المؤلفون: Mark M. Iles, Jennifer H. Barrett, Matthew Law, Andrew Vu, Leandro M. Colli, Bogdan Pasaniuc, Michiel Vermeulen, Stephen J. Chanock, Cathrin Gräwe, Karen M. Funderburk, John C. Taylor, Harriet Rothschild, Myriam Brossard, Leonard I. Zon, Raj Chari, Clive J. Hoggart, Kevin M. Brown, Rebecca C Hennessey, Jiyeon Choi, Kai Yu, Mai Xu, Jinhu Yin, Julien Ablain, Michael A. Kovacs, Matthew M. Makowski, Tongwu Zhang, Florence Demenais

المساهمون: Bodescot, Myriam, National Cancer Institute [Bethesda] (NCI-NIH), National Institutes of Health [Bethesda] (NIH), Dana-Farber Cancer Institute [Boston], Radboud University [Nijmegen], 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 Paris Cité (UPCité), University of Leeds, University of California [Los Angeles] (UCLA), University of California (UC), Frederick National Laboratory for Cancer Research (FNLCR), Imperial College London, QIMR Berghofer Medical Research Institute, This work has been supported by the Intramural Research Program (IRP) of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, US National Institutes of Health. This work was also supported by grants from the National Institutes of Health (R01 CA10384, P01 CA163222, R01 CA083115), Cancer Research UK (C588/A19167), Institut National du Cancer, France (INCa_5982), Programme Hospitalier de Recherche Clinique (AOM-07-195), Fondation pour la Recherche Médicale (FDT20130928343), and the Howard Hughes Medical Institute Investigator Program (L.I.Z.). The Vermeulen lab is part of the Oncode Institute, which is partly funded by the Dutch Cancer Society (KWF)., Radboud university [Nijmegen], Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of California

المصدر: Nature Communications
Nature Communications, 2020, 11 (1), pp.2718. ⟨10.1038/s41467-020-16590-1⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.2718. ⟨10.1038/s41467-020-16590-1⟩
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature Communications, 11, 1-16
Nature Communications, 11, 1, pp. 1-16

مصطلحات موضوعية: Myxovirus Resistance Proteins, 0301 basic medicine, General Physics and Astronomy, MELANOMA, Genome-wide association study, 02 engineering and technology, Genome-wide association studies, Genes, Reporter, lcsh:Science, Cancer genetics, Melanoma, Zebrafish, Genetics, Regulation of gene expression, Multidisciplinary, Proteomics and Chromatin Biology, 021001 nanoscience & nanotechnology, Melanocytes, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], 0210 nano-technology, Proto-Oncogene Proteins B-raf, Science, Quantitative Trait Loci, [SDV.CAN]Life Sciences [q-bio]/Cancer, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, [SDV.CAN] Life Sciences [q-bio]/Cancer, Cell Line, Tumor, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Animals, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Gene, YY1, General Chemistry, Epigenome, Disease Models, Animal, HEK293 Cells, 030104 developmental biology, Gene Expression Regulation, Mutation, Expression quantitative trait loci, lcsh:Q, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85a4367fecae45d7f1bac0aa41d00adfTest
https://doi.org/10.1038/s41467-020-16590-1Test

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: Anne E. Cust, Julia Newton-Bishop, John R. Davies, Jennifer H. Barrett, Mark A. Jenkins, G.G. Giles, John L. Hopper, Kylie Vuong, Martin Drummond, H. Schmid, Kevin McGeechan, Joanne F. Aitken, Graham J. Mann, D T Bishop, Bruce K. Armstrong

المصدر: Br J Dermatol

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Skin Neoplasms, Adolescent, Dermatology, Logistic regression, Article, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Internal medicine, medicine, Humans, Family history, Risk factor, Melanoma, Lentigo, Nevus, Pigmented, business.industry, Case-control study, Australia, Cancer, medicine.disease, Confidence interval, Case-Control Studies, Cutaneous melanoma, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c23682d9c17d611c43fa128841434dfTest
https://pubmed.ncbi.nlm.nih.gov/31608432Test

المؤلفون: Anne E, Cust, Martin, Drummond, Peter A, Kanetsky, Alisa M, Goldstein, Jennifer H, Barrett, Stuart, MacGregor, Matthew H, Law, Mark M, Iles, Minh, Bui, John L, Hopper, Myriam, Brossard, Florence, Demenais, John C, Taylor, Clive, Hoggart, Kevin M, Brown, Maria Teresa, Landi, Julia A, Newton-Bishop, Graham J, Mann, Paul, King

المصدر: The Journal of Investigative Dermatology

مصطلحات موضوعية: Adult, Male, Skin Neoplasms, Adolescent, Risk Assessment, Article, Young Adult, Population Groups, Ethnicity, Humans, Genetic Predisposition to Disease, Pathology, Molecular, Melanoma, Alleles, Aged, Polymorphism, Genetic, Australia, Middle Aged, SNP, single nucleotide polymorphism, Prognosis, United Kingdom, CI, confidence interval, NRI, net reclassification improvement, OR, odds ratio, AUC, area under receiver operating characteristic curves, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::fa691e18cc2edaaefe3129929267b496Test
https://pubmed.ncbi.nlm.nih.gov/29890168Test

المؤلفون: Felicity Mackenzie, Robert Spiera, Javier Martin, Alexandre E. Voskuyl, Ora Gewurz-Singer, Luc Mouthon, Eamonn S. Molloy, Giacomo Emmi, Cisca Wijmenga, B. Marí-Alfonso, Sharon A. Chung, Augusto Vaglio, John G. Taylor, Cee Seng Yee, Christoph Berger, Abdel Salih, Santos Castañeda, Paul A. Monach, Luigi Boiardi, Verena Schönau, David Cuthbertson, Jenny Spimpolo, Asanka Nugaliyadde, Andrew Gough, Lorraine O'Neill, Christine Routledge, Neil McHugh, Michael D Morgan, Yannick Allanore, Stephen Jarrett, Elisabeth Brouwer, Raquel Fernández, Larry W. Moreland, Eugenio de Miguel, Carol A. Langford, Lisa Carr, Sarah L. Mackie, J. Sanchez-Martin, Marc Ramentol-Sintas, Lorenzo Beretta, Steve Martin, Emma Sanders, Sergio Prieto-González, Kathleen Maksimowicz-McKinnon, Inmaculada C. Morado, Lesley Hordon, Yusuf Patel, Thomas Neumann, Genessa Peters, Marco A. Cimmino, Kenneth J. Warrington, Simon Carette, Louise Sorensen, Agustín Martínez Berriochoa, Antoine G. Sreih, Rosanna Fong, M J García-Villanueva, Gary S. Hoffman, Andy Kempa, Javier Narváez, Víctor M. Martínez-Taboada, Karen Culfear, Carlo Salvarani, Francesco Bonatti, Roser Solans, Carol A. McAlear, Susan P Mollan, Luis Caminal-Montero, Laura Tío, Thomas Daikeler, Enrique Raya, Mercedes Pérez-Conesa, José Hernández-Rodríguez, Aleida Martínez Zapico, Philip Seo, Torsten Witte, Charles Li, Julia U Holle, Robert Stevens, Miguel A. González-Gay, Daniel Engelbert Blockmans, Lubna Haroon Rashid, Mohammed Nisar, Rose Wood, A. Unzurrunzaga, Richard A. Watts, Michael H. Weisman, Andreas P. Diamantopoulos, Sanjeet Kamath, Peter A. Merkel, Julien Haroche, Christian Pagnoux, Pradip Nandi, Lynne James, Marc Corbera-Bellalta, Colin T. Pease, Anne Gill, Michael J. Green, J. Bernardino Díaz López, Benedicte A. Lie, Carmen Gómez-Vaquero, Øyvind Molberg, Ulrich Specks, Esme Roads, Sarah Levy, Bhaskar Dasgupta, Steven R. Ytterberg, Zahira Masqood, Ann W. Morgan, Thomas Papo, Anupama Nandagudi, Mercedes Guijarro-Rojas, Curry L. Koening, Bridie Rowbotham, A. Hidalgo-Conde, Nader Khalidi, Jennifer H. Barrett, Norberto Ortego-Centeno, Marcello Govoni, José Luis Callejas, F. David Carmona, Laurent Sailler, James I. Robinson, Bernardo Sopeña, José A. Miranda-Filloy, Lindsy J. Forbess, Maria C. Cid, Jordi Monfort, Alfred Mahr, Oliver Wordsworth, Prisca Gondo, Bobby P. C. Koeleman, Paul J. McLaren, John D. Isaacs, Timothy J. Vyse, Jane Hollywood

المساهمون: Rheumatology, AII - Inflammatory diseases, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Translational Immunology Groningen (TRIGR), Department of Health and Life Sciences

المصدر: American journal of human genetics, 100(1), 64-74. Cell Press
American Journal of Human Genetics, 100(1), 64. Cell Press
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Carmona, F D, Vaglio, A, Mackie, S L, Hernández-Rodríguez, J, Monach, P A, Castañeda, S, Solans, R, Morado, I C, Narváez, J, Ramentol-Sintas, M, Pease, C T, Dasgupta, B, Watts, R, Khalidi, N, Langford, C A, Ytterberg, S, Boiardi, L, Beretta, L, Govoni, M, Emmi, G, Bonatti, F, Cimmino, M A, Witte, T, Neumann, T, Holle, J, Schönau, V, Sailler, L, Papo, T, Haroche, J, Mahr, A, Mouthon, L, Molberg, Ø, Diamantopoulos, A P, Voskuyl, A, Brouwer, E, Daikeler, T, Berger, C T, Molloy, E S, O'Neill, L, Blockmans, D, Lie, B A, Mclaren, P, Vyse, T J, Wijmenga, C, Allanore, Y, Koeleman, B P C, Callejas, J L, Caminal-Montero, L, Corbera-Bellalta, M, de Miguel, E, López, J B D, García-Villanueva, M J, Gómez-Vaquero, C, Guijarro-Rojas, M, Hidalgo-Conde, A, Marí-Alfonso, B, Berriochoa, A M, Zapico, A M, Martínez-Taboada, V M, Miranda-Filloy, J A, Monfort, J, Ortego-Centeno, N, Pérez-Conesa, M, Prieto-González, S, Raya, E, Fernández, R R, Sánchez-Martín, J, Sopeña, B, Tío, L, Unzurrunzaga, A, Gough, A, Isaacs, J D, Green, M, McHugh, N, Hordon, L, Kamath, S, Nisar, M, Patel, Y, Yee, C S, Stevens, R, Nandi, P, Nandagudi, A, Jarrett, S, Li, C, Levy, S, Mollan, S, Salih, A, Wordsworth, O, Sanders, E, Roads, E, Gill, A, Carr, L, Routledge, C, Culfear, K, Nugaliyadde, A, James, L, Spimpolo, J, Kempa, A, Mackenzie, F, Fong, R, Peters, G, Rowbotham, B, Masqood, Z, Hollywood, J, Gondo, P, Wood, R, Martin, S, Rashid, L H, Robinson, J I, Morgan, M, Sorensen, L, Taylor, J, Carette, S, Chung, S, Cuthbertson, D, Forbess, L J, Gewurz-Singer, O, Hoffman, G S, Koening, C L, Maksimowicz-McKinnon, K M, McAlear, C A, Moreland, L W, Pagnoux, C, Seo, P, Specks, U, Spiera, R F, Sreih, A, Warrington, K J, Weisman, M, Barrett, J H, Cid, M C, Salvarani, C, Merkel, P A, Morgan, A W, González-Gay, M A & Martín, J 2017, ' A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis ', American Journal of Human Genetics, vol. 100, no. 1, pp. 64-74 . https://doi.org/10.1016/j.ajhg.2016.11.013Test
American journal of human genetics
Carmona, F D, Vaglio, A, Mackie, S L, Hernández-Rodríguez, J, Monach, P A, Castañeda, S, Solans, R, Morado, I C, Narváez, J, Ramentol-Sintas, M, Pease, C T, Dasgupta, B, Watts, R, Khalidi, N, Langford, C A, Ytterberg, S, Boiardi, L, Beretta, L, Govoni, M, Emmi, G, Bonatti, F, Cimmino, M A, Witte, T, Neumann, T, Holle, J, Schönau, V, Sailler, L, Papo, T, Haroche, J, Mahr, A, Mouthon, L, Molberg, Ø, Diamantopoulos, A P, Voskuyl, A, Brouwer, E, Daikeler, T, Berger, C T, Molloy, E S, O'Neill, L, Blockmans, D, Lie, B A, Mclaren, P, Vyse, T J, Wijmenga, C, Allanore, Y, Koeleman, B P C, Spanish CGA Group, UKGCA Consortium, Vasculitis Clinical Research Consortium, UKGCA Consortium, Vasculitis Clinical Research Consortium & Vasculitis Clinical Research Consortium 2017, ' A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis ', American journal of human genetics, vol. 100, no. 1, pp. 64-74 . https://doi.org/10.1016/j.ajhg.2016.11.013Test
American Journal of Human Genetics, 100(1), 64-74. CELL PRESS

مصطلحات موضوعية: 0301 basic medicine, Male, ANCA-ASSOCIATED VASCULITIS, PATHOGENESIS, Genome-wide association study, HYPOXIA, SUSCEPTIBILITY, DISEASE, Cohort Studies, GENETIC-VARIANTS, GWAS, Genetics(clinical), FUNCTIONAL VARIATION, Genetics (clinical), Giant cell arteritis, Genetics, Aged, 80 and over, 3. Good health, Europe, INSIGHTS, Female, Vasculitis, Risk, EXPRESSION, Giant Cell Arteritis, Neovascularization, Physiologic, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Prolyl Hydroxylases, NO, 03 medical and health sciences, Genetic variation, medicine, Journal Article, LOCUS, Humans, Genetic Predisposition to Disease, Allele, Gene, Alleles, Aged, P4HA2, Genetic Variation, Genetics (clinical), Giant cell arteritis, GWAS, Plasminogen, P4HA2, Plasminogen, medicine.disease, 030104 developmental biology, Immunology, Imputation (genetics), Genome-Wide Association Study

وصف الملف: image/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e168ba29f9ffe061385948122e8e7a17Test
https://research.vumc.nl/en/publications/d0dbec2c-2c52-44f8-9c8b-33e370454337Test

المؤلفون: Frederik J. Hes, Richard S. Houlston, Ceres Fernandez-Rozadilla, Maggie Gorman, Harry Campbell, Ben Kinnersley, Albert Tenesa, Carli M. J. Tops, Melanie Schrumpf, Nicola Whiffin, Asta Försti, D. Timothy Bishop, Ella Barclay, Robert M.W. Hofstra, Fay J. Hosking, L. Y. Ooi, Claire Smillie, Graeme R. Grimes, Caroline Hayward, Arnoud Boot, Amy Lloyd, Stephan Buch, Manuela Pinheiro, Sara E. Dobbins, Clemens Schafmayer, Jennifer H. Barrett, Kari Hemminki, Helga Westers, Tom van Wezel, David J. Porteous, Archie Campbell, Sergi Castellví-Bel, Carla M. A. Pinto, Evropi Theodoratou, Lina Zgaga, Antoni Castells, Roland Wolf, Juul T. Wijnen, Hans Morreau, Peter Broderick, Susan M. Farrington, Victoria Svinti, Sarah E. Harris, Emma Northwood, Angel Carracedo, Andre Franke, Lynn Martin, Gillian Smith, Peter Propping, David Forman, Hans F. A. Vasen, Malcolm G. Dunlop, Ian Tomlinson, Dina Ruano, Wolgang Lieb, Claire Palles, Manuel R. Teixeira, Ian J. Deary, Clara Ruiz-Ponte, Maria Timofeeva, Jochen Hampe

المساهمون: Neurology, Internal Medicine, Medical Genetics

المصدر: Scientific Reports, 5
Scientific Reports
Scientific Reports, 5:16286. Nature Publishing Group
Scientific Reports, 5. Nature Publishing Group
Timofeeva, M N, Kinnersley, B, Farrington, S M, Whiffin, N, Palles, C, Svinti, V, Lloyd, A, Gorman, M, Ooi, L, Hosking, F, Barclay, E, Zgaga, L, Dobbins, S, Martin, L, Theodoratou, E, Broderick, P, Tenesa, A, Smillie, C, Grimes, G, Hayward, C, Campbell, A, Porteous, D, Deary, I J, Harris, S E, Northwood, E L, Barrett, J H, Smith, G, Wolf, R, Forman, D, Morreau, H, Ruano, D, Tops, C, Wijnen, J, Schrumpf, M, Boot, A, Vasen, H F A, Hes, F J, Van Wezel, T, Franke, A, Lieb, W, Schafmayer, C, Hampe, J, Buch, S, Propping, P, Hemminki, K, F??rsti, A, Westers, H, Hofstra, R, Pinheiro, M, Pinto, C, Teixeira, M, Ruiz-ponte, C, Fern??ndez-rozadilla, C, Carracedo, A, Castells, A, Castellv??-bel, S, Campbell, H, Bishop, D T, Tomlinson, I P M, Dunlop, M G & Houlston, R S 2015, ' Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ', Scientific Reports, vol. 5, pp. 16286 . https://doi.org/10.1038/srep16286Test

مصطلحات موضوعية: Activating Transcription Factor 1/genetics, EXPRESSION, Linkage disequilibrium, SUSCEPTIBILITY LOCI, Genotype, VARIANT, European Continental Ancestry Group, IDENTIFIES 6, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Article, Linkage Disequilibrium, White People, SDG 3 - Good Health and Well-being, Gene Frequency, Genetic variation, Odds Ratio, Coding region, Humans, HETEROGENEITY, European Continental Ancestry Group/genetics, Allele, GENOME-WIDE ASSOCIATION, Allele frequency, Gene, METAANALYSIS, Alleles, Adaptor Proteins, Signal Transducing, Medicine(all), Genetics, RISK, Activating Transcription Factor 1, Multidisciplinary, Cadherins/genetics, Intracellular Signaling Peptides and Proteins, Genetic Variation, Proteins, Cadherins, Colorectal Neoplasms/genetics, 3. Good health, DISCOVERY, Case-Control Studies, Proteins/genetics, Colorectal Neoplasms, SCAN, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9238dafb31e9af55e1a3a42fc1fdfb4Test

المؤلفون: Eitan Friedman, Shenying Fang, Jeffrey E. Lee, Esther Azizi, Marie-Françoise Avril, Douglas F. Easton, Julia A. Newton Bishop, Julie Lang, Elizabeth M. Gillanders, Juliette Randerson-Moor, Jan Lubinski, D. Timothy Bishop, Bruce K. Armstrong, Donato Calista, Florence Demenais, Joan Anton Puig-Butille, Anne E. Cust, Tadeusz Dȩbniak, Graham G. Giles, Grant W. Montgomery, Lorenza Pastorino, David C. Whiteman, Kevin M. Brown, Nicholas G. Martin, Diana Zelenika, Maria Teresa Landi, Jennifer H. Barrett, Veronica Höiom, Pilar Galan, Qingyi Wei, Johan Hansson, Lars A. Akslen, Bert Bakker, Brigitte Bressac-de Paillerets, Josep Malvehy, Rainer Tuominen, Wilma Bergman, Mark M. Iles, Stuart MacGregor, Jiali Han, Rona M. MacKie, Nicholas K. Hayward, Richard F. Kefford, Mark A. Jenkins, Christian Ingvar, Anders Molven, Graham J. Mann, Lisa A. Cannon-Albright, David E. Elder, Göran Jönsson, Joanne F. Aitken, Mark Harland, John L. Hopper, David L. Duffy, Eve Corda, Helen Snowden, Peter A. Kanetsky, Alisa M. Goldstein, Alison M. Dunning, John C. Taylor, Giorgio Landi, Håkan Olsson, Paola Ghiorzo, Nienke van der Stoep, Bart Janssen, Per Arne Andresen, Susana Puig, Nelleke A. Gruis, Marko Hočevar, Frans A. van Nieuwpoort, Srdjan Novaković, G. Mark Lathrop, Patricia Van Belle, Giovanna Bianchi-Scarrà, Christopher I. Amos

المساهمون: St. James's University Hospital, Cancer Council, Partenaires INRAE, Oslo University Hospital [Oslo], University of Bergen (UiB), Haukeland University Hospital, The Westmead Institute for Medical Research, Université Paris Descartes - Paris 5 (UPD5), Sheba Med Ctr, Tel Aviv University [Tel Aviv], Leiden University, University of Genoa (UNIGE), Fdn Jean Daussel CEPH, Institut Gustave Roussy (IGR), Département de biologie et pathologie médicales [Gustave Roussy], Maurizio Bufalini Hosp, University of Utah, University of Melbourne, University of Sydney, Pomeranian Med Univ, Unité de Recherche en Epidémiologie Nutritionnelle (UREN), Université Paris 13 (UP13)-Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Wellcome Trust [076113], European Commission [LSHC-CT-2006-018702], Cancer Research UK [C588/A4994, C588/A10589, C8216/A6129], US National Institutes of Health (NIH) [CA83115], NIH, National Cancer Institute (NCI), Division of Cancer Epidemiology and Genetics

المصدر: Nature genetics
Nature Genetics, 43(11), 1108-U98
Nature Genetics
Nature Genetics, Nature Publishing Group, 2011, 43 (11), pp.1108-U98. ⟨10.1038/ng.959⟩
Dipòsit Digital de la UB
Universidad de Barcelona

مصطلحات موضوعية: Skin Neoplasms, NEVI, [SDV]Life Sciences [q-bio], PHENOTYPIC CHARACTERISTICS, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Genètica mèdica, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, SEQUENCE VARIANTS, Skin cancer, Nevus, SNP, Humans, Genetic Predisposition to Disease, Gene, Melanoma, Càncer de pell, METAANALYSIS, POPULATION, 030304 developmental biology, RISK, 0303 health sciences, CUTANEOUS MALIGNANT-MELANOMA, Medical genetics, Case-control study, WOMEN, medicine.disease, GENE, CANCER, 030220 oncology & carcinogenesis, Case-Control Studies, Cutaneous melanoma, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::709d559a17530681126b93462d532230Test
http://europepmc.org/articles/PMC3251256Test

المؤلفون: Yu-Mei Chang, Julia Newton-Bishop, Jennifer H. Barrett, D. Timothy Bishop, Birute Karpavicius, Juliette Randerson-Moor, David E. Elder, Sue Haynes, Faye Elliott, Elaine Fitzgibbon, Kairen Kukalizch, Susan Leake, May Chan

المصدر: European Journal of Cancer. 47:732-741

مصطلحات موضوعية: Adult, Male, Cancer Research, medicine.medical_specialty, Skin Neoplasms, Population, Sunburn, Skin Pigmentation, Article, Young Adult, Risk Factors, medicine, Vitamin D and neurology, Humans, Risk factor, Young adult, skin and connective tissue diseases, education, Melanoma, Aged, education.field_of_study, Eye Color, integumentary system, Hydroxycholecalciferols, business.industry, Case-control study, Environmental Exposure, Odds ratio, Middle Aged, medicine.disease, Adaptation, Physiological, Dermatology, Surgery, Phenotype, England, Oncology, Case-Control Studies, Sunlight, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3625ca42884842d181f58fe826bb8f4Test
https://doi.org/10.1016/j.ejca.2010.10.008Test

المؤلفون: Martin G. Cook, Julia Newton-Bishop, Barry Powell, Andy Boon, Caroline Conway, Samira Lobo, Ian A. Cree, Margaret A. Knowles, Sara Edward, Jérémie Nsengimana, Mark Harland, Angana Mitra, D. Timothy Bishop, Maria Marples, Juliette Randerson-Moor, Floor de Kort, Katharine A. Parker, Rosalyn Jewell, Jennifer H. Barrett

المصدر: Clinical Cancer Research. 16:5211-5221

مصطلحات موضوعية: Male, Cancer Research, Skin Neoplasms, DNA Repair, DNA repair, Biology, Biomarkers, Pharmacological, Disease-Free Survival, Gene Expression Regulation, Enzymologic, Article, Cohort Studies, Recurrence, Antineoplastic Combined Chemotherapy Protocols, Gene expression, medicine, Humans, Melanoma, Gene, Regulation of gene expression, Gene Expression Profiling, Hazard ratio, Cancer, medicine.disease, Gene Expression Regulation, Neoplastic, Gene expression profiling, DNA Repair Enzymes, Oncology, Cancer research, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4df0c3a433b4ce575c16121eeed38aTest
https://doi.org/10.1158/1078-0432.ccr-10-1521Test

المؤلفون: Gunnar Steineck, Michael A. van Es, Eliane Kellen, Augustine Kong, Faye Elliott, Giuseppe Matullo, Carolyn D. Hurst, Margaret A. Knowles, Maurice P. Zeegers, Gerald W. Verhaegh, Simonetta Guarrera, Kristleifur Kristjansson, Rajesh Kumar, Sei C. Sak, Jennifer H. Barrett, N. Aydin Mungan, Charlotta Ryk, Berta Saez Gutierrez, Thorunn Rafnar, Annika Lindblom, Maria D. Garcia-Prats, Cecilia Arici, Stefan T Palsson, Patrick Sulem, Oskar B Skarphedinsson, Lambertus A. Kiemeney, Julius Gudmundsson, Gudmundur Geirsson, Unnur Thorsteinsdottir, Jan G. Hengstler, Petra J. de Verdier, Sigfus Nikulasson, Sita H. Vermeulen, Marcello Campagna, Carlotta Sacerdote, Gabriel Valdivia, D. Timothy Bishop, Silvia Polidoro, Anne E. Kiltie, Sigurjon A. Gudjonsson, Katja K H Aben, Asgeir Sigurdsson, Anne J. Grotenhuis, Peter Rudnai, Leonard H. van den Berg, Thorgeir E. Thorgeirsson, Roel A. Ophoff, Daniel F. Gudbjartsson, Eirikur Jonsson, J. Alfred Witjes, José I Sanz-Velez, Klaus Golka, Søren Besenbacher, Paolo Vineis, Kari Stefansson, Gisli Masson, Stefano Porru, Carlo Zanon, Ananya Choudhury, Holger Dietrich, Vigdis Petursdottir, Jelena Kostic, Frank Buntinx, Donatella Placidi, Jose I. Mayordomo, Meinolf Blaszkewicz, Kristin Alexiusdottir, Manuel Sanchez-Zalabardo, Gudmar Thorleifsson, Kvetoslava Koppova, Simon N. Stacey, Eugene Gurzau, Hjordis Bjarnason

المساهمون: Complexe Genetica, Family Medicine, RS: CAPHRI School for Public Health and Primary Care, RS: NUTRIM - R4 - Gene-environment interaction, Genetica & Celbiologie, Zonguldak Bülent Ecevit Üniversitesi, Department of Epidemiology, Biostatistics and Health Technology Assessment, Nijmegen, The Netherlands. b.kiemeney@ebh.umcn.nl

المصدر: Nature Genetics
Nature Genetics, 42(5), 415-419. Nature Publishing Group
Nature Genetics, 42, 415-9
Nature Genetics, 42, 5, pp. 415-9
Kiemeney, L A, Sulem, P, Besenbacher, S, Vermeulen, S H, Sigurdsson, A, Thorleifsson, G, Gudbjartsson, D F, Stacey, S N, Gudmundsson, J, Zanon, C, Kostic, J, Masson, G, Bjarnason, H, Palsson, S T, Skarphedinsson, O B, Gudjonsson, S A, Witjes, J A, Grotenhuis, A J, Verhaegh, G W, Bishop, D T, Sak, S C, Choudhury, A, Elliott, F, Barrett, J H, Hurst, C D, de Verdier, P J, Ryk, C, Rudnai, P, Gurzau, E, Koppova, K, Vineis, P, Polidoro, S, Guarrera, S, Sacerdote, C, Campagna, M, Placidi, D, Arici, C, Zeegers, M P, Kellen, E, Gutierrez, B S, Sanz-Velez, J I, Sanchez-Zalabardo, M, Valdivia, G, Garcia-Prats, M D, Hengstler, J G, Blaszkewicz, M, Dietrich, H, Ophoff, R A, van den Berg, L H, Alexiusdottir, K, Kristjansson, K, Geirsson, G, Nikulasson, S, Petursdottir, V, Kong, A, Thorgeirsson, T, Mungan, N A, Lindblom, A, van Es, M A, Porru, S, Buntinx, F, Golka, K, Mayordomo, J I, Kumar, R, Matullo, G, Steineck, G, Kiltie, A E, Aben, K K H, Jonsson, E, Thorsteinsdottir, U, Knowles, M A, Rafnar, T & Stefansson, K 2010, ' A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer ', Nature Genetics, vol. 42, no. 5, pp. 415-9 . https://doi.org/https://www.ncbi.nlm.nih.gov/pubmed/20348956Test

مصطلحات موضوعية: Male, Somatic cell, Genome-wide association study, Aetiology, screening and detection [ONCOL 5], medicine.disease_cause, Germline, DISEASE, 0302 clinical medicine, Recurrence, Genotype, Genetics, RISK, 0303 health sciences, Mutation, Manchester Cancer Research Centre, Smoking, Urinary Bladder Neoplasms/genetics, 3. Good health, Receptor, Fibroblast Growth Factor, Type 3/genetics, Europe, 030220 oncology & carcinogenesis, bladder cancer, Female, Chromosomes, Human, Pair 4, Risk, EXPRESSION, medicine.medical_specialty, genome-wide association study, FGFR3, Urology, Biology, Article, Disease-Free Survival, Molecular epidemiology [NCEBP 1], 03 medical and health sciences, Text mining, Translational research [ONCOL 3], medicine, UROTHELIAL CELL-CARCINOMA, Humans, Receptor, Fibroblast Growth Factor, Type 3, Genetic Predisposition to Disease, Allele, Alleles, Sequence (medicine), 030304 developmental biology, Bladder cancer, Models, Genetic, Urinary Bladder Cancer, business.industry, ResearchInstitutes_Networks_Beacons/mcrc, fungi, Genetic Variation, Cancer, medicine.disease, Neck of urinary bladder, Urinary Bladder Neoplasms, Evaluation of complex medical interventions [NCEBP 2], FGFR3 MUTATIONS, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5528d06d2a2b285b8a4ec5eb5bf0c6d7Test
https://doi.org/10.1038/ng.558Test