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المؤلفون: Janey L. Wiggs, C.M. vanDuijn, Vincent Laville, Adriana I Iglesias, Daniel I. Chasman, Bernard Rosner, Jessica N. Cooke Bailey, James F. Wilson, Michael A. Hauser, Jae H. Kang, William G. Christen, Christopher J Hammond, Hugues Aschard, Puya Gharahkhani, John H. Fingert, Alex W. Hewitt, Stuart MacGregor, Frank B. Hu, Peter Kraft, Louis R. Pasquale, Robert P. Igo, Yeunjoo E. Song, David A. Mackey, Pirro G. Hysi, Jonathan L. Haines, UK Biobank, Anthony P Khawaja, Clara C. Cousins, Reka Nagy, Veronique Vitart
المساهمون: Département de Biologie Computationnelle - Department of Computational Biology, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Brigham & Women’s Hospital [Boston] (BWH), Harvard Medical School [Boston] (HMS), Erasmus University Medical Center [Rotterdam] (Erasmus MC), University of Edinburgh, Case Western Reserve University [Cleveland], Harvard T.H. Chan School of Public Health, QIMR Berghofer Medical Research Institute, University of Melbourne, University of Tasmania [Hobart, Australia] (UTAS), The University of Western Australia (UWA), King‘s College London, University of Oxford [Oxford], University of Iowa [Iowa City], Duke University [Durham], University of Cambridge [UK] (CAM), Icahn School of Medicine at Mount Sinai [New York] (MSSM), The Orkney Complex Disease Study was supported by the Chief Scientist Office of the Scottish Government (CZB/4/276, CZB/4/710), a Royal Society URF to Dr Wilson, the MRC Human Genetics Unit quinquennial programme 'QTL in Health and Disease,' Arthritis Research UK, and the European Union framework program 6 EUROSPAN project (contract no. LSHG-CT-2006-018947)., The Viking Health Study – Shetland (VIKING) was supported by the MRC Human Genetics Unit quinquennial programme grant 'QTL in Health and Disease.', European Project: 35103,EUROSPAN, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), University of Oxford, Clinical Genetics, Ophthalmology
المصدر: American Journal of Ophthalmology
American Journal of Ophthalmology, Elsevier Masson, 2019, 206, pp.245-255. ⟨10.1016/j.ajo.2019.05.015⟩
American Journal of Ophthalmology, 2019, 206, pp.245-255. ⟨10.1016/j.ajo.2019.05.015⟩
American Journal of Ophthalmology, 206, 245-255. Elsevier Inc.
Am J Ophthalmol
Laville, V, Kang, J H, Cousins, C, Iglesias, A I, Nagy, R, Cooke Bailey, J N, Igo, R P, Song, Y E, Chasman, D I, Christen, W, Kraft, P & Wilson, J F & Vitart, V 2019, ' Genetic correlations between diabetes and glaucoma: an analysis of continuous and dichotomous phenotypes ', American journal of ophthalmology . https://doi.org/10.1016/j.ajo.2019.05.015Testمصطلحات موضوعية: Male, Linkage disequilibrium, genetic structures, Glaucoma, Genome-wide association study, Type 2 diabetes, 0302 clinical medicine, MESH: Aged, 80 and over, MESH: Incidence, Aged, 80 and over, 2. Zero hunger, MESH: Aged, 0303 health sciences, [STAT.AP]Statistics [stat]/Applications [stat.AP], MESH: Middle Aged, Incidence, MESH: Tonometry, Ocular, Middle Aged, Pedigree, 3. Good health, Europe, Phenotype, MESH: Young Adult, Female, [STAT.ME]Statistics [stat]/Methodology [stat.ME], Glaucoma, Open-Angle, MESH: Diabetes Mellitus, Type 2, Adult, medicine.medical_specialty, Adolescent, MESH: Pedigree, Biology, MESH: Phenotype, Genetic correlation, Article, Tonometry, Ocular, Young Adult, 03 medical and health sciences, MESH: Cross-Sectional Studies, SDG 3 - Good Health and Well-being, MESH: Intraocular Pressure, Genetic linkage, Ophthalmology, medicine, MESH: United States, Humans, Intraocular Pressure, Aged, 030304 developmental biology, MESH: Adolescent, MESH: Humans, MESH: Adult, Heritability, medicine.disease, United States, Human genetics, eye diseases, MESH: Male, Cross-Sectional Studies, Diabetes Mellitus, Type 2, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: Genome-Wide Association Study, 030221 ophthalmology & optometry, MESH: Glaucoma, Open-Angle, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, sense organs, MESH: Europe, [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___::f37eb2ae4c5d9cebd21d3aa695a2b922Test
https://hal-pasteur.archives-ouvertes.fr/pasteur-03278624Test -
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المؤلفون: Anamika Tandon, Wallace L.M. Alward, Young H. Kwon, John H. Fingert, Ze Zhang, Kai Wang
المصدر: Am J Ophthalmol
مصطلحات موضوعية: Adult, Male, Intraocular pressure, medicine.medical_specialty, genetic structures, Adolescent, Ocular hypertension, Glaucoma, Transillumination, Slit Lamp Microscopy, Article, 03 medical and health sciences, Tonometry, Ocular, Young Adult, 0302 clinical medicine, Trabecular Meshwork, Ophthalmology, Medicine, Humans, Genetic Predisposition to Disease, Prospective Studies, Prospective cohort study, Child, Intraocular Pressure, 030304 developmental biology, Aged, 0303 health sciences, business.industry, food and beverages, Middle Aged, medicine.disease, eye diseases, Pedigree, medicine.anatomical_structure, Cross-Sectional Studies, Pigment dispersion syndrome, 030221 ophthalmology & optometry, Optic nerve, Female, sense organs, Trabecular meshwork, business, Glaucoma, Open-Angle, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::809c4067c9f087aad75b697444dde948Test
https://pubmed.ncbi.nlm.nih.gov/30796891Test -
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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 Geneticsمصطلحات 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 -
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المؤلفون: Frances Solivan-Timpe, Alan L. Robin, Luke A Wiley, Ben R. Roos, Budd A. Tucker, Robert F. Mullins, John H. Fingert, Kristin R. Anfinson
المصدر: Journal of stem cell research & therapy
مصطلحات موضوعية: Pathology, medicine.medical_specialty, TBK1, Stem cells, Retinal ganglion cells, Retinal ganglion, Article, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, SOX2, Gene duplication, Autophagy, medicine, Induced pluripotent stem cell, 030304 developmental biology, 0303 health sciences, Retina, iPSC, business.industry, Glaucoma, Retinal, 3. Good health, Cell biology, medicine.anatomical_structure, Retinal ganglion cell, chemistry, 030221 ophthalmology & optometry, sense organs, Stem cell, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdc93a6f3a88354c3a18c63794ef1eaTest
https://doi.org/10.4172/2157-7633.1000161Test -
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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 ONEمصطلحات 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 -
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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