المؤلفون: Kathryn P. Burdon, Marianne O. Price, Natalie A. Afshari, Simon G. Gregory, Jiagang Zhao, S. Amer Riazuddin, Sanjay V. Patel, Elmer Balajonda, Sudha K. Iyengar, Christopher R. Croasdale, Jamie E Craig, Venkateswara Mootha, Gordon K. Klintworth, Barbara Truitt, John F. Stamler, George O D Rosenwasser, Shiwani Sharma, Abraham Kuot, Jonathan H. Lass, Mollie A. Minear, Richard A. Mills, Steven P. Dunn, Sonja Klebe, Keith H. Baratz, John H. Fingert, Anthony J. Aldave, Xuejun Qin, Dwight Stambolian, V. Lakshmi Pulagam, John D. Gottsch, Joan E. Bailey-Wilson, Francis W. Price, Nathan Morris, Yi-Ju Li, Robert P. Igo, J. B. Rimmler

المصدر: Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Nature Communications

مصطلحات موضوعية: 0301 basic medicine, Science, General Physics and Astronomy, Locus (genetics), Genome-wide association study, Biology, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Cornea, medicine, Humans, Genetics, Multidisciplinary, Fuchs' Endothelial Dystrophy, Reproducibility of Results, General Chemistry, TCF4, eye diseases, 3. Good health, Transplantation, Corneal Disorder, 030104 developmental biology, medicine.anatomical_structure, ROC Curve, Genetic Loci, 030221 ophthalmology & optometry, Etiology, sense organs, Fuchs Endothelial Corneal Dystrophy, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78aba81960472d88ac8bad9b04f110f5Test
https://doaj.org/article/d1c65f3362014583bd22c5188abefc76Test

المؤلفون: David C. Whiteman, Jessica N. Cooke Bailey, William K. Scott, Michael Coote, Ivan Goldberg, Mark J Walland, David J. Lynn, Paul R. Healey, Paul Mitchell, John Landers, Terry Gaasterland, Kathryn P. Burdon, Arthur J. Sit, Jonathan B Ruddle, Nicholas G. Martin, Douglas Vollrath, R. Rand Allingham, Richard K. Lee, Julia E. Richards, Yutao Liu, David A. Mackey, Kuldev Singh, Mitchell Lawlor, Doug Rhee, Stuart MacGregor, Jamie E Craig, Robert Ritch, Graham L. Radford-Smith, Donald L. Budenz, Murray H. Brilliant, Robert P. Igo, John R. Grigg, Robert J Casson, Janey L. Wiggs, Bronwyn Ridge, Stuart L. Graham, Stephen Best, Louis R. Pasquale, S.E. Moroi, Peter Kraft, Anthony Realini, Lisa A Hark, Mona S Awadalla, Gadi Wollstein, Jesse Gale, Donald J. Zack, Owen M. Siggs, Puya Gharahkhani, Andrea L Vincent, Tiger Zhou, Alex W. Hewitt, Emmanuelle Souzeau, Margaret A. Pericak-Vance, Michael A. Hauser, Shiwani Sharma, John H. Fingert, Andrew White, Grant W. Montgomery, Douglas E. Gaasterland, Paul R. Lichter, Richard A. Mills, Joel S. Schuman, Jae H. Kang, Matthew Law, Jonathan L. Haines

المصدر: Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)

مصطلحات موضوعية: Male, 0301 basic medicine, Intraocular pressure, genetic structures, Optic disk, lcsh:Medicine, Muscle Proteins, Glaucoma, Genome-wide association study, 0302 clinical medicine, Risk Factors, lcsh:Science, Genetics, Multidisciplinary, LIM Domain Proteins, Middle Aged, Retinoic Acid 4-Hydroxylase, 3. Good health, Phenotype, Female, Glaucoma, Open-Angle, Genotype, Open angle glaucoma, Endophenotypes, LIM-Homeodomain Proteins, Optic Disk, Locus (genetics), Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Article, Tonometry, Ocular, 03 medical and health sciences, medicine, Humans, Genetic Predisposition to Disease, gamma-Crystallins, Intraocular Pressure, Aged, lcsh:R, Calcium-Binding Proteins, Membrane Proteins, Macular degeneration, medicine.disease, eye diseases, 030104 developmental biology, Case-Control Studies, 030221 ophthalmology & optometry, lcsh:Q, sense organs, Visual Fields, Genome-Wide Association Study, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b51aa370db671dce4d05df4cd7c4455bTest
https://doi.org/10.1038/s41598-018-20435-9Test

المؤلفون: Jim Gauderman, Veronique Vitart, Jonathan L. Haines, S.E. Moroi, Srinivasan Sacikala, René Höhn, Angela J. Cree, Xueli Chen, Terri L. Young, Francesca Pasutto, Robert N. Weinreb, Joel S. Schuman, William K. Scott, Jae H. Kang, Pirro G. Hysi, Richard K. Lee, Tin Aung, Kuldev Singh, Anthony P Khawaja, Michael A. Hauser, Henriette Springelkamp, David S. Friedman, Anthony Realini, Rashima Asokan, Donald J. Zack, D. L. Budenz, Gadi Wollstein, Unnur Thorsteinsdottir, Robert P. Igo, Lingam Vijaya, Caroline C W Klaver, Jessica N. Cooke Bailey, Kathryn P. Burdon, Tien Wong, Paul Mitchell, Jerome I. Rotter, Robert Wojciechowski, Julia R. Richards, Terry Gaasterland, Douglas Vollrath, Adriana I. Iglesias Gonzalez, David A. Mackey, Puya Gharahkhani, X. Raymond Gao, Yutao Liu, R. Rand Allingham, Rohit Varma, Stuart MacGregor, Arthur J. Sit, John H. Fingert, Nisha Sondhi, Baojian Fan, Cornelia M. van Duijn, Nagasamy Soumittra, Calvin C P Pang, Doug Rhee, Paul R. Lichter, P. Ferdinamarie Sharmila, Douglas E. Gaasterland, Sarangapani Sripriya, Murray H. Brilliant, Jamie E Craig, Ching-Yu Cheng, Aniket Mishra, Alex W. Hewitt, Ananth C. Viswanathan, Janey L. Wiggs, Peter Kraft, Jost B. Jonas, Tanja Zeller, Louis R. Pasquale, Gudmar Thorleifsson, Ronnie George, Robert Ritch, Chiea Chuen Khor, Christopher J Hammond

المساهمون: Clinical Genetics, Ophthalmology, Epidemiology, Obstetrics & Gynecology, Psychiatry

المصدر: Investigative Ophthalmology & Visual Science
Investigative Ophthalmology and Visual Science, 59(6), 2495-2502. Association for Research in Vision and Ophthalmology Inc.
George, R J & Wiggs, J L 2018, ' Family-based Genome-wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus ', Investigative Ophthalmology & Visual Science . https://doi.org/10.1167/iovs.17-23536Test

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Corneal Pachymetry, Genotyping Techniques, genetic association, WNT7B, genetic structures, Quantitative Trait Loci, Population, India, Locus (genetics), Genome-wide association study, Single-nucleotide polymorphism, Pedigree chart, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, Cohort Studies, Cornea, quantitative trait, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Asian People, Genetics, Humans, SNP, education, ocular PheWAS, Aged, Genetic association, Aged, 80 and over, Family Health, education.field_of_study, cornea central thickness, Organ Size, Middle Aged, Introns, eye diseases, Pedigree, Wnt Proteins, 030104 developmental biology, 030221 ophthalmology & optometry, Female, sense organs, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec0b756e8f509c3f68563df07ffb3c7Test
https://doi.org/10.1167/iovs.17-23536Test

المؤلفون: Hemin R. Chin, Donald J. Zack, Yangfan P. Liu, Kang Zhang, Richard K. Lee, Edwin C. Oh, Robert N. Weinreb, Jonathan L. Haines, Terry Gaasterland, David S. Friedman, Douglas Vollrath, Louis R. Pasquale, Nicholas Katsanis, Kuldev Singh, Paul R. Lichter, Benjamin T. Whigham, Allison E. Ashley-Koch, Brian L. Yaspan, Janey L. Wiggs, Douglas E. Gaasterland, Megan U. Carnes, Jessica N. Cooke Bailey, Chunyan Qiao, Jae H. Kang, William K. Scott, Cathy Essentia McCarty, Sayoko E. Moroi, Donald L. Budenz, Stephanie Loomis, Arthur J. Sit, Michael A. Hauser, Melanie E. Garrett, Anthony Realini, Margaret A. Pericak-Vance, Gadi Wollstein, R. Rand Allingham, Julia E. Richards, Shane J. Havens, Murray H. Brilliant, Joel S. Schuman, John H. Fingert, Yutao Liu

المساهمون: Gibson, Greg

المصدر: PLoS genetics, vol 10, iss 5
PLoS Genetics, Vol 10, Iss 5, p e1004372 (2014)
PLoS Genetics

مصطلحات موضوعية: Aging, Cancer Research, genetic structures, Glaucoma, Genome-wide association study, Neurodegenerative, Bioinformatics, Eye, NEIGHBORHOOD Consortium Investigators, 0302 clinical medicine, 2.1 Biological and endogenous factors, Aetiology, Genetics (clinical), Genetics, 0303 health sciences, medicine.anatomical_structure, Open-Angle, Optic nerve, Female, Chromosomes, Human, Pair 9, Glaucoma, Open-Angle, Biotechnology, Research Article, Human, Pair 9, lcsh:QH426-470, Single-nucleotide polymorphism, Locus (genetics), Biology, Retinal ganglion, Chromosomes, 03 medical and health sciences, medicine, Humans, Allele, Eye Disease and Disorders of Vision, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Intraocular Pressure, Alleles, 030304 developmental biology, Aged, Homeodomain Proteins, Retina, Human Genome, Neurosciences, Biology and Life Sciences, Human Genetics, Optic Nerve, medicine.disease, eye diseases, lcsh:Genetics, Genetics of Disease, 030221 ophthalmology & optometry, Trans-Activators, sense organs, Gene Function, Genome-Wide Association Study, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb8177ed75c16a3fd6be331c812b4daaTest
https://escholarship.org/uc/item/8gv231gqTest