المؤلفون: R. Rand Allingham, Douglas J Rhee, Julia E. Richards, Donald J. Zack, Mariusz Butkiewicz, Margaret A. Pericak-Vance, Janey L. Wiggs, Richard K. Lee, William K. Scott, Hugues Aschard, Lisa A Hark, Arthur J. Sit, Alex W. Hewitt, Felipe A. Medeiros, Gadi Wollstein, Sayoko E. Moroi, Louis R. Pasquale, Jessica N. Cooke Bailey, Murray H. Brilliant, Stuart MacGregor, Donald L. Budenz, William G. Christen, John H. Fingert, Yeunjoo E. Song, Jamie E Craig, Thasarat S. Vajaranant, Tony Realini, David A. Sullivan, Daniel I. Chasman, Peter Kraft, Jonathan L. Haines, Robert P. Igo, Jae H. Kang, Robert N. Weinreb, Joel S. Schuman, Kuldev Singh, Robert Ritch, Kathryn P. Burdon, Yutao Liu, Puya Gharahkhani, David A. Mackey, Michael A. Hauser, Terry Gaasterland, Douglas Vollrath, Bernard Rosner, Allison E. Ashley-Koch

المساهمون: Harvard Medical School [Boston] (HMS), University of California [San Diego] (UC San Diego), University of California, Harvard T.H. Chan School of Public Health

المصدر: Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2018, 59 (2), pp.629. ⟨10.1167/iovs.17-22708⟩
Investigative ophthalmology & visual science, vol 59, iss 2

مصطلحات موضوعية: Male, 0301 basic medicine, primary open-angle glaucoma, genetic structures, Datasets as Topic, Genome-wide association study, Ophthalmology & Optometry, Medical and Health Sciences, MESH: Genotype, 0302 clinical medicine, Gene Frequency, genetics, MESH: Datasets as Topic, Low Tension Glaucoma, MESH: Low Tension Glaucoma, Genetics, [STAT.AP]Statistics [stat]/Applications [stat.AP], MESH: Middle Aged, MESH: Polymorphism, Single Nucleotide, Single Nucleotide, Middle Aged, Biological Sciences, Pathway analysis, pathway analysis, Open-Angle, Female, [STAT.ME]Statistics [stat]/Methodology [stat.ME], Glaucoma, Open-Angle, Metabolic Networks and Pathways, Genotype, Open angle glaucoma, MESH: Testosterone, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Australian and New Zealand Registry of Advanced Glaucoma (ANZRAG) Consortium, 03 medical and health sciences, MESH: Intraocular Pressure, MESH: Gene Frequency, Humans, Polymorphism, 1000 Genomes Project, Estrogen Metabolism, Allele frequency, Intraocular Pressure, MESH: Humans, Glaucoma, Testosterone (patch), eye diseases, MESH: Male, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: Metabolic Networks and Pathways, testosterone, MESH: Genome-Wide Association Study, 030221 ophthalmology & optometry, MESH: Glaucoma, Open-Angle, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, sense organs, [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM], MESH: Female, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085d9740d37a72c5216216334f75d84cTest
https://hal-pasteur.archives-ouvertes.fr/pasteur-03278714Test

المؤلفون: Robert F. Mullins, Carly J. Lewis, Todd E. Scheetz, Kathleen R. Chirco, Budd A. Tucker, Edwin M. Stone, Rebecca M. Johnston, John H. Fingert

المصدر: Ophthalmic genetics. 39(1)

مصطلحات موضوعية: 0301 basic medicine, Male, genetic structures, Genotyping Techniques, Blotting, Western, Single-nucleotide polymorphism, Enzyme-Linked Immunosorbent Assay, Retinal Pigment Epithelium, Biology, Real-Time Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Retina, Article, Andrology, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), medicine, SNP, Humans, Genetics (clinical), Aged, Aged, 80 and over, Retinal pigment epithelium, Vascular Endothelial Growth Factor Receptor-1, Choroid, Anatomy, Macular degeneration, Middle Aged, medicine.disease, eye diseases, Tissue Donors, Blot, Ophthalmology, 030104 developmental biology, medicine.anatomical_structure, Pediatrics, Perinatology and Child Health, 030221 ophthalmology & optometry, Wet Macular Degeneration, Female, sense organs

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::979c1bf546d87f41567150cdf98c4627Test
https://pubmed.ncbi.nlm.nih.gov/28949775Test

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

المؤلفون: Todd E. Scheetz, James C. Folk, H. Culver Boldt, Edwin M. Stone, Terry A. Braun, Stephen R. Russell, Wallace L.M. Alward, Markus H. Kuehn, John H. Fingert, Val C. Sheffield, Abbot F. Clark, Thomas L. Casavant, Kai Wang, Kevin L. Knudtson

المصدر: PLoS ONE, Vol 8, Iss 3, p e58657 (2013)
PLoS ONE

مصطلحات موضوعية: Male, Anatomy and Physiology, genetic structures, Glaucoma, lcsh:Medicine, Genome-wide association study, Bioinformatics, Cornea, Macular Degeneration, 0302 clinical medicine, lcsh:Science, 0303 health sciences, Multidisciplinary, Complement component 7, Middle Aged, Complement C7, Medicine, Female, Glaucoma, Open-Angle, Research Article, medicine.medical_specialty, Open angle glaucoma, Genotype, Molecular Sequence Data, Quantitative Trait Loci, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Quantitative Trait, Heritable, Ocular System, Ophthalmology, medicine, Genetics, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Inherited Eye Disorders, Amino Acid Sequence, Allele, Risk factor, Alleles, 030304 developmental biology, Aged, lcsh:R, Human Genetics, Macular degeneration, medicine.disease, eye diseases, Macular Disorders, Genetics of Disease, 030221 ophthalmology & optometry, lcsh:Q, sense organs, Sequence Alignment, Population Genetics, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19c6e05cb2184d62705a51b3a57cb303Test
http://europepmc.org/articles/PMC3594156?pdf=renderTest

المؤلفون: Robert F. Mullins, Jian Huang, Edwin M. Stone, Kai Wang, Thomas A. Oetting, Frances Solivan-Timpe, James C. Folk, John H. Fingert, Jessica M. Skeie

المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 12, Iss 1, p 58 (2011)

مصطلحات موضوعية: Risk, lcsh:Internal medicine, lcsh:QH426-470, genetic structures, Genotype, Single-nucleotide polymorphism, Drusen, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Retina, Pathogenesis, 03 medical and health sciences, Macular Degeneration, 0302 clinical medicine, Genetics, medicine, SNP, Animals, Humans, Genetics(clinical), Allele, L-Selectin, lcsh:RC31-1245, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Choroid, Genetic Variation, Macular degeneration, medicine.disease, eye diseases, Genotype frequency, lcsh:Genetics, Disease Models, Animal, P-Selectin, Microscopy, Fluorescence, 030221 ophthalmology & optometry, sense organs, E-Selectin, Genetic screen, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::879242f1c0beda8accb508685a72235eTest
https://pubmed.ncbi.nlm.nih.gov/21521525Test