Browsing by Author Lázaro, Conxi

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Showing results 1 to 11 of 11
Issue DateTitleAuthor(s)
1-Jan-2024A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical AnalysisPorras, Luz Marina; Padilla, Natàlia; Moles Fernández, Alejandro; Feliubadaló, Lidia; Santamariña Pena, Marta; Sánchez, Alysson T.; López Novo, Anael; Blanco, Ana; De La Hoya, Miguel; Molina, Ignacio J.; Osorio, Ana; Pineda, Marta; Rueda, Daniel; Ruiz Ponte, Clara; Vega, Ana; Lázaro, Conxi; Díez, Orland; Gutiérrez Enríquez, Sara; De La Cruz, Xavier
2-Feb-2024Biological basis of extensive pleiotropy between blood traits and cancer riskGómez, Antonio; Pardo Cea, Miguel A.; Farré, Xavier; Esteve, Anna; Palade, Joanna; Espín, Roderic; Mateo González, Francesca; Alsop, Eric; Alorda, Marc; Blay, Natalia; Baiges, Alexandra; Shabbir, Arzoo; Comellas, Francesc; Arnan, Montserrat; Teulé Vega, Àlex; Salinas Masdeu, Mònica; Berrocal, Laura; Brunet, Joan; Rofes, Paula; Lázaro, Conxi; Conesa, Miquel; Rojas, Juan Jose; Velten, Lars; Fendler, Wojciech; Smyczynska, Urszula; Chowdhury, Dipanjan; Zeng, Yong; Hansen He, Housheng; Li, Rong; Van Keuren‑Jensen, Kendall; Cid, Rafael de; Pujana Genestar, M. Ángel
12-Jan-2022CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer SurvivalMinguillón, Jordi; Ramírez, María José; Rovirosa, Llorenç; Bustamante Madrid, Pilar; Camps i Fajol, Cristina; Ruiz de Garibay, Gorka; Shimelis, Hermela; Montanuy, Helena; Pujol, Roser; Hernandez, Gonzalo; Bogliolo, Massimo; Castillo, Pau; Soucy, Penny; Martrat, Griselda; Gómez, Antonio; Cuadras, Daniel; García, María J.; Gayarre, Javier; Lázaro, Conxi; Benítez, Javier; Couch, Fergus J.; Pujana, Miquel Angel; Surrallés, Jordi; CIMBA Consortium
13-May-2021CNVfilteR: an R/bioconductor package to identify false positives produced by germline NGS CNV detection tools.Moreno Cabrera, José Marcos; Valle, Jesús del; Castellanos, Elisabeth; Feliubadaló i Elorza, Maria Lídia; Pineda Riu, Marta; Serra Arenas, Eduard; Capellá, G. (Gabriel); Lázaro, Conxi; Gel, Bernat
26-Jan-2024Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndromeSánchez 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
1-Jan-2023Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesGarcia 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, 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
1-Feb-2022Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromasMazuelas, Helena; Magallón Lorenz, Míriam; Fernández Rodríguez, Juana; Uriarte Arrazola, Itziar; Richaud Patin, Yvonne; Terribas, Ernest; Villanueva Garatachea, Alberto; Castellanos, Elisabeth; Blanco Guillermo, Ignacio; Raya Chamorro, Ángel; Chojnacki, Jakub; Heyn, Holger; Romagosa Pérez-Portabella, Cleofé; Lázaro, Conxi; Gel, Bernat; Carrió, Meritxell; Serra Arenas, Eduard
1-Dec-2023Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centreMosteiro, Miguel; Azuara García, Daniel; Alay, Ania; Gausachs Romero, Mireia; Varela, M.; Baixeras, N.; Pijuan, Lara; Ajenjo-Bauza, M.; López Dóriga Guerra, Adriana; Teulé-Vega, Àlex; Solanes, Aleix; Palmero, Ramón; Brenes, Jesús; Jové, M.; Padrones, Susana; Moreno Aguado, Víctor; Cordero, D.; Matias-Guiu, Xavier; Lázaro, Conxi; Nadal, Ernest
25-Nov-2021RNA assay identifies a previous misclassification of BARD1 c.1977A>G variantRofes, Paula; Pineda, Marta; Feliubadaló, Lídia; Menéndez, Mireia; Cid, Rafael de; Gómez, Carolina; Montes, Eva; Capellá, G. (Gabriel); Brunet, Joan; Valle, Jesús del; Lázaro, Conxi
May-2022Systematic collaborative reanalysis of genomic data improves diagnostic yield in neurologic rare diseasesBullich, Gemma; Matalonga, Leslie; Pujadas, Montserrat; Papakonstantinou, Anastasios; Piscia, Davide; Tonda, Raúl; Artuch, Rafael; Gallano, Pia; Garrabou Tornos, Glòria; González, Juan R.; Grinberg Vaisman, Daniel Raúl; Guitart, Míriam; Laurie, Steven; Lázaro, Conxi; Luengo, Critina; Martí, Ramon; Milà, Montserrat; Ovelleiro, David; Parra, Genís; Pujol, Aurora; Tizzano, Eduardo; Macaya, Alfonso; Palau, Francesc; Ribes, Antonio; Pérez-Jurado, Luis A.; Beltran, Sergi; Undiagnosed Rare Disease Program of Catalonia (URD-Cat) Consortium.; Rabionet Janssen, Raquel; Balcells Comas, Susana
4-Jan-2024Unbalancing cAMP and Ras/MAPK pathways as a therapeutic strategy for cutaneous neurofibromasMazuelas, Helena; Magallón-lorenz, Miriam; Uriarte-arrazola, Itziar; Negro, Alejandro; Rosas, Inma; Blanco, Ignacio; Castellanos, Elisabeth; Lázaro, Conxi; Gel, Bernat; Carrió, Meritxell; Serra, Eduard