Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome von Allegue, Catarina, Coll, Mònica, Mates, Jesus, Campuzano, Oscar, Iglesias, Anna, Sobrino, Beatriz, Brion, Maria, Amigo, Jorge, Carracedo, Angel, Brugada, Pedro, Brugada, Josep, Brugada, Ramon

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

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Chromatin establishes an immature version of neuronal protocadherin selection during the naive-to-primed conversion of pluripotent stem cells von Almenar-Queralt, Angels, Merkurjev, Daria, Kim, Hong Sook, Navarro, Michael, Ma, Qi, Chaves, Rodrigo S., Allegue, Catarina, Driscoll, Shawn P., Chen, Andrew G., Kohlnhofer, Bridget, Fong, Lauren K., Woodruff, Grace, Mackintosh, Carlos, Bohaciakova, Dasa, Hruska-Plochan, Marian, Tadokoro, Takahiro, Young, Jessica E., El Hajj, Nady, Dittrich, Marcus, Marsala, Martin, Goldstein, Lawrence S. B., Garcia-Bassets, Ivan

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Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene von Toro, Rocio, Pérez-Serra, Alexandra, Campuzano, Oscar, Moncayo-Arlandi, Javier, Allegue, Catarina, Iglesias, Anna, Mangas, Alipio, Brugada, Ramon

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Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia von Wangüemert, Fernando, PhD, MD, Bosch Calero, Cristina, MSc, Pérez, Carmelo, BD, Campuzano, Oscar, PhD, Beltran-Alvarez, Pedro, PhD, Scornik, Fabiana S., PhD, Iglesias, Anna, MSc, Berne, Paola, MD, Allegue, Catarina, PhD, Ruiz Hernandez, Pablo M., PhD, MD, Brugada, Josep, PhD, MD, Pérez, Guillermo J., PhD, Brugada, Ramon, PhD, MD

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

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

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A Genetically Vulnerable Myocardium May Predispose to Myocarditis von Campuzano, Oscar, PhD, Fernández-Falgueras, Anna, MSc, Sarquella-Brugada, Georgia, MD, Sanchez, Olallo, MSc, Cesar, Sergi, MD, Mademont, Irene, PhD, Allegue, Catarina, PhD, Mates, Jesus, MSc, Pérez-Serra, Alexandra, MSc, Coll, Monica, PhD, Alcalde, Mireia, MSc, Iglesias, Anna, MSc, Tiron, Coloma, MD, Gallego, María Ángeles, MD, Ferrer-Costa, Carles, PhD, Hospital, Anna, MD, Escribano, Carme, MD, Dasí, Concha, MD, Borondo, Juan Carlos, MD, PhD, Castellà, Josep, MD, PhD, Arbelo, Elena, MD, PhD, Medallo, Jordi, MD, PhD, Brugada, Josep, MD, PhD, Brugada, Ramon, MD, PhD

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Identification of Sodium Transients Through NaV1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons von Martínez, Antón L., Brea, José, Domínguez, Eduardo, Varela, María J., Allegue, Catarina, Cruz, Raquel, Monroy, Xavier, Merlos, Manuel, Burgueño, Javier, Carracedo, Ángel, Loza, María Isabel

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

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Post-mortem genetic analysis in juvenile cases of sudden cardiac death von Campuzano, Oscar, Sanchez-Molero, Olallo, Allegue, Catarina, Coll, Monica, Mademont-Soler, Irene, Selga, Elisabet, Ferrer-Costa, Carles, Mates, Jesus, Iglesias, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Brugada, Josep, Castellà, Josep, Medallo, Jordi, Brugada, Ramon

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Genetic Kidney Diseases (GKDs) Modeling Using Genome Editing Technologies von Gómez-García, Fernando, Martínez-Pulleiro, Raquel, Carrera, Noa, Allegue, Catarina, Garcia-Gonzalez, Miguel A

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Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series von Partemi, Sara, Vidal, Monica Coll, Striano, Pasquale, Campuzano, Oscar, Allegue, Catarina, Pezzella, Marianna, Elia, Maurizio, Parisi, Pasquale, Belcastro, Vincenzo, Casellato, Susanna, Giordano, Lucio, Mastrangelo, Massimo, Pietrafusa, Nicola, Striano, Salvatore, Zara, Federico, Bianchi, Amedeo, Buti, Daniela, La Neve, Angela, Tassinari, Carlo Alberto, Oliva, Antonio, Brugada, Ramon

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

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

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

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The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution von Mosquera Orgueira, Adrián, Antelo Rodríguez, Beatriz, Alonso Vence, Natalia, Díaz Arias, José Ángel, Díaz Varela, Nicolás, Pérez Encinas, Manuel Mateo, Allegue Toscano, Catarina, Goiricelaya Seco, Elena María, Carracedo Álvarez, Ángel, Bello López, José Luis

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Negative autopsy and sudden cardiac death von Campuzano, Oscar, Allegue, Catarina, Partemi, Sara, Iglesias, Anna, Oliva, Antonio, Brugada, Ramon

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Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies von Campuzano, Oscar, Allegue, Catarina, Fernandez, Anna, Iglesias, Anna, Brugada, Ramon

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CARTAR: a comprehensive web tool for identifying potential targets in chimeric antigen receptor therapies using TCGA and GTEx data von Hernandez-Gamarra, Miguel, Salgado-Roo, Alba, Dominguez, Eduardo, Goiricelaya Seco, Elena María, Veiga-Rúa, Sara, Pedrera-Garbayo, Lucía F, Carracedo, Ángel, Allegue, Catarina

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