Browsing by Author Lázaro, Conxi
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 2-Feb-2024 | Biological basis of extensive pleiotropy between blood traits and cancer risk | Gómez, 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 |
| 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, 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-Dec-2023 | Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centre | Mosteiro, 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, S.; Moreno Aguado, Víctor; Cordero, D.; Matias-Guiu, Xavier; Lázaro, Conxi; Nadal, Ernest |
| 25-Nov-2021 | RNA assay identifies a previous misclassification of BARD1 c.1977A>G variant | Rofes, 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-2022 | Systematic collaborative reanalysis of genomic data improves diagnostic yield in neurologic rare diseases | Bullich, 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 |