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by Hysi, Pirro G and Cheng, Ching-Yu and Springelkamp, Henriët and Macgregor, Stuart and Bailey, Jessica N Cooke and Wojciechowski, Robert and Vitart, Veronique and Nag, Abhishek and Hewitt, Alex W and Höhn, René and Venturini, Cristina and Mirshahi, Alireza and Ramdas, Wishal D and Thorleifsson, Gudmar and Vithana, Eranga and Khor, Chiea-Chuen and Stefansson, Arni B and Liao, Jiemin and Haines, Jonathan L and Amin, Najaf and Wang, Ya Xing and Wild, Philipp S and Ozel, Ayse B and Li, Jun Z and Fleck, Brian W and Zeller, Tanja and Staffieri, Sandra E and Teo, Yik-Ying and Cuellar-Partida, Gabriel and Luo, Xiaoyan and Allingham, R Rand and Richards, Julia E and Senft, Andrea and Karssen, Lennart C and Zheng, Yingfeng and Bellenguez, Céline and Xu, Liang and Iglesias, Adriana I and Wilson, James F and Kang, Jae H and van Leeuwen, Elisabeth M and Jonsson, Vesteinn and Thorsteinsdottir, Unnur and Despriet, Dominiek D G and Ennis, Sarah and Moroi, Sayoko E and Martin, Nicholas G and Jansonius, Nomdo M and Yazar, Seyhan and Tai, E-Shyong and Amouyel, Philippe and Kirwan, James and van Koolwijk, Leonieke M E and Hauser, Michael A and Jonasson, Fridbert and Leo, Paul and Loomis, Stephanie J and Fogarty, Rhys and Rivadeneira, Fernando and Kearns, Lisa and Lackner, Karl J and de Jong, Paulus T V M and Simpson, Claire L and Pennell, Craig E and Oostra, Ben A and Uitterlinden, André G and Saw, Seang-Mei and Lotery, Andrew J and Bailey-Wilson, Joan E and Hofman, Albert and Vingerling, Johannes R and Maubaret, Cécilia and Pfeiffer, Norbert and Wolfs, Roger C W and Lemij, Hans G and Young, Terri L and Pasquale, Louis R and Delcourt, Cécile and Spector, Timothy D and Klaver, Caroline C W and Small, Kerrin S and Burdon, Kathryn P and Stefansson, Kari and Wong, Tien-Yin and Viswanathan, Ananth and Mackey, David A and Craig, Jamie E and Wiggs, Janey L and van Duijn, Cornelia M and Hammond, Christopher J and Aung, Tin and NEIGHBORHOOD Consortium and Wellcome Trust Case Control Consortium 2 and BMES GWAS Group and BMES GWAS Grp and Wellcome Trust Case Control Conso
Nature genetics, ISSN 1546-1718, 2014, Volume 46, Issue 10, pp. 1126 - 1130
Journal Article
PLoS genetics, ISSN 1553-7404, 2012, Volume 8, Issue 4, pp. e1002654 - 424
Journal Article
PLoS genetics, ISSN 1553-7404, 2019, Volume 15, Issue 5, p. e1008130
Journal Article
by Bailey, Jessica N Cooke and Loomis, Stephanie J and Kang, Jae H and Allingham, R Rand and Gharahkhani, Puya and Khor, Chiea Chuen and Burdon, Kathryn P and Aschard, Hugues and Chasman, Daniel I and Igo, Robert P and Hysi, Pirro G and Glastonbury, Craig A and Ashley-Koch, Allison and Brilliant, Murray and Brown, Andrew A and Budenz, Donald L and Buil, Alfonso and Cheng, Ching-Yu and Choi, Hyon and Christen, William G and Curhan, Gary and De Vivo, Immaculata and Fingert, John H and Foster, Paul J and Fuchs, Charles and Gaasterland, Douglas and Gaasterland, Terry and Hewitt, Alex W and Hu, Frank and Hunter, David J and Khawaja, Anthony P and Lee, Richard K and Li, Zheng and Lichter, Paul R and Mackey, David A and McGuffin, Peter and Mitchell, Paul and Moroi, Sayoko E and Perera, Shamira A and Pepper, Keating W and Qi, Qibin and Realini, Tony and Richards, Julia E and Ridker, Paul M and Rimm, Eric and Ritch, Robert and Ritchie, Marylyn and Schuman, Joel S and Scott, William K and Singh, Kuldev and Sit, Arthur J and Song, Yeunjoo E and Tamimi, Rulla M and Topouzis, Fotis and Viswanathan, Ananth C and Verma, Shefali Setia and Vollrath, Douglas and Wang, Jie Jin and Weisschuh, Nicole and Wissinger, Bernd and Wollstein, Gadi and Wong, Tien Y and Yaspan, Brian L and Zack, Donald J and Zhang, Kang and Study, EPIC-Norfolk Eye and Weinreb, Robert N and Pericak-Vance, Margaret A and Small, Kerrin and Hammond, Christopher J and Aung, Tin and Liu, Yutao and Vithana, Eranga N and MacGregor, Stuart and Craig, Jamie E and Kraft, Peter and Howell, Gareth and Hauser, Michael A and Pasquale, Louis R and Haines, Jonathan L and Wiggs, Janey L and ANZRAG Consortium and EPIC Norfolk Eye Study
Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 2, pp. 189 - 194
Journal Article
by Lu, Yi and Vitart, Veronique and Burdon, Kathryn P and Khor, Chiea Chuen and Bykhovskaya, Yelena and Mirshahi, Alireza and Hewitt, Alex W and Koehn, Demelza and Hysi, Pirro G and Ramdas, Wishal D and Zeller, Tanja and Vithana, Eranga N and Cornes, Belinda K and Tay, Wan-Ting and Tai, E Shyong and Cheng, Ching-Yu and Liu, Jianjun and Foo, Jia-Nee and Saw, Seang Mei and Thorleifsson, Gudmar and Stefansson, Kari and Dimasi, David P and Mills, Richard A and Mountain, Jenny and Ang, Wei and Hoehn, René and Verhoeven, Virginie J M and Grus, Franz and Wolfs, Roger and Castagne, Raphaële and Lackner, Karl J and Springelkamp, Henriët and Yang, Jian and Jonasson, Fridbert and Leung, Dexter Y L and Chen, Li J and Tham, Clement C Y and Rudan, Igor and Vatavuk, Zoran and Hayward, Caroline and Gibson, Jane and Cree, Angela J and MacLeod, Alex and Ennis, Sarah and Polasek, Ozren and Campbell, Harry and Wilson, James F and Viswanathan, Ananth C and Fleck, Brian and Li, Xiaohui and Siscovick, David and Taylor, Kent D and Rotter, Jerome I and Yazar, Seyhan and Ulmer, Megan and Li, Jun and Yaspan, Brian L and Ozel, Ayse B and Richards, Julia E and Moroi, Sayoko E and Haines, Jonathan L and Kang, Jae H and Pasquale, Louis R and Allingham, R Rand and Ashley-Koch, Allison and Mitchell, Paul and Wang, Jie Jin and Wright, Alan F and Pennell, Craig and Spector, Timothy D and Young, Terri L and Klaver, Caroline C W and Martin, Nicholas G and Montgomery, Grant W and Anderson, Michael G and Aung, Tin and Willoughby, Colin E and Wiggs, Janey L and Pang, Chi P and Thorsteinsdottir, Unnur and Lotery, Andrew J and Hammond, Christopher J and van Duijn, Cornelia M and Hauser, Michael A and Rabinowitz, Yaron S and Pfeiffer, Norbert and Mackey, David A and Craig, Jamie E and Macgregor, Stuart and Wong, Tien Y and NEIGHBOR Consortium
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 2, pp. 155 - 163
Journal Article
Clinical Ophthalmology, ISSN 1177-5467, 06/2017, Volume 11, pp. 1119 - 1120
Joshua R Ehrlich, Sayoko E MoroiDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, USAWe read with great interest the article by Patodia et al entitled, "Clinical... 
Glaucoma | Patient-Reported Outcomes | Rehabilitation | Mixed Methods | Low Vision
Journal Article
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 1864 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
DECORIN | CHROMATIN STATES | POLYMORPHISMS | RISK-FACTOR | MULTIDISCIPLINARY SCIENCES | MOUSE | GENE-EXPRESSION | MUTATIONS | HERITABILITY | LUMICAN | KERATOCONUS | Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix
Journal Article