Azhany, Chia, Kee-Seng, Allingham, R Rand, Hauser, Michael A, Lam, Dennis S C, Hibberd, Martin L, Bhattacharya, Shomi S, Zhang, Mingzhi, Teo, Yik Ying, Tan, Donald T, Jonas, Jost B, Tai, E-Shyong, Saw, Seang-Mei, Hon, Do Nhu, Al-Obeidan, Saleh A, Liu, Jianjun, Chau, Tran Nguyen Bich, Simmons, Cameron P, Bei, Jin-Xin, Zeng, Yi-Xin, Foster, Paul J, Vijaya, Lingam, Wong, Tien-Yin, Pang, Chi-Pui, Wang, Ningli, Aung, Tin
Published in Nature genetics (01.10.2012)
Published in Nature genetics (01.10.2012)
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A common variant near TGFBR3 is associated with primary open angle glaucoma
Li, Zheng, Allingham, R Rand, Nakano, Masakazu, Jia, Liyun, Chen, Yuhong, Ikeda, Yoko, Mani, Baskaran, Chen, Li-Jia, Kee, Changwon, Garway-Heath, David F, Sripriya, Sarangapani, Fuse, Nobuo, Abu-Amero, Khaled K, Huang, Chukai, Namburi, Prasanthi, Burdon, Kathryn, Perera, Shamira A, Gharahkhani, Puya, Lin, Ying, Ueno, Morio, Ozaki, Mineo, Mizoguchi, Takanori, Krishnadas, Subbiah Ramasamy, Osman, Essam A, Lee, Mei Chin, Chan, Anita S Y, Tajudin, Liza-Sharmini A, Do, Tan, Goncalves, Aurelien, Reynier, Pascal, Zhang, Hong, Bourne, Rupert, Goh, David, Broadway, David, Husain, Rahat, Negi, Anil K, Su, Daniel H, Ho, Ching-Lin, Blanco, Augusto Azuara, Leung, Christopher K S, Wong, Tina T, Yakub, Azhany, Liu, Yutao, Nongpiur, Monisha E, Han, Jong Chul, Hon, Do Nhu, Shantha, Balekudaru, Zhao, Bowen, Sang, Jinghong, Zhang, NiHong, Sato, Ryuichi, Yoshii, Kengo, Panda-Jonas, Songhomita, Ashley Koch, Allison E, Herndon, Leon W, Moroi, Sayoko E, Challa, Pratap, Foo, Jia Nee, Bei, Jin-Xin, Zeng, Yi-Xin, Simmons, Cameron P, Bich Chau, Tran Nguyen, Sharmila, Philomenadin Ferdinamarie, Chew, Merwyn, Lim, Blanche, Tam, Pansy O S, Chua, Elaine, Ng, Xiao Yu, Yong, Victor H K, Chong, Yaan Fun, Meah, Wee Yang, Vijayan, Saravanan, Seongsoo, Sohn, Xu, Wang, Teo, Yik Ying, Cooke Bailey, Jessica N, Kang, Jae H, Haines, Jonathan L, Cheng, Ching Yu, Saw, Seang-Mei, Tai, E-Shyong, Richards, Julia E, Ritch, Robert, Gaasterland, Douglas E, Pasquale, Louis R, Liu, Jianjun, Jonas, Jost B, Milea, Dan, George, Ronnie, Al-Obeidan, Saleh A, Mori, Kazuhiko, Macgregor, Stuart, Hewitt, Alex W, Girkin, Christopher A, Zhang, Mingzhi, Sundaresan, Periasamy, Vijaya, Lingam, Mackey, David A, Wong, Tien Yin, Craig, Jamie E
Published in Human molecular genetics (01.07.2015)
Published in Human molecular genetics (01.07.2015)
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ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur, Monisha E, Khor, Chiea Chuen, Jia, Hongyan, Cornes, Belinda K, Chen, Li-Jia, Qiao, Chunyan, Nair, K Saidas, Cheng, Ching-Yu, Xu, Liang, George, Ronnie, Tan, Do, Abu-Amero, Khaled, Perera, Shamira A, Ozaki, Mineo, Mizoguchi, Takanori, Kurimoto, Yasuo, Low, Sancy, Tajudin, Liza-Sharmini A, Ho, Ching-Lin, Tham, Clement C Y, Soto, Ileana, Chew, Paul T K, Wong, Hon-Tym, Shantha, Balekudaru, Kuroda, Masako, Osman, Essam A, Tang, Guangxian, Fan, Sujie, Meng, Hailin, Wang, Hua, Feng, Bo, Yong, Victor H K, Ting, Serena M L, Li, Yang, Wang, Ya-Xing, Li, Zheng, Lavanya, Raghavan, Wu, Ren-Yi, Zheng, Ying-Feng, Su, Daniel H, Loon, Seng-Chee, Yong, Vernon K Y, Allingham, R Rand, Hauser, Michael A, Soumittra, Nagaswamy, Ramprasad, Vedam L, Waseem, Naushin, Yaakub, Azhany, Chia, Kee-Seng, Kumaramanickavel, Govindasamy, Wong, Tina T, How, Alicia C, Chau, Tran Nguyen Bich, Simmons, Cameron P, Bei, Jin-Xin, Zeng, Yi-Xin, Bhattacharya, Shomi S, Zhang, Mingzhi, Tan, Donald T, Teo, Yik-Ying, Al-Obeidan, Saleh A, Hon, Do Nhu, Tai, E-Shyong, Saw, Seang-Mei, Foster, Paul J, Vijaya, Lingam, Jonas, Jost B, Wong, Tien-Yin, John, Simon W M, Pang, Chi-Pui, Vithana, Eranga N, Wang, Ningli, Aung, Tin
Published in PLoS genetics (01.03.2014)
Published in PLoS genetics (01.03.2014)
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Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online
Ramprasad, Vedam L, Ebenezer, Neil D, Aung, Tin, Rajagopal, Rama, Yong, Victor H K, Tuft, Stephen J, Viswanathan, Deepa, El-Ashry, Mohamed F, Liskova, Petra, Tan, Donald T H, Bhattacharya, Shomi S, Kumaramanickavel, Govindasamy, Vithana, Eranga N
Published in Human mutation (01.05.2007)
Published in Human mutation (01.05.2007)
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