المؤلفون: Caroline C W Klaver, Xiaoyan Luo, Albert Hofman, Arni B Stefansson, Christopher J Hammond, Fridbert Jonasson, Louis R. Pasquale, Norbert Pfeiffer, Jun Li, Johannes R. Vingerling, Gudmar Thorleifsson, Nicholas G. Martin, René Höhn, Ananth C. Viswanathan, Sarah Ennis, Jonathan L. Haines, Craig E. Pennell, Vesteinn Jonsson, Jessica N. Cooke Bailey, Kathryn P. Burdon, Lennart C. Karssen, Céline Bellenguez, Pirro G. Hysi, Philipp S. Wild, Dominiek D. G. Despriet, James F. Wilson, Cécile Delcourt, Jamie E Craig, Michael A. Hauser, Philippe Amouyel, Leonieke M E van Koolwijk, Andrea Senft, Chiea Chuen Khor, Tien Yin Wong, Tin Aung, Tanja Zeller, Nomdo M. Jansonius, Yik Ying Teo, Yingfeng Zheng, Terri L. Young, David A. Mackey, Brian W Fleck, Roger C. W. Wolfs, Veronique Vitart, Ching-Yu Cheng, Paulus T. V. M. de Jong, Joan E. Bailey-Wilson, Kari Stefansson, Alireza Mirshahi, Lisa S. Kearns, James F Kirwan, Ben A. Oostra, Andrew J. Lotery, Sayoko E. Moroi, Rhys Fogarty, Henriët Springelkamp, R. Rand Allingham, Eranga N. Vithana, Julia E. Richards, André G. Uitterlinden, Wishal D. Ramdas, Cristina Venturini, Paul Leo, Kerrin S. Small, Fernando Rivadeneira, Stuart MacGregor, Jiemin Liao, Karl J. Lackner, Cornelia M. van Duijn, Sandra E Staffieri, Alex W. Hewitt, Hans G Lemij, Seang-Mei Saw, Seyhan Yazar, Janey L. Wiggs, Gabriel Cuellar-Partida, Jae H. Kang, Abhishek Nag, Adriana I Iglesias, Najaf Amin, Tim D. Spector, Claire L. Simpson, Cécilia Maubaret, Robert Wojciechowski, E-Shyong Tai, Liang Xu, Ya Xing Wang, Elisabeth M. van Leeuwen, Ayse Bilge Ozel, Unnur Thorsteinsdottir, Stephanie J. Loomis

المساهمون: Ophthalmology, Epidemiology, Internal Medicine, Clinical Genetics, Obstetrics & Gynecology, Perceptual and Cognitive Neuroscience (PCN), Netherlands Institute for Neuroscience (NIN)

المصدر: Nature Genetics, 46(10), 1126-1130. Nature Publishing Group
Nature Genetics, 46(10), 1126-1130
Nature genetics, 46(10), 1126-1130. Nature Publishing Group
Nature genetics
Nature Genetics, 46(10), 1126-30. Nature Publishing Group

مصطلحات موضوعية: Male, Intraocular pressure, genetic structures, Glaucoma, Genome-wide association study, Cohort Studies, 0302 clinical medicine, Polymorphism (computer science), Risk Factors, POPULATION, Genetics, Aged, 80 and over, RISK, 0303 health sciences, education.field_of_study, COMMON VARIANTS, ASSOCIATION, Middle Aged, Female, TRIAL, Chromosomes, Human, Pair 3, OPEN-ANGLE GLAUCOMA, Chromosomes, Human, Pair 9, Glaucoma, Open-Angle, ATP Binding Cassette Transporter 1, Adult, EXPRESSION, medicine.medical_specialty, Open angle glaucoma, Genotype, Population, Chromosome 9, Biology, Polymorphism, Single Nucleotide, Article, ABO Blood-Group System, 03 medical and health sciences, Young Adult, Meta-Analysis as Topic, Ophthalmology, medicine, Humans, Genetic Predisposition to Disease, education, CENTRAL CORNEAL THICKNESS, Intraocular Pressure, METAANALYSIS, 030304 developmental biology, Genetic association, Aged, Chromosomes, Human, Pair 11, medicine.disease, eye diseases, Fibronectins, REDUCTION, Genetic Loci, 030221 ophthalmology & optometry, sense organs, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168e3aecc686f9a55eaa1e094fb26ae4Test
https://pure.eur.nl/en/publications/4b859410-3363-4564-9294-9cc3251696e5Test

المؤلفون: Gonneke Willemsen, Cathryn M. Lewis, Dorret I. Boomsma, Michele L. Pergadia, Peter McGuffin, Brenda W.J.H. Penninx, Douglas Blackwood, Pa Madden, Dixie J. Statham, Nicholas G. Martin, Jouke-Jan Hottenga, Enda M. Byrne, Dale R. Nyholt, Grant W. Montgomery, Patrick F. Sullivan, Stephan Ripke, E. J. C. G. van den Oord, Brian P. McEvoy, Naomi R. Wray, Anjali K. Henders, Donald J. MacIntyre, Sarah E. Medland, Kevin A. McGhee, Jimmy Z. Liu, Jan H. Smit, Ian B. Hickie, Scott D. Gordon, Stuart MacGregor, Alan W Maclean, A. C. Heath, E.J.C. de Geus, Christel M. Middeldorp

المساهمون: Psychiatry, EMGO - Mental health, NCA - Anxiety & Depression, Biological Psychology, Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Mental Health

المصدر: Molecular Psychiatry, 17(1), 36-48. Nature Publishing Group
Wray, N R, Pergadia, M L, Blackwood, D H, Penninx, B W J H, Gordon, S D, Nyholt, DR, Ripke, S, MacIntyre, D J, McGhee, K A, Maclean, A W, Smit, J H, Hottenga, J J, Willemsen, G, Middeldorp, C M, de Geus, E J C, Lewis, C M, McGuffin, P, Hickie, I B, van den Oord, E J C G, Liu, J Z, Macgregor, S, McEvoy, B P, Byrne, E M, Medland, S E, Statham, D J, Henders, A K, Heath, A C, Montgomery, G W, Martin, N G, Boomsma, D I, Madden, P A F & Sullivan, P F 2012, ' Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned ', Molecular Psychiatry, vol. 17, no. 1, pp. 36-48 . https://doi.org/10.1038/mp.2010.109Test
Molecular Psychiatry
Wray, N R, Pergadia, M L, Blackwood, D H R, Penninx, B W J H, Gordon, S D, Nyholt, D R, Ripke, S, MacIntyre, D J, McGhee, K A, Maclean, A W, Smit, J H, Hottenga, J J, Willemsen, G, Middeldorp, C M, de Geus, E J C, Lewis, C M, McGuffin, P, Hickie, I B, van den Oord, E J C G, Liu, J Z, Macgregor, S, McEvoy, B P, Byrne, E M, Medland, S E, Statham, D J, Henders, A K, Heath, A C, Montgomery, G W, Martin, N G, Boomsma, D I, Madden, P A F, Sullivan, P F & MacIntyre, D 2012, ' Genome-wide association study of major depressive disorder : new results, meta-analysis, and lessons learned ', Molecular Psychiatry, vol. 17, no. 1, pp. 36-48 . https://doi.org/10.1038/mp.2010.109Test

مصطلحات موضوعية: Adenylate Cyclase, Adult, Male, Netherlands Twin Register (NTR), Adolescent, Calcium Channels, L-Type, Genotype, Galanin, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, Sex Factors, 0302 clinical medicine, Odds Ratio, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Molecular Biology, 030304 developmental biology, Genetic association, Genetics, Depressive Disorder, Major, Principal Component Analysis, 0303 health sciences, genome-wide association study, major depressive disorder, Odds ratio, Middle Aged, medicine.disease, GAL, 3. Good health, Psychiatry and Mental health, CACNA1C, ADCY3, Schizophrenia, Meta-analysis, depression, Major depressive disorder, Female, Original Article, 030217 neurology & neurosurgery, Genome-Wide Association Study, Adenylyl Cyclases

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb7428e1d6fadc2d4e5e05385f97d28aTest
https://hdl.handle.net/1871/41675Test

المؤلفون: Alex W. Hewitt, Abbas M Solouki, Jugnoo S Rahi, Margarida C. Lopes, M. Kamran Ikram, Stuart MacGregor, Terri L. Young, David A. Mackey, Cornelia M. van Duijn, Toby Andrew, Samantha J. Fahy, Eugenio Santos, Yi-Ju Li, Caroline C W Klaver, Alberto Fernández-Medarde, Tim D. Spector, Francis Carbonaro, Christopher J Hammond, Angel Porteros, Nicholas G. Martin, Pak C. Sham, Pirro G. Hysi, Lara Manyes, Johannes R. Vingerling, Lee Yiu Fai

المساهمون: Ophthalmology, Epidemiology

المصدر: Nature Genetics; Vol 42
Nature Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Genetics, 42(10), 902-+. Nature Publishing Group

مصطلحات موضوعية: Adult, Male, Refractive error, Genotype, genetic structures, Eye disease, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Cohort Studies, Mice, 03 medical and health sciences, 0302 clinical medicine, Myopia, Genetics, medicine, Animals, Humans, Genetic Predisposition to Disease, 030304 developmental biology, Mice, Knockout, Chromosomes, Human, Pair 15, 0303 health sciences, Retina, Genome, Human, ras-GRF1, Case-control study, Middle Aged, medicine.disease, eye diseases, 3. Good health, medicine.anatomical_structure, Case-Control Studies, 030221 ophthalmology & optometry, Twin Studies as Topic, Female, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2e4b6f383678aefc9b6bffdc693f171Test

المؤلفون: Rui Zhang, Alan G. Casson, Isabel Caldas, Nicholas K. Hayward, Carlos Caldas, Stuart MacGregor, Liam J. Murray, Olof Nyrén, Leslie Bernstein, Xinxue Liu, Douglas A. Corley, David C. Whiteman, Thomas L. Vaughan, Brian J. Reid, Harvey A. Risch, Stephen J. Chanock, Paul D.P. Pharoah, Irene Debiram-Beecham, Cassandra L. Sather, Nicholas J. Shaheen, Marilie D. Gammon, Weronica E. Ek, Pierre Lao-Sirieix, Weimin Ye, Geoffrey Liu, David M. Levine, Patricia Harrington, Yvonne Romero, Rebecca C. Fitzgerald, Nigel C. Bird, Laura J. Hardie, Lynn Onstad, Wong Ho Chow, Anna H. Wu

المساهمون: Caldas, Carlos [0000-0003-3547-1489], Pharoah, Paul [0000-0001-8494-732X], Fitzgerald, Rebecca [0000-0002-3434-3568], Apollo - University of Cambridge Repository

المصدر: Nature genetics

مصطلحات موضوعية: Male, Esophageal Neoplasms, Genotype, Tumor suppressor gene, Genome-wide association study, Adenocarcinoma, Biology, Polymorphism, Single Nucleotide, Article, Barrett Esophagus, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Esophagus, Cancer, FOXP1, medicine.disease, digestive system diseases, 3. Good health, medicine.anatomical_structure, Genetic Loci, Case-Control Studies, 030220 oncology & carcinogenesis, Transcription Coactivator, Barrett's esophagus, Cancer research, Female, 030211 gastroenterology & hepatology, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7a2bd4a5444db3b5983aa227cddf64Test