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.2019.05.015Test

مصطلحات 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

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: R. Rand Allingham, Julia E. Richards, William K. Scott, Janey L. Wiggs, Jessica N. Cooke Bailey, Robert Ritch, Michael A. Hauser, Arthur J. Sit, Joel S. Schuman, Jonathan L. Haines, Donald L. Budenz, Jae H. Kang, Margaret A. Pericak-Vance, Douglas E. Gaasterland, William G. Christen, Yutao Liu, Kang Zhang, Robert N. Weinreb, Donald J. Zack, Kuldev Singh, Felipe A. Medeiros, Terry Gaasterland, Gadi Wollstein, Douglas Vollrath, Louis R. Pasquale, Tony Realini, Richard K. Lee, Anthony P Khawaja, Murray H. Brilliant, S.E. Moroi, Paul R. Lichter, John H. Fingert, Peter Kraft

المصدر: Investigative Ophthalmology & Visual Science
Khawaja, AP; Cooke Bailey, JN; Kang, JH; Rand Allingham, R; Hauser, MA; Brilliant, M; et al.(2016). Assessing the association of mitochondrial genetic variation with primary open-angle glaucoma using gene-set analyses. Investigative Ophthalmology and Visual Science, 57(11), 5046-5052. doi: 10.1167/iovs.16-20017. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/6tq4q4qpTest
Investigative ophthalmology & visual science, vol 57, iss 11

مصطلحات موضوعية: 0301 basic medicine, Genetics, genetic structures, Carbohydrate Metabolism Pathway, Lipid metabolism, Biological Sciences, Biology, Carbohydrate metabolism, Mitochondrion, Ophthalmology & Optometry, Medical and Health Sciences, eye diseases, mitochondria, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, glaucoma, Genetic variation, 030221 ophthalmology & optometry, Fatty acid elongation, genetics, sense organs, KEGG, Gene

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ad174fa9e24c4b05e595ebdff19f71Test
http://europepmc.org/articles/PMC5040191Test

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: S.E. Moroi, Christopher J Hammond, Peter Kraft, Terri L. Young, Tin Aung, Unnar Thorsteinsdottir, R. Rand Allingham, Francesca Pasutto, Murray H. Brilliant, Robert P. Igo, Joel S. Schuman, Paul R. Lichter, Adriana I. Iglesias Gonzalez, Jessica N. Cooke Bailey, Jonathan L. Haines, Chiea Chuen Khor, Robert Ritch, René Hoehn, John H. Fingert, Puya Gharahkhani, Terry Gaasterland, Calvin C P Pang, Cheng Yu Cheng, Louis R. Pasquale, Lisa A Hark, Andrew J. Lotery, Douglas Vollrath, Yutao Liu, David A. Mackey, Stuart MacGregor, William K. Scott, Pirro G. Hysi, Alex W. Hewitt, Jae H. Kang, Cornelia M. van Duijn, Arthur J. Sit, Margaret A. Pericak-Vance, Michael A. Hauser, Peter Bonnemaijer, Veronique Vitart, Kuldev Singh, D. L. Budenz, Doaa Nabih Maria, Gudmar Thorleifsson, Julia R. Richards, Kari Stefansson, Sumana R Chintalapudi, Doug Rhee, Richard K. Lee, Anthony P Khawaja, Anthony Realini, Robert W. Williams, Eranga N. Vithana, Gadi Wollstein, Fridbert Jonansson, Jamie E Craig, Xiang Di Wang, Tanja Zeller, Douglas E. Gaasterland, Donald J. Zack, Caroline C W Klaver, Janey L. Wiggs, Monica M. Jablonski

المساهمون: Psychiatry, Epidemiology, Clinical Genetics, Ophthalmology

المصدر: Chintalapudi, S R, Maria, D, Di Wang, X, Bailey, J N C, Allingham, R, Brilliant, M, Budenz, D, Fingert, J, Gaasterland, D, Gaasterland, T, Haines, J L, Hark, L, Hauser, M, Igo, R, Hee Kang, J, Kraft, P, Lee, R, Lichter, P, Liu, Y, Moroi, S, Pasquale, L R, Pericak-Vance, M, Realini, A, Rhee, D, Richards, J R, Ritch, R, Schuman, J, Scott, W K, Singh, K, Sit, A, Vollrath, D, Wollstein, G, Zack, D, Aung, T, Bonnemaijer, P, Cheng, C Y, Craig, J, Van Duijn, C, Gharahkhani, P, Iglesias Gonzalez, A, Hammond, C J, Hewitt, A, Hoehn, R, Jonansson, F, Khawaja, A, Chuen Khor, C, Klaver, C C W, Lotery, A, MacKey, D, MacGregor, S, Pang, C, Pasutto, F, Stefansson, K, Thorleifsson, G, Thorsteinsdottir, U, Vitart, V, Vithana, E, Young, T, Zeller, T, Hysi, P G, Wiggs, J L, Williams, R W & Jablonski, M M 2017, ' Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility ', Nature Communications, vol. 8, no. 1, 1755 . https://doi.org/10.1038/s41467-017-00837-5Test
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Nature Communications
Nature Communications, 8(1):1755. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Male, Intraocular pressure, Candidate gene, genetic structures, General Physics and Astronomy, Glaucoma, Genome-wide association study, Disease, Bioinformatics, Cohort Studies, Mice, 0302 clinical medicine, lcsh:Science, Multidisciplinary, biology, 3. Good health, Mice, Inbred DBA, CACNA2D1, Female, Glaucoma, Open-Angle, Open angle glaucoma, Science, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Genetic variation, medicine, Animals, Humans, Genetic Predisposition to Disease, Intraocular Pressure, Aged, business.industry, General Chemistry, medicine.disease, eye diseases, Mice, Inbred C57BL, Disease Models, Animal, 030104 developmental biology, 030221 ophthalmology & optometry, biology.protein, lcsh:Q, Calcium Channels, sense organs, business, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b10ace24e0c92bcd94cc63b53e0738fTest
http://www.scopus.com/inward/record.url?scp=85035018930&partnerID=8YFLogxKTest

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: Michael D. Abràmoff, Alex W. Hewitt, Todd E. Scheetz, David A. Mackey, Young H. Kwon, Gwenole Quellec, Li Tang, Joseph M. Reinhardt, John H. Fingert

المصدر: Investigative ophthalmology and visual science, 51(11), 5870. Association for Research in Vision and Ophthalmology

مصطلحات موضوعية: Adult, medicine.medical_specialty, genetic structures, Adolescent, Optic Disk, Optic disk, Biology, Head shape, 030218 nuclear medicine & medical imaging, Geneeskunde, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Imaging, Three-Dimensional, Quantitative Trait, Heritable, Ophthalmology, medicine, Photography, Twins, Dizygotic, Humans, Genetics, Articles, Twins, Monozygotic, Heritability, Middle Aged, Phenotype, Twin study, eye diseases, medicine.anatomical_structure, Automated algorithm, 030221 ophthalmology & optometry, Optic nerve, sense organs, Optic disc

وصف الملف: image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd021f717808c6b1844a3a89f710904Test
https://europepmc.org/articles/PMC3061515Test/