Browsing by Author Valle Domínguez, Jesús del
Showing results 4 to 11 of 11
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| Issue Date | Title | Author(s) |
|---|---|---|
| 4-Jan-2017 | Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer | Feliubadaló i Elorza, Maria Lídia; Tonda, Raul; Gausachs Romero, Mireia; Trotta, Jean Rémi; Castellanos, Elisabeth; López Dóriga Guerra, Adriana; Teulé-Vega, Àlex; Tornero, Eva; Valle Domínguez, Jesús del; Gel, Bernat; Gut, Marta; Pineda Riu, Marta; González, Sara; Menéndez Vilà, Mireia; Navarro, Matilde; Capellá, G. (Gabriel); Gut, Ivo G.; Serra Arenas, Eduard; Brunet, Joan; Beltran i Agulló, Sergi; Lázaro García, Conxi |
| 28-Jul-2021 | Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores | Barnes, Daniel R.; Angel Pujana, Miquel; Teulé Vega, Àlex; Balmaña, Judith; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; Consortium Of Investigators Of Modifiers Of Brca1 And Brca2, The; Brunet, Joan; Darder, Esther; Valle Domínguez, Jesús del; Diez, Orland; Feliubadaló i Elorza, Maria Lídia; Izquierdo, Angel; Lazaro, Conxi; López Fernández, Adrià |
| 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 |
| 31-Mar-2022 | Genetic approaches to improve hereditary cancer diagnosis based on next-generation sequencing data | Rofes Terrón, Paula |
| 28-Nov-2019 | Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation | Dámaso, Estela; Canet Hermida, Júlia; Vargas Parra, Gardenía María; Velasco, Àngela; Marín, Fátima; Darder, Esther; Valle Domínguez, Jesús del; Fernández, Anna; Izquierdo i Font, Àngel Xavier; Mateu, Gemma; Oliveras, Glòria; Escribano, Carmen; Piñol, Virgínia; Uchima, Hugo Ikuo; Soto, José Luis; Hitchins, Megan; Farrés, Ramon; Lázaro García, Conxi; Queralt, Bernat; Brunet, Joan; Capellá, G. (Gabriel); Pineda Riu, Marta |
| Oct-2018 | Primary constitutional MLH1 epimutations: a focal epigenetic event | Dámaso, Estela; Castillejo, Adela; Arias, María del Mar; Canet Hermida, Júlia; Navarro, Matilde; Valle Domínguez, Jesús del; Campos, Olga; Fernández, Anna; Marín, Fátima; Turchetti, Daniela; García Díaz, Juan de Dios; Lázaro García, Conxi; Genuardi, Maurizio; Rueda, Daniel; Alonso, Ángel; Soto, Jose Luis; Hitchins, Megan; Pineda Riu, Marta; Capellá, G. (Gabriel) |
| 28-Apr-2021 | The Challenge of Diagnosing Constitutional Mismatch Repair Deficiency Syndrome in Brain Malignancies from Young Individuals | Carrato, Cristina; Sanz, Carolina; Muñoz Mármol, Ana María; Blanco Guillermo, Ignacio; Pineda Riu, Marta; Valle Domínguez, Jesús del; Dámaso, Estela; Esteller, Manel; Musulén, Eva |
| 1-Feb-2020 | The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases | Brunet, Joan; Darder, Esther; Valle Domínguez, Jesús del; Lázaro García, Conxi; ENIGMA Consortium; GENESIS Study Collaborators; SWE-BRCA Group |