Browsing by Author Lázaro García, Conxi
Showing results 29 to 48 of 101
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| Issue Date | Title | Author(s) |
|---|---|---|
| 6-Mar-2018 | Decapping Protein Edc4 Regulates Dna Repair And Phenocopies Brca1 | Hernández, Gonzalo; Ramírez, María José; Minguillón, Jordi; Quiles, Paco; Ruiz de Garibay, Gorka; Aza-Carmona, Miriam; Bogliolo, Massimo; Pujol, Roser; Prados-Carvajal, Rosario; Fernandez, Juana; Garcia, Nadia; López, Adriá; Gutiérrez Enríquez, Sara; Díez Gibert, Orland; Benitez, Javier; Salinas Masdeu, Mònica; Teulé-Vega, Àlex; Brunet, Joan; Radice, Paolo; Peterlongo, Paolo; Schindler, Detlev; Huertas, Pablo; Puente, Xose S.; Lázaro García, Conxi; Pujana Genestar, M. Ángel; Surrallés, Jordi |
| 1-Feb-2023 | Deep genomic analysis of malignant peripheral nerve sheath tumor cell lines challenges current malignant peripheral nerve sheath tumor diagnosis | Magallón Lorenz, Miriam; Terribas, Ernest; Ortega Bertran, Sara; Creus Bachiller, Edgar; Fernández, Marco; Requena, Gerard; Rosas, Inma; Mazuelas, Helena; Uriarte Arrazola, Itziar; Negro, Alex; Lausová, Tereza; Castellanos, Elisabeth; Blanco, Ignacio; Devries, George; Kawashima, Hiroyuki; Legius, Eric; Brems, Hilde; Mautner, Viktor; Kluwe, Lan; Ratner, Nancy; Wallace, Margaret; Fernández Rodríguez, Juana; Lázaro García, Conxi; Fletcher, Jonathan A.; Reuss, David; Carrió, Meritxell; Gel, Bernat; Serra Arenas, Eduard |
| 6-Apr-2014 | DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers | Menéndez Vilà, Mireia; Lázaro García, Conxi; Blanco Guillermo, Ignacio |
| 22-Dec-2018 | Does multilocus inherited neoplasia alleles syndrome have severe clinical expression? | Stradella, Agostina; Valle, Jesús del; Rofes, Paula; Feliubadaló i Elorza, Maria Lídia; Grau Garcés, Èlia; Velasco, Àngela; González, Sara; Vargas Parra, Gardenía María; Izquierdo, Ángel; Campos, Olga; Tornero, Eva; Navarro, Matilde; Balmaña, Judith; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan; Lázaro García, Conxi |
| 28-Nov-2014 | Estratègies terapèutiques per la Neurofibromatosi de tipus 1 | Castellsagué, Joan |
| 1-Dec-2020 | Evaluation of CNV detection tools for NGS panel data in genetic diagnostics | Moreno Cabrera, José Marcos; Valle Domínguez, Jesús del; Castellanos, Elisabeth; Feliubadaló i Elorza, Maria Lídia; Pineda Riu, Marta; Brunet, Joan; Serra, Eduard; Capellá, G. (Gabriel); Lázaro García, Conxi; Gel, Bernat |
| 1-Feb-2017 | Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers | Lázaro García, Conxi; BCFR Investigators; EMBRACE Collaborators; GEMO Study Collaborators; HEBON Investigators; KConFab Investigators |
| 13-Mar-2024 | Expansion of a Malignant Peripheral Nerve Sheath Tumor preclinical platform and its application in a high-throughput screening strategy to identify novel drug treatments | Creus Bachiller, Edgar |
| 22-Nov-2010 | Exploring the Link Between Germline and Somatic Genetic Alterations in Breast Carcinogenesis | Bonifaci Cano, Núria; Gorski, Bohdan; Masojć, Bartlomiej; Wokolorczyk, Dominika; Jakubowska, Anna; Dębniak, Tadeusz; Berenguer, Antoni; Serra-Musach, Jordi; Brunet, Joan; Dopazo, Joaquín; Narod, Steven A.; Lubinski, Jan; Lázaro García, Conxi; Cybulski, Cezary; Pujana Genestar, M. Ángel |
| 5-Apr-2011 | Exploring the link between MORF4L1 and risk of breast cancer | Martrat Sànchez, Griselda; Maxwell, Christopher A.; Porta de la Riva, Montserrat; Bonifaci Cano, Núria; Gómez Baldó, Laia; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Aguilar, Helena; Fernández Rodríguez, Juana; Cuadras, Daniel; Moreno Aguado, Víctor; Cerón Madrigal, Julián; Pujana Genestar, M. Ángel |
| 1-Apr-2020 | Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients | Valle, Jesús del; Rofes, Paula; Moreno Cabrera, José Marcos; López Dóriga Guerra, Adriana; Belhadj, Sami; Vargas Parra, Gardenía María; Teulé-Vega, Àlex; Cuesta, Raquel; Muñoz, Xavier; Campos, Olga; Salinas Masdeu, Mònica; Cid, Rafael de; Brunet, Joan; González, Sara; Capellá, G. (Gabriel); Pineda Riu, Marta; Feliubadaló i Elorza, Maria Lídia; Lázaro García, Conxi |
| 17-Apr-2013 | Functional and Structural Analysis of C-Terminal BRCA1 Missense Variants | Quiles Vidal, Francisco de Asís; Fernández Rodríguez, Juana; Mosca, Roberto; Feliubadaló i Elorza, Maria Lídia; Tornero, Eva; Brunet, Joan; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Pujana Genestar, M. Ángel; Aloy, Patrick, 1972-; Monteiro, Alvaro N.; Lázaro García, Conxi |
| 26-Jan-2024 | Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome | Sánchez Heras, Ana Beatriz; Dámaso, Estela; Castillejo, Adela; Robledo, Mercedes; Teulé, Alexandre; Lázaro García, 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 |
| 31-Mar-2022 | Genetic approaches to improve hereditary cancer diagnosis based on next-generation sequencing data | Rofes Terrón, Paula |
| 23-Jul-2021 | Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19 | Solanich, Xavier; Vargas Parra, Gardenía María; Van Der Made, Caspar I.; Simons, Annet; Schuurs Hoeijmakers, Janneke; Antolí, Arnau; Valle, Jesús del; Rocamora Blanch, Gemma; Setién, Fernando; Esteller, Manel; Van Reijmersdal, Simon V.; Riera Mestre, Antoni; Sabater Riera, Joan; Capellá, G. (Gabriel); Van De Veerdonk, Frank L.; Van Der Hoven, Ben; Corbella, Xavier; Hoischen, Alexander; Lázaro García, Conxi |
| 15-Apr-2019 | Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer | Lázaro García, Conxi; GC-HBOC Study Collaborators; GEMO Study Collaborators; EMBRACE Collaborators; HEBON Investigators; BCFR Investigators; ABCTB Investigators |
| 1-Jun-2020 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses | Zhan, Haoyu; Ahearn, Thomas U.; Lecarpentier, Julie; Lázaro García, Conxi; EMBRACE Collaborators; GEMO Study Collaborators |
| 9-Jan-2013 | Genomic imbalance of HMMR/RHAMM regulates the sensitivity and response of malignant peripheral nerve sheath tumour cells to aurora kinase inhibition | Mohan, Pooja; Castellsagué, Joan; Jiang, Jihong; Allen, Kristi; Chen, Helen; Nemirovsky, Oksana; Spyra, Melanie; Hu, Kaiji; Kluwe, Lan; Pujana Genestar, M. Ángel; Villanueva Garatachea, Alberto; Mautner, Victor-Felix; Keats, Jonathan J.; Dunn, Sandra E.; Lázaro García, Conxi; Maxwell, Christopher A. |
| 1-Jan-2023 | Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes | Garcia Pelaez, José; Barbosa Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sérgio; Sousa, Sónia; Pinheiro, Hugo; Sousa, Liliana; Monteiro, Rita; Maqueda, Joaquin J.; Fernandes, Susana; Carneiro, Fátima; Pinto, Nádia; Lemos, Carolina; Pinto, Carla; Teixeira, Manuel R.; Aretz, Stefan; Bajalica Lagercrantz, Svetlana; Balmaña, Judith; Blatnik, Ana; Benusiglio, Patrick R.; Blanluet, Maud; Bours, Vincent; Brems, Hilde; Brunet, Joan; Calistri, Daniele; Capella, Gabriel; Carrera, Sergio; Colas, Chrystelle; Dahan, Karin; Putter, Robin de; Desseignés, Camille; Domínguez Garrido, Elena; Egas, Conceição; Evans, D. Gareth; Feret, Damien; Fewings, Eleanor; Fitzgerald, Rebecca C.; Coulet, Florence; Garcia Barcina, María; Genuardi, Maurizio; Golmard, Lisa; Hackmann, Karl; Hanson, Helen; Holinski Feder, Elke; Hüneburg, Robert; Krajc, Mateja; Lagerstedt Robinson, Kristina; Lázaro García, Conxi; Ligtenberg, Marjolijn J. L.; Martínez Bouzas, Cristina; Merino, Sonia; Michils, Geneviève; Novaković, Srdjan; Patiño García, Ana; Ranzani, Guglielmina Nadia; Schröck, Evelin; Silva, Inês; Silveira, Catarina; Soto, José L.; Spier, Isabel; Steinke Lange, Verena; Tedaldi, Gianluca; Tejada, María isabel; Woodward, Emma R; Tischkowitz, Marc; Hoogerbrugge, Nicoline; Oliveira, Carla |
| 15-Feb-2018 | Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis | Mur, Pilar; de Voer, Richarda M.; Olivera-Salguero, Rubén; Rodriguez Perales, Sandra; Pons, Tirso; Setién, Fernando; Aiza, Gemma; Valdés Mas, Rafael; Bertini, Angelo; Pineda Riu, Marta; Vreede, Lilian; Navarro, Matilde; Iglesias Casals, Sílvia; González, Sara; Brunet, Joan; Valencia, Alfonso; Esteller, Manel; Lázaro García, Conxi; Kops, Geert J. P. L.; Urioste, Miguel; Puente, Xose S.; Capellá, G. (Gabriel); Valle Velasco, Laura |