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Lancet, The, ISSN 0140-6736, 2015, Volume 386, Issue 9991, pp. 360 - 368
Journal Article
Nature genetics, ISSN 1061-4036, 10/2014, Volume 46, Issue 10, pp. 1120 - 1125
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 | Life Sciences | Populations and Evolution | Microbiology and Parasitology | Parasitology | Quantitative Methods | Computer Science | Genetics | Santé publique et épidémiologie | Bioinformatics | Human genetics | Virology
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0172427
Purpose To identify biological processes associated with POAG and its subtypes, high-tension (HTG) and normal -tension glaucoma (NTG), by analyzing rare... 
CENTRAL CORNEAL THICKNESS | WILD-TYPE | CHEMICAL CHAPERONE | COPY NUMBER VARIATIONS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | ENDOPLASMIC-RETICULUM STRESS | MUTATIONS | MYOCILIN | GENOME-WIDE ASSOCIATION | CELL-DEATH | Computational Biology - methods | Genetic Predisposition to Disease | Unfolded Protein Response - genetics | Glaucoma, Open-Angle - genetics | Humans | Middle Aged | Gene Expression Regulation | Apoptosis - genetics | Male | Gene Expression Profiling | Gene Regulatory Networks | Case-Control Studies | Exome | Organogenesis - genetics | Adult | Female | Glaucoma, Open-Angle - metabolism | Cell Membrane - metabolism | High-Throughput Nucleotide Sequencing | Mutation | Gene Ontology | Homeostasis - genetics | Usage | Care and treatment | Molecular chaperones | Open-angle glaucoma | Exome sequencing | Cell membranes | Genetic aspects | Research | Glaucoma | Enrichment | Regulators | Neurosciences | Calcium | Pathogenesis | Genes | Science | Homeostasis | Retina | Genomes | Phospholipids | Kinases | Eye | Proteins | Protein folding | Network analysis | Ion channels | Tension | Discipline | Deoxyribonucleic acid--DNA | Antigen presentation | Medical research | Gene expression | Minority & ethnic groups | Disease control | Biological activity | Membrane proteins | Calcium chloride | Studies | Genetic variance | Hospitals | Major histocompatibility complex | Transport processes | Aberration | Apoptosis | Deoxyribonucleic acid | DNA
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 3124 - 12
Open-angle glaucoma (OAG) is a major cause of blindness worldwide. To identify new risk loci for OAG, we performed a genome-wide association study in 3,071 OAG... 
COMMON VARIANTS | RETINOIC ACID | GENOTYPE IMPUTATION | TRABECULAR MESHWORK | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | MACULAR DEGENERATION | TO-DISC RATIO | INTRAOCULAR-PRESSURE | EYE DEVELOPMENT | GENOME-WIDE ASSOCIATION | Macular degeneration | Glaucoma | Blindness | Myopia | Fluid flow | Eye diseases | Retina | Genomes | Mechanical stimuli | Gene mapping | Age
Journal Article
Lancet Respiratory Medicine, The, ISSN 2213-2600, 2017, Volume 5, Issue 1, pp. 51 - 60
Journal Article
Australian Family Physician, ISSN 0300-8495, 08/2015, Volume 44, Issue 8, pp. 554 - 557
Journal Article
by Khor, Chiea Chuen and Do, Tan and Jia, Hongyan and Nakano, Masakazu and George, Ronnie and Abu-Amero, Khaled and Duvesh, Roopam and Chen, Li Jia and Li, Zheng and Nongpiur, Monisha E and Perera, Shamira A and Qiao, Chunyan and Wong, Hon-Tym and Sakai, Hiroshi and De Melo, Mônica Barbosa and Lee, Mei-Chin and SChan, Anita and Azhany, Yaakub and Dao, Thi Lam Huong and Ikeda, Yoko and Perez-Grossmann, Rodolfo A and Zarnowski, Tomasz and Day, Alexander C and Jonas, Jost B and Tam, Pancy O.S and Tran, Tuan Anh and Ayub, Humaira and Akhtar, Farah and Micheal, Shazia and Chew, Paul T.K and Aljasim, Leyla A and Dada, Tanuj and Luu, Tam Thi and Awadalla, Mona S and Kitnarong, Naris and Wanichwecharungruang, Boonsong and Aung, Yee Yee and Mohamed-Noor, Jelinar and Vijayan, Saravanan and Sarangapani, Sripriya and Husain, Rahat and Jap, Aliza and Baskaran, Mani and Goh, David and Su, Daniel H and Wang, Huaizhou and Yong, Vernon K and Yip, Leonard W and Trinh, Tuyet Bach and Makornwattana, Manchima and Nguyen, Thanh Thu and Leuenberger, Edgar U and Park, Ki-Ho and Wiyogo, Widya Artini and SKumar, Rajesh and Tello, Celso and Kurimoto, Yasuo and Thapa, Suman S and Pathanapitoon, Kessara and Salmon, John F and Sohn, Yong Ho and Fea, Antonio and Ozaki, Mineo and Lai, Jimmy S.M and Tantisevi, Visanee and Khaing, Chaw Chaw and Mizoguchi, Takanori and Nakano, Satoko and Kim, Chan-Yun and Tang, Guangxian and Fan, Sujie and Wu, Renyi and Meng, Hailin and Nguyen, Thi Thuy Giang and Tran, Tien Dat and Ueno, Morio and Martinez, Jose Maria and Ramli, Norlina and Aung, Yin Mon and Reyes, Rigo Daniel and Vernon, Stephen A and Fang, Seng Kheong and Xie, Zhicheng and Chen, Xiao Yin and Foo, Jia Nee and Sim, Kar Seng and Wong, Tina T and Quek, Desmond T and Venkatesh, Rengaraj and Kavitha, Srinivasan and Krishnadas, Subbiah R and Soumittra, Nagaswamy and Shantha, Balekudaru and Lim, Boon-Ang and Ogle, Jeanne and Vasconcellos, José P. Cde and Costa, Vital P and Abe, Ricardo Y and De Souza, Bruno B and Sng, Chelvin C and ...
Nature Genetics, ISSN 1061-4036, 05/2016, Volume 48, Issue 5, pp. 556 - 562
Journal Article
by Verhoeven, Virginie J. M and Hysi, Pirro G and Wojciechowski, Robert and Fan, Qiao and Guggenheim, Jeremy A and Höhn, René and Macgregor, Stuart and Hewitt, Alex W and Nag, Abhishek and Cheng, Ching-Yu and Yonova-Doing, Ekaterina and Zhou, Xin and Ikram, M. Kamran and Buitendijk, Gabriëlle H. S and McMahon, George and Kemp, John P and Pourcain, Beate St and Simpson, Claire L and Mäkelä, Kari-Matti and Lehtimäki, Terho and Kähönen, Mika and Paterson, Anew D and Hosseini, S. Mohsen and Wong, Hoi Suen and Xu, Liang and Jonas, Jost B and Pärssinen, Olavi and Wedenoja, Juho and Yip, Shea Ping and Ho, Daniel W. H and Pang, Chi Pui and Chen, Li Jia and Burdon, Kathryn P and Craig, Jamie E and Klein, Barbara E. K and Klein, Ronald and Haller, Toomas and Metspalu, Anes and Khor, Chiea-Chuen and Tai, E.-Shyong and Aung, Tin and Vithana, Eranga and Tay, Wan-Ting and Barathi, Veluchamy A and Chen, Peng and Li, Ruoying and Liao, Jiemin and Zheng, Yingfeng and Ong, Rick T and Döring, Angela and Evans, David M and Timpson, Nicholas J and Verkerk, Annemieke J. M. H and Meitinger, Thomas and Raitakari, Olli and Hawthorne, Felicia and Spector, Tim D and Karssen, Lennart C and Pirastu, Mario and Murgia, Federico and Ang, Wei and Mishra, Aniket and Montgomery, Grant W and Pennell, Craig E and Cumberland, Phillippa M and Cotlarciuc, Ioana and Mitchell, Paul and Wang, Jie Jin and Schache, Maria and Janmahasathian, Sarayut and Igo, Robert P and Lass, Jonathan H and Chew, Emily and Iyengar, Sudha K and Gorgels, Theo G. M. F and Rudan, Igor and Hayward, Caroline and Wright, Alan F and Polasek, Ozren and Vatavuk, Zoran and Wilson, James F and Fleck, Brian and Zeller, Tanja and Mirshahi, Alireza and Müller, Christian and Uitterlinden, Ané G and Rivadeneira, Fernando and Vingerling, Johannes R and Hofman, Albert and Oostra, Ben A and Amin, Najaf and Bergen, Arthur A. B and teo, Yik-Ying and Rahi, Jugnoo S and Vitart, Veronique and Williams, Cathy and Baird, Paul N and Wong, Tien-Yin and Oexle, Konrad and Pfeiffer, Norbert and ... and Fuchs' Genetics Multi-Ctr Study Gr and Diabet Control Complications Trial and WTCCC2 and CREAM and Consortium for Refractive Error and Myopia (CREAM) and Fuchs' Genetics Multi-Center Study Group and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and Wellcome Trust Case Control Consortium 2 (WTCCC2) and The Fuchs' Genetics Multi-Center Study Group and The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 3, pp. 314 - 318
Journal Article