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PLoS genetics, ISSN 1553-7404, 04/2013, Volume 9, Issue 4, pp. e1003442 - e1003442
  [...]the exact mechanisms through which these genes act to regulate ocular refraction are unknown, and current animal models may be inadequate to hypothesize... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Myopia - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Myopia - physiopathology | Humans | Eye | Genetic aspects | Refractive errors | Myopia | Testing | Index Medicus | Studies | Survival analysis | Genetics | Retina | Public health | Risk factors
Journal Article
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, 08/2014, Volume 46, Issue 10, pp. 1126 - 1130
Journal Article
PLoS genetics, ISSN 1553-7390, 09/2012, Volume 8, Issue 9, pp. e1002932 - e1002932
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, 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... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Index Medicus
Journal Article
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 5, pp. e1002611 - e1002611
Journal Article
by Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjoerg and Hotze, Melanie and Strachan, David P and Curtin, John A and Bonnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P and den Dekker, Herman T and Ferreira, Manuel A and Altmaier, Elisabeth and Sleiman, Patrick M. A and Xiao, Feng Li and Gonzalez, Juan R and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Chengjian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M and Venturini, Cristina and Pennell, Craig E and Barton, Sheila J and Levin, Albert M and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Moller, Eskil and Lockett, Gabrielle A and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L and Henderson, A. John and Kemp, John P and Zheng, Jie and Smith, George Davey and Rueschendorf, Franz and Postma, Dirkje S and Weiss, Scott T and Koppelman, Gerard H and the EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium and AAGC and EArly Genetics Lifecourse Epidemio and Australian Asthma Genetics Consortium (AAGC) and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Department of Obstetrics and Gynecology and Sahlgrenska Academy
Nature genetics, ISSN 1546-1718, 10/2015, Volume 47, Issue 12, pp. 1449 - 1456
Journal Article