المؤلفون: Judith Abarca-Zabalía, Pilar López-Cotarelo, Manuel Comabella, Yolanda Aladro, Teresa Agudo-Jiménez, Belen Pilo, Elena Urcelay, Adela González-Jiménez, Laura Espino-Paisán

المساهمون: Institut Català de la Salut, [López-Cotarelo P, González-Jiménez A] Laboratorio de Investigación en Genética y Bases Moleculares de Enfermedades Complejas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. Red Española de Esclerosis Múltiple (REEM), Madrid, Spain. [Agudo-Jiménez T, Abarca-Zabalía J] Laboratorio de Investigación en Genética y Bases Moleculares de Enfermedades Complejas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. [Aladro Y, Pilo B] Neurology Department, Hospital Universitario de Getafe, Madrid, Spain. [Comabella M] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Red Española de Esclerosis Múltiple (REEM), Madrid, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientia

مصطلحات موضوعية: Male, Esclerosi múltiple - Aspectes genètics, T-Lymphocytes, Gene Expression, Autoimmunity, Basal (phylogenetics), fenómenos genéticos::variación genética::polimorfismo genético::polimorfismo de nucleótido único [FENÓMENOS Y PROCESOS], B-Lymphocytes, Multidisciplinary, Genètica humana, medicine.diagnostic_test, Otros calificadores::Otros calificadores::/genética [Otros calificadores], CD69, Nervous System Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis [DISEASES], Middle Aged, Genetic Phenomena::Genetic Variation [PHENOMENA AND PROCESSES], enfermedades del sistema nervioso::enfermedades autoinmunitarias del sistema nervioso::enfermedades autoinmunes desmielinizantes del SNC::esclerosis múltiple [ENFERMEDADES], Medicine, Female, Adult, medicine.medical_specialty, Multiple Sclerosis, Science, Biology, Peripheral blood mononuclear cell, Polymorphism, Single Nucleotide, Article, Immune system, Western blot, Downregulation and upregulation, Internal medicine, fenómenos genéticos::variación genética [FENÓMENOS Y PROCESOS], medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], Immunogenetics, Humans, Allele, Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [PHENOMENA AND PROCESSES], Multiple sclerosis, Polimorfisme genètic, Genetic Variation, Membrane Proteins, medicine.disease, Gene regulation in immune cells, Endocrinology, Genetic markers, Carrier Proteins, Neurological disorders

وصف الملف: application/pdf; image/jpeg

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f388d85995737210bb8c4ee2f6acde1Test
http://europepmc.org/articles/PMC8560952Test

المؤلفون: Lurdes Planas-Cerezales, Elena G. Arias-Salgado, Cristina Berastegui, Ana Montes-Worboys, Rafaela González-Montelongo, José. M. Lorenzo-Salazar, Vanesa Vicens-Zygmunt, Marta Garcia-Moyano, Jordi Dorca, Carlos Flores, Rosario Perona, Antonio Román, María Molina-Molina

المساهمون: Institut Català de la Salut, [Planas-Cerezales L, Montes-Worboys A] ILD Multidisciplinary Unit, Hospital Universitari Bellvitge, IDIBELL, Universitat de Barcelona, Hospitalet de Llobregat, Spain. [Arias-Salgado EG] Biomedical Research Institute CSIC/UAM, IdIPAZ, Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain. [Berastegui C, Román A] Servei de Pneumologia, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [González-Montelongo R, Lorenzo-Salazar JM] Genomics Division, Instituto Tecnológico y de Energías Renovables, Santa Cruz de Tenerife, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Frontiers in Medicine, Vol 8 (2021)
Dipòsit Digital de la UB
Universidad de Barcelona
Frontiers in Medicine
Scientia

مصطلحات موضوعية: 0301 basic medicine, Telomerase, Medicine (General), Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial [DISEASES], medicine.medical_treatment, law.invention, 0302 clinical medicine, telomere shortening, law, telomere disorders, Pulmonary fibrosis, Medicine, genetics, Surgical Procedures, Operative::Surgical Procedures, Operative::Transplantation::Organ Transplantation::Lung Transplantation [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Original Research, interstitial lung disease, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Interstitial lung disease, General Medicine, Intensive care unit, medicine.anatomical_structure, medicine.medical_specialty, 03 medical and health sciences, R5-920, Internal medicine, Transplantation of organs, tissues, etc, Other subheadings::Other subheadings::/genetics [Other subheadings], lung transplantation, Lung transplantation, Fibrosi pulmonar - Aspectes genètics, Lung, pulmonary fibrosis, business.industry, Extracorporeal circulation, diagnóstico::pronóstico::resultado del tratamiento [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Pulmó, Diagnosis::Prognosis::Treatment Outcome [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], medicine.disease, Transplantation, Trasplantament d'òrgans, Pulmons - Trasplantació, 030104 developmental biology, Anomalies cromosòmiques, 030228 respiratory system, enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales [ENFERMEDADES], Chromosome abnormalities, Avaluació de resultats (Assistència sanitària), intervenciones quirúrgicas::intervenciones quirúrgicas::trasplante::trasplante de órganos::trasplante de pulmón [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Lungs, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0aa4da58bf0be019cbc0238aee38019Test
https://www.frontiersin.org/articles/10.3389/fmed.2021.695919/fullTest

المؤلفون: Remuzgo-Martínez, Sara, Genre, Fernanda, Pulito-Cueto, Verónica, Atienza-Mateo, Belén, Mora Cuesta, Víctor Manuel, Iturbe Fernández, David, Fernández Rozas, Sonia María, Lera-Gómez, Leticia, Alonso Lecue, Pilar, Ussetti, María Piedad, Laporta, Rosalía, Berastegui García, Cristina, Solé, Amparo, Pérez González, Virginia Luz, De Pablo Gafas, Alicia, Gualillo, Oreste, Cifrián, José Manuel, López-Mejías, Raquel, Gonzalez-Gay, MA, Universitat Autònoma de Barcelona

المساهمون: Institut Català de la Salut, Vall d'Hebron Barcelona Hospital Campus, Universidad de Cantabria

المصدر: Biomedicines, Vol 9, Iss 458, p 458 (2021)
Biomedicines
Volume 9
Issue 5
Scientia
Biomedicines . 2021 Apr 22;9(5):458
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona

مصطلحات موضوعية: idiopathic interstitial pneumonia, medicine.medical_specialty, Pulmons - Malalties - Aspectes genètics, Respiratory Tract Diseases::Lung Diseases::Lung Diseases, Interstitial [DISEASES], QH301-705.5, Medicine (miscellaneous), Interstitial lung disease, Gastroenterology, General Biochemistry, Genetics and Molecular Biology, Pulmonary function testing, Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptors, Vascular Endothelial Growth Factor [CHEMICALS AND DRUGS], Lung Disorder, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Internal medicine, Genotype, Proteïnes quinases - Receptors, medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], Genetics, genetics, Idiopathic interstitial pneumonia, Biology (General), health care economics and organizations, interstitial lung disease, vascular endothelial growth factor, business.industry, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Haplotype, Biomarker, respiratory system, medicine.disease, respiratory tract diseases, Vascular endothelial growth factor, 030228 respiratory system, chemistry, enfermedades respiratorias::enfermedades pulmonares::enfermedades pulmonares intersticiales [ENFERMEDADES], 030220 oncology & carcinogenesis, Biomarker (medicine), enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::proteína cinasas::proteína-tirosina cinasas::receptores proteína-tirosina cinasas::receptores del factor de crecimiento del endotelio vascular [COMPUESTOS QUÍMICOS Y DROGAS], biomarker, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b03977d86c2562597f540c38ff3003Test
https://www.mdpi.com/2227-9059/9/5/458Test

المؤلفون: Maria Rosario Chica Parrado, Maria Auxiliadora Gómez-España, Eduardo Díaz-Rubio, Manuel Benavides, Ana Vivancos, Marta Toledano, Enrique Aranda, Vanesa García-Barberán, Martina Alvarez, Elena Elez

المساهمون: Institut Català de la Salut, [Vivancos A] Grup de genòmica del Càncer, Vall d'Hebron Institut d'Oncologia, Barcelona, Spain. [Aranda E, Gómez-España MA] Department of Medical Oncology, Reina Sofía University Hospital, CIBERONC, Córdoba, Spain. [Benavides M] Department of Medical Oncology, Hospital Universitario Regional y Virgen de la Victoria, Málaga, Spain. [Élez E] Servei d’Oncologia Mèdica, Vall d'Hebron Institut d'Oncologia, Barcelona, Spain. [Toledano M] IMIBIC Instituto Maimonides Investigación Biomédica de Córdoba, Córdoba, Spain., Hospital Verge de la Cinta de Tortosa

المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientia
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Scientific Reports

مصطلحات موضوعية: 0301 basic medicine, Male, Colorectal cancer, Mutant, DNA Mutational Analysis, lcsh:Medicine, medicine.disease_cause, Gastroenterology, 0302 clinical medicine, Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Cytodiagnosis::Biopsy::Liquid Biopsy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Other subheadings::/diagnosis [Other subheadings], lcsh:Science, Early Detection of Cancer, enzimas y coenzimas::enzimas::hidrolasas::ácido anhídrido hidrolasas::GTP fosfohidrolasas::proteínas de unión al GTP::proteínas de unión al GTP monoméricas::proteínas ras::proteínas protooncogénicas p21(ras) [COMPUESTOS QUÍMICOS Y DROGAS], Aged, 80 and over, Mutation, Multidisciplinary, Otros calificadores::Otros calificadores::/genética [Otros calificadores], neoplasias::neoplasias por localización::neoplasias del sistema digestivo::neoplasias gastrointestinales::neoplasias intestinales::neoplasias colorrectales [ENFERMEDADES], Enzimas y Coenzimas::Enzimas::Hidrolasas::Ácido Anhídrido Hidrolasas::GTP Fosfohidrolasas::Proteínas de Unión al GTP::Proteínas de Unión al GTP Monoméricas::Proteínas ras::Proteínas Proto-Oncogénicas p21(ras) [COMPUESTOS QUÍMICOS Y DROGAS], Middle Aged, Prognosis, diagnóstico::técnicas y procedimientos diagnósticos::técnicas de laboratorio clínico::técnicas citológicas::citodiagnóstico::biopsia::biopsia líquida [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Female, KRAS, Colorectal Neoplasms, Biòpsia, Cell-Free Nucleic Acids, Oncogens Ras, Neoplasias::Neoplasias por Localización::Neoplasias del Sistema Digestivo::Neoplasias Gastrointestinales::Neoplasias Intestinales::Neoplasias Colorrectales [ENFERMEDADES], Adult, medicine.medical_specialty, Concordance, Otros calificadores::/diagnóstico [Otros calificadores], Article, Cancer screening, Proto-Oncogene Proteins p21(ras), 03 medical and health sciences, Gastrointestinal cancer, Neoplasms::Neoplasms by Site::Digestive System Neoplasms::Gastrointestinal Neoplasms::Intestinal Neoplasms::Colorectal Neoplasms [DISEASES], Internal medicine, medicine, Biomarkers, Tumor, Other subheadings::Other subheadings::/genetics [Other subheadings], Humans, Liquid biopsy, Allele, neoplasms, Aged, Enzymes and Coenzymes::Enzymes::Hydrolases::Acid Anhydride Hydrolases::GTP Phosphohydrolases::GTP-Binding Proteins::Monomeric GTP-Binding Proteins::ras Proteins::Proto-Oncogene Proteins p21(ras) [CHEMICALS AND DRUGS], business.industry, lcsh:R, Liquid Biopsy, medicine.disease, digestive system diseases, 030104 developmental biology, Còlon - Càncer - Diagnòstic, lcsh:Q, business, 030217 neurology & neurosurgery, Kras mutation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c48f78c860ebc9726fe6397f0efd05Test
http://link.springer.com/article/10.1038/s41598-019-45616-yTest

المؤلفون: Espen Saxhaug Kristoffersen, Ko Willems van Dijk, Aster V.E. Harder, Rigmor H. Jensen, Patricia Pozo-Rosich, Lisanne S. Vijfhuizen, Michel D. Ferrari, John-Anker Zwart, Laurent F. Thomas, Thomas F. Hansen, Emer O'Connor, G.M. Terwindt, Raymond Noordam, Frits R. Rosendaal, Lisette J. A. Kogelman, Rolf Fronczek, Erling Tronvik, Sigrid Børte, Arn M. J. M. van den Maagdenberg, Irene de Boer, Bendik S. Winsvold, Carmen Fourier

المساهمون: Institut Català de la Salut, [Harder AVE] Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. [Winsvold BS] Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. Department of Neurology, Oslo University Hospital, Oslo, Norway. [Noordam R] Department of Internal Medicine, Section of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, The Netherlands. [Vijfhuizen LS] Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. [Børte S] Department of Research, Innovation and Education, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway. Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway. [Kogelman LJA] Department of Neurology, Danish Headache Center, Rigshospitalet, Glostrup, Denmark. [Pozo-Rosich P] Grup de Recerca en Cefalea, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Unitat de Cefalea, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus, Complex Disease Genetics, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, University of Helsinki

المصدر: Annals of Neurology, 90(2), 203-216. WILEY
Scientia
Annals of Neurology
Harder, A V E, Winsvold, B S, Noordam, R, Vijfhuizen, L S, Børte, S, Kogelman, L J A, Boer, I, Tronvik, E, Rosendaal, F R, Willems Van Dijk, K, O'connor, E, Fourier, C, Thomas, L F, Kristoffersen, E S, Fronczek, R, Pozo-rosich, P, Jensen, R H, Ferrari, M D, Hansen, T F, Zwart, J, Terwindt, G M & Maagdenberg, A M J M 2021, ' Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache ', Annals of Neurology, vol. 90, no. 2, pp. 203-216 . https://doi.org/10.1002/ana.26146Test
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona

مصطلحات موضوعية: medicine.medical_specialty, Linkage disequilibrium, Genetic Phenomena::Genotype::Genetic Predisposition to Disease [PHENOMENA AND PROCESSES], Diàtesi, Single-nucleotide polymorphism, Genome-wide association study, 3124 Neurology and psychiatry, afecciones patológicas, signos y síntomas::procesos patológicos::atributos de la enfermedad::susceptibilidad a enfermedades::predisposición genética a la enfermedad [ENFERMEDADES], Internal medicine, medicine, Genetic predisposition, Other subheadings::Other subheadings::/genetics [Other subheadings], enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::trastornos con cefaleas::cefaleas primarias::cefalalgia autónoma del trigémino::cefalea histamínica [ENFERMEDADES], Research Articles, business.industry, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Cluster headache, 3112 Neurosciences, Cefalàlgia - Aspectes genètics, Odds ratio, medicine.disease, Confidence interval, 3. Good health, Neurology, Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Headache Disorders::Headache Disorders, Primary::Trigeminal Autonomic Cephalalgias::Cluster Headache [DISEASES], Population study, Neurology (clinical), business, Research Article

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dcff5fa4403ed4b892b048f6c58b55cTest
https://ddd.uab.cat/record/256417Test

المؤلفون: Graham G. Giles, Diana Eccles, Cezary Cybulski, Catherine M. Tangen, Leon Raskin, Per Hall, Ana Vega, Hedy S. Rennert, Andrew T. Chan, Stephan Lam, Michael Hoffmeister, Angeline S. Andrew, Claudine Isaacs, Matthias W. Beckmann, Vessela N. Kristensen, Julia A. Knight, Mark S. Goldberg, Jonathan Tyrer, Jane C. Figueiredo, Katherine L. Nathanson, Anna deFazio, Ian G. Campbell, Nora Pashayan, Liene Nikitina-Zake, Goska Leslie, Rosalind A. Eeles, Line Bjørge, Adonina Tardón, Angela Cox, Gregory Idos, Evgeny N. Imyanitov, Manolis Kogevinas, Marc Tischkowitz, Hilary K. Finucane, Hardev Pandha, Rayjean J. Hung, Davor Lessel, Richard S. Houlston, Andrew F. Olshan, André Lopes Carvalho, James D. McKay, Kenneth Offit, Penelope M. Webb, Barry S. Rosenstein, Melinda C. Aldrich, Alice S. Whittemore, Austin Miller, Miguel E. Aguado-Barrera, Amanda E. Toland, Anna Marie Mulligan, Catharine M L West, Susan J. Ramus, Jennifer Stone, David C. Christiani, Clarice R. Weinberg, Olivia Fletcher, Kyriaki Michailidou, Demetrius Albanes, Chu Chen, Jenny L Donovan, Linda E. Kelemen, Carolina Ellberg, Hermann Brenner, Eitan Friedman, Sara Margolin, Jacek Gronwald, Argyrios Ziogas, Elisa V. Bandera, Qin Wang, Christopher I. Amos, Swe-Brca, Douglas F. Easton, Karin Sundfeldt, John L. Hopper, Jong Y. Park, Børge G. Nordestgaard, Johanna Schleutker, Freddie C. Hamdy, Alicja Wolk, Graham Casey, Radka Kaneva, Joe Dennis, Francesmary Modugno, Paolo Radice, Aage Haugen, Ralf Bützow, Barbara Burwinkel, Maria A. Caligo, Paul A. Townsend, Daniel D. Buchanan, Håkan Olsson, Li Li, Elza Khusnutdinova, Karina Dalsgaard Sørensen, Marco Montagna, Patricia A. Ganz, Kirsten B. Moysich, Stephen B. Gruber, Geraldine Cancel-Tassin, Mary Anne Rossing, Mads Thomassen, Manuela Gago-Dominguez, Marjanka K. Schmidt, Jolanta Kupryjanczyk, Melissa C. Southey, Finn Cilius Nielsen, Sara Benlloch, Roger L. Milne, Manuel R. Teixeira, Taymaa May, David V. Conti, Thilo Dörk, Kathleen Claes, Manjeet K. Bolla, Douglas A. Levine, Lorelei A. Mucci, Irene L. Andrulis, Carl Blomqvist, Sara Lindström, Marjorie J. Riggan, Ellen L. Goode, Jenny Lester, Jack A. Taylor, Adam S. Kibel, Jyotsna Batra, Stephen N. Thibodeau, Elinor J. Sawyer, Stefania Boccia, Jacques Simard, Robert J. MacInnis, Fredrik Wiklund, Geoffrey Liu, Robert Winqvist, Robert J. Hamilton, Joan Brunet, Olufunmilayo I. Olopade, Jeffrey N. Weitzel, Susan L. Neuhausen, Robert L. Ferris, Georgia Chenevix-Trench, Elizabeth J. van Rensburg, Amanda B. Spurdle, Jeroen R. Huyghe, Stig E. Bojesen, Eric J. Duell, Christopher A. Haiman, Bogdan Pasaniuc, Wilbert H.M. Peters, M. Dawn Teare, Marc T. Goodman, Richa Saxena, Renée T. Fortner, Shanbeh Zienolddiny, Mia M. Gaudet, Stephanie J. Weinstein, Mikael Johansson, Heli Nevanlinna, Nhu D. Le, Rolando Herrero, Peter Kraft, Steven Gallinger, David E. Goldgar, Anna Jakubowska, Paul D.P. Pharoah, Erin M. Siegel, Gabriella Cadoni, Weiva Sieh, Esther M. John, Rebecca Sutphen, Kari Stefansson, Loic Le Marchand, David J. Hunter, Alkes L. Price, Judy Garber, Mary B. Daly, Flavio Lejbkowicz, Lambertus A. Kiemeney, Martha L. Slattery, Arto Mannermaa, Christian F. Singer, Daniele Campa, Hans Brunnström, Hongbing Shen, Els Van Nieuwenhuysen, V. Wendy Setiawan, Penella J. Woll, Catherine M. Phelan, Christopher I. Li, Robert L. Nussbaum, Niclas Håkansson, Triantafillos Liloglou, Stella Koutros, Kjell Grankvist, James D. Brenton, Annika Lindblom, Gad Rennert, Karoline Kuchenbaecker, Martin Lacko, Gary E. Goodman, Fredrick R. Schumacher, Henrik Grönberg, Diana Torres, J. Margriet Collée, Rosa B. Barkardottir, Amit Joshi, Trinidad Caldés, Mary Beth Terry, Jenny Chang-Claude, Paul Brennan, Simon A. Gayther, Mark H. Greene, Daniel R. Barnes, Janet L. Stanford, Miriam Dwek, Christiane Maier, Susanne K. Kjaer, Florentia Fostira, Miranda Pring, Noralane M. Lindor, Harvey A. Risch, David G. Huntsman, Kim De Ruyck, Judith A. Clements, Pooja Middha, Alison M. Dunning, Nadine Tung, Sebastian Stintzing, Michael O. Woods, Stephen J. Chanock, Andrew K. Godwin, Kenneth Muir, Eloiza H. Tajara, Silvia Franceschi, Xia Jiang, Li Hsu, Emily White, Peter T. Campbell, Paul A. James, Josef Heinz-Lenz, Ali Amin Al Olama, Victoria L. Stevens, Lovise Maehle, Fotios Loupakis, Peter Devilee, Orland Diez, Kristin K. Zorn, Stephanie A. Bien, Maria Teresa Landi, Mark A. Jenkins, Amanda I. Phipps, Alfons Meindl, Frank Claessens, Mark N. Brook, Kathryn L. Penney, Digna R. Velez Edwards, Montserrat Garcia-Closas, Diether Lambrechts, Zsofia Kote-Jarai, Fergus J. Couch, Duncan Thomas, Kathryn L. Terry, Ute Hamann, Heike Bickeböller, Christopher K. Edlund, Ana Osorio, Younghun Han, Jochen Hampe, Tee Kay-Khaw, Corina Lesseur, Peter A. Fasching, Lesley McGuffog, Eunjung Lee, Tabea Kühl, Andy R Ness, Kamila Czene, Angela Risch, Aocs Mod SQuaD, Jeri Kim, Anna H. Wu, Jacqueline M. Lane, Brenda Diergaarde, Ruth C. Travis, Julie M. Cunningham, Philip Lazarus, Shelley S. Tworoger, Natalia Antonenkova, Emmanouil Saloustros, Wei Zheng, Javier Benitez, Dijana Plaseska-Karanfilska, Mark C. Weissler, Marcia Cruz Correa, Hoda Anton-Culver, Neil E. Caporaso, Cornelia M. Ulrich, Stephanie L. Schmit, Antonis C. Antoniou, Victor Moreno, David E. Neal, Tanja Pejovic, Erich H-Wichmann, Pascal Guénel, Mattias Johansson, Florian Heitz, Beth Y. Karlan, Sonja I. Berndt, Anthony J. Swerdlow, Estrid Høgdall, Hiltrud Brauch, Ulrike Peters, D. Gareth Evans, Celine M. Vachon, Edith Olah, Dale P. Sandler, Lisa F. Newcomb, Michael T. Parsons, Lisa A. Cannon-Albright, Peter J. Hulick, José A. García-Sáenz, Sue A. Ingles, Andrew Berchuck, Peter Hillemanns, Matthew B. Schabath, Polly A. Newcomb, Banu Arun, Xifeng Wu, Darya Prokofyeva, Jan Lubinski, Susanne M. Arnold, Natalia Bogdanova, Drakoulis Yannoukakos, Nawaid Usmani, Kristan J. Aronson, Chul Yun-Hong, Monique J. Roobol

المساهمون: Clinical Genetics, Urology, Læknadeild (HÍ), Faculty of Medicine (UI), Lífvísindasetur (HÍ), Biomedical Center (UI), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland, Finucane, Hilary K [0000-0003-3864-9828], Schumacher, Fredrick R [0000-0002-3073-7463], Schmit, Stephanie L [0000-0001-5931-1194], Michailidou, Kyriaki [0000-0001-7065-1237], Kuchenbaecker, Karoline B [0000-0001-9726-603X], Dennis, Joe [0000-0003-4591-1214], Huyghe, Jeroen R [0000-0001-6027-9806], Andrulis, Irene L [0000-0002-4226-6435], Arnold, Susanne M [0000-0001-6542-9551], Barnes, Daniel R [0000-0002-3781-7570], Batra, Jyotsna [0000-0003-4646-6247], Bojesen, Stig E [0000-0002-4061-4133], Brauch, Hiltrud [0000-0001-7531-2736], Brenton, James D [0000-0002-5738-6683], Brook, Mark N [0000-0002-8969-2378], Brunet, Joan [0000-0003-1945-3512], Brunnström, Hans [0000-0001-7402-138X], Buchanan, Daniel D [0000-0003-2225-6675], Campbell, Ian [0000-0002-7773-4155], Cancel-Tassin, Géraldine [0000-0002-9583-6382], Chan, Andrew T [0000-0001-7284-6767], Chanock, Stephen J [0000-0002-2324-3393], Claes, Kathleen BM [0000-0003-0841-7372], Cunningham, Julie M [0000-0002-8159-3025], Devilee, Peter [0000-0002-8023-2009], Ellberg, Carolina [0000-0001-7297-0645], Fasching, Peter A [0000-0003-4885-8471], Liloglou, Triantafillos [0000-0003-0460-1404], Fletcher, Olivia [0000-0001-9387-7116], García-Sáenz, José A [0000-0001-6880-0301], Grankvist, Kjell [0000-0003-4289-2097], Greene, Mark H [0000-0003-1852-9239], Gronberg, Henrik [0000-0002-1073-2753], Guénel, Pascal [0000-0002-8359-518X], Hampe, Jochen [0000-0002-2421-6127], Houlston, Richard [0000-0002-5268-0242], Hulick, Peter J [0000-0001-8397-4078], James, Paul [0000-0002-4361-4657], Jenkins, Mark A [0000-0002-8964-6160], Joshi, Amit D [0000-0001-7581-6934], Lambrechts, Diether [0000-0002-3429-302X], Leslie, Goska [0000-0001-5756-6222], Lessel, Davor [0000-0003-4496-244X], Levine, Douglas A [0000-0003-1038-8232], Miller, Austin [0000-0001-9739-8462], Milne, Roger L [0000-0001-5764-7268], Moreno, Victor [0000-0002-2818-5487], Muir, Kenneth [0000-0001-6429-988X], Nathanson, Katherine L [0000-0002-6740-0901], Nevanlinna, Heli [0000-0002-0916-2976], Newcomb, Polly A [0000-0001-8786-0043], Nikitina-Zake, Liene [0000-0003-2491-5187], Nordestgaard, Børge G [0000-0002-1954-7220], Olama, Ali Amin Al [0000-0002-7178-3431], Olopade, Olufunmilayo I [0000-0002-9936-1599], Pashayan, Nora [0000-0003-0843-2468], Parsons, Michael T [0000-0003-3242-8477], Plaseska-Karanfilska, Dijana [0000-0001-8877-2416], Raskin, Leon [0000-0003-1195-7214], Rennert, Gad [0000-0002-8512-068X], Risch, Angela [0000-0002-8026-5505], Roobol, Monique J [0000-0001-6967-1708], Saloustros, Emmanouil [0000-0002-0485-0120], Schabath, Matthew B [0000-0003-3241-3216], Schleutker, Johanna [0000-0002-1863-0305], Schmidt, Marjanka K [0000-0002-2228-429X], Sorensen, Karina Dalsgaard [0000-0002-4902-5490], Stintzing, Sebastian [0000-0002-3297-5801], Stone, Jennifer [0000-0001-5077-0124], Tardon, Adonina [0000-0001-5150-1209], Teixeira, Manuel R [0000-0002-4896-5982], Toland, Amanda E [0000-0002-0271-1792], Aguado-Barrera, Miguel Elías [0000-0002-7822-6726], Webb, Penelope M [0000-0003-0733-5930], Wolk, Alicja [0000-0001-7387-6845], Yannoukakos, Drakoulis [0000-0001-7509-3510], Zheng, Wei [0000-0003-1226-070X], Ziogas, Argyrios [0000-0003-4529-3727], Peters, Ulrike [0000-0001-5666-9318], Eeles, Rosalind A [0000-0002-3698-6241], Brennan, Paul J [0000-0002-0518-8714], Easton, Douglas F [0000-0003-2444-3247], Pharoah, Paul DP [0000-0001-8494-732X], Price, Alkes L [0000-0002-2971-7975], Apollo - University of Cambridge Repository, Institut Català de la Salut, [Jiang X] Program in Genetic Epidemiology and Statistical Genetics, Harvard T.H. Chan School of Public Health, Boston, MA, USA. Unit of Cardiovascular Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden. [Finucane HK] Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA. Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. [Schumacher FR] Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, USA. Seidman Cancer Center, University Hospitals, Cleveland, OH, USA. [Schmit SL] Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA. Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA. [Tyrer JP] Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK. [Han Y] Department of Biomedical Data Science, The Geisel School of Medicine at Dartmouth, Lebanon, NH, USA. [Diez O] Grup d'Oncogenètica, Vall d'Hebron Institut d'Oncologia, Barcelona, Spain. Hospital Universitari Vall d'Hebron, Barcelona, Spain, Hospital Universitari Vall d'Hebron, Lääketieteen ja terveysteknologian tiedekunta - Faculty of Medicine and Health Technology, Tampere University, Cancer Research UK (Reino Unido), NIHR - Comprehensive Biomedical Research Centre, Guy ’ s & St. Thomas ’ NHS Foundation Trust, NIHR - Oxford Biomedical Research Centre (Reino Unido), German Cancer Research Center, Consejo Nacional de Ciencia y Tecnología (CONACyT), King College London, National Health and Medical Research Council (Australia), Canadian Institutes of Health Research, The BREast Oncology GAlician Network (BREOGAN, Dietmar-Hopp Foundation, Helmholtz Society and the German Cancer Research Center (DKFZ), Asociación Española Contra el Cáncer, Vall d'Hebron Barcelona Hospital Campus, Clinicum, Department of Oncology, University of Helsinki, Department of Pathology, Medicum, Department of Obstetrics and Gynecology, HUS Comprehensive Cancer Center

المصدر: Jiang, X, Finucane, H K, Schumacher, F R, Schmit, S L, Tyrer, J P, Han, Y, Michailidou, K, Lesseur, C, Kuchenbaecker, K B, Dennis, J, Conti, D V, Casey, G, Gaudet, M M, Huyghe, J R, Albanes, D, Aldrich, M C, Andrew, A S, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Antonenkova, N N, Arnold, S M, Aronson, K J, Arun, B K, Bandera, E V, Barkardottir, R B, Barnes, D R, Batra, J, Beckmann, M W, Benitez, J, Benlloch, S, Berchuck, A, Berndt, S I, Bickeböller, H, Bien, S A, Blomqvist, C, Boccia, S, Bogdanova, N V, Bojesen, S E, Bolla, M K, Brauch, H, Brenner, H, Brenton, J D, Brook, M N, Brunet, J, Brunnström, H, Buchanan, D D, Burwinkel, B, Butzow, R, Cadoni, G, Caldés, T, Caligo, M A, Campbell, I, Campbell, P T, Cancel-Tassin, G, Cannon-Albright, L, Campa, D, Caporaso, N, Carvalho, A L, Chan, A T, Chang-Claude, J, Chanock, S J, Chen, C, Christiani, D C, Claes, K B M, Claessens, F, Clements, J, Collée, J M, Correa, M C, Couch, F J, Cox, A, Cunningham, J M, Cybulski, C, Czene, K, Daly, M B, deFazio, A, Devilee, P, Diez, O, Gago-Dominguez, M, Donovan, J L, Dörk, T, Duell, E J, Dunning, A M, Dwek, M, Eccles, D M, Edlund, C K, Edwards, D R V, Ellberg, C, Evans, D G, Fasching, P A, Ferris, R L, Liloglou, T, Figueiredo, J C, Fletcher, O, Fortner, R T, Fostira, F, Franceschi, S, Friedman, E, Gallinger, S J, Ganz, P A, Garber, J, García-Sáenz, J A, Gayther, S A, Giles, G G, Godwin, A K, Goldberg, M S, Goldgar, D E, Goode, E L, Goodman, M T, Goodman, G, Grankvist, K, Greene, M H, Gronberg, H, Gronwald, J, Guénel, P, Håkansson, N, Hall, P, Hamann, U, Hamdy, F C, Hamilton, R J, Hampe, J, Haugen, A, Heitz, F, Herrero, R, Hillemanns, P, Hoffmeister, M, Høgdall, E, Hong, Y-C, Hopper, J L, Houlston, R, Hulick, P J, Hunter, D J, Huntsman, D G, Idos, G, Imyanitov, E N, Ingles, S A, Isaacs, C, Jakubowska, A, James, P, Jenkins, M A, Johansson, M, Johansson, M, John, E M, Joshi, A D, Kaneva, R, Karlan, B Y, Kelemen, L E, Kühl, T, Khaw, K-T, Khusnutdinova, E, Kibel, A S, Kiemeney, L A, Kim, J, Kjaer, S K, Knight, J A, Kogevinas, M, Kote-Jarai, Z, Koutros, S, Kristensen, V N, Kupryjanczyk, J, Lacko, M, Lam, S, Lambrechts, D, Landi, M T, Lazarus, P, Le, N D, Lee, E, Lejbkowicz, F, Lenz, H-J, Leslie, G, Lessel, D, Lester, J, Levine, D A, Li, L, Li, C I, Lindblom, A, Lindor, N M, Liu, G, Loupakis, F, Lubiński, J, Maehle, L, Maier, C, Mannermaa, A, Marchand, L L, Margolin, S, May, T, McGuffog, L, Meindl, A, Middha, P, Miller, A, Milne, R L, MacInnis, R J, Modugno, F, Montagna, M, Moreno, V, Moysich, K B, Mucci, L, Muir, K, Mulligan, A M, Nathanson, K L, Neal, D E, Ness, A R, Neuhausen, S L, Nevanlinna, H, Newcomb, P A, Newcomb, L F, Nielsen, F C, Nikitina-Zake, L, Nordestgaard, B G, Nussbaum, R L, Offit, K, Olah, E, Olama, A A A, Olopade, O I, Olshan, A F, Olsson, H, Osorio, A, Pandha, H, Park, J Y, Pashayan, N, Parsons, M T, Pejovic, T, Penney, K L, Peters, W H M, Phelan, C M, Phipps, A I, Plaseska-Karanfilska, D, Pring, M, Prokofyeva, D, Radice, P, Stefansson, K, Ramus, S J, Raskin, L, Rennert, G, Rennert, H S, van Rensburg, E J, Riggan, M J, Risch, H A, Risch, A, Roobol, M J, Rosenstein, B S, Rossing, M A, De Ruyck, K, Saloustros, E, Sandler, D P, Sawyer, E J, Schabath, M B, Schleutker, J, Schmidt, M K, Setiawan, V W, Shen, H, Siegel, E M, Sieh, W, Singer, C F, Slattery, M L, Sorensen, K D, Southey, M C, Spurdle, A B, Stanford, J L, Stevens, V L, Stintzing, S, Stone, J, Sundfeldt, K, Sutphen, R, Swerdlow, A J, Tajara, E H, Tangen, C M, Tardon, A, Taylor, J A, Teare, M D, Teixeira, M R, Terry, M B, Terry, K L, Thibodeau, S N, Thomassen, M, Bjørge, L, Tischkowitz, M, Toland, A E, Torres, D, Townsend, P A, Travis, R C, Tung, N, Tworoger, S S, Ulrich, C M, Usmani, N, Vachon, C M, Van Nieuwenhuysen, E, Vega, A, Aguado-Barrera, M E, Wang, Q, Webb, P M, Weinberg, C R, Weinstein, S, Weissler, M C, Weitzel, J N, West, C M L, White, E, Whittemore, A S, Wichmann, H-E, Wiklund, F, Winqvist, R, Wolk, A, Woll, P, Woods, M, Wu, A H, Wu, X, Yannoukakos, D, Zheng, W, Zienolddiny, S, Ziogas, A, Zorn, K K, Lane, J M, Saxena, R, Thomas, D, Hung, R J, Diergaarde, B, McKay, J, Peters, U, Hsu, L, García-Closas, M, Eeles, R A, Chenevix-Trench, G, Brennan, P J, Haiman, C A, Simard, J, Easton, D F, Gruber, S B, Pharoah, P D P, Price, A L, Pasaniuc, B, Amos, C I, Kraft, P & Lindström, S 2019, ' Shared heritability and functional enrichment across six solid cancers ', Nature Communications, vol. 10, no. 1, 431, pp. 1-23 . https://doi.org/10.1038/s41467-018-08054-4Test
Nature Communications, 10
Nature Communications
Dipòsit Digital de la UB
Universidad de Barcelona
Jiang, X, Finucane, H K, Schumacher, F R, Schmit, S L, Tyrer, J P, Han, Y, Michailidou, K, Lesseur, C, Kuchenbaecker, K B, Dennis, J, Conti, D V, Casey, G, Gaudet, M M, Huyghe, J R, Albanes, D, Aldrich, M C, Andrew, A S, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Antonenkova, N N, Arnold, S M, Aronson, K J, Arun, B K, Bandera, E V, Barkardottir, R B, Barnes, D R, Batra, J, Beckmann, M W, Benitez, J, Benlloch, S, Berchuck, A, Berndt, S I, Bickeböller, H, Bien, S A, Blomqvist, C, Boccia, S, Bogdanova, N V, Bojesen, S E, Bolla, M K, Brauch, H, Brenner, H, Brenton, J D, Brook, M N, Brunet, J, Brunnström, H, Buchanan, D D, Burwinkel, B, Butzow, R, Cadoni, G, Caldés, T, Caligo, M A, Campbell, I, Campbell, P T, Cancel-Tassin, G, Cannon-Albright, L, Campa, D, Caporaso, N, Carvalho, A L, Chan, A T, Chang-Claude, J, Chanock, S J, Chen, C, Christiani, D C, Claes, K B M, Claessens, F, Clements, J, Collée, J M, Correa, M C, Couch, F J, Cox, A, Cunningham, J M, Cybulski, C, Czene, K, Daly, M B, deFazio, A, Devilee, P, Diez, O, Gago-Dominguez, M, Donovan, J L, Dörk, T, Duell, E J, Dunning, A M, Dwek, M, Eccles, D M, Edlund, C K, Edwards, D R V, Ellberg, C, Evans, D G, Fasching, P A, Ferris, R L, Liloglou, T, Figueiredo, J C, Fletcher, O, Fortner, R T, Fostira, F, Franceschi, S, Friedman, E, Gallinger, S J, Ganz, P A, Garber, J, García-Sáenz, J A, Gayther, S A, Giles, G G, Godwin, A K, Goldberg, M S, Goldgar, D E, Goode, E L, Goodman, M T, Goodman, G, Grankvist, K, Greene, M H, Gronberg, H, Gronwald, J, Guénel, P, Håkansson, N, Hall, P, Hamann, U, Hamdy, F C, Hamilton, R J, Hampe, J, Haugen, A, Heitz, F, Herrero, R, Hillemanns, P, Hoffmeister, M, Høgdall, E, Hong, Y-C, Hopper, J L, Houlston, R, Hulick, P J, Hunter, D J, Huntsman, D G, Idos, G, Imyanitov, E N, Ingles, S A, Isaacs, C, Jakubowska, A, James, P, Jenkins, M A, Johansson, M, Johansson, M, John, E M, Joshi, A D, Kaneva, R, Karlan, B Y, Kelemen, L E, Kühl, T, Khaw, K-T, Khusnutdinova, E, Kibel, A S, Kiemeney, L A, Kim, J, Kjaer, S K, Knight, J A, Kogevinas, M, Kote-Jarai, Z, Koutros, S, Kristensen, V N, Kupryjanczyk, J, Lacko, M, Lam, S, Lambrechts, D, Landi, M T, Lazarus, P, Le, N D, Lee, E, Lejbkowicz, F, Lenz, H-J, Leslie, G, Lessel, D, Lester, J, Levine, D A, Li, L, Li, C I, Lindblom, A, Lindor, N M, Liu, G, Loupakis, F, Lubiński, J, Maehle, L, Maier, C, Mannermaa, A, Marchand, L L, Margolin, S, May, T, McGuffog, L, Meindl, A, Middha, P, Miller, A, Milne, R L, MacInnis, R J, Modugno, F, Montagna, M, Moreno, V, Moysich, K B, Mucci, L, Muir, K, Mulligan, A M, Nathanson, K L, Neal, D E, Ness, A R, Neuhausen, S L, Nevanlinna, H, Newcomb, P A, Newcomb, L F, Nielsen, F C, Nikitina-Zake, L, Nordestgaard, B G, Nussbaum, R L, Offit, K, Olah, E, Olama, A A A, Olopade, O I, Olshan, A F, Olsson, H, Osorio, A, Pandha, H, Park, J Y, Pashayan, N, Parsons, M T, Pejovic, T, Penney, K L, Peters, W H M, Phelan, C M, Phipps, A I, Plaseska-Karanfilska, D, Pring, M, Prokofyeva, D, Radice, P, Stefansson, K, Ramus, S J, Raskin, L, Rennert, G, Rennert, H S, van Rensburg, E J, Riggan, M J, Risch, H A, Risch, A, Roobol, M J, Rosenstein, B S, Rossing, M A, De Ruyck, K, Saloustros, E, Sandler, D P, Sawyer, E J, Schabath, M B, Schleutker, J, Schmidt, M K, Setiawan, V W, Shen, H, Siegel, E M, Sieh, W, Singer, C F, Slattery, M L, Sorensen, K D, Southey, M C, Spurdle, A B, Stanford, J L, Stevens, V L, Stintzing, S, Stone, J, Sundfeldt, K, Sutphen, R, Swerdlow, A J, Tajara, E H, Tangen, C M, Tardon, A, Taylor, J A, Teare, M D, Teixeira, M R, Terry, M B, Terry, K L, Thibodeau, S N, Thomassen, M, Bjørge, L, Tischkowitz, M, Toland, A E, Torres, D, Townsend, P A, Travis, R C, Tung, N, Tworoger, S S, Ulrich, C M, Usmani, N, Vachon, C M, Van Nieuwenhuysen, E, Vega, A, Aguado-Barrera, M E, Wang, Q, Webb, P M, Weinberg, C R, Weinstein, S, Weissler, M C, Weitzel, J N, West, C M L, White, E, Whittemore, A S, Wichmann, H-E, Wiklund, F, Winqvist, R, Wolk, A, Woll, P, Woods, M, Wu, A H, Wu, X, Yannoukakos, D, Zheng, W, Zienolddiny, S, Ziogas, A, Zorn, K K, Lane, J M, Saxena, R, Thomas, D, Hung, R J, Diergaarde, B, McKay, J, Peters, U, Hsu, L, García-Closas, M, Eeles, R A, Chenevix-Trench, G, Brennan, P J, Haiman, C A, Simard, J, Easton, D F, Gruber, S B, Pharoah, P D P, Price, A L, Pasaniuc, B, Amos, C I, Kraft, P & Lindström, S 2019, ' Shared heritability and functional enrichment across six solid cancers ', Nature Communications, vol. 10, no. 1, 431 . https://doi.org/10.1038/s41467-018-08054-4Test
Nature Communications, 10(1):431. Nature Publishing Group
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Scientia
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Nat. Commun. 10:431 (2019)
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
Jiang, X, Lindström, S & et al. 2019, ' Shared heritability and functional enrichment across six solid cancers ', Nature Communications, vol. 10, no. 1, 431 . https://doi.org/10.1038/s41467-018-08054-4Test
Jiang, Xia; Finucane, Hilary K; Schumacher, Fredrick R; Schmit, Stephanie L; Tyrer, Jonathan P; Han, Younghun; et al.(2019). Shared heritability and functional enrichment across six solid cancers. NATURE COMMUNICATIONS, 10(1), 431. doi: 10.1038/s41467-018-08054-4. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/42x44002Test
Repisalud
Instituto de Salud Carlos III (ISCIII)
Recercat. Dipósit de la Recerca de Catalunya
Nature Communications, Vol 10, Iss 1, Pp 1-23 (2019)
Jiang, X, Finucane, H K, Schumacher, F R, Schmit, S L, Tyrer, J P, Han, Y, Michailidou, K, Lesseur, C, Kuchenbaecker, K B, Dennis, J, Conti, D V, Casey, G, Gaudet, M M, Huyghe, J R, Albanes, D, Aldrich, M C, Andrew, A S, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Antonenkova, N N, Arnold, S M, Aronson, K J, Arun, B K, Bandera, E V, Barkardottir, R B, Barnes, D R, Batra, J, Beckmann, M W, Benitez, J, Benlloch, S, Berchuck, A, Berndt, S I, Bickeböller, H, Bien, S A, Blomqvist, C, Boccia, S, Bogdanova, N V, Bojesen, S E, Bolla, M K, Brauch, H, Brenner, H, Brenton, J D, Brook, M N, Brunet, J, Brunnström, H, Buchanan, D D, Burwinkel, B, Butzow, R, Cadoni, G, Caldés, T, Caligo, M A, Campbell, I, Campbell, P T, Cancel-Tassin, G, Cannon-Albright, L, Campa, D, Caporaso, N, Carvalho, A L, Chan, A T, Chang-Claude, J, Chanock, S J, Chen, C, Christiani, D C, Claes, K B M, Claessens, F, Clements, J, Collée, J M, Correa, M C, Couch, F J, Cox, A, Cunningham, J M, Cybulski, C, Czene, K, Daly, M B, deFazio, A, Devilee, P, Diez, O, Gago-Dominguez, M, Donovan, J L, Dörk, T, Duell, E J, Dunning, A M, Dwek, M, Eccles, D M, Edlund, C K, Edwards, D R V, Ellberg, C, Evans, D G, Fasching, P A, Ferris, R L, Liloglou, T, Figueiredo, J C, Fletcher, O, Fortner, R T, Fostira, F, Franceschi, S, Friedman, E, Gallinger, S J, Ganz, P A, Garber, J, García-Sáenz, J A, Gayther, S A, Giles, G G, Godwin, A K, Goldberg, M S, Goldgar, D E, Goode, E L, Goodman, M T, Goodman, G, Grankvist, K, Greene, M H, Gronberg, H, Gronwald, J, Guénel, P, Håkansson, N, Hall, P, Hamann, U, Hamdy, F C, Hamilton, R J, Hampe, J, Haugen, A, Heitz, F, Herrero, R, Hillemanns, P, Hoffmeister, M, Høgdall, E, Hong, Y-C, Hopper, J L, Houlston, R, Hulick, P J, Hunter, D J, Huntsman, D G, Idos, G, Imyanitov, E N, Ingles, S A, Isaacs, C, Jakubowska, A, James, P, Jenkins, M A, Johansson, M, Johansson, M, John, E M, Joshi, A D, Kaneva, R, Karlan, B Y, Kelemen, L E, Kühl, T, Khaw, K-T, Khusnutdinova, E, Kibel, A S, Kiemeney, L A, Kim, J, Kjaer, S K, Knight, J A, Kogevinas, M, Kote-Jarai, Z, Koutros, S, Kristensen, V N, Kupryjanczyk, J, Lacko, M, Lam, S, Lambrechts, D, Landi, M T, Lazarus, P, Le, N D, Lee, E, Lejbkowicz, F, Lenz, H-J, Leslie, G, Lessel, D, Lester, J, Levine, D A, Li, L, Li, C I, Lindblom, A, Lindor, N M, Liu, G, Loupakis, F, Lubiński, J, Maehle, L, Maier, C, Mannermaa, A, Marchand, L L, Margolin, S, May, T, McGuffog, L, Meindl, A, Middha, P, Miller, A, Milne, R L, MacInnis, R J, Modugno, F, Montagna, M, Moreno, V, Moysich, K B, Mucci, L, Muir, K, Mulligan, A M, Nathanson, K L, Neal, D E, Ness, A R, Neuhausen, S L, Nevanlinna, H, Newcomb, P A, Newcomb, L F, Nielsen, F C, Nikitina-Zake, L, Nordestgaard, B G, Nussbaum, R L, Offit, K, Olah, E, Olama, A A A, Olopade, O I, Olshan, A F, Olsson, H, Osorio, A, Pandha, H, Park, J Y, Pashayan, N, Parsons, M T, Pejovic, T, Penney, K L, Peters, W H M, Phelan, C M, Phipps, A I, Plaseska-Karanfilska, D, Pring, M, Prokofyeva, D, Radice, P, Stefansson, K, Ramus, S J, Raskin, L, Rennert, G, Rennert, H S, van Rensburg, E J, Riggan, M J, Risch, H A, Risch, A, Roobol, M J, Rosenstein, B S, Rossing, M A, De Ruyck, K, Saloustros, E, Sandler, D P, Sawyer, E J, Schabath, M B, Schleutker, J, Schmidt, M K, Setiawan, V W, Shen, H, Siegel, E M, Sieh, W, Singer, C F, Slattery, M L, Sorensen, K D, Southey, M C, Spurdle, A B, Stanford, J L, Stevens, V L, Stintzing, S, Stone, J, Sundfeldt, K, Sutphen, R, Swerdlow, A J, Tajara, E H, Tangen, C M, Tardon, A, Taylor, J A, Teare, M D, Teixeira, M R, Terry, M B, Terry, K L, Thibodeau, S N, Thomassen, M, Bjørge, L, Tischkowitz, M, Toland, A E, Torres, D, Townsend, P A, Travis, R C, Tung, N, Tworoger, S S, Ulrich, C M, Usmani, N, Vachon, C M, Van Nieuwenhuysen, E, Vega, A, Aguado-Barrera, M E, Wang, Q, Webb, P M, Weinberg, C R, Weinstein, S, Weissler, M C, Weitzel, J N, West, C M L, White, E, Whittemore, A S, Wichmann, H-E, Wiklund, F, Winqvist, R, Wolk, A, Woll, P, Woods, M, Wu, A H, Wu, X, Yannoukakos, D, Zheng, W, Zienolddiny, S, Ziogas, A, Zorn, K K, Lane, J M, Saxena, R, Thomas, D, Hung, R J, Diergaarde, B, McKay, J, Peters, U, Hsu, L, García-Closas, M, Eeles, R A, Chenevix-Trench, G, Brennan, P J, Haiman, C A, Simard, J, Easton, D F, Gruber, S B, Pharoah, P D P, Price, A L, Pasaniuc, B, Amos, C I, Kraft, P & Lindström, S 2019, ' Shared heritability and functional enrichment across six solid cancers ', Nature Communications, vol. 10, no. 1, pp. 431 . https://doi.org/10.1038/s41467-018-08054-4Test
Nature Communications, 2019, vol. 10, art. núm. 431
Articles publicats (IdIBGi)
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مصطلحات موضوعية: Oncology, Male, Lung Neoplasms, Colorectal cancer, Epidemiology, Inheritance Patterns, Genome-wide association study, 02 engineering and technology, Colorectal Neoplasms/diagnosis, Càncer - Aspectes genètics, 0302 clinical medicine, Neoplasm Proteins/genetics, Brjóstakrabbamein, PARTITIONING HERITABILITY, lcsh:Science, Càncer, Cancer genetics, Cancer, Càncer - Estudi de casos, Ovarian Neoplasms, Prostatic Neoplasms/diagnosis, 0303 health sciences, Otros calificadores::Otros calificadores::/genética [Otros calificadores], 1184 Genetics, developmental biology, physiology, Genomics, Publisher Correction, ddc, 3. Good health, Neoplasm Proteins, Head and Neck Neoplasms, 030220 oncology & carcinogenesis, Etiologia, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], Neoplasias [ENFERMEDADES], ICEP, Erfðarannsóknir, 0210 nano-technology, Genetic Phenomena::Inheritance Patterns [PHENOMENA AND PROCESSES], medicine.medical_specialty, Biolääketieteet - Biomedicine, Science, Lung Neoplasms/diagnosis, European Continental Ancestry Group, Genetic correlation, Article, General Biochemistry, Genetics and Molecular Biology, White People, GENETIC ARCHITECTURE, 03 medical and health sciences, Breast cancer, SDG 3 - Good Health and Well-being, Syöpätaudit - Cancers, BREAST-CANCER, Humans, Otros calificadores::Otros calificadores::Otros calificadores::/etnología [Otros calificadores], Polymorphism, GENOME-WIDE ASSOCIATION, solid cancers, heritability, enrichment, Settore MED/42 - IGIENE GENERALE E APPLICATA, ResearchInstitutes_Networks_Beacons/mcrc, Fenómenos Genéticos::Patrón de Herencia [FENÓMENOS Y PROCESOS], ANALYSES IDENTIFY, Biology and Life Sciences, fenómenos genéticos::patrones de herencia [FENÓMENOS Y PROCESOS], medicine.disease, Càncer -- Etiologia, 030104 developmental biology, Case-Control Studies, RISK-FACTORS, lcsh:Q, 0301 basic medicine, Etiology, Medizin, General Physics and Astronomy, técnicas de investigación::métodos epidemiológicos::características de los estudios epidemiológicos::estudios epidemiológicos::estudios de casos y controles [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], head and neck, Prostate cancer, Medicine and Health Sciences, Càncer -- Aspectes genètics, Multidisciplinary, Manchester Cancer Research Centre, Mental Disorders, Codi genètic, Smoking, Single Nucleotide, 021001 nanoscience & nanotechnology, Phenotype, Centre for Surgical Research, Cancer -- Etiology, MENDELIAN RANDOMIZATION, Female, Smoking/ethnology, Colorectal Neoplasms, Mental Disorders/ethnology, Medical Genetics, Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics::Epidemiologic Studies::Case-Control Studies [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES AND EQUIPMENT], Cancer Etiology, Técnicas de Investigación::Métodos Epidemiológicos::Características de Estudios Epidemiológicos::Estudios Epidemiológicos::Estudios de Casos y Controles [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], SUSCEPTIBILITY LOCI, 3122 Cancers, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, LUNG-CANCER, All institutes and research themes of the Radboud University Medical Center, Internal medicine, MD Multidisciplinary, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Erfðafræði, Genetic Predisposition to Disease, CELL-TYPES, Lung cancer, Krabbamein, Medicinsk genetik, 030304 developmental biology, Ovarian Neoplasms/diagnosis, Faraldsfræði, Prostatic Neoplasms, Breast Neoplasms/diagnosis, General Chemistry, Heritability, Head and Neck Neoplasms/diagnosis, Neoplasms [DISEASES], Genome-Wide Association Study, 3111 Biomedicine, Ovarian cancer, Other subheadings::Other subheadings::Other subheadings::/ethnology [Other subheadings]

وصف الملف: application/pdf; fulltext; text; Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2165621cdfac3fe75b5749d07f6c68eTest
https://findresearcher.sdu.dk:8443/ws/files/146391474/Shared_heritability_and_functional_enrichment.pdfTest

المؤلفون: Madariaga, Leire, García-Castaño, Alejandro, Ariceta Iraola, Gema, Martínez-Salazar, Rosa, Aguayo, Aníbal, Castaño, Luis, Universitat Autònoma de Barcelona

المساهمون: Institut Català de la Salut, [Madariaga L] Pediatric Nephrology Department, Cruces University Hospital, Barakaldo, Spain. Universidad del País Vasco, Barakaldo, Spain. Biocruces Health Research Institute, Barakaldo, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. [García-Castaño A] Biocruces Health Research Institute, Barakaldo, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. [Ariceta G] Servei de Nefrologia Pediàtrica, Hospital Universitari Vall d'Hebron, Barcelona, Spain. Universitat Autònoma de Barcelona, Barcelona, Spain. [Martínez-Salazar R, Aguayo A] Biocruces Health Research Institute, Barakaldo, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Madrid, Spain. [Castaño L] Pediatric Nephrology Department, Cruces University Hospital, Barakaldo, Spain. Universidad del País Vasco, Barakaldo, Spain. Biocruces Health Research Institute, Barakaldo, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Madrid, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia
Clinical Kidney Journal
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Addi. Archivo Digital para la Docencia y la Investigación
instname

مصطلحات موضوعية: medicine.medical_specialty, HNF1B, Urinary system, Population, Genetic Phenomena::Genetic Variation::Mutation [PHENOMENA AND PROCESSES], hypomagnesaemia, 030232 urology & nephrology, enfermedades nutricionales y metabólicas::enfermedades metabólicas::trastornos del metabolismo de la glucosa [ENFERMEDADES], Ciliopathies, Gastroenterology, Nutritional and Metabolic Diseases::Metabolic Diseases::Glucose Metabolism Disorders [DISEASES], Pancreatic structural anomalies, enfermedades urogenitales masculinas::anomalías urogenitales [ENFERMEDADES], 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Hypomagnesaemia, Amino Acids, Peptides, and Proteins::Proteins::DNA-Binding Proteins::Hepatocyte Nuclear Factors::Hepatocyte Nuclear Factor 1::Hepatocyte Nuclear Factor 1-beta [CHEMICALS AND DRUGS], pancreatic structural anomalie, pancreatic structural anomalies, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Prediabetes, Aparell genitourinari - Malalties, education, Genetic Kidney Disease, fenómenos genéticos::variación genética::mutación [FENÓMENOS Y PROCESOS], CAKUT, Transplantation, education.field_of_study, Kidney, Otros calificadores::Otros calificadores::/genética [Otros calificadores], business.industry, Mutació (Biologia), aminoácidos, péptidos y proteínas::proteínas::proteínas de unión al ADN::factores nucleares del hepatocito::factor nuclear 1 del hepatocito::factor nuclear 1-beta del hepatocito [COMPUESTOS QUÍMICOS Y DROGAS], medicine.disease, Penetrance, Male Urogenital Diseases::Urogenital Abnormalities [DISEASES], medicine.anatomical_structure, Nephrology, Dysplasia, MODY, Glucosa - Metabolisme, Malalties congènites, business, Proteïnes

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305b6a9859d0868320518ecc2bcf47d1Test
https://ddd.uab.cat/record/226497Test

المؤلفون: Antonia Felzen, Daan B.E. van Wessel, Emmanuel Gonzales, Richard J. Thompson, Irena Jankowska, Benjamin L. Shneider, Etienne Sokal, Tassos Grammatikopoulos, Agustina Kadaristiana, Emmanuel Jacquemin, Anne Spraul, Patryk Lipiński, Piotr Czubkowski, Nathalie Rock, Mohammad Shagrani, Dieter Broering, Emanuele Nicastro, Deirdre Kelly, Gabriella Nebbia, Henrik Arnell, Björn Fischler, Jan B.F. Hulscher, Daniele Serranti, Cigdem Arikan, Esra Polat, Dominique Debray, Florence Lacaille, Cristina Goncalves, Loreto Hierro, Gema Muñoz Bartolo, Yael Mozer-Glassberg, Amer Azaz, Jernej Brecelj, Antal Dezsőfi, Pier Luigi Calvo, Enke Grabhorn, Steffen Hartleif, Wendy J. van der Woerd, Binita M. Kamath, Jian-She Wang, Liting Li, Özlem Durmaz, Nanda Kerkar, Marianne Hørby Jørgensen, Ryan Fischer, Carolina Jimenez-Rivera, Seema Alam, Mara Cananzi, Noemie Laverdure, Cristina Targa Ferreira, Felipe Ordoñez Guerrero, Heng Wang, Valerie Sency, Kyung Mo Kim, Huey-Ling Chen, Elisa de Carvalho, Alexandre Fabre, Jesus Quintero Bernabeu, Aglaia Zellos, Estella M. Alonso, Ronald J. Sokol, Frederick J. Suchy, Kathleen M. Loomes, Patrick J. McKiernan, Philip Rosenthal, Yumirle Turmelle, Simon Horslen, Kathleen Schwarz, Jorge A. Bezerra, Kasper Wang, Bettina E. Hansen, Henkjan J. Verkade

المساهمون: Gastroenterology & Hepatology, Center for Liver, Digestive and Metabolic Diseases (CLDM), Institut Català de la Salut, [Felzen A, van Wessel DBE] Pediatric Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, the Netherlands. [Gonzales E] Pediatric Hepatology & Pediatric Liver Transplant Department, Centre de Référence de l'Atrésie des Voies Biliaires et des Cholestases Génétiques, Filière de Santé des Maladies Rares du Foie de l'enfant et de l'adulte, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Paris-Saclay, CHU Bicêtre, Paris, France. European Reference Network on Hepatological Diseases (ERN RARE-LIVER). INSERM, Hepatinov, Université Paris-Saclay, Orsay, France. [Thompson RJ] Institute of Liver Studies, King's College London, London, United Kingdom. [Jankowska I] European Reference Network on Hepatological Diseases (ERN RARE-LIVER). Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, The Children’s Memorial Health Institute, Warsaw, Poland. [Shneider BL] Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA. Childhood Liver Disease Research Network (ChiLDReN). [Quintero Bernabeu J] European Reference Network on Hepatological Diseases (ERN RARE-LIVER). Unitat de Gastroenterologia, Hepatologia, Suport Nutricional i Trasplantaments Hepàtics Pediàtrics, Vall d'Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus, UCL - SSS/IREC/PEDI - Pôle de Pédiatrie, UCL - (SLuc) Service de gastro-entérologie et hépatologie pédiatrique

المصدر: JHEP Reports, 5(2):100626. Elsevier
JHEP reports : innovation in hepatology, 5(2):100626. Elsevier
Scientia
JHEP Reports, Vol. 5, no.2, p. 100626 (2023)

مصطلحات موضوعية: Fetge - Malalties - Aspectes genètics, Surgical Procedures, Operative::Digestive System Surgical Procedures::Surgical Procedures, Operative::Surgical Procedures, Operative::Liver Transplantation [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Hepatology, Otros calificadores::Otros calificadores::/genética [Otros calificadores], phenotype, genotype, Genetic Phenomena::Genetic Variation::Mutation [PHENOMENA AND PROCESSES], Gastroenterology, Fetge - Trasplantació, Polycyclic Compounds::Fused-Ring Compounds::Steroids::Bile Acids and Salts [CHEMICALS AND DRUGS], interruption of the enterohepatic circulation, compuestos policíclicos::compuestos con anillos de fusión::esteroides::ácidos y sales biliares [COMPUESTOS QUÍMICOS Y DROGAS], PFIC2, enfermedades del sistema digestivo::enfermedades hepáticas [ENFERMEDADES], Anomalies cromosòmiques, Digestive System Diseases::Liver Diseases [DISEASES], Àcids biliars - Secrecions, BSEP, COMPOUND HETEROZYGOSITY, Other subheadings::Other subheadings::/genetics [Other subheadings], Internal Medicine, Immunology and Allergy, intervenciones quirúrgicas::procedimientos quirúrgicos del sistema digestivo::intervenciones quirúrgicas::intervenciones quirúrgicas::trasplante de hígado [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], fenómenos genéticos::variación genética::mutación [FENÓMENOS Y PROCESOS]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9a4bf0cbb88ad99b95105970a79be1Test
https://pure.eur.nl/en/publications/48dc60fd-d2f3-4015-b5b3-25d845d0ca1aTest