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Nature communications, ISSN 2041-1723, 01/2019, Volume 10, Issue 1, pp. 155 - 155
Emmanuelle Souzeau, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this Article.... 
Association analysis | Eye diseases | Data processing | Cornea | Genomes
Journal Article
by Springelkamp, Henriët and Iglesias, Aiana I and Mishra, Aniket and Höhn, René and Wojciechowski, Robert and Khawaja, Anthony P and Nag, Abhishek and Wang, Ya Xing and Wang, Jie Jin and Cuellar-Partida, Gabriel and Gibson, Jane and Bailey, Jessica N. Cooke and Vithana, Eranga N and Gharahkhani, Puya and Boutin, Thibaud and Ramdas, Wishal D and Zeller, Tanja and Luben, Robert N and Yonova-Doing, Ekaterina and Viswanathan, Ananth C and Yazar, Seyhan and Cree, Angela J and Haines, Jonathan L and Koh, Jia Yu and Souzeau, Emmanuelle and Wilson, James F and Amin, Najaf and Müller, Christian and Venturini, Cristina and Kearns, Lisa S and Kang, Jae Hee and Tham, Yih Chung and Zhou, Tiger and van Leeuwen, Elisabeth M and Nickels, Stefan and Sanfilippo, Paul and Liao, Jiemin and van der Linde, Herma and Zhao, Wanting and van Koolwijk, Leonieke M. E and Zheng, Li and Rivadeneira, Fernando and Baskaran, Mani and van der Lee, Sven J and Perera, Shamira and de Jong, Paulus T. V. M and Oostra, Ben A and Uitterlinden, Ané G and Fan, Qiao and Hofman, Albert and Tai, E.-Shyong and Vingerling, Johannes R and Sim, Xueling and Wolfs, Roger C. W and teo, Yik Ying and Lemij, Hans G and Khor, Chiea Chuen and Willemsen, Rob and Lackner, Karl J and Aung, Tin and Jansonius, Nomdo M and Montgomery, Grant and Wild, Philipp S and Young, Terri L and Burdon, Kathryn P and Hysi, Pirro G and Pasquale, Louis R and Wong, Tien Yin and Klaver, Caroline C. W and Hewitt, Alex W and Jonas, Jost B and Mitchell, Paul and Lotery, Anew J and Foster, Paul J and Vitart, Veronique and Pfeiffer, Norbert and Craig, Jamie E and Mackey, David A and Hammond, Christopher J and Wiggs, Janey L and Cheng, Ching-Yu and van Duijn, Cornelia M and Macgregor, Stuart and NEIGHBORHOOD Consortium
Human molecular genetics, ISSN 0964-6906, 2017, Volume 26, Issue 2, pp. 438 - 453
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
by Iglesias, Adriana I and Mishra, Aniket and Vitart, Veronique and Bykhovskaya, Yelena and Höhn, René and Springelkamp, Henriët and Cuellar-Partida, Gabriel and Gharahkhani, Puya and Bailey, Jessica N. Cooke and Willoughby, Colin E and Li, Xiaohui and Yazar, Seyhan and Nag, Abhishek and Khawaja, Anthony P and Polašek, Ozren and Siscovick, David and Mitchell, Paul and Tham, Yih Chung and Haines, Jonathan L and Kearns, Lisa S and Hayward, Caroline and Shi, Yuan and Van Leeuwen, Elisabeth M and Taylor, Kent D and Wang, Jie Jin and Rochtchina, Elena and Attia, John and Scott, Rodney and Holliday, Elizabeth G and Baird, Paul N and Xie, Jing and Inouye, Michael and Viswanathan, Ananth and Sim, Xueling and Bonnemaijer, Pieter and Rotter, Jerome I and Martin, Nicholas G and Zeller, Tanja and Mills, Richard A and Staffieri, Sandra E and Jonas, Jost B and Schmidtmann, Irene and Boutin, Thibaud and Kang, Jae H and Lucas, Sionne E. M and Wong, Tien Yin and Beutel, Manfred E and Wilson, James F and Allingham, R. Rand and Brilliant, Murray H and Budenz, Donald L and Christen, William G and Fingert, John and Friedman, David S and Gaasterland, Douglas and Gaasterland, Terry and Hauser, Michael A and Kraft, Peter and Lee, Richard K and Lichter, Paul R and Liu, Yutao and Loomis, Stephanie J and Moroi, Sayoko E and Pericak-Vance, Margaret A and Realini, Anthony and Richards, Julia E and Schuman, Joel S and Scott, William K and Singh, Kuldev and Sit, Arthur J and Vollrath, Douglas and Weinreb, Robert N and Wollstein, Gadi and Zack, Donald J and Zhang, Kang and Donnelly, Peter and Barroso, Ines and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Deloukas, Panos and Duncanson, Audrey and Jankowski, Janusz and Markus, Hugh S and Mathew, Christopher G and Palmer, Colin N. A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Wood, Nicholas W and Spencer, Chris C. A and Band, Gavin and Bellenguez, Céline and Freeman, Colin and Hellenthal, Garrett and Giannoulatou, Eleni and Pirinen, Matti and ... and Blue Mountains Eye Study-GWAS Grp and NEIGHBORHOOD Consortium and Wellcome Trust Case Control Consor and Blue Mountains Eye Study—GWAS group and Wellcome Trust Case Control Consortium 2 (WTCCC2)
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1 - 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 | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
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 | Degeneration | Mechanical stimuli | Gene mapping | Age
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, p. 1864
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
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 | Cornea | Decorin | Corneal Dystrophies, Hereditary | Myopia | Corneal Diseases | Marfan Syndrome | Keratoconus | ADAMTS Proteins | Lumican | Transforming Growth Factor beta2 | Ehlers-Danlos Syndrome | Glaucoma, Open-Angle | Fibrillin-1 | Eye Diseases, Hereditary | Proteoglycans | Wellcome Trust Case Control Consortium 2 (WTCCC2) | Blue Mountains Eye Study—GWAS group | Loeys-Dietz Syndrome | NEIGHBORHOOD Consortium
Journal Article
by King, Rebecca and Struebing, Felix L and Li, Ying and Wang, Jiaxing and Koch, Allison Ashley and Cooke Bailey, Jessica N and Gharahkhani, Puya and MacGregor, Stuart and Allingham, R. Rand and Hauser, Michael A and Wiggs, Janey L and Geisert, Eldon E and Allingham, Rand and Brilliant, Murray and Budenz, Don and Bailey, Jessica Cooke and Fingert, John and Gaasterland, Douglas and Gaasterland, Teresa and Haines, Jonathan L and Hark, Lisa and Hauser, Michael and Igo, Rob and Kang, Jae Hee and Kraft, Peter and Lee, Richard and Lichter, Paul and Liu, Yutao and Moroi, Syoko and Pasquale, Louis R and Pericak-Vance, Margaret and Realini, Anthony and Rhee, Doug and Richards, Julia R and Ritch, Robert and Schuman, Joel and Scott, William K and Singh, Kuldev and Sit, Arthur and Vollrath, Douglas and Weinreb, Robert N and Wollstein, Gadi and Zack, Don and Aung, Tin and Burdon, Kathryn P and Cheng, Ching-Yu and Bailey, Jessica N. Cooke and Craig, Jamie E and Cree, Angela J and Hammond, Christopher J and Hewitt, Alex W and Höhn, René and Hysi, Pirro and Gonzalez, Adriana I Iglesias and Jonas, Jost and Khawaja, Anthony and Khor, Chiea-Cheun and Klaver, Caroline CW and Pasutto, Francesca and Mackey, David and Mitchell, Paul and Mishra, Aniket and Pang, Calvin and Springelkamp, Henriette and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and van Duijn, Cornelia M and Viswanathan, Ananth and Vitart, Veronique and Wojciechowski, Robert and Wong, Tien and Young, Terrri L and Zeller, Tanja and NEIGHBORHOOD Consortium and Int Glaucoma Genetics Consortium and International Glaucoma Genetics Consortium
PLoS Genetics, ISSN 1553-7390, 01/2018, Volume 14, Issue 1, pp. e1007145 - e1007145
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1755 - 12
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2014, Volume 10, Issue 5
  Glaucoma is a leading cause of blindness worldwide. Primary open-angle glaucoma (POAG) is the most common subtype and is a complex trait with multigenic... 
Glaucoma | Neighborhoods | Optic nerve | Disease | Physicians | Medical treatment | Genes | Colleges & universities | Zebrafish | Retina | Genomes | Medicine | Insects | Genetic research
Journal Article
by Springelkamp, Henriët and Iglesias, Aiana I and Mishra, Aniket and Höhn, René and Wojciechowski, Robert and Khawaja, Anthony P and Nag, Abhishek and Wang, Ya Xing and Wang, Jie Jin and Cuellar-Partida, Gabriel and Gibson, Jane and Cooke Bailey, Jessica N and Vithana, Eranga N and Gharahkhani, Puya and Boutin, Thibaud and Ramdas, Wishal D and Zeller, Tanja and Luben, Robert N and Yonova-Doing, Ekaterina and Viswanathan, Ananth C and Yazar, Seyhan and Cree, Angela J and Haines, Jonathan L and Koh, Jia Yu and Souzeau, Emmanuelle and Wilson, James F and Amin, Najaf and Müller, Christian and Venturini, Cristina and Kearns, Lisa S and Hee Kang, Jae and Consortium, Neighborhood and Tham, Yih Chung and Zhou, Tiger and van Leeuwen, Elisabeth M and Nickels, Stefan and Sanfilippo, Paul and Liao, Jiemin and Linde, Herma van der and Zhao, Wanting and van Koolwijk, Leonieke M E and Zheng, Li and Rivadeneira, Fernando and Baskaran, Mani and van der Lee, Sven J and Perera, Shamira and de Jong, Paulus T V M and Oostra, Ben A and Uitterlinden, Ané G and Fan, Qiao and Hofman, Albert and Shyong Tai, E and Vingerling, Johannes R and Sim, Xueling and Wolfs, Roger C W and Teo, Yik Ying and Lemij, Hans G and Khor, Chiea Chuen and Willemsen, Rob and Lackner, Karl J and Aung, Tin and Jansonius, Nomdo M and Montgomery, Grant and Wild, Philipp S and Young, Terri L and Burdon, Kathryn P and Hysi, Pirro G and Pasquale, Louis R and Wong, Tien Yin and Klaver, Caroline C W and Hewitt, Alex W and Jonas, Jost B and Mitchell, Paul and Lotery, Anew J and Foster, Paul J and Vitart, Veronique and Pfeiffer, Norbert and Craig, Jamie E and Mackey, David A and Hammond, Christopher J and Wiggs, Janey L and Cheng, Ching-Yu and van Duijn, Cornelia M and MacGregor, Stuart
Human Molecular Genetics, ISSN 0964-6906, 2017, Volume 26, pp. 438 - 453
Primary open-angle glaucoma (POAG), the most common optic neuropathy, is a heritable disease. Siblings of POAG cases have a ten-fold increase risk of... 
Journal Article