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1995, ISBN 9780471106012, xii, 240
Book
JAMA Ophthalmology, ISSN 2168-6165, 12/2017, Volume 135, Issue 12, pp. 1385 - 1386
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 06/2019, Volume 202, pp. 1 - 5
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 2019, Volume 137, Issue 5, pp. 559 - 563
IMPORTANCE Mutations in the myocilin (MYOC) gene are the most common molecularly defined cause of primary open-angle glaucoma that typically occurs in patients... 
OPHTHALMOLOGY | ANGLE | GENE | FAMILIES | Polymerase chain reaction | Glaucoma | Genotyping | Nucleotide sequence | Genomes | Mutation | Ophthalmology
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 02/2019, Volume 137, Issue 2, pp. 129 - 137
IMPORTANCE Elevated intraocular pressure is a major risk factor for glaucoma, a leading cause of irreversible blindness worldwide. Environmental air pollution... 
WORLDWIDE | OPEN-ANGLE GLAUCOMA | AIR-POLLUTION | GENE VARIANTS | DNA METHYLATION AGE | REGRESSION-MODELS | OPHTHALMOLOGY | FINE PARTICLES | HEALTH | BLOOD-PRESSURE | INDOOR | Glaucoma | Oxidative stress | Toxicity | Blindness | Aging | Air pollution | Models | Ophthalmology | Carbon | Pressure | Black carbon
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 03/2016, Volume 134, Issue 3, p. 294
  Nitric oxide signaling alterations in outflow facility and retinal blood flow autoregulation are implicated in primary open-angle glaucoma (POAG). Nitric... 
Glaucoma | Signal transduction | Vegetables | Diet | Nitric oxide | Nitrates | Ophthalmology
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 05/2019, Volume 10, Issue 2, pp. 180 - 185
Muir-Torre syndrome, a variant of Lynch syndrome or hereditary nonpolyposis colorectal cancer, is an autosomal dominant disease characterized by skin neoplasms... 
Case Report | Muir-Torre syndrome | Sebaceous carcinoma | Lynch syndrome
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 05/2014, Volume 132, Issue 5, p. 549
  Effective strategies for primary prevention are lacking for exfoliation glaucoma (EG), which is the most common type of secondary glaucoma. To examine the... 
Glaucoma | Physical examinations | Nurses | Questionnaires | Preventive medicine | Vitamins | Meta-analysis
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2012, Volume 8, Issue 4, pp. 413 - 424
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2017, Volume 23, p. 548
Purpose: Inherited optic neuropathy is genetically heterogeneous, and genetic testing has an important role in risk assessment and counseling. The purpose of... 
Demography | Optic nerve | Optic neuropathy | Copy number | Visual field | Genomes | Mitochondrial DNA | Family medical history | Neuropathy | Genetic screening | Eye | Atrophy | Optic atrophy | Risk assessment | Genetic testing | Mutation | DNA sequencing
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 642 - 650
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
Nature genetics, ISSN 1061-4036, 10/2014, Volume 46, Issue 10, pp. 1120 - 1125
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2014, Volume 10, Issue 5, p. e1004372
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 1061-4036, 02/2013, Volume 45, Issue 2, pp. 155 - 163