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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
JAMA Ophthalmology, ISSN 2168-6165, 01/2017, Volume 135, Issue 1, p. 31
  Importance Measurement of ganglion cell complex (GCC) thickness may be more sensitive than current methods for glaucoma diagnosis and research. However,... 
Glaucoma | Body mass index | Aging | Regression analysis | Ophthalmology | Medical diagnosis
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
Scientific Reports, ISSN 2045-2322, 04/2017, Volume 7, Issue 1, pp. 45977 - 45977
Myopia, or near-sightedness, is our most common eye condition and the prevalence is increasing globally. Visual impairment will occur if uncorrected, whilst... 
REFRACTIVE ERROR | RISK-FACTORS | MULTIDISCIPLINARY SCIENCES | GEM TWIN | WORK | JUVENILE-ONSET MYOPIA | SCHOOL-CHILDREN | PREVALENCE | EDUCATIONAL-ATTAINMENT | ASSOCIATION | OUTDOOR ACTIVITY | Eye | Genotype & phenotype | Pleiotropy | Intelligence | Lasers | Myopia | Genomes | Genetic factors | Polygenic inheritance | Index Medicus
Journal Article
Journal Article
The Lancet Neurology, ISSN 1474-4422, 07/2018, Volume 17, Issue 7, pp. 597 - 608
Most patients with Parkinson's disease, Parkinson's disease dementia, and dementia with Lewy bodies do not carry mutations in known disease-causing genes. The... 
DIAGNOSIS | MULTICENTER | MANAGEMENT | VPS35 | GLUCOCEREBROSIDASE MUTATIONS | ASSOCIATION | CLINICAL NEUROLOGY | FEATURES | REVEALS | Parkinson Disease - complications | Genome-Wide Association Study | Humans | Middle Aged | RNA, Messenger - genetics | Male | Dementia - epidemiology | Parkinson Disease - genetics | Dementia - genetics | LDL-Receptor Related Proteins - genetics | Lewy Body Disease - epidemiology | Pluripotent Stem Cells - metabolism | Dementia - etiology | Lewy Body Disease - genetics | Pedigree | Brain - pathology | Parkinson Disease - epidemiology | Family | Female | Heterozygote | Italy | RNA, Messenger - chemistry | Chromosomes, Human, Pair 14 - genetics | Genetic Linkage | Genetic research | Genetic aspects | Analysis | Genomics | Dementia | Parkinson's disease | Laboratories | Neuropathology | Immunocytochemistry | Genes | Parkinsons disease | Aneurysm | Genomes | Proteins | Neurodegeneration | Autopsy | Dementia disorders | Aorta | Chromosome 14 | Movement disorders | Deoxyribonucleic acid--DNA | Linkage analysis | Neurodegenerative diseases | Therapeutic applications | Gene expression | Lewy bodies | Genetic variance | Pathology | Cycloheximide | Brain research | Molecular modelling | Pluripotency | mRNA stability | Index Medicus | Neurologi | Clinical Medicine | Neurology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Scientific Reports, ISSN 2045-2322, 09/2016, Volume 6, Issue 1, pp. 34116 - 34116
Retinal nerve fibre layer (RNFL) thickness has been associated with cognitive function but it is unclear whether RNFL thinning is secondary to cortical loss,... 
EYE | NORMALS | MINI-MENTAL-STATE | OPTICAL COHERENCE TOMOGRAPHY | MULTIDISCIPLINARY SCIENCES | COHORT | ALZHEIMERS-DISEASE PATIENTS | GLAUCOMA | MORPHOLOGY | MULTIPLE | IMPAIRMENT | Eye | Thinning | Cortex | Cognitive ability | Myopia | Retina | Heritability | Genetic factors | Regression analysis | Twins
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
by Cheng, Ching-Yu and Schache, Maria and Ikram, M. Kamran and Ikram, M. Kamran and Young, Terri L and Young, Terri L and Guggenheim, Jeremy A and Guggenheim, Jeremy A and Vitart, Veronique and MacGregor, Stuart and Verhoeven, Virginie J.M and Verhoeven, Virginie J.M and Barathi, Veluchamy A and Liao, Jiemin and Hysi, Pirro G and Hysi, Pirro G and Bailey-Wilson, Joan E and St. Pourcain, Beate and Kemp, John P and McMahon, George and Timpson, Nicholas J and Evans, David M and Montgomery, Grant W and Mishra, Aniket and Wang, Jie Jin and Wang, Jie Jin and Wang, Ya Xing and Rochtchina, Elena and Polasek, Ozren and Wright, Alan F and Wright, Alan F and Amin, Najaf and van Leeuwen, Elisabeth M and Wilson, James F and Wilson, James F and Wilson, Joan E. Bailey and Pennell, Craig E and van Duijn, Cornelia M and de Jong, Paulus T.V.M and Vingerling, Johannes R and Zhou, Xin and Zhou, Xiangtian and Chen, Peng and Chen, Li Jia and Chen, Wei and Li, Ruoying and Tay, Wan-Ting and Zheng, Yingfeng and Zheng, D and Chew, Merwyn and Chew, Emily Y and Chew, Emily and Rahi, Jugnoo S and Yoshimura, Nagahisa and Yamashiro, Kenji and Miyake, Masahiro and Delcourt, Cécile and Maubaret, Cecilia and Williams, T and Williams, Katie M and Williams, Cathy and Northstone, Kate and Ring, Susan M and Davey-Smith, George and Craig, Jamie E and Burdon, Kathryn P and Fogarty, Rhys D and Iyengar, Sudha K and Igo, Robert P and Janmahasathian, Sarayut and Stambolian, Dwight and Lu, Yi and Jonas, Jost B and Xu, Liang and Saw, Seang-Mei and Baird, Paul N and Mitchell, Paul and Nangia, Vinay and Hayward, Caroline and Campbell, C and Campbell, Harry and Rudan, Igor and Vatavuk, Zoran and Paterson, Andrew D and Hosseini, S. Mohsen and Fondran, Jeremy R and Feng, Sheng and Klaver, Caroline C and Klaver, Caroline C.W and van Duijn, Cornelia M and Metspalu, Andres and Haller, Toomas and Mihailov, Evelin and Pärssinen, Olavi and Wedenoja, Juho and Wojciechowski, Robert and Pfeiffer, Norbert and Höhn, René and Pang, Chi Pui and Meitinger, Thomas and ... and Consortium Refractive Error Myopia and Fuchs Genetics Multictr Study Grp and Diabet Control Complications Trial and Wellcome Trust Case Control Consor and Fuchs' Genetics Multi-Center Study Group and Consortium for Refractive Error and Myopia and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group and Wellcome Trust Case Control Consortium 2
The American Journal of Human Genetics, ISSN 0002-9297, 08/2013, Volume 93, Issue 2, pp. 264 - 277
Journal Article