المؤلفون: Eva Gimeno, Margarita Ortega, Silvia Ramos-Campoy, Francesc Bosch, Tycho Baumann, Sandrine Bougeon, Florence Nguyen-Khac, Helen Parker, Carolina Moreno, Anna Puiggros, Blanca Espinet, Xavier Calvo, María José Calasanz, María José Larrayoz, David Oscier, Rosa Collado, Claudia Haferlach, María Laura Blanco, Jacqueline Schoumans, Rocío Salgado, Gian Matteo Rigolin, Sílvia Beà, Antonio Cuneo, Jonathan C. Strefford, Dolors Costa

المساهمون: Institut Català de la Salut, [Ramos-Campoy S, Puiggros A] Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain. Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d’Investigacions Mèdiques (IMIM), Barcelona, Spain. [Beà S, Costa D] Hematopathology Unit, Hospital Clínic, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBERONC, Barcelona, Spain. [Bougeon S] Oncogenomic Laboratory, Hematology Service, Lausanne University Hospital, Lausanne, Switzerland. [Larráyoz MJ] Cytogenetics and Hematological Genetics Services, Department of Genetics, University of Navarra, Pamplona, Spain. [Ortega M, Bosch F] Servei d’Hematologia, Vall d'Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: HAEMATOLOGICA
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
Dadun. Depósito Académico Digital de la Universidad de Navarra
Scientia
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Chronic lymphocytic leukemia, Leucèmia limfocítica crònica - Aspectes genètics, Biology, Genetic Phenomena::Genetic Variation::Mutation::Chromosome Aberrations [PHENOMENA AND PROCESSES], Risk Assessment, NO, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Complex Karyotype, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Humans, In patient, microarrays, Chromosome Aberrations, Natural Science Disciplines::Biological Science Disciplines::Biology::Computational Biology::Genomics [DISCIPLINES AND OCCUPATIONS], Chronic lymphocytic leukmia, genomic complexity, Genome complexity, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Karyotype, Genomics, Hematology, Prognosis, medicine.disease, Leukemia, Lymphocytic, Chronic, B-Cell, Chromosome Banding, Genòmica, Anomalies cromosòmiques, Neoplasms::Neoplasms by Histologic Type::Leukemia::Leukemia, Lymphoid::Leukemia, B-Cell::Leukemia, Lymphocytic, Chronic, B-Cell [DISEASES], Área de Biomedicina, 030220 oncology & carcinogenesis, disciplinas de las ciencias naturales::disciplinas de las ciencias biológicas::biología::biología computacional::genómica [DISCIPLINAS Y OCUPACIONES], Mutation, Risk stratification, Cohort, DNA microarray, fenómenos genéticos::variación genética::mutación::aberraciones cromosómicas [FENÓMENOS Y PROCESOS], neoplasias::neoplasias por tipo histológico::leucemia::leucemia linfoide::leucemia de células B::leucemia linfocítica crónica de células B [ENFERMEDADES], 030215 immunology

وصف الملف: application/pdf; text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0246e8a7bd7915b1adde1b3996bc485eTest
https://doi.org/10.3324/haematol.2020.274456Test

المؤلفون: David Gonzalez, Alexander W. Wyatt, Joaquin Mateo, Michelle Shiller, Leonard G. Gomella, Albrecht Stenzinger, Ros Eeles, Anders Bjartell, Frédérique Penault-Llorca, Federico Rojo

المساهمون: Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA), Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP), UNICANCER, Institut Català de la Salut, [Gonzalez D] Patrick G Johnston Centre for Cancer Research, Queen’s University, Belfast, UK. [Mateo J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Stenzinger A] Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany. [Rojo F] Department of Pathology, IIS-Hospital Universitario Fundación Jiménez Díaz-CIBERONC, Madrid, Spain. [Shiller M] Department of Pathology, Baylor University Medical Center, Dallas, TX, USA. [Wyatt AW] Vancouver Prostate Centre, Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada, Vall d'Hebron Barcelona Hospital Campus

المصدر: Journal of Pathology: Clinical Research
Journal of Pathology: Clinical Research, Wiley Open Access, In press, ⟨10.1002/cjp2.203⟩
Scientia
The Journal of Pathology: Clinical Research
Gonzalez, D, Mateo, J, Stenzinger, A, Rojo, F, Shiller, M, Wyatt, A W, Penault-Llorca, F, Gomella, L G, Eeles, R & Bjartell, A 2021, ' Practical considerations for optimising homologous recombination repair mutation testing in patients with metastatic prostate cancer ', The Journal of Pathology: Clinical Research . https://doi.org/10.1002/cjp2.203Test
The Journal of Pathology: Clinical Research, Vol 7, Iss 4, Pp 311-325 (2021)

مصطلحات موضوعية: Male, Oncology, ADN - Reparació, Indoles, [SDV]Life Sciences [q-bio], Review, Other subheadings::Other subheadings::/drug therapy [Other subheadings], Poly (ADP-Ribose) Polymerase Inhibitor, Piperazines, Prostate cancer, chemistry.chemical_compound, 0302 clinical medicine, Clinical pathway, Pathology, RB1-214, Pathology, Molecular, ComputingMilieux_MISCELLANEOUS, 0303 health sciences, Otros calificadores::Otros calificadores::/genética [Otros calificadores], mCRPC, 3. Good health, Prostatic Neoplasms, Castration-Resistant, 030220 oncology & carcinogenesis, medicine.medical_specialty, Otros calificadores::Otros calificadores::/farmacoterapia [Otros calificadores], Poly(ADP-ribose) Polymerase Inhibitors, metastatic prostate cancer, homologous recombination repair, Pathology and Forensic Medicine, Olaparib, molecular diagnostics, fenómenos químicos::fenómenos bioquímicos::reparación del ADN::reparación del ADN por recombinación [FENÓMENOS Y PROCESOS], 03 medical and health sciences, SDG 3 - Good Health and Well-being, Metàstasi, Internal medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Humans, Rucaparib, 030304 developmental biology, Chemical Phenomena::Biochemical Phenomena::DNA Repair::Recombinational DNA Repair [PHENOMENA AND PROCESSES], business.industry, Prostatic Neoplasms, Recombinational DNA Repair, Pròstata - Càncer - Tractament, medicine.disease, Molecular diagnostics, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms::Prostatic Neoplasms, Castration-Resistant [DISEASES], chemistry, poly(ADP‐ribose) polymerase inhibitors, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata::neoplasias prostáticas resistentes a la castración [ENFERMEDADES], Mutation, Phthalazines, Personalized medicine, business, Homologous recombination

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ac0b84518f6ea72980fcece1d656c4Test
https://doi.org/10.1002/cjp2.203Test

المؤلفون: Marzia Del Re, David T. Miyamoto, Kenneth J. Pienta, Alejandro Athie, Arnulf Stenzl, Adam G. Sowalsky, Alexander W. Wyatt, Paul C. Boutros, Irene Casanova-Salas, Edwin M. Posadas, Joaquin Mateo

المساهمون: Institut Català de la Salut, [Casanova-Salas I, Athie A, Mateo J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Boutros PC] Departments of Human Genetics and Urology, Institute for Precision Health and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA, USA. [Del Re M] Unit of Clinical Pharmacology and Pharmacogenetics, Department of Clinical and Experimental Medicine, University Hospital of Pisa, Pisa, Italy. [Miyamoto DT] Department of Radiation Oncology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA. [Pienta KJ] The James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA, Vall d'Hebron Barcelona Hospital Campus

المصدر: European urology, vol 79, iss 6
Scientia

مصطلحات موضوعية: Oncology, Male, diagnóstico::toma de decisiones clínicas [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], 030232 urology & nephrology, Neoplastic Cells, Circulating Tumor DNA, Transcriptome, Prostate cancer, 0302 clinical medicine, Circulating tumor cell, Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Cytodiagnosis::Biopsy::Liquid Biopsy [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Circulating, Cancer, screening and diagnosis, Tumor, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Precision medicine, Genomics, Extracellular vesicles, Urology & Nephrology, Neoplastic Cells, Circulating, diagnóstico::técnicas y procedimientos diagnósticos::técnicas de laboratorio clínico::técnicas citológicas::citodiagnóstico::biopsia::biopsia líquida [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Detection, 030220 oncology & carcinogenesis, Diagnosis::Clinical Decision-Making [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Pròstata - Càncer - Aspectes genètics, Biòpsia, Pròstata - Càncer - Presa de decisions, Biotechnology, 4.2 Evaluation of markers and technologies, Urologic Diseases, medicine.medical_specialty, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms [DISEASES], Urology, Clinical Decision-Making, Clinical Sciences, Context (language use), 03 medical and health sciences, Clinical Research, Internal medicine, Biomarkers, Tumor, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Genetics, Humans, Liquid biopsy, Circulating tumor DNA, business.industry, Human Genome, Prostatic Neoplasms, Epigenome, medicine.disease, 4.1 Discovery and preclinical testing of markers and technologies, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata [ENFERMEDADES], Good Health and Well Being, Liquid Biopsy, Tumor progression, business, Biomarkers

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44876dd37defa804cb9ab8692907b642Test
https://escholarship.org/uc/item/8h9111fjTest

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: Stephen J. Pettitt, Antje Neeb, Lorna Pope, Jane Goodall, Suzanne Carreira, Joe Baxter, Pasquale Rescigno, Harry Parr, Diletta Bianchini, Claudia Bertan, Stéphane Oudard, Christine Geffriaud-Ricouard, Christopher J. Lord, Sandrine Macé, Oliver Sartor, Ayse Ozatilgan, Rossitza Christova, Gemma Fowler, Maryou B. Lambros, Wei Yuan, Ines Figueiredo, Niven Mehra, Joaquin Mateo, Jan Rekowski, Penelope Flohr, George Seed, Mario A. Eisenberger, Semini Sumanasuriya, Adam Sharp, Mustapha Chadjaa, Johann S. de Bono

المساهمون: Institut Català de la Salut, [Sumanasuriya S] The Institute of Cancer Research, University of London, London, UK. The Royal Marsden Hospital, London, UK. [Seed G, Parr H, Christova R, Pope L, Bertan C] The Institute of Cancer Research, University of London, London, UK. [Mateo J] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia
European Urology
European Urology, 80, 2, pp. 243-253
European Urology, 80, 243-253

مصطلحات موضوعية: Oncology, Male, 030232 urology & nephrology, Docetaxel, Tumour fraction, Other subheadings::Other subheadings::/drug therapy [Other subheadings], Circulating Tumor DNA, Prostate cancer, chemistry.chemical_compound, Cell-free DNA, 0302 clinical medicine, Prospective Studies, cfDNA, Elements genètics mòbils, Cabazitaxel, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Prostate Cancer, Hazard ratio, DNA, Neoplasm, mCRPC, Prostatic Neoplasms, Castration-Resistant, Cell-free fetal DNA, Pharmaceutical Preparations, 030220 oncology & carcinogenesis, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], Pròstata - Càncer - Aspectes genètics, medicine.drug, medicine.medical_specialty, lpWGS, Urology, Otros calificadores::Otros calificadores::/farmacoterapia [Otros calificadores], Context (language use), nucleótidos y nucleósidos de ácidos nucleicos::ácidos nucleicos::ácidos nucleicos libres de células::ADN tumoral circulante [COMPUESTOS QUÍMICOS Y DROGAS], 03 medical and health sciences, Taxanes, Internal medicine, medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], Enzalutamide, Humans, Taxane, Nucleic Acids, Nucleotides, and Nucleosides::Nucleic Acids::Cell-Free Nucleic Acids::Circulating Tumor DNA [CHEMICALS AND DRUGS], business.industry, ctDNA, medicine.disease, Pròstata - Càncer - Tractament, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms::Prostatic Neoplasms, Castration-Resistant [DISEASES], Metastatic castration-resistant prostate cancer, chemistry, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata::neoplasias prostáticas resistentes a la castración [ENFERMEDADES], Low-pass whole-genome sequencing, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bcfbe9a4e19be1664cf6e141fe2f9cbTest
https://doi.org/10.1016/j.eururo.2021.05.030Test

المؤلفون: Miguel Martín, Laia Paré, Barbara Adamo, Roberta Fasani, Blanca Gonzalez-Farre, Benedetta Conte, Giovanna Sabarese, Carlos H. Barrios, Fara Brasó-Maristany, Esther Sanfeliu, Mariavittoria Locci, Giuseppe Perrone, Francesca Zalfa, Esther Barnadas, Olga Martínez-Sáez, Aranzazu Fernandez-Martinez, Ana Lluch, Maria Vidal, Joaquín Gavilá, Tomás Pascual, Aleix Prat, Francesco Schettini, Sabino De Placido, Patricia Villagrasa, Vicente Peg, Nuria Chic, Juan Miguel Cejalvo

المساهمون: Schettini, F., Chic, N., Braso-Maristany, F., Pare, L., Pascual, T., Conte, B., Martinez-Saez, O., Adamo, B., Vidal, M., Barnadas, E., Fernandez-Martinez, A., Gonzalez-Farre, B., Sanfeliu, E., Cejalvo, J. M., Perrone, G., Sabarese, G., Zalfa, F., Peg, V., Fasani, R., Villagrasa, P., Gavila, J., Barrios, C. H., Lluch, A., Martin, M., Locci, M., De Placido, S., Prat, A., Institut Català de la Salut, [Schettini F] Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy. Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. SOLTI Breast Cancer Research Group, Barcelona, Spain. [Chic N] Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. SOLTI Breast Cancer Research Group, Barcelona, Spain. Department of Medical Oncology, Hospital Clínic, Barcelona, Spain. [Brasó-Maristany F] Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. Department of Medical Oncology, Hospital Clínic, Barcelona, Spain. [Paré L] SOLTI Breast Cancer Research Group, Barcelona, Spain. [Pascual T] Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. SOLTI Breast Cancer Research Group, Barcelona, Spain. Department of Medical Oncology, Hospital Clínic, Barcelona, Spain. Department of Genetics, University of North Carolina, Chapel Hill, NC, USA. [Conte B] Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. Department of Medical Oncology, Ospedale Policlinico San Martino, University of Genova, Genova, Italy. [Peg V] Vall d’Hebron Hospital Universitari, Barcelona, Spain. GEICAM, Grupo Español de Investigación en Cáncer de Mama, Madrid, Spain. [Fasani R] Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Dipòsit Digital de la UB
Universidad de Barcelona
Scientia
NPJ Breast Cancer
npj Breast Cancer, Vol 7, Iss 1, Pp 1-13 (2021)

مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Neoplasms::Neoplasms by Site::Breast Neoplasms [DISEASES], Disease, Article, Càncer de mama, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Mama - Càncer, Internal medicine, Gene expression, Cancer genomics, Other subheadings::Other subheadings::/genetics [Other subheadings], Medicine, High activity, Pharmacology (medical), Radiology, Nuclear Medicine and imaging, skin and connective tissue diseases, Gene, Pathological, neoplasms, RC254-282, neoplasias::neoplasias por localización::neoplasias de la mama [ENFERMEDADES], Her2 expression, business.industry, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Investigative Techniques::Genetic Techniques::Gene Expression Profiling [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Translational research, medicine.disease, Expressió gènica, 3. Good health, ERBB2 Amplification, técnicas de investigación::técnicas genéticas::perfiles de expresión génica [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], 030104 developmental biology, 030220 oncology & carcinogenesis, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c10b99479fa39b069aa421ecf890520Test
http://hdl.handle.net/2445/175264Test

المؤلفون: Consol López San Martin, Enrique Lastra, Mercedes Robledo, José María Mesa-Latorre, Gemma Llort, María Fonfria, Luis Gómez, Judith Balmaña, A Beatriz Sánchez-Heras, Adela Castillejo, Alexandre Teulé, Pere Berbel, Teresa Ramón y Cajal, Juan de Dios García-Díaz, Ángel Zúñiga, Mercedes Durán, Adrià López-Fernández, Isabel Chirivella, M. Isabel Castillejo, Luis Robles, Inés Escandell, Raquel Perea Ibañez, Carmen Yagüe, Rosario Sánchez, José Luis Soto

المساهمون: Universidad de Alicante. Departamento de Biotecnología, Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología, Biotecnología, Genética Humana y de Mamíferos (GHM), Institut Català de la Salut, [Sánchez-Heras AB] Cancer Genetic Counselling Unit, Medical Oncology Department, Hospital General Universitario de Elche, Elche, Spain. [Castillejo A] Molecular Genetics Unit, Hospital General Universitario de Elche, Elche, Spain. [García-Díaz JD] Clinical Genetics Unit, Department of Internal Medicine, University Hospital Príncipe de Asturias, Alcalá de Henares, Spain. [Robledo M] Hereditary Endocrine Cancer Group, Spanish National Cancer Research Center (CNIO), Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras, CIBERER, Madrid, Spain. [Teulé A] Hereditary Cancer Program, Catalan Institute of Oncology, Instituto de Investigación Biomédica de Bellvitge, Hospitalet de Llobregat, Spain. [Sánchez R] Unidad Multidisciplinar de Enfermedades de Baja Prevalencia, Instituto de Investigación Sanitaria y Biomédica de Alicante (ISABIAL), Hospital General Universitario de Alicante, Alicante, Spain. [López-Fernández A, Balmaña J] Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Cancers
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Scientia
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Dipòsit Digital de la UB
Universidad de Barcelona
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Volume 12
Issue 11
r-FHPC. Repositorio Institucional de Producción Científica de la Fundación del Hospital Provincial de Castellón
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
r-FISABIO. Repositorio Institucional de Producción Científica
Cancers, Vol 12, Iss 3277, p 3277 (2020)

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, Cancer cells, medicine.disease_cause, urologic and male genital diseases, Male Urogenital Diseases::Urogenital Neoplasms::Urologic Neoplasms::Kidney Neoplasms::Male Urogenital Diseases::Carcinoma, Renal Cell [DISEASES], FH gene, 0302 clinical medicine, Malalties hereditàries, Missense mutation, FH gene, hereditary leiomyomatosis, leiomyomas, missense pathogenic variants, renal cell cancer, Renal cell cancer, Mutation, Kidney diseases, Hereditary leiomyomatosis, Otros calificadores::Otros calificadores::/genética [Otros calificadores], enfermedades urogenitales masculinas::neoplasias urogenitales::neoplasias urológicas::neoplasias renales::enfermedades urogenitales masculinas::carcinoma de células renales [ENFERMEDADES], leiomyomas, missense pathogenic variants, renal cell cancer, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Rare diseases, Geographic Locations::Europe::Spain [GEOGRAPHICALS], 030220 oncology & carcinogenesis, Cohort, Cèl·lules canceroses, Malalties rares, Renal Cell Cancers, Genetic disorders, medicine.medical_specialty, Missense pathogenic variants, Biología Celular, lcsh:RC254-282, Article, 03 medical and health sciences, Leiomyomas, Internal medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, Ronyons - Malalties - Espanya, localizaciones geográficas::Europa (continente)::España [DENOMINACIONES GEOGRÁFICAS], business.industry, neoplasias::neoplasias por tipo histológico::neoplasias de tejido conjuntivo y de tejidos blandos::neoplasias de tejido muscular::leiomioma::leiomiomatosis [ENFERMEDADES], Retrospective cohort study, medicine.disease, Genética, 030104 developmental biology, Fumarase, Clinical diagnosis, Hereditary leiomyomatosis and renal cell cancer syndrome, Malalties del ronyó, Neoplasms::Neoplasms by Histologic Type::Neoplasms, Connective and Soft Tissue::Neoplasms, Muscle Tissue::Leiomyoma::Leiomyomatosis [DISEASES], hereditary leiomyomatosis, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e93ce3b0db93156404976e82b01c35c8Test
http://hdl.handle.net/10045/110274Test

المؤلفون: Palomo Sanchís, Laura, Acha, Pamela, Sole, F., Universitat Autònoma de Barcelona

المساهمون: Institut Català de la Salut, [Palomo L] MDS Group, Institut de Recerca Contra la Leucèmia Josep Carreras, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Bellaterra, Spain. Experimental Hematology, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Acha P, Solé F] MDS Group, Institut de Recerca Contra la Leucèmia Josep Carreras, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Cancers
Scientia
Cancers, Vol 13, Iss 2120, p 2120 (2021)

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, Myeloid, Myelodysplastic/myeloproliferative neoplasms, Genetic Phenomena::Genetic Variation::Mutation [PHENOMENA AND PROCESSES], Review, Disease, Gene mutation, cytogenetics, Cytogenetics, 03 medical and health sciences, 0302 clinical medicine, hemic and lymphatic diseases, Internal medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, RC254-282, fenómenos genéticos::variación genética::mutación [FENÓMENOS Y PROCESOS], molecular landscape, gene mutations, Otros calificadores::Otros calificadores::/genética [Otros calificadores], business.industry, Myelodysplastic syndromes, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, food and beverages, medicine.disease, Molecular landscape, Peripheral blood, Trastorns mieloproliferatius - Aspectes genètics, enfermedades hematológicas y linfáticas::enfermedades hematológicas::enfermedades de la médula ósea::enfermedades mielodisplásicas-mieloproliferativas [ENFERMEDADES], Síndromes mielodisplàsiques - Aspectes genètics, Anomalies cromosòmiques, 030104 developmental biology, medicine.anatomical_structure, myelodysplastic/myeloproliferative neoplasms, 030220 oncology & carcinogenesis, Gene mutations, Bone marrow, Differential diagnosis, business, Hemic and Lymphatic Diseases::Hematologic Diseases::Bone Marrow Diseases::Myelodysplastic-Myeloproliferative Diseases [DISEASES]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc669533d1a1d37254d4e6974e28209Test
https://doi.org/10.3390/cancers13092120Test

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
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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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Nat. Commun. 10:431 (2019)
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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
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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
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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]

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https://findresearcher.sdu.dk:8443/ws/files/146391474/Shared_heritability_and_functional_enrichment.pdfTest

المؤلفون: Johanna I. Kiiski, Miguel Urioste, Melissa C. Southey, Ramunas Janavicius, Finn Cilius Nielsen, Ana Vega, Irene Konstantopoulou, Ana Blanco, Jesús del Valle, Joan Brunet, Emma Tham, Daniele Calistri, Esther Darder, Taru A. Muranen, Maria Rossing, Åke Borg, Aleksander Myszka, Marketa Janatova, Drakoulis Yannoukakos, Laura Papi, Paolo Peterlongo, Bernardo Bonanni, Florentia Fostira, Catarina Santos, Séverine Eon-Marchais, Anders Kvist, Petra Kleiblova, Snezhana Smichkoska, Manuel R. Teixeira, Vilius Rudaitis, Dijana Plaseska-Karanfilska, Conxi Lázaro, Alicia Barroso, Ugnius Mickys, Mariarosaria Calvello, Edith Olah, Virginie Moncoutier, Zdenek Kleibl, Nadine Andrieu, Rimvydas Norvilas, Stepan Chvojka, Paolo Radice, Jana Soukupova, Birgitte Bertelsen, Siranoush Manoukian, Claude Houdayer, Marta Santamariña, Bernard Peissel, Zdenka Vlckova, Ana Osorio, Laura Cortesi, Jacopo Azzollini, Katerina Kubelka-Sabit, Fabienne Lesueur, Valentina Zampiga, Tu Nguyen-Dumont, Javier Benitez, Gisella Figlioli, Hans Ehrencrona, Orland Diez, Therese Törngren, Judith Balmaña, Francesca Gensini, Ruta Marcinkute, Timea Pocza, Angela Toss, Dominique Stoppa-Lyonnet, Ana Peixoto, Heli Nevanlinna

المساهمون: Institut Català de la Salut, [Figlioli G] Genome Diagnostics Program, IFOM - the FIRC Institute for Molecular Oncology, Milan, Italy. [Kvist A] Division of Oncology and Pathology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. [Tham E] Department of Clinical Genetics, Karolinska University Hospital and Department of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden. [Soukupova J] Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University, Prague, Czech Republic. [Kleiblova P] Institute of Biology and Medical Genetics, General University Hospital and First Faculty of Medicine, Charles University, Prague, Czech Republic. [Muranen TA] Department of Obstetrics and Gynecology, Helsinki University Hospital and University of Helsinki, HUS, Helsinki, Finland. [Balmaña J] Hereditary Cancer Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Diez O] Hereditary Cancer Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Àrea de Genètica Clínica i Molecular, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus, Italian Association for Cancer Research, Fondazione Umberto Veronesi, Ministero della Salute (Italia), Region Stockholm (ALF), Ministry of Health (República Checa), Unión Europea. Comisión Europea, Instituto de Salud Carlos III, Centro de Investigación Biomédica en Red - CIBERER (Enfermedades Raras), French National Institute of Cancer (INCa grant), National Health and Medical Research Council (Australia), Hungarian Research Grants, Lietuvos Mokslo Taryba (Lituania), Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF), Associazione Italiana per la Ricerca sul Cancro (AIRC), Ministry of Health, Italy, Ministry of Health, Czech Republic, European Commission, Instituto de Salud Carlos III - ISCIII, Spanish Network on Rare Diseases (CIBERER), National Health and Medical Research Council of Australia, Research Council of Lithuania (LMTLT), European Regional Development Fund (ERDF/FEDER), HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, Helsinki University Hospital Area, University of Helsinki, INDIVIDRUG - Individualized Drug Therapy, Clinicum

المصدر: Scientia
Cancers, Basel : MDPI AG, 2020, vol. 12, no. 2, art. no. 292, p. [1-14]
Dipòsit Digital de la UB
Universidad de Barcelona
Repisalud
Instituto de Salud Carlos III (ISCIII)
Cancers, Vol 12, Iss 2, p 292 (2020)
Cancers
Figlioli, G, Kvist, A, Tham, E, Soukupova, J, Kleiblova, P, Muranen, T A, Andrieu, N, Azzollini, J, Balmaña, J, Barroso, A, Benítez, J, Bertelsen, B, Blanco, A, Bonanni, B, Borg, Å, Brunet, J, Calistri, D, Calvello, M, Chvojka, S, Cortesi, L, Darder, E, Del Valle, J, Diez, O, Eon-Marchais, S, Fostira, F, Gensini, F, Houdayer, C, Janatova, M, Kiiski, J I, Konstantopoulou, I, Kubelka-Sabit, K, Lázaro, C, Lesueur, F, Manoukian, S, Marcinkute, R, Mickys, U, Moncoutier, V, Myszka, A, Nguyen-Dumont, T, Nielsen, F C, Norvilas, R, Olah, E, Osorio, A, Papi, L, Peissel, B, Peixoto, A, Plaseska-Karanfilska, D, Pócza, T, Rossing, M, Rudaitis, V & ENIGMA Consortium 2020, ' The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases ', Cancers, vol. 12, no. 2, 292 . https://doi.org/10.3390/cancers12020292Test
Volume 12
Issue 2

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, Breast cancer risk factors, Neoplasms::Neoplasms by Site::Breast Neoplasms [DISEASES], ptvs, Càncer - Aspectes genètics, Basic medicine, Breast cancer, 0302 clinical medicine, Mama - Càncer, hemic and lymphatic diseases, FANCM, Breast cancer predisposition, FANCM truncating variants, Mutation spectrum, PTVs, RISK, neoplasias::neoplasias por localización::neoplasias de la mama [ENFERMEDADES], Factors de risc en les malalties, Otros calificadores::Otros calificadores::/genética [Otros calificadores], FANCM GENE, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, 3. Good health, 030220 oncology & carcinogenesis, Gene sequence, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Risk factors in diseases, 3122 Cancers, lcsh:RC254-282, fancm truncating variants, Càncer de mama, breast cancer predisposition, breast cancer risk factors, mutation spectrum, 03 medical and health sciences, Internal medicine, Other subheadings::Other subheadings::/genetics [Other subheadings], medicine, ANEMIA, Allele frequency, Female breast cancer, MUTATIONS, business.industry, nutritional and metabolic diseases, BRCA1, medicine.disease, GENE, 030104 developmental biology, Clinical medicine, C.5791C-GREATER-THAN-T, FANCM Protein, business

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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50814983c51d7b6f93b23792330c61faTest
https://doi.org/10.3390/cancers12020292Test