Lidia Feliubadaló
13PUBLICATIONS
204CO-AUTHORS

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Publications (13)
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|Mar 17, 2026
Evaluation of BoostDM, a somatic variant prediction tool, for the interpretation of germline variants in hereditary cancer genes.Elisabet Munté, Ferran Muiños, Raúl Marín
|Mar 17, 2026
Optimizing GRIDSS for clinical use: A targeted NGS filtering strategy for germline structural variant detection.Elisabet Munté, Paula Rofes, Miriam Millán-Castillo
|Jul 05, 2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.José M Moreno-Cabrera, Lidia Feliubadaló, Marta Pineda
|Jul 29, 2023
Choosing Variant Interpretation Tools for Clinical Applications: Context Matters.Josu Aguirre, Natàlia Padilla, Selen Özkan
|Jul 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.Lenka Stolarova, Petra Kleiblova, Petra Zemankova
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Frequent Collaborators
8 joint publications
Conxi Lázaro
7 joint publications
Joan Brunet
6 joint publications
Jesús Del Valle
4 joint publications
Elisabet Munté
3 joint publications
Paula Rofes
3 joint publications
José Marcos Moreno-Cabrera
2 joint publications
Bernat Gel
2 joint publications
Ian Campbell
2 joint publications
Marinus J Blok
2 joint publications
Joe Dennis