المؤلفون: Sánchez Heras, Ana Beatriz, Dámaso, Estela, Castillejo, Adela, Robledo, Mercedes, Teulé, Alexandre, Lázaro, Conxi, Sánchez Martínez, Rosario, Zúñiga, Ángel, López Fernández, Adrià, Balmaña, Judith, Robles, Luis, Ramon y Cajal, Teresa, Castillejo, M. Isabel, Ibañez, Raquel Perea, Sevila, Carmen Martínez, Sánchez Mira, Andrea, Escandell, Inés, Gómez, Luís, Berbel, Pere, Soto, José Luis

المصدر: Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

مصطلحات موضوعية: Mutació (Biologia), Càncer de ronyó, Malalties hereditàries, Mutation (Biology), Renal cancer, Genetic diseases

وصف الملف: 7 p.; application/pdf

العلاقة: Reproducció del document publicat a: https://doi.org/10.1186/s13023-024-03017-zTest; Orphanet Journal of Rare Diseases, 2024, vol. 19, num. 1; https://doi.org/10.1186/s13023-024-03017-zTest; http://hdl.handle.net/2445/207940Test

الإتاحة: https://doi.org/10.1186/s13023-024-03017-zTest
http://hdl.handle.net/2445/207940Test

المؤلفون: Dámaso, Estela, Castillejo Castillo, Adela, Robledo, Mercedes, Teule, Alex, LAZARO GARCIA, CONXI, Lopez-Fernandez, Adrià, Sanchez-Heras, Ana Beatriz, Balmaña, Judith

المساهمون: Institut Català de la Salut, Sánchez Heras AB Cancer Genetic Counselling Unit, Medical Oncology Department, Hospital General Universitario de Elche, Elche, Alicante, Spain. Dámaso E, Castillejo A Molecular Genetics Laboratory, Hospital General Universitario de Elche, Elche, Alicante, Spain. Foundation for the Promotion of Health and Biomedical Research of Valencia Region (FISABIO), FISABIO-Elche Health Department, Elche, Spain. Robledo M Hereditary Endocrine Cancer, Human Cancer Genetics Programme Spanish National Cancer Centre (CNIO), Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Raras, CIBERER, Madrid, Spain. Teulé A, Lázaro C Hereditary Cancer Program, Program in Molecular Mechanisms and Experimental Therapy in Oncology (Oncobell), IDIBELL, Catalan Institute of Oncology, L’Hospitalet del Llobregat, Barcelona, 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: Scientia

مصطلحات موضوعية: Anomalies cromosòmiques, Músculs - Càncer - Aspectes genètics, Ronyons - Càncer - Aspectes genètics, Malalties congènites, DISEASES::Neoplasms::Neoplastic Syndromes, Hereditary, DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Connective and Soft Tissue::Neoplasms, Muscle Tissue::Leiomyoma::Leiomyomatosis, DISEASES::Neoplasms::Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Urologic Neoplasms::Kidney Neoplasms::Carcinoma, Renal Cell, PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Variation::Mutation, ENFERMEDADES::neoplasias::síndromes neoplásicos hereditarios, ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de tejido conjuntivo y de tejidos blandos::neoplasias de tejido muscular::leiomioma::leiomiomatosis, ENFERMEDADES::neoplasias::neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias urológicas::neoplasias renales::carcinoma de células renales, FENÓMENOS Y PROCESOS::fenómenos genéticos::variación genética::mutación

وصف الملف: application/pdf

العلاقة: Orphanet Journal of Rare Diseases;19; https://doi.org/10.1186/s13023-024-03017-zTest; Sánchez-Heras AB, Dámaso E, Castillejo A, Robledo M, Teulé A, Lázaro C, et al. Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome. Orphanet J Rare Dis. 2024 Jan 26;19:26.; https://hdl.handle.net/11351/11062Test; 001150660000001

الإتاحة: https://doi.org/10.1186/s13023-024-03017-zTest
https://hdl.handle.net/11351/11062Test

المؤلفون: Sánchez-Heras, Ana Beatriz, Dámaso, Estela, Castillejo, Adela, Robledo, Mercedes, Teulé, Alexandre, Lázaro, Conxi, Sánchez-Martínez, Rosario, Zúñiga, Ángel, López-Fernández, Adrià, Balmaña, Judith, Robles, Luis, Ramon y Cajal, Teresa, Castillejo, M. Isabel, Ibañez, Raquel Perea, Sevila, Carmen Martínez, Sánchez-Mira, Andrea, Escandell, Inés, Gómez, Luís, Berbel, Pere, Soto, José Luis

المساهمون: Sociedad Española de Oncología Médica

المصدر: Orphanet Journal of Rare Diseases ; volume 19, issue 1 ; ISSN 1750-1172

مصطلحات موضوعية: Pharmacology (medical), Genetics (clinical), General Medicine

الإتاحة: https://doi.org/10.1186/s13023-024-03017-zTest

المؤلفون: Mellid, Sara, Gil, Eduardo, Letón, Rocío, Caleiras, Eduardo, Honrado, Emiliano, Richter, Susan, Palacios, Nuria, Lahera, Marcos, Galofré, Juan C., López-Fernández, Adriá, Calatayud, Maria, Herrera-Martínez, Aura D., Galvez, María A., Matias-Guiu, Xavier, Balbín, Milagros, Korpershoek, Esther, Lim, Eugénie S., Maletta, Francesca, Lider, Sofia, Fliedner, Stephanie M.J., Bechmann, Nicole, Eisenhofer, Graeme, Canu, Letizia, Rapizzi, Elena, Bancos, Irina, Robledo, Mercedes, Cascón, Alberto

المصدر: Mellid , S , Gil , E , Letón , R , Caleiras , E , Honrado , E , Richter , S , Palacios , N , Lahera , M , Galofré , J C , López-Fernández , A , Calatayud , M , Herrera-Martínez , A D , Galvez , M A , Matias-Guiu , X , Balbín , M , Korpershoek , E , Lim , E S , Maletta , F , Lider , S , Fliedner , S M J , Bechmann , N , Eisenhofer , G , Canu , L , Rapizzi ....

مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being

وصف الملف: application/pdf

العلاقة: https://pure.eur.nl/en/publications/db30a476-e175-4e33-a86b-f08a09712e2fTest

الإتاحة: https://doi.org/10.3389/fendo.2022.1070074Test
https://pure.eur.nl/en/publications/db30a476-e175-4e33-a86b-f08a09712e2fTest
https://pure.eur.nl/ws/files/86746272/Co_occurrence_of_mutations_in_NF1_and_other_susceptibility_genes_in_pheochromocytoma_and_paraganglioma.pdfTest
http://www.scopus.com/inward/record.url?scp=85147675003&partnerID=8YFLogxKTest

المؤلفون: Barnes, Daniel R., Silvestri, Valentina, Leslie, Goska, McGuffog, Lesley, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A., Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arason, Adalgeir, Arnold, Norbert, Auber, Bernd, Azzollini, Jacopo, Balmana, Judith, Barkardottir, Rosa B., Barrowdale, Daniel, Barwell, Julian, Belotti, Muriel, Benitez, Javier, Berthet, Pascaline, Boonen, Susanne E., Borg, Ake, Bozsik, Aniko, Brady, Angela F., Brennan, Paul, Brewer, Carole, Brunet, Joan, Bucalo, Agostino, Buys, Saundra S., Caldes, Trinidad, Caligo, Maria A., Campbell, Ian, Cassingham, Hayley, Christensen, Lise Lotte, Cini, Giulia, Claes, Kathleen B. M., Cook, Jackie, Coppa, Anna, Cortesi, Laura, Damante, Giuseppe, Darder, Esther, Davidson, Rosemarie, de la Hoya, Miguel, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesus, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Donaldson, Alan, Eason, Jacqueline, Eeles, Ros, Engel, Christoph, Evans, D. Gareth, Feliubadalo, Lidia, Fostira, Florentia, Frone, Megan, Frost, Debra, Gallagher, David, Gehrig, Andrea, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K., Goldgar, David E., Greene, Mark H., Gregory, Helen, Gross, Eva, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V. O., Hanson, Helen, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Izquierdo, Angel, James, Paul A., Janavicius, Ramunas, Jensen, Uffe Birk, Johannsson, Oskar Th, John, Esther M., Kramer, Gero, Kroeldrup, Lone, Kruse, Torben A., Lautrup, Charlotte, Lazaro, Conxi, Lesueur, Fabienne, Lopez-Fernandez, Adria, Mai, Phuong L., Manoukian, Siranoush, Matrai, Zoltan, Matricardi, Laura, Maxwell, Kara N., Mebirouk, Noura, Meindl, Alfons, Montagna, Marco, Monteiro, Alvaro N., Morrison, Patrick J., Muranen, Taru A., Murray, Alex, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Nguyen-Dumont, Tu, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo, Palli, Domenico, Parsons, Michael T., Pedersen, Inge Sokilde, Peissel, Bernard, Perez-Segura, Pedro, Peterlongo, Paolo, Petersen, Annabeth H., Pinto, Pedro, Porteous, Mary E., Pottinger, Caroline, Pujana, Miquel Angel, Radice, Paolo, Ramser, Juliane, Rantala, Johanna, Robson, Mark, Rogers, Mark T., Ronlund, Karina, Rump, Andreas, Sanchez de Abajo, Ana Maria, Shah, Payal D., Sharif, Saba, Side, Lucy E., Singer, Christian F., Stadler, Zsofia, Steele, Linda, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel R., Teule, Alex, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Tommasi, Stefania, Toss, Angela, Trainer, Alison H., Tripathi, Vishakha, Valentini, Virginia, van Asperen, Christi J., Venturelli, Marta, Viel, Alessandra, Vijai, Joseph, Walker, Lisa, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Whaite, Anna, Zanna, Ines, Offit, Kenneth, Thomassen, Mads, Couch, Fergus J., Schmutzler, Rita K., Simard, Jacques, Easton, Douglas F., Chenevix-Trench, Georgia, Antoniou, Antonis C., Ottini, Laura

المساهمون: Medicum, Research Programs Unit, Kristiina Aittomäki / Principal Investigator, HUSLAB, Department of Medical and Clinical Genetics, University of Helsinki, Helsinki University Hospital Area, Research Program in Systems Oncology, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, Clinicum

مصطلحات موضوعية: Mutation carriers, Association, Ovarian, Cancers

وصف الملف: application/pdf

العلاقة: Barnes , D R , Silvestri , V , Leslie , G , McGuffog , L , Dennis , J , Yang , X , Adlard , J , Agnarsson , B A , Ahmed , M , Aittomäki , K , Andrulis , I L , Arason , A , Arnold , N , Auber , B , Azzollini , J , Balmana , J , Barkardottir , R B , Barrowdale , D , Barwell , J , Belotti , M , Benitez , J , Berthet , P , Boonen , S E , Borg , A , Bozsik , A , Brady , A F , Brennan , P , Brewer , C , Brunet , J , Bucalo , A , Buys , S S , Caldes , T , Caligo , M A , Campbell , I , Cassingham , H , Christensen , L L , Cini , G , Claes , K B M , Cook , J , Coppa , A , Cortesi , L , Damante , G , Darder , E , Davidson , R , de la Hoya , M , De Leeneer , K , de Putter , R , Del Valle , J , Diez , O , Ding , Y C , Domchek , S M , Donaldson , A , Eason , J , Eeles , R , Engel , C , Evans , D G , Feliubadalo , L , Fostira , F , Frone , M , Frost , D , Gallagher , D , Gehrig , A , Giraud , S , Glendon , G , Godwin , A K , Goldgar , D E , Greene , M H , Gregory , H , Gross , E , Hahnen , E , Hamann , U , Hansen , T V O , Hanson , H , Hentschel , J , Horvath , J , Izatt , L , Izquierdo , A , James , P A , Janavicius , R , Jensen , U B , Johannsson , O T , John , E M , Kramer , G , Kroeldrup , L , Kruse , T A , Lautrup , C , Lazaro , C , Lesueur , F , Lopez-Fernandez , A , Mai , P L , Manoukian , S , Matrai , Z , Matricardi , L , Maxwell , K N , Mebirouk , N , Meindl , A , Montagna , M , Monteiro , A N , Morrison , P J , Muranen , T A , Murray , A , Nathanson , K L , Neuhausen , S L , Nevanlinna , H , Nguyen-Dumont , T , Niederacher , D , Olah , E , Olopade , O , Palli , D , Parsons , M T , Pedersen , I S , Peissel , B , Perez-Segura , P , Peterlongo , P , Petersen , A H , Pinto , P , Porteous , M E , Pottinger , C , Pujana , M A , Radice , P , Ramser , J , Rantala , J , Robson , M , Rogers , M T , Ronlund , K , Rump , A , Sanchez de Abajo , A M , Shah , P D , Sharif , S , Side , L E , Singer , C F , Stadler , Z , Steele , L , Stoppa-Lyonnet , D , Sutter , C , Tan , Y Y , Teixeira , M R , Teule , A , Thull , D L , Tischkowitz , M , Toland , A E , Tommasi , S , Toss , A , Trainer , A H , Tripathi , V , Valentini , V , van Asperen , C J , Venturelli , M , Viel , A , Vijai , J , Walker , L , Wang-Gohrke , S , Wappenschmidt , B , Whaite , A , Zanna , I , Offit , K , Thomassen , M , Couch , F J , Schmutzler , R K , Simard , J , Easton , D F , Chenevix-Trench , G , Antoniou , A C & Ottini , L 2022 , ' Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores ' , Journal of the National Cancer Institute , vol. 114 , no. 1 , pp. 109-122 . https://doi.org/10.1093/jnci/djab147Test; ORCID: /0000-0002-5895-1808/work/128027373; http://hdl.handle.net/10138/354035Test; 02a50b1f-2bb2-430e-9d88-e585b49420fd; 000748167200017

الإتاحة: http://hdl.handle.net/10138/354035Test

المؤلفون: Calsina, Bruna, Piñeiro-Yáñez, Elena, Martínez-Montes, Ángel M., Caleiras, Eduardo, Fernández-Sanromán, Ángel, Monteagudo, María, Lopez Fernandez, Adrià, De Almeida Toledo, Rodrigo

المساهمون: Institut Català de la Salut, Calsina B, Martínez-Montes ÁM, Fernández-Sanromán Á, Monteagudo M Hereditary Endocrine Cancer Group, Human Cancer Genetics Program, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. Piñeiro-Yáñez E Bioinformatics Unit, Structural Biology Program, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. Caleiras E Histopathology Core Unit, Biotechnology Program, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. López-Fernández A Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Toledo RA Gastrointestinal and Endocrine Tumors, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Institute of Health Carlos III (ISCIII), Madrid, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Genòmica, Tumors neuroendocrins - Aspectes genètics, Metàstasi, DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Germ Cell and Embryonal::Neuroectodermal Tumors::Neuroendocrine Tumors::Paraganglioma::Pheochromocytoma, Germ Cell and Embryonal::Neuroectodermal Tumors::Neuroendocrine Tumors::Paraganglioma, PHENOMENA AND PROCESSES::Cell Physiological Phenomena::Cellular Microenvironment::Tumor Microenvironment, DISCIPLINES AND OCCUPATIONS::Natural Science Disciplines::Biological Science Disciplines::Biology::Computational Biology::Genomics, ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::tumores neuroendocrinos::paraganglioma::feocromocitoma, ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de células germinales y embrionarias::tumores neuroectodérmicos::tumores neuroendocrinos::paraganglioma, FENÓMENOS Y PROCESOS::fenómenos fisiológicos celulares::microambiente celular::microambiente tumoral, DISCIPLINAS Y OCUPACIONES::disciplinas de las ciencias naturales::disciplinas de las ciencias biológicas::biología::biología computacional::genómica

وصف الملف: application/pdf

العلاقة: Nature Communications;14; https://doi.org/10.1038/s41467-023-36769-6Test; Calsina B, Piñeiro-Yáñez E, Martínez-Montes ÁM, Caleiras E, Fernández-Sanromán Á, Monteagudo M, et al. Genomic and immune landscape Of metastatic pheochromocytoma and paraganglioma. Nat Commun. 2023 Feb 28;14:1122.; https://hdl.handle.net/11351/9205Test

الإتاحة: https://doi.org/10.1038/s41467-023-36769-6Test
https://hdl.handle.net/11351/9205Test

المؤلفون: Carrasco, Estela, López-Fernández, Adrià, Codina-Sola, Marta, Valenzuela, Irene, Cueto-González, AM, Villacampa, Guillermo, Navarro, Victor, Torres-Esquius, Sara, Palau, Dolors, Cruellas, Mara, Torres, Maite, Perez-Dueñas, Belen, Abulí, Anna, Diez, Orland, Sábado-Álvarez, Constantino, García-Arumí, Elena, Tizzano, Eduardo F, Moreno, Lucas, Balmaña, Judith

مصطلحات موضوعية: Cancer genetics

وصف الملف: text/html

العلاقة: http://jmg.bmj.com/cgi/content/short/60/7/685Test; http://dx.doi.org/10.1136/jmg-2022-108929Test

الإتاحة: https://doi.org/10.1136/jmg-2022-108929Test
http://jmg.bmj.com/cgi/content/short/60/7/685Test

المؤلفون: Barnes, Daniel R, Silvestri, Valentina, Leslie, Goska, McGuffog, Lesley, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L, Arason, Adalgeir, Arnold, Norbert, Auber, Bernd, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barrowdale, Daniel, Barwell, Julian, Belotti, Muriel, Benitez, Javier, Berthet, Pascaline, Boonen, Susanne E, Borg, Åke, Bozsik, Aniko, Brady, Angela, Brennan, Paul, Brewer, Carole, Brunet, Joan, Bucalo, Agostino, Buys, Saundra S, Caldés, Trinidad, Caligo, Maria A, Campbell, Ian, Cassingham, Hayley, Lotte Christensen, Lise, Cini, Giulia, Claes, Kathleen B M, Cook, Jackie, Coppa, Anna, Cortesi, Laura, Damante, Giuseppe, Darder, Esther, Davidson, Rosemarie, de la Hoya, Miguel, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesús, Diez, Orland, Chun Ding, Yuan, Domchek, Susan M, Donaldson, Alan, Eason, Jacqueline, Eeles, Ros, Engel, Christoph, Gareth Evans, D, Feliubadaló, Lidia, Fostira, Florentia, Frone, Megan, Frost, Debra, Gallagher, David, Gehrig, Andrea, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Greene, Mark H, Gregory, Helen, Gross, Eva, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hanson, Helen, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Izquierdo, Angel, James, Paul A, Janavicius, Ramunas, Birk Jensen, Uffe, Johannsson, Oskar Th, John, Esther M, Kramer, Gero, Kroeldrup, Lone, Kruse, Torben A, Lautrup, Charlotte, Lazaro, Conxi, Lesueur, Fabienne, Lopez-Fernández, Adria, Mai, Phuong L, Manoukian, Siranoush, Matrai, Zoltan, Matricardi, Laura, Maxwell, Kara N, Mebirouk, Noura, Meindl, Alfons, Montagna, Marco, Monteiro, Alvaro N, Morrison, Patrick J, Muranen, Taru A, Murray, Alex, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nguyen-Dumont, Tu, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Palli, Domenico, Parsons, Michael T, Sokilde Pedersen, Inge, Peissel, Bernard, Perez-Segura, Pedro, Peterlongo, Paolo, Petersen, Annabeth H, Pinto, Pedro, Porteous, Mary E, Pottinger, Caroline, Angel Pujana, Miquel, Radice, Paolo, Ramser, Juliane, Rantala, Johanna, Robson, Mark, Rogers, Mark T, Rønlund, Karina, Rump, Andreas, María Sánchez de Abajo, Ana, Shah, Payal D, Sharif, Saba, Side, Lucy E, Singer, Christian F, Stadler, Zsofia, Steele, Linda, Stoppa-Lyonnet, Dominique, Sutter, Christian, Yen Tan, Yen, Teixeira, Manuel R, Teulé, Alex, Thull, Darcy L, Tischkowitz, Marc, Toland, Amanda E, Tommasi, Stefania, Toss, Angela, Trainer, Alison H, Tripathi, Vishakha, Valentini, Virginia, van Asperen, Christi J, Venturelli, Marta, Viel, Alessandra, Vijai, Joseph, Walker, Lisa, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Whaite, Anna, Zanna, Ines, Offit, Kenneth, Thomassen, Mads, Couch, Fergus J, Schmutzler, Rita K, Simard, Jacques, Easton, Douglas F, Chenevix-Trench, Georgia, Antoniou, Antonis C, Ottini, Laura

المساهمون: Barnes, Daniel R, Silvestri, Valentina, Leslie, Goska, Mcguffog, Lesley, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L, Arason, Adalgeir, Arnold, Norbert, Auber, Bernd, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barrowdale, Daniel, Barwell, Julian, Belotti, Muriel, Benitez, Javier, Berthet, Pascaline, Boonen, Susanne E, Borg, Åke, Bozsik, Aniko, Brady, Angela, Brennan, Paul, Brewer, Carole, Brunet, Joan, Bucalo, Agostino, Buys, Saundra S, Caldés, Trinidad, Caligo, Maria A, Campbell, Ian, Cassingham, Hayley, Lotte Christensen, Lise, Cini, Giulia, Claes, Kathleen B M, Cook, Jackie, Coppa, Anna, Cortesi, Laura, Damante, Giuseppe, Darder, Esther, Davidson, Rosemarie, de la Hoya, Miguel, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesú, Diez, Orland, Chun Ding, Yuan, Domchek, Susan M, Donaldson, Alan, Eason, Jacqueline, Eeles, Ro, Engel, Christoph, Gareth Evans, D, Feliubadaló, Lidia, Fostira, Florentia, Frone, Megan, Frost, Debra, Gallagher, David, Gehrig, Andrea, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Greene, Mark H, Gregory, Helen, Gross, Eva, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hanson, Helen, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Izquierdo, Angel, James, Paul A, Janavicius, Ramuna, Birk Jensen, Uffe, Johannsson, Oskar Th, John, Esther M, Kramer, Gero, Kroeldrup, Lone, Kruse, Torben A, Lautrup, Charlotte, Lazaro, Conxi, Lesueur, Fabienne, Lopez-Fernández, Adria, Mai, Phuong L, Manoukian, Siranoush, Matrai, Zoltan, Matricardi, Laura, Maxwell, Kara N, Mebirouk, Noura, Meindl, Alfon, Montagna, Marco, Monteiro, Alvaro N, Morrison, Patrick J, Muranen, Taru A

مصطلحات موضوعية: BRCA1, BRCA2, PRS, genetic, male breast cancer, polygenic, prostate cancer

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34320204; info:eu-repo/semantics/altIdentifier/wos/WOS:000748167200017; volume:114; issue:1; firstpage:109; lastpage:122; numberofpages:14; journal:JOURNAL OF THE NATIONAL CANCER INSTITUTE; http://hdl.handle.net/11573/1574218Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85122613384

الإتاحة: https://doi.org/10.1093/jnci/djab147Test
http://hdl.handle.net/11573/1574218Test

المؤلفون: Tamborero, David, Haj Rachid, Maan, Boekel, Jorrit, Lopez Fernandez, Adrià, Jonsson, Markus, Braña Garcia, Irene, Balmaña Gelpí, Judith, Villalobos Alberú, Xenia, Chavarria, Elena, Garralda Cabanas, Elena, Tabernero Caturla, Josep, Rodon Ahnert, Jordi, Dienstmann, Rodrigo

المساهمون: Institut Català de la Salut, Tamborero D, Rachid MH, Boekel J, Jonsson M Department of Oncology and Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden. Dienstmann R Medical Oncology, Oncology Data Science, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Lopez-Fernandez A, Balmaña J Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Braña I, Garralda E, Tabernero J Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Villalobos X, Chavarria E Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Rodon J Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Department of Investigational Cancer Therapeutics, University of Texas MD Anderson Cancer Center, Houston, USA, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Medicina personalitzada, Càncer - Diagnòstic, Medicina clínica - Presa de decisions, DISCIPLINES AND OCCUPATIONS::Health Occupations::Medicine::Internal Medicine::Medical Oncology, DISCIPLINAS Y OCUPACIONES::profesiones sanitarias::medicina::medicina interna::oncología médica

وصف الملف: application/pdf

العلاقة: Nature Cancer;3; https://doi.org/10.1038/s43018-022-00332-xTest; Tamborero D, Dienstmann R, Rachid MH, Boekel J, Lopez-Fernandez A, Jonsson M, et al. The Molecular Tumor Board Portal supports clinical decisions and automated reporting for precision oncology. Nat Cancer. 2022 Feb;3:251–61.; https://hdl.handle.net/11351/7882Test; 000761593600008

الإتاحة: https://doi.org/10.1038/s43018-022-00332-xTest
https://hdl.handle.net/11351/7882Test

المؤلفون: Tamborero, David, Dienstmann, Rodrigo, Rachid, Maan Haj, Boekel, Jorrit, Lopez-Fernandez, Adria, Jonsson, Markus, Razzak, Ali, Braña, Irene, De Petris, Luigi, Yachnin, Jeffrey, Baird, Richard D., Loriot, Yohann, Massard, Christophe, Martin-Romano, Patricia, Opdam, Frans, Schlenk, Richard F., Vernieri, Claudio, Masucci, Michele, Villalobos, Xenia, Chavarria, Elena, Anand, Shubha, Baars, Danny, Bajalica-Lagercrantz, Svetlana, Baird, Richard, Bierkens, Mariska, Blomqvist, Lennart, Bono, Costanza, Doherty, Gary J., Forest, Arnauld, Fornerone, Valentina, Gabaldi, Paola, Haglund, Felix, Hartman, Johan, Horak, Peter, Jutzi, Tanja, Kasanicki, Mary, Kreutzfeldt, Simon, Le Cornet, Lucian, Lewensohn, Rolf, Lindberg, Johan, Lopez, Carlos, Lundqvist, Andreas, Martin, Jose-Ezequiel, Meijer, Gerrit, Muñoz, Susana, Camus, Maud Ngo, Nicotra, Claudio, Nuciforo, Paolo, Oberrauch, Petra

المصدر: Nature Cancer ; volume 3, issue 5, page 649-649 ; ISSN 2662-1347

مصطلحات موضوعية: Cancer Research, Oncology

الإتاحة: https://doi.org/10.1038/s43018-022-00378-xTest
https://www.nature.com/articles/s43018-022-00378-x.pdfTest
https://www.nature.com/articles/s43018-022-00378-xTest