The Selectivity for Tumor Cells of Nuclear-Directed Cytotoxic RNases Is Mediated by the Nuclear/Cytoplasmic Distribution of p27(KIP1)

por García-Galindo, Glòria, Castro, Jessica, Matés, Jesús, Bravo, Marlon, Ribó, Marc, Vilanova, Maria, Benito, Antoni
Publicado 2021

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

por Allegue, Catarina, Coll, Mònica, Mates, Jesus, Campuzano, Oscar, Iglesias, Anna, Sobrino, Beatriz, Brion, Maria, Amigo, Jorge, Carracedo, Angel, Brugada, Pedro, Brugada, Josep, Brugada, Ramon
Publicado 2015

Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology

por Campuzano, Oscar, Sarquella-Brugada, Georgia, Mademont-Soler, Irene, Allegue, Catarina, Cesar, Sergi, Ferrer-Costa, Carles, Coll, Monica, Mates, Jesus, Iglesias, Anna, Brugada, Josep, Brugada, Ramon
Publicado 2014

Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death

por Campuzano, Oscar, Sanchez-Molero, Olallo, Mademont-Soler, Irene, Riuró, Helena, Allegue, Catarina, Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, Picó, Ferran, Iglesias, Anna, Brugada, Ramon
Publicado 2015

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

por Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, del Olmo, Bernat, Puigmulé, Marta, Fernandez-Falgueras, Anna, Iglesias, Anna, Picó, Ferran, Lopez, Laura, Brugada, Ramon, Campuzano, Oscar
Publicado 2017

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP

por Coll, Monica, Striano, Pasquale, Ferrer-Costa, Carles, Campuzano, Oscar, Matés, Jesús, del Olmo, Bernat, Iglesias, Anna, Pérez-Serra, Alexandra, Mademont, Irene, Picó, Ferran, Oliva, Antonio, Brugada, Ramon
Publicado 2017

Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients

por Coll, Monica, Ferrer-Costa, Carles, Pich, Sara, Allegue, Catarina, Rodrigo, Emilio, Fernández-Fresnedo, Gema, Barreda, Paloma, Mates, Jesus, Martinez de Francisco, Angel Luis, Ortega, Israel, Iglesias, Anna, Campuzano, Oscar, Salas, Eduardo, Arias, Manuel, Brugada, Ramon
Publicado 2018

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

por Campuzano, Oscar, Fernandez-Falgueras, Anna, Lemus, Ximena, Sarquella-Brugada, Georgia, Cesar, Sergi, Coll, Monica, Mates, Jesus, Arbelo, Elena, Jordà, Paloma, Perez-Serra, Alexandra, del Olmo, Bernat, Ferrer-Costa, Carles, Iglesias, Anna, Fiol, Victoria, Puigmulé, Marta, Lopez, Laura, Pico, Ferran, Brugada, Josep, Brugada, Ramon
Publicado 2019

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

por Pinsach-Abuin, Mel·lina, del Olmo, Bernat, Pérez-Agustin, Adrian, Mates, Jesus, Allegue, Catarina, Iglesias, Anna, Ma, Qi, Merkurjev, Daria, Konovalov, Sergiy, Zhang, Jing, Sheikh, Farah, Telenti, Amalio, Brugada, Josep, Brugada, Ramon, Gymrek, Melissa, di Iulio, Julia, Garcia-Bassets, Ivan, Pagans, Sara
Publicado 2021

Large Genomic Imbalances in Brugada Syndrome

por Mademont-Soler, Irene, Pinsach-Abuin, Mel·lina, Riuró, Helena, Mates, Jesus, Pérez-Serra, Alexandra, Coll, Mònica, Porres, José Manuel, del Olmo, Bernat, Iglesias, Anna, Selga, Elisabet, Picó, Ferran, Pagans, Sara, Ferrer-Costa, Carles, Sarquella-Brugada, Geòrgia, Arbelo, Elena, Cesar, Sergi, Brugada, Josep, Campuzano, Óscar, Brugada, Ramon
Publicado 2016

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies

por Campuzano, Oscar, Fernandez-Falgueras, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Arbelo, Elena, García-Álvarez, Ana, Jordà, Paloma, Coll, Monica, Fiol, Victoria, Iglesias, Anna, Perez-Serra, Alexandra, Mates, Jesus, del Olmo, Bernat, Ferrer, Carles, Alcalde, Mireia, Puigmulé, Marta, Mademont-Soler, Irene, Pico, Ferran, Lopez, Laura, Tiron, Coloma, Brugada, Josep, Brugada, Ramon
Publicado 2019

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

por Sanchez, Olallo, Campuzano, Oscar, Fernández-Falgueras, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Mademont, Irene, Mates, Jesus, Pérez-Serra, Alexandra, Coll, Monica, Pico, Ferran, Iglesias, Anna, Tirón, Coloma, Allegue, Catarina, Carro, Esther, Gallego, María Ángeles, Ferrer-Costa, Carles, Hospital, Anna, Bardalet, Narcís, Borondo, Juan Carlos, Vingut, Albert, Arbelo, Elena, Brugada, Josep, Castellà, Josep, Medallo, Jordi, Brugada, Ramon
Publicado 2016

Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

por Sanchez, Olallo, Campuzano, Oscar, Fernández-Falgueras, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Mademont, Irene, Mates, Jesus, Pérez-Serra, Alexandra, Coll, Monica, Pico, Ferran, Iglesias, Anna, Tirón, Coloma, Allegue, Catarina, Carro, Esther, Gallego, María Ángeles, Ferrer-Costa, Carles, Hospital, Anna, Bardalet, Narcís, Borondo, Juan Carlos, Vingut, Albert, Arbelo, Elena, Brugada, Josep, Castellà, Josep, Medallo, Jordi, Brugada, Ramon
Publicado 2017

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy

por Mademont-Soler, Irene, Mates, Jesus, Yotti, Raquel, Espinosa, Maria Angeles, Pérez-Serra, Alexandra, Fernandez-Avila, Ana Isabel, Coll, Monica, Méndez, Irene, Iglesias, Anna, del Olmo, Bernat, Riuró, Helena, Cuenca, Sofía, Allegue, Catarina, Campuzano, Oscar, Picó, Ferran, Ferrer-Costa, Carles, Álvarez, Patricia, Castillo, Sergio, Garcia-Pavia, Pablo, Gonzalez-Lopez, Esther, Padron-Barthe, Laura, Díaz de Bustamante, Aranzazu, Darnaude, María Teresa, González-Hevia, José Ignacio, Brugada, Josep, Fernandez-Aviles, Francisco, Brugada, Ramon
Publicado 2017