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by Vithana, Eranga N and Khor, Chiea-Chuen and Qiao, Chunyan and Nongpiur, Monisha E and George, Ronnie and Chen, Li-Jia and Do, Tan and Abu-Amero, Khaled and Huang, Chor Kai and Low, Sancy and Tajudin, Liza-Sharmini A and Perera, Shamira A and Cheng, Ching-Yu and Xu, Liang and Jia, Hongyan and Ho, Ching-Lin and Sim, Kar Seng and Wu, Ren-Yi and Tham, Clement C. Y and Chew, Paul T. K and Su, Daniel H and Oen, Francis T and Sarangapani, Sripriya and Soumittra, Nagaswamy and Osman, Essam A and Wong, Hon-Tym and Tang, Guangxian and Fan, Sujie and Meng, Hailin and Huong, Dao T. L and Wang, Hua and Feng, Bo and Baskaran, Mani and Shantha, Balekudaru and Ramprasad, Vedam L and Kumaramanickavel, Govindasamy and Iyengar, Sudha K and How, Alicia C and Lee, Kelvin Y and Sivakumaran, Theru A and Yong, Victor H. K and Ting, Serena M. L and Li, Yang and Wang, Ya-Xing and Tay, Wan-Ting and Sim, Xueling and Lavanya, Raghavan and Cornes, Belinda K and Zheng, Ying-Feng and Wong, Tina T and Loon, Seng-Chee and Yong, Vernon K. Y and Waseem, Naushin and Yaakub, Azhany and Chia, Kee-Seng and Rand Allingham, R and Hauser, Michael A and Lam, Dennis S. C and Hibberd, Martin L and Bhattacharya, Shomi S and Zhang, Mingzhi and Teo, Yik Ying and Tan, Donald T and Jonas, Jost B and Tai, E-Shyong and Saw, Seang-Mei and Hon, Do Nhu and Al-Obeidan, Saleh A and Liu, Jianjun and Chau, Tran Nguyen Bich and Simmons, Cameron P and Bei, Jin-Xin and Zeng, Yi-Xin and Foster, Paul J and Vijaya, Lingam and Wong, Tien-Yin and Pang, Chi-Pui and Wang, Ningli and Aung, Tin
Nature Genetics, ISSN 1061-4036, 10/2012, Volume 44, Issue 10, pp. 1142 - 1146
Journal Article
by Aung, T and Ozaki, M and Lee, M.C and Schlotzer-Schrehardt, U and Thorleifsson, G and Mizoguchi, T and Igo, R.P., Jr and Haripriya, A and Williams, S.E and Astakhov, Y.S and Orr, A.C and Burdon, K.P and Nakano, S and Mori, K and Abu-Amero, K and Hauser, M and Li, Z and Prakadeeswari, G and Bailey, J.N and Cherecheanu, A.P and Kang, J.H and Nelson, S and Hayashi, K and Manabe, S.I and Kazama, S and Zarnowski, T and Inoue, K and Irkec, M and Coca-Prados, M and Sugiyama, K and Jarvela, I and Schlottmann, P and Lerner, S.F and Lamari, H and Nilgun, Y and Bikbov, M and Park, K.H and Cha, S.C and Yamashiro, K and Zenteno, J.C and Jonas, J.B and Kumar, R.S.S and Perera, S.A and Chan, A.S.Y and Kobakhidze, N and George, R and Vijaya, L and Do, T and Edward, D.P and Juan Marcos, L. de and Pakravan, M and Moghimi, S and Ideta, R and Bach-Holm, D and Kappelgaard, P and Wirostko, B and Thomas, S and Gaston, D and Bedard, K and Greer, W.L and Yang, Z and Chen, X and Huang, L and Sang, J and Jia, H and Jia, L and Qiao, C and Zhang, H and Liu, X and Zhao, B and Wang, Y.X and Xu, L and Leruez, S and Reynier, P and Chichua, G and Tabagari, S and Uebe, S and Zenkel, M and Berner, D and Mossbock, G and Weisschuh, N and Hoja, U and Welge-Luessen, U.C and Mardin, C and Founti, P and Chatzikyriakidou, A and Pappas, T and Anastasopoulos, E and Lambropoulos, A and Ghosh, A and Shetty, R and Porporato, N and Saravanan, V and Venkatesh, R and Shivkumar, C and Kalpana, N and Sarangapani, S and Kanavi, M.R and Beni, A.N and Yazdani, S and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 7, pp. 993 - 1004
Exfoliation syndrome (XFS) is the most common known risk factor for secondary glaucoma and a major cause of blindness worldwide. Variants in two genes, LOXL1... 
INDIVIDUALS | RISK LOCI | PSEUDOEXFOLIATION SYNDROME | INFLAMMATORY-BOWEL-DISEASE | METAANALYSIS | POLYMORPHISMS | COMMON SEQUENCE VARIANTS | GENETICS & HEREDITY | GLAUCOMA | BLOOD-PRESSURE | GENOME-WIDE ASSOCIATION | Haplotypes | Humans | Asian Continental Ancestry Group - genetics | Extracellular Matrix - metabolism | Male | Gene Expression Profiling | Mutation, Missense | Amino Acid Oxidoreductases - genetics | Exfoliation Syndrome - ethnology | RNA, Messenger - biosynthesis | Aged, 80 and over | Female | Spheroids, Cellular | Calcium Channels - genetics | Molecular Chaperones - biosynthesis | Eye - metabolism | Genetic Predisposition to Disease | Genome-Wide Association Study | Amino Acid Oxidoreductases - physiology | Molecular Chaperones - genetics | Cell Adhesion | Point Mutation | Alleles | Exfoliation Syndrome - genetics | Amino Acid Substitution | Exfoliatins | Disease susceptibility | Genetic aspects | Analysis | Risk factors | Glaucoma | Genes | Principal components analysis | Cardiovascular disease | Genomes | Biology | Loci | Exfoliation | Studies | Collaboration | Blindness | Alzheimers disease | Index Medicus | Life Sciences | Populations and Evolution | Microbiology and Parasitology | Parasitology | Quantitative Methods | Computer Science | Genetics | Santé publique et épidémiologie | Bioinformatics | Human genetics | Virology
Journal Article
by Li, Zheng and Allingham, R. Rand and Nakano, Masakazu and Jia, Liyun and Chen, Yuhong and Ikeda, Yoko and Mani, Baskaran and Chen, Li-Jia and Kee, Changwon and Garway-Heath, David F and Sripriya, Sarangapani and Fuse, Nobuo and Abu-Amero, Khaled K and Huang, Chukai and Namburi, Prasanthi and Burdon, Kathryn and Perera, Shamira A and Gharahkhani, Puya and Lin, Ying and Ueno, Morio and Ozaki, Mineo and Mizoguchi, Takanori and Krishnadas, Subbiah Ramasamy and Osman, Essam A and Lee, Mei Chin and Chan, Anita S.Y and Tajudin, Liza-Sharmini A and Do, Tan and Goncalves, Aurelien and Reynier, Pascal and Zhang, Hong and Bourne, Rupert and Goh, David and Broadway, David and Husain, Rahat and Negi, Anil K and Su, Daniel H and Ho, Ching-Lin and Blanco, Augusto Azuara and Leung, Christopher K.S and Wong, Tina T and Yakub, Azhany and Liu, Yutao and Nongpiur, Monisha E and Han, Jong Chul and Hon, Do Nhu and Shantha, Balekudaru and Zhao, Bowen and Sang, Jinghong and Zhang, NiHong and Sato, Ryuichi and Yoshii, Kengo and Panda-Jonas, Songhomita and Ashley Koch, Allison E and Herndon, Leon W and Moroi, Sayoko E and Challa, Pratap and Foo, Jia Nee and Bei, Jin-Xin and Zeng, Yi-Xin and Simmons, Cameron P and Bich Chau, Tran Nguyen and Sharmila, Philomenadin Ferdinamarie and Chew, Merwyn and Lim, Blanche and Tam, Pansy O.S and Chua, Elaine and Ng, Xiao Yu and Yong, Victor H.K and Chong, Yaan Fun and Meah, Wee Yang and Vijayan, Saravanan and Seongsoo, Sohn and Xu, Wang and Teo, Yik Ying and Cooke Bailey, Jessica N and Kang, Jae H and Haines, Jonathan L and Cheng, Ching Yu and Saw, Seang-Mei and Tai, E.-Shyong and Richards, Julia E and Ritch, Robert and Gaasterland, Douglas E and Pasquale, Louis R and Liu, Jianjun and Jonas, Jost B and Milea, Dan and George, Ronnie and Al-Obeidan, Saleh A and Mori, Kazuhiko and Macgregor, Stuart and Hewitt, Alex W and Girkin, Christopher A and Zhang, Mingzhi and Sundaresan, Periasamy and Vijaya, Lingam and Mackey, David A and Wong, Tien Yin and Craig, Jamie E and ... and ICAARE-Glaucoma Consortium and NEIGHBORHOOD Consortium
Human Molecular Genetics, ISSN 0964-6906, 07/2015, Volume 24, Issue 13, pp. 3880 - 3892
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 3, pp. e1004089 - e1004089
Journal Article
Journal Article
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 01/2008, Volume 49, Issue 1, pp. 184 - 188
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 10/2005, Volume 46, Issue 10, pp. 3812 - 3816
Journal Article
Human mutation, 2007, Volume 28, Issue 5, pp. 522 - 523
Autosomal recessive congenital hereditary endothelial dystrophy (CHED2) is a severe and rare corneal disorder that presents at birth or shortly thereafter,... 
Corneal Diseases - genetics | United States | Humans | Antiporters - genetics | Mutation | Genes, Recessive | Anion Transport Proteins - genetics | Genetic Carrier Screening | India | Index Medicus
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2014, Volume 10, Issue 3
  Anterior chamber depth (ACD) is a key anatomical risk factor for primary angle closure glaucoma (PACG). We conducted a genome-wide association study (GWAS)... 
Confidence intervals | Glaucoma | Ethnicity | Biomedical research | Genes | Genomics | Cardiovascular disease | Population | Influence | Genomes | Collections
Journal Article