المؤلفون: Stacey L. Edwards, Francesmary Modugno, Michael E. Carney, Jonathan Tyrer, Klaus Bauman, Jue-Sheng Ong, Tanja Pejovic, Rosalind Glasspool, Matthias Dürst, Bryan M. McCauley, Javier Benitez, Andreas du Bois, Ann-Marie Patch, Karen McCue, Florian Heitz, Diether Lambrechts, Paul D.P. Pharoah, Beth Y. Karlan, David G. Huntsman, Matthias W. Beckmann, Wei Shi, Penelope M. Webb, Michelle M.M. Woo, Kathryn L. Terry, Georgia Chenevix-Trench, Puya Gharahkhani, Melissa C. Larson, Kirsten B. Moysich, Estrid Høgdall, Sian Fereday, Julie M. Cunningham, Joellen M. Schildkraut, Andrew Civitarese, Jenny Lester, Peter A. Fasching, Ellen L. Goode, Stuart MacGregor, Jonathan Beesley, Allan Jensen, Michael Friedlander, Claus Høgdall, Stacey J. Winham, Yi Lu, Marc T. Goodman, Thilo Dörk, Dylan M. Glubb, Sharon E. Johnatty, Digna R. Velez Edwards, Tracy A. O'Mara, Melissa Moffitt, Taymaa May, Marjorie J. Riggan, Andrew Berchuck, Jacobus Pfisterer, Bo Gao, María Josefa Mosteiro García, Samantha Hinsley, Alicia Beeghly-Fadiel, Ignace Vergote, Michael C.J. Quinn, Sebastian M. Armasu, Anna deFazio, Line Bjørge, Daniel W. Cramer, Gabrielle Ene, Catherine J. Kennedy, Susanne K. Kjaer

المصدر: Cancer Epidemiology, Biomarkers & Prevention. 30:1669-1680

مصطلحات موضوعية: EXPRESSION, Oncology, medicine.medical_specialty, SUSCEPTIBILITY LOCI, endocrine system diseases, Epidemiology, Single-nucleotide polymorphism, Locus (genetics), Genome-wide association study, LIKELIHOOD, chemistry.chemical_compound, Internal medicine, KINASE, Medicine, Progression-free survival, POLYMORPHISMS, METAANALYSIS, Public, Environmental & Occupational Health, OUTCOMES, Science & Technology, business.industry, CONSORTIUM, Cancer, medicine.disease, Carboplatin, 3. Good health, SEROUS OVARIAN, chemistry, Genetic marker, AUTOPHAGY, business, Ovarian cancer, Life Sciences & Biomedicine

وصف الملف: Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8ac710ae2dcb38fedaee1b1c6710611Test
https://doi.org/10.1158/1055-9965.epi-20-1817Test

المؤلفون: Catherine M. Olsen, Rachel E. Neale, Stuart MacGregor, Alisa M. Goldstein, Jean Claude Dusingize, Bridie S. Thompson, Jiyuan An, Jue-Sheng Ong, David C. Whiteman, Nirmala Pandeya, Penelope M. Webb, Matthew Law, Mark M. Iles

المصدر: Int J Epidemiol

مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Skin Neoplasms, Epidemiology, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Body Mass Index, 03 medical and health sciences, 0302 clinical medicine, Mendelian Randomization, Risk Factors, Internal medicine, Mendelian randomization, medicine, Humans, Melanoma, business.industry, Confounding, Mendelian Randomization Analysis, General Medicine, Odds ratio, Body Height, Confidence interval, 030104 developmental biology, 030220 oncology & carcinogenesis, Cutaneous melanoma, business, Body mass index, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c008eb06415e566c06e57059c0991e3Test
https://doi.org/10.1093/ije/dyaa009Test

المؤلفون: Upekha E Liyanage, Jiyuan An, David C. Whiteman, Matthew Law, Stuart MacGregor, Scott D. Gordon, Xikun Han, Catherine M. Olsen, Puya Gharahkhani, Jue-Sheng Ong, Rachel E. Neale

المصدر: Human Molecular Genetics

مصطلحات موضوعية: Keratinocytes, Linkage disequilibrium, Skin Neoplasms, Quantitative Trait Loci, Single-nucleotide polymorphism, Genome-wide association study, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Quantitative Trait, Heritable, Genetic variation, Genetics, medicine, Odds Ratio, Humans, Genetic Predisposition to Disease, Association Studies Article, Molecular Biology, Genetics (clinical), Alleles, 030304 developmental biology, Genetic association, 0303 health sciences, Gene Expression Profiling, Cancer, Computational Biology, Molecular Sequence Annotation, General Medicine, medicine.disease, Genetic architecture, 3. Good health, Carcinoma, Basal Cell, 030220 oncology & carcinogenesis, Case-Control Studies, Carcinoma, Squamous Cell, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004f10d7b23a88a3e18df5533d560aefTest
http://europepmc.org/articles/PMC6737293Test

المؤلفون: David M. Levine, Tania Noder, Jakob R. Izbicki, Hauke Lang, Marino Venerito, Hugh Barr, Laura Chegwidden, Timo Hess, Horst Neuhaus, Kirsten B. Moysich, David C. Whiteman, Christine B. Ambrosone, Peter H. Watson, Douglas A. Corley, Harvey A. Risch, Jessica Becker, Rebecca Harrison, Sharon B. Love, James Y. Dai, Arnulf H. Hölscher, Jesper Lagergren, Andrea May, Leslie Bernstein, Anna H. Wu, Thomas Rösch, Geoffrey Liu, Markus M. Nöthen, Paul Moayyedi, Katja Ott, Mario Anders, Michael Vieth, Stuart MacGregor, Johannes Schumacher, Oliver Pech, Qianchuan He, Brigitte Schumacher, Rupert Mayershofer, Lothar Veits, Wong Ho Chow, Matthew F. Buas, Lesley A. Anderson, Puya Gharahkhani, John deCaestecker, Margaret M. Madeleine, Josef Weismüller, Claire Palles, Lynn Onstad, Nicholas J. Shaheen, Susanne Moebus, Christian Gerges, Marilie D. Gammon, Christian Ell, Yogesh K. Vashist, Anne C. Böhmer, Laura J. Hardie, Ines Gockel, Thomas Schmidt, David MacDonald, Stephen Attwood, Shruti G. Dighe, Hendrik Manner, Jianhong Chen, Nicole Kreuser, Dietmar Lorenz, Janusz Jankowski, Hans Prenen, Prasad G. Iyer, Weimin Ye, Michael Knapp, Li Yan, Thomas L. Vaughan, Ian Tomlinson, Claudia Schmidt

المصدر: Carcinogenesis
Dighe, S G, Chen, J, Yan, L, He, Q, Gharahkhani, P, Onstad, L, Levine, D M, Palles, C, Ye, W, Gammon, M D, Iyer, P G, Anderson, L A, Liu, G, Wu, A H, Dai, J Y, Chow, W, Risch, H A, Lagergren, J, Shaheen, N J, Bernstein, L, Corley, D A, Prenen, H, Decaestecker, J, Macdonald, D, Moayyedi, P, Barr, H, Love, S B, Chegwidden, L, Attwood, S, Watson, P, Harrison, R, Ott, K, Moebus, S, Venerito, M, Lang, H, Mayershofer, R, Knapp, M, Veits, L, Gerges, C, Weismüller, J, Gockel, I, Vashist, Y, Nöthen, M M, Izbicki, J R, Manner, H, Neuhaus, H, Rösch, T, Böhmer, A C, Hölscher, A H, Anders, M, Pech, O, Schumacher, B, Schmidt, C, Schmidt, T, Noder, T, Lorenz, D, Vieth, M, May, A, Hess, T, Kreuser, N, Becker, J, Ell, C, Ambrosone, C B, Moysich, K B, Macgregor, S, Tomlinson, I, Whiteman, D C, Jankowski, J, Schumacher, J, Vaughan, T L, Madeleine, M M, Hardie, L J & Buas, M F 2020, ' Germline variation in the insulin-like growth factor pathway and risk of Barrett’s esophagus and esophageal adenocarcinoma ', Carcinogenesis . https://doi.org/10.1093/carcin/bgaa132Test
Carcinogenesis, 42, 3, pp. 369-377
Carcinogenesis, 42, 369-377

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Cancer Research, medicine.medical_specialty, Esophageal Neoplasms, Medizin, Single-nucleotide polymorphism, Genome-wide association study, Biology, Adenocarcinoma, Polymorphism, Single Nucleotide, Receptor, IGF Type 1, 03 medical and health sciences, Barrett Esophagus, 0302 clinical medicine, Risk Factors, Somatomedins, Internal medicine, Genetic variation, medicine, Biomarkers, Tumor, SNP, Humans, Genetic Predisposition to Disease, Risk factor, Germ-Line Mutation, Cancer Biomarkers and Molecular Epidemiology, Insulin-like growth factor 1 receptor, Genetic association, Aged, General Medicine, Middle Aged, medicine.disease, Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11], 030104 developmental biology, 030220 oncology & carcinogenesis, Barrett's esophagus, Female, Human medicine, Carrier Proteins, Genome-Wide Association Study, Signal Transduction

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e124a3a63391422b5fb226f753ce64b6Test
https://hdl.handle.net/10067/1758980151162165141Test

المؤلفون: Jue-Sheng Ong, Benjamin Elsworth, Konstantinos K. Tsilidis, Stuart MacGregor, Merete Ellingjord-Dale, Sarah J Lewis, Niki Dimou, Nikos Papadimitriou, Richard M. Martin, Michail Katsoulis, Dipender Gill, Chew Yee, Elio Riboli, Dagfinn Aune

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Inverse Association, Randomization, business.industry, Estrogen receptor, Single-nucleotide polymorphism, Odds ratio, medicine.disease, Confidence interval, Breast cancer, Internal medicine, Mendelian randomization, medicine, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d323c6a060f7f75f9cf6002c850f1decTest
https://doi.org/10.1101/2020.07.17.208421Test

المؤلفون: Upekha E Liyanage, Amanda B. Spurdle, K. E. Huber, Anna H. Wu, J. Fah Sathirapongsasuti, Douglas A. Corley, C. Tian, Anne Böhmer, David A. Hinds, A. Auton, Xikun Han, Matt Buas, M. Agee, Rebecca C. Fitzgerald, Puya Gharahkhani, Yvonne Romero, S. L. Elson, Ines Gockel, Johannes Schumacher, Leslie Bernstein, Nigel C. Bird, Thomas L. Vaughan, E. S. Noblin, P. Fontanillas, Laura J. Hardie, Brian J. Reid, V. Vacic, M. H. McIntyre, Jiyuan An, Andrew Berchuck, Claire Palles, Weimin Ye, K. Bryc, S. J. Pitts, Jue-Sheng Ong, Geoffrey Liu, R. K. Bell, Rachel E. Neale, Marilie D. Gammon, J. L. Mountain, C. A. M. Northover, Catherine M. Olsen, C. H. Wilson, Janusz Jankowski, Matthew Law, A. Kleinman, Suzanne C. Dixon-Suen, J. Y. Tung, Aaron P. Thrift, Wong-Ho Chow, Paul Pharoah, Jean-Cluade Dusingize, Suyash Shringarpure, Mark M. Iles, Wei Zheng, N. A. Furlotte, Penelope M. Webb, B. Alipanahi, O. V. Sazonova, Stuart MacGregor, David Whiteman, J. F. Shelton, Harvey A. Risch, N. K. Litterman, Tracy A. O'Mara, Nicholas J. Shaheen

المساهمون: Ong, Jue-Sheng [0000-0002-6062-710X], Dixon-Suen, Suzanne C [0000-0003-3714-8386], Han, Xikun [0000-0002-3823-7308], Gockel, Ines [0000-0001-7423-713X], Böhmer, Anne [0000-0002-5716-786X], O'Mara, Tracy [0000-0002-5436-3232], Spurdle, Amanda [0000-0003-1337-7897], Law, Matthew H [0000-0002-4303-8821], Iles, Mark M [0000-0002-2603-6509], Pharoah, Paul [0000-0001-8494-732X], Zheng, Wei [0000-0003-1226-070X], Thrift, Aaron P [0000-0002-0084-5308], Olsen, Catherine [0000-0003-4483-1888], Gharahkhani, Puya [0000-0002-4203-5952], Webb, Penelope M [0000-0003-0733-5930], MacGregor, Stuart [0000-0001-6731-8142], Apollo - University of Cambridge Repository

المصدر: Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)

مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Science, General Physics and Astronomy, Sunburn, Single-nucleotide polymorphism, General Biochemistry, Genetics and Molecular Biology, Article, Cancer prevention, 03 medical and health sciences, 0302 clinical medicine, Cancer epidemiology, Risk Factors, Internal medicine, Neoplasms, Mendelian randomization, Vitamin D and neurology, medicine, Humans, Genetic Predisposition to Disease, 030212 general & internal medicine, Risk factor, Vitamin D, Child, Cancer genetics, Multidisciplinary, business.industry, Pigmentation, Case-control study, Cancer, Mendelian Randomization Analysis, General Chemistry, medicine.disease, Confidence interval, 030104 developmental biology, Case-Control Studies, Multivariate Analysis, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf9bc87b026a463b5cb1c5ed0f8e4f2eTest
https://pubmed.ncbi.nlm.nih.gov/33431812Test

المؤلفون: Eduardo Nagore, Caroline Hayward, Christopher I. Amos, Douglas F. Easton, Zaida García-Casado, Julie Lang, Anjali K. Henders, Veronica Höiom, Lisa Bowdler, Kathryn P. Burdon, Laura Del Regno, Nick Orr, Per Arne Andresen, Tongwu Zhang, Rose Yang, Myriam Brossard, Eric K. Moses, Dirk Schadendorf, Laura Cattaneo, Casey Rowe, Essen-Heidelberg Investigators, Hans-Joachim Schulze, Jamie E Craig, D. Timothy Bishop, Anne E. Cust, Johan Hansson, David E. Elder, Nelleke A. Gruis, Donato Calista, Wei V. Chen, Abrar A. Qureshi, Amy Hutchinson, Pilar Galan, Leanne Wallace, Jennifer H. Barrett, Nilesh J. Samani, Maria Teresa Landi, Per Helsing, Andreas Hadjisavvas, Fengju Song, Celia Requena, Elizabeth M. Gillanders, Arantxa Rodriguez, Joan Anton Puig-Butille, Blair H. Smith, Mark Smithers, Michael Malasky, Marianna Sanna, Miriam Potrony, Maria A. Loizidou, Evangelos Evangelou, Richard A. Scolyer, Karen A. Pooley, Rachel E. Neale, Mario Falchi, Adèle C. Green, Monica Rodolfo, Ketty Peris, Licia Rivoltini, Mark M. Iles, Catherine M. Olsen, Alexander J. Stratigos, Tadeusz Dębniak, Weiyin Zhou, H. Peter Soyer, Xin Li, Margaret A. Tucker, Rajesh Kumar, Håkan Olsson, Anders Molven, Nicholas G. Martin, Anthony J. Swerdlow, Aurelie Vogt, Lars A. Akslen, Stuart MacGregor, Sarah V. Ward, Hamida Mohamdi, Bruna Dalmasso, Grant W. Montgomery, Rona M. MacKie, Esther Azizi, Gonçalo R. Abecasis, Chiara Menin, Alison M. Dunning, Ibd investigators, Kevin M. Brown, Jiali Han, Veryan Codd, Graham J. Mann, Nicholas K. Hayward, Marko Hočevar, Eitan Friedman, Richard A. Sturm, Paola Queirolo, Qtwin Investigators, Lawrie Wheeler, Lars G. Fritsche, Shenying Fang, Kiarash Khosrotehrani, Nicole A Kukutsch, Pol Gimenez-Xavier, Belynda Hicks, Matthew Zawistowski, Alessia Visconti, Jessica Harris, Chad M. Brummett, Paola Ghiorzo, andMe, David G. Hunter, Veronique Bataille, Julia Newton-Bishop, Srdjan Novaković, Amfs Investigators, Siranoush Manoukian, Jianxin Shi, Mitchell J. Machiela, G. Mark Lathrop, Josep Malvehy, Katerina P. Kypreou, Susana Puig, Dale R. Nyholt, I. Stefanaki, Maria Concetta Fargnoli, Lisa A. Simms, Kerrie McAloney, M. Malt, Adam J. Trower, Matthew Law, Lei Song, Paul D.P. Pharoah, Christian Ingvar, Jiyeon Choi, Alisa M. Goldstein, Jeffrey E. Lee, Mark Harland, Cristina Pellegrini, Daniela Massi, Sarah Simi, Scott D. Gordon, Jacobo Martinez, Florence Demenais, Kristine Jones, Graham L. Radford-Smith, David C. Whiteman, Lorenza Pastorino, Lisa Elefanti, Arcangela De Nicolo, Mario Mandalà, Juliette Randerson-Moor, Q-Mega, Jan Lubinski, Stephen J. Chanock, Marie-Françoise Avril, David L. Duffy, Helen Gogas, Nienke van der Stoep, Peter A. Kanetsky, Georgina V. Long

المساهمون: National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH), University of Leeds, QIMR Berghofer Medical Research Institute, National and Kapodistrian University of Athens (NKUA), Ospedale Policlinico San Martino [Genoa], Universita degli studi di Genova, Toxicité environnementale, cibles thérapeutiques, signalisation cellulaire (T3S - UMR_S 1124), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Maurizio Bufalini Hospital, University of L'Aquila [Italy] (UNIVAQ), Fondazione IRCCS Istituto Nazionale Tumori - National Cancer Institute [Milan], Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana [Espagne] (FISABIO), Cyprus Institute of Neurology and Genetics, University of Athens Medical School [Athens], The University of Sydney, Universitat de Barcelona (UB), Azienda Ospedaliera Ospedale Papa Giovanni XXIII [Bergamo, Italy], University of Michigan [Ann Arbor], University of Michigan System, Instituto Valenciano de Oncologia, Veneto Institute of Oncology IOV-IRCCS [Padua, Italy], IRCCS Istituto Nazionale dei Tumori [Milano], Ninewells Hospital and Medical School [Dundee], Cyprus Institute (CyI), Fondazione 'Policlinico Universitario A. Gemelli' [Rome], Università degli Studi di Firenze = University of Florence [Firenze] (UNIFI), University of Queensland [Brisbane], Haukeland University Hospital, University of Bergen (UiB), Geisel School of Medicine at Dartmouth, Oslo University Hospital [Oslo], Service de Dermatologie [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Sackler Faculty of Medicine, Tel Aviv University [Tel Aviv], King‘s College London, Menzies School of Health Research [Australia], Charles Darwin University, The University of Texas M.D. Anderson Cancer Center [Houston], University of Leicester, Flinders University [Adelaide, Australia], West Pomeranian University of Technology Szczecin, Equipe 3: EREN- Equipe de Recherche en Epidémiologie Nutritionnelle (CRESS - U1153), Université Sorbonne Paris Nord-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), National Human Genome Research Institute (NHGRI), Leiden University Medical Center (LUMC), Karolinska Institutet [Stockholm], Queensland University of Technology [Brisbane] (QUT), Institute of Oncology Ljubljana, Harvard T.H. Chan School of Public Health, Lund University [Lund], German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ), University of Glasgow, Statistical Genetics, Intramural Research Program of the Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health (NIH) United States Department of Health & Human ServicesNational Institutes of Health (NIH) - USAU19CA148112SEARCH team (Cancer Research UK) C490/A16561AOCS (US Army Medical Research and Material Command) DAMD17-01-1-0729Canadian Institutes of Health Research (CIHR)Cancer Council Victoria Queensland Cancer Fund Cancer Council New South Wales Cancer Council South Australia Cancer Council Western Australia Cancer Council Tasmania National Health and Medical Research Council of AustraliaID400413ID400281National Health and Medical Research Council of Australia National Health and Medical Research Council of Australia National Health and Medical Research Council of Australia National Health and Medical Research Council of Australia Intramural Research Program of the Division of Cancer Epidemiology and Genetics, NCI, NIH, DHHS Ministry of Health, Italy Associazione Italiana per la Ricerca sul Cancro (AIRC)IG 15460Spanish Fondo de Investigaciones Sanitarias grant - FEDER 'Una manera de hacer Europa' PI15/00716PI15/00956CIBER de Enfermedades Raras of the Instituto de Salud Carlos III, Spain - European Development Regional Fund 'A way to achieve Europe' ERDF AGAUR of the Catalan Government, Spain 2014_SGR_603European CommissionEuropean Commission Joint Research CentreLSHC-CT-2006-018702European Union (EU) 'Fundacio La Marato de TV3', Catalonia, Spain 201331-30'Fundacion Cientifica de la Asociacion Espanola Contra el Cancer', Spain GCB15152978SOENCERCA Programme/Generalitat de Catalunya Italian Ministry of the University and Scientific Research (PRIN-2012 grant) 2012JJX494Melanoma Research Alliance United States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI)CA88363CA83115CA122838CA87969CA055075CA100264CA133996CA49449National Health and Medical Research Council of Australia200071241944339462380385389927389875389891389892389938443036442915442981496610496675496739552485552498APP1049894Cancer Council Queensland Cancer Institute New South Wales Australian GovernmentDepartment of Industry, Innovation and ScienceCooperative Research Centres (CRC) Programme Australian Cancer Research Foundation Wellcome TrustWT084766/Z/08/ZNational Health and Medical Research Council of Australia Australian Research Council Department of Health and Human Services (DHHS)

المصدر: Nature Genetics
Nature Genetics, Nature Publishing Group, 2020, 52 (5), pp.494-504. ⟨10.1038/s41588-020-0611-8⟩
Nature genetics
Nature Genetics, 52(5), 494-504. NATURE PUBLISHING GROUP

مصطلحات موضوعية: Sequence Variants, Male, medicine.medical_specialty, Skin Neoplasms, Genotype, Medizin, Identifies 3, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Malignant-melanoma, 0302 clinical medicine, Genetics, medicine, Genetic predisposition, Nevus, Humans, Hla Class-i, Genetic Predisposition to Disease, Polymorphism, Melanoma, 030304 developmental biology, Telomere Length, Cancer, 0303 health sciences, [SDV.GEN]Life Sciences [q-bio]/Genetics, Loci, Pigmentation, E-cadherin, Single Nucleotide, medicine.disease, Genetic architecture, Attributable Fraction, 3. Good health, Phenotype, Female, Genetic Loci, Genome-Wide Association Study, Cutaneous melanoma, Medical genetics, Settore MED/35 - MALATTIE CUTANEE E VENEREE, 030217 neurology & neurosurgery, Familial Melanoma

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0663ba533ad6d0d069e8827e0d374241Test
https://discovery.dundee.ac.uk/files/49101915/Landi_2019_main_text_NG_A52232R2_15012020_2_.pdfTest

المؤلفون: Nicholas G. Martin, Jiyuan An, Jacqueline M. Vink, Eske M. Derks, Stuart MacGregor, Joëlle A. Pasman, Karin J. H. Verweij, Mengzhen Liu, Jue-Sheng Ong, Marilyn C. Cornelis, Lun Hsien Chang

المساهمون: Adult Psychiatry, APH - Mental Health

المصدر: Drug and Alcohol Dependence, 210
Drug and alcohol dependence, 210:107966. Elsevier Ireland Ltd

مصطلحات موضوعية: Male, Nicotine, Alcohol Drinking, Genome-wide association study, Single-nucleotide polymorphism, Substance use, Toxicology, Genetic correlation, Coffee, Cigarette Smoking, Cohort Studies, 03 medical and health sciences, Cognition, 0302 clinical medicine, Pleiotropy, Caffeine, Tobacco, Humans, Medicine, SNP, Pharmacology (medical), 030212 general & internal medicine, Cannabis, Pharmacology, Genetic instruments, biology, Tea, business.industry, Two-sample Mendelian randomisation, Mendelian Randomization Analysis, biology.organism_classification, Single nucleotide polymorphism, Psychiatry and Mental health, Trait, Female, Marijuana Use, business, Developmental Psychopathology, 030217 neurology & neurosurgery, Genome-Wide Association Study, Demography, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee618148e78636c61ba892c7b280182Test
http://hdl.handle.net/2066/217711Test

المؤلفون: Alex W. Hewitt, Yukihiro Shiga, Yukihide Momozawa, Adeyinka O. Ashaye, Koichi Matsuda, Shoichiro Tsugane, Haruo Mikami, Koh Hei Sonoda, Koji M. Nishiguchi, Makoto Araie, Kenji Kashiwagi, Yoichiro Kamatani, Mamoru Satoh, Tetsuya Yamamoto, Chiea Chuen Khor, Janey L. Wiggs, Toru Nakazawa, Takeshi Iwata, Puya Gharahkhani, Shamira A. Perera, Kazuhide Kawase, Mariko Naito, Masahiro Miyake, Taiki Yamaji, Koji Nitta, Nobuo Fuse, Micheal Hauser, Susan Williams, Nobuhiro Shimozawa, Kota Sato, Ching-Yu Cheng, Atsushi Takahashi, Masato Akiyama, Tin Aung, Makoto Aihara, Tatsuro Ishibashi, Aiko Iwase, Eranga N. Vithana, Mitsuko Takamoto, R. Rand Allingham, Kenji Wakai, Mineo Ozaki, Mani Baskaran, Makoto Sasaki, Munemitsu Yoshikawa, Yasuhiro Ikeda, Louis R. Pasquale, Motoki Iwasaki, Donald L. Budenz, Jamie E Craig, Kathryn P. Burdon, Yoshitaka Oka, Stuart MacGregor, Fumihiko Mabuchi, Kenji Yamashiro, Stephan Akafo, David A. Mackey, Jae H. Kang, Yoshiaki Kiuchi, Michiaki Kubo, Makoto Nakamura, Yoichi Suzuki, Isao Oze, Shiroaki Shirato, Jessica N. Cooke Bailey, Makoto Hirata, Jonathan L. Haines

المصدر: Human Molecular Genetics. 27:1486-1496

مصطلحات موضوعية: Male, 0301 basic medicine, Candidate gene, genetic structures, Black People, Gene Expression, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, 0302 clinical medicine, Asian People, Polymorphism (computer science), Genetics, Humans, Genetic Predisposition to Disease, Eye Proteins, Association Studies Article, Molecular Biology, Genetics (clinical), Genetic association, Case-control study, General Medicine, eye diseases, Genetic architecture, ErbB Receptors, 030104 developmental biology, Diabetes Mellitus, Type 2, Cardiovascular Diseases, Genetic Loci, Case-Control Studies, Mutation, 030221 ophthalmology & optometry, Female, sense organs, Candidate Disease Gene, Glaucoma, Open-Angle, Genome-Wide Association Study, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298869a72354e1a0ffbbd8fec9552469Test
https://doi.org/10.1093/hmg/ddy053Test

المؤلفون: Robert Wojciechowski, Myopia (Cream), Jost B. Jonas, Tin Aung, Paul Mitchell, Terri L. Young, Katie M Williams, Ching-Yu Cheng, Pik Fang Kho, David A. Mackey, Cathy Williams, Pirro G. Hysi, Stuart MacGregor, Jeremy A. Guggenheim, Dwight Stambolian, J. Willem L. Tideman, Alex W. Hewitt, Robyn M. Lucas, Jie Jin Wang, Christopher J Hammond, Tien Yin Wong, Seyhan Yazar, Gabriel Cuellar-Partida, Seang-Mei Saw

المساهمون: Ophthalmology

المصدر: Cuellar-Partida, G, Williams, K M, Yazar, S, Guggenheim, J A, Hewitt, A W, Williams, C, Wang, J J, Kho, P-F, Saw, S M, Cheng, C-Y, Wong, T Y, Aung, T, Young, T L, Tideman, J W L, Jonas, J B, Mitchell, P, Wojciechowski, R, Stambolian, D, Hysi, P, Hammond, C J, Mackey, D A, Lucas, R M, MacGregor, S 2017, ' Genetically low vitamin D concentrations and myopic refractive error : a Mendelian randomization study ', International Journal of Epidemiology, vol. 46, no. 6, dyx068, pp. 1882–1890 . https://doi.org/10.1093/ije/dyx068Test
International Journal of Epidemiology, 46(6), 1882-1890. Oxford University Press
Cuellar-Partida, G, Williams, K M, Yazar, S, Guggenheim, J A, Hewitt, A W, Williams, C, JinWang, J, Kho, P F, Saw, S M, Cheng, C Y, YinWong, T, Aung, T, LYoung, T, Tideman, J W L, Jonas, J B, Mitchell, P, Wojciechowski, R, Stambolian, D, Hysi, P, Hammond, C J, Mackey, D A, Lucas, R M, MacGregor, S 2017, ' Genetically low vitamin D concentrations and myopic refractive error : A Mendelian randomization study ', International Journal of Epidemiology, vol. 46, no. 6, pp. 1882-1890 . https://doi.org/10.1093/ije/dyx068Test

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Refractive error, Vision, Epidemiology, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, 0302 clinical medicine, Blood serum, Asian People, Meta-Analysis as Topic, Risk Factors, Internal medicine, Mendelian randomization, Myopia, Vitamin D and neurology, Humans, Medicine, Genetic Predisposition to Disease, 030212 general & internal medicine, Vitamin D, Aged, business.industry, Confounding, Australia, Mendelian Randomization Analysis, General Medicine, Middle Aged, medicine.disease, Confidence interval, Endocrinology, 030221 ophthalmology & optometry, Female, business, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f37459da2a15673c10d84ad366c1fe9Test
https://hdl.handle.net/1765/108251Test