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British Journal of Ophthalmology, ISSN 0007-1161, 08/2019, Volume 103, Issue 8, pp. 1078 - 1084
PurposeMyopia is an increasingly prevalent condition globally. A greater understanding of contemporaneous, early life factors associated with myopia risk is... 
Studies | Ethnicity | Child development | Myopia | Questionnaires | DNA methylation | Families & family life | Systematic review | Twins | Age | Educational attainment | Index Medicus
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2013, Volume 9, Issue 4
  [...]the exact mechanisms through which these genes act to regulate ocular refraction are unknown, and current animal models may be inadequate to hypothesize... 
Studies | Survival analysis | Myopia | Genetics | Retina | Public health | Risk factors
Journal Article
Ophthalmology, ISSN 0161-6420, 06/2016, Volume 123, Issue 6, pp. 1237 - 1244
Purpose To determine the heritability of nuclear cataract progression and to explore prospectively the effect of dietary micronutrients on the progression of... 
Journal Article
Canadian Journal of Ophthalmology, ISSN 0008-4182, 08/2018, Volume 53, Issue 4, p. 420
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.jcjo.2017.10.006 Temporal... 
Complications and side effects | Sickle cell anemia | Genetic aspects | Research | Retinal diseases | Risk factors
Journal Article
PLoS Genetics, ISSN 1553-7390, 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... 
REFRACTIVE ERROR | SCHOOLCHILDREN | VISUAL IMPAIRMENT | GENETICS & HEREDITY | SUSCEPTIBILITY LOCUS | PREVALENCE | GENOME-WIDE ASSOCIATION | CHILDREN | 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
Canadian Journal of Ophthalmology/Journal canadien d'ophtalmologie, ISSN 0008-4182, 08/2018, Volume 53, Issue 4, pp. 420 - 424
Journal Article
Canadian Journal of Ophthalmology, ISSN 0008-4182, 08/2016, Volume 51, Issue 4, p. 282
To perform a pilot study to explore use of a generic patient-reported outcome measure to assess patient-perceived improvements in quality of life within 2-4... 
Cataract | Surgery | Patient outcomes | Health aspects | Quality of life
Journal Article
PL o S Genetics (Online), ISSN 1553-7390, 09/2012, Volume 8, Issue 9, pp. e1002932 - e1002932
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1684 - 7
Journal Article
by Winkler, Thomas W and Justice, Anne E and Graff, Mariaelisa and Barata, Llilda and Feitosa, Mary F and Chu, Su and Czajkowski, Jacek and Esko, Tõnu and Fall, Tove and Kilpeläinen, Tuomas O and Lu, Yingchang and Mägi, Reedik and Mihailov, Evelin and Pers, Tune H and Rüeger, Sina and Teumer, Alexander and Ehret, Georg B and Ferreira, Teresa and Heard-Costa, Nancy L and Karjalainen, Juha and Lagou, Vasiliki and Mahajan, Anubha and Neinast, Michael D and Prokopenko, Inga and Simino, Jeannette and Teslovich, Tanya M and Jansen, Rick and Westra, Harm-Jan and White, Charles C and Absher, Devin and Ahluwalia, Tarunveer S and Ahmad, Shafqat and Albrecht, Eva and Alves, Alexessander Couto and Bragg-Gresham, Jennifer L and de Craen, Anton J. M and Bis, Joshua C and Bonnefond, Amélie and Boucher, Gabrielle and Cadby, Gemma and Cheng, Yu-Ching and Chiang, Charleston W. K and Delgado, Graciela and Demirkan, Ayse and Dueker, Nicole and Eklund, Niina and Eiriksdottir, Gudny and Eriksson, Joel and Feenstra, Bjarke and Fischer, Krista and Frau, Francesca and Galesloot, Tessel E and Geller, Frank and Goel, Anuj and Gorski, Mathias and Grammer, Tanja B and Gustafsson, Stefan and Haitjema, Saskia and Hottenga, Jouke-Jan and Huffman, Jennifer E and Jackson, Anne U and Jacobs, Kevin B and Johansson, Åsa and Kaakinen, Marika and Kleber, Marcus E and Lahti, Jari and Mateo Leach, Irene and Lehne, Benjamin and Liu, Youfang and Lo, Ken Sin and Lorentzon, Mattias and Luan, Jian'an and Madden, Pamela A. F and Mangino, Massimo and McKnight, Barbara and Medina-Gomez, Carolina and Monda, Keri L and Montasser, May E and Müller, Gabriele and Müller-Nurasyid, Martina and Nolte, Ilja M and Panoutsopoulou, Kalliope and Pascoe, Laura and Paternoster, Lavinia and Rayner, Nigel W and Renström, Frida and Rizzi, Federica and Rose, Lynda M and Ryan, Kathy A and Salo, Perttu and Sanna, Serena and Scharnagl, Hubert and Shi, Jianxin and Smith, Albert Vernon and Southam, Lorraine and Stančáková, Alena and Steinthorsdottir, Valgerdur and Strawbridge, Rona J and Sung, Yun Ju and Tachmazidou, Ioanna and ... and DIAGRAM Consortium and CHARGE Consortium and GLGC Consortium and MAGIC Consortium and ICBP Consortium and Global-BPGen Consortium
PLoS genetics, ISSN 1553-7390, 2015, Volume 11, Issue 10, pp. 1 - 42
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
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 5, pp. 492 - 497
Common multi-allelic copy number variants (CNVs) appear enriched for phenotypic associations compared to their biallelic counterparts(1-4). Here we... 
VARIANTS | GENETICS & HEREDITY | EARLY-ONSET | BODY-MASS INDEX | SEGMENTAL DUPLICATIONS | MICROBIOTA | POLYMORPHISM | DELETIONS | HERITABILITY | GENOME-WIDE ASSOCIATION | ACCURACY | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Salivary alpha-Amylases - genetics | Microarray Analysis | Humans | Salivary alpha-Amylases - blood | Carbohydrate Metabolism - genetics | Genomics - methods | Odds Ratio | Obesity - genetics | Obesity | Amylases | Genetic susceptibility | Salivary glands | Genetic research | Genetic aspects | Research | Health aspects | Saliva | Risk factors | secretions | Studies | Medical research | Hospitals | Biomedical research | Genomes | Grants | Gene expression | Deoxyribonucleic acid--DNA | Index Medicus | Life Sciences | Genetics | Human genetics | body mass | major clinical study | Genomics | genetic association | gene cluster | heritability | copy number variation | enzyme activity | gene mapping | genetic risk | genetic predisposition | sugar intake | female | obesity | Genetic Predisposition to Disease | Salivary alpha-Amylases | adipose tissue | European | article | Clinical Medicine | alpha amylase saliva isoenzyme | adult | gene expression | male | carbohydrate metabolism | fat mass | gene identification | Klinisk medicin | insulin release | subcutaneous fat | priority journal | saliva level | human | gene replication | enzyme blood level | human tissue | gene linkage disequilibrium | Gene Dosage | genetic variability | nucleotide sequence | controlled study | Chinese | overlapping gene | alpha amylase pancreas isoenzyme | principal component analysis
Journal Article