Genetics of feline hypertrophic cardiomyopathy von Gil-Ortuno, Cristina, Sebastian-Marcos, Patricia, Sabater-Molina, Maria, Nicolas-Rocamora, Elisa, Gimeno-Blanes, Juan R., del Palacio, Maria J. Fernandez

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Whole Sequencing and Detailed Analysis of SARS-CoV-2 Genomes in Southeast Spain: Identification of Recurrent Mutations in the 20E (EU1) Variant with Some Clinical Implications von López-Andreo, María José, Vicente-Romero, María Rosario, Bernal, Enrique, Navarro-González, Inmaculada, Salazar-Martínez, Francisco, Cánovas-Cánovas, Vanesa, Gil-Ortuño, Cristina, Riquelme-Rocamora, María Gema, Solano, Francisco, Ibáñez-López, Francisco Javier, Tomás, Cristina, Candel-Pérez, Carmen, Pérez-Parra, Santiago, Flores-Flores, César

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Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease von Sabater Molina, Maria, Nicolás Rocamora, Elisa, Bendicho, Asunción Iborra, Vázquez, Elisa García, Zorio, Esther, Rodriguez, Fernando Domínguez, Gil Ortuño, Cristina, Rodríguez, Ana Isabel, Sánchez-López, Antonio J, Jara Rubio, Rubén, Moreno-Docón, Antonio, Marcos, Pedro J, García Pavía, Pablo, Villa, Roberto Barriales, Gimeno Blanes, Juan R

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Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases von Hernandez del Rincon, Juan P., Olmo Conesa, Mari C., Rodriguez Serrano, Ana, Garcia Pulgar, Helena, Lopez Cuenca, David, Munoz Esparza, Carmen, Navarro Penalver, Marina, Santos Mateo, Juan Jose, Nicolas Rocamora, Elisa, Gil Ortuno, Cristina, Sabater-Molina, Maria, Gimeno Blanes, Juan Ramon, Pastor Quirante, Francisco

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Glinge, Charlotte, Nannenberg, Eline A., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Clauss, Sebastian, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Ellinor, Patrick T., Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C., Kurabayashi, Masahiko, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Sahin, Hatice, Sarquella-Brugada, Georgia, Sharma, Sanjay, Sheppard, Mary N., Shoemaker, M.Benjamin, Stallmeyer, Birgit, Tanaka, Yuji, Tester, David J., van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A., Lubitz, Steven A., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Arnaout, Alain Al, Amelot, Mathieu, Anselme, Frédéric, Billon, Olivier, Jesel, Laurence, Laurent, Gabriel, Maury, Philippe, Pasquie, Jean-Luc, Wiart, Francois, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.

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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility von Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y, Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J, Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A, Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O, Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D, Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuno, Cristina Gil, Lacunza, Javier, Giachino, Daniela F, Cerrato, Natascia, Martins, Raphael P, Campuzano, Oscar, Van Dooren, Sonia, Thollet, Aurelie, Kyndt, Florence, Mazzanti, Andrea, Clementy, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noel, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K, Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P, Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B, Boukens, Bas J, Skoric-Milosavljevic, Doris, Bikker, Hennie, Manevy, Federico C, Lichtner, Peter, Ribases, Marta, Meitinger, Thomas, Muller-Nurasyid, Martina, Veldink, Jan H, van den Berg, Leonard H, Van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stephanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Herve, Chatel, Stephanie, Karakachoff, Matilde, Bezieau, Stephane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E, Cerrone, Marina, Chinitz, Larry A, Volders, Paul G, van de Berg, Maarten P, Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kaab, Stefan, Al Arnaout, Alain, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D, Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D, Mansourati, Jacques

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter G, Amin, Ahmad S, Nannenberg, Eline A, Ware, James S, Whiffin, Nicola, Mazzarotto, Francesco, Skoric-Milosavljevic, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M, Bezieau, Stephane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick T, Ortuno, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jorgen K, Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C, Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L, Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphael P, Mazzanti, Andrea, Morner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Sabater Molina, Maria, Sacher, Frederic, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary N, Shimamoto, Keiko, Shoemaker, M. Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David J, Usuda, Keisuke, van der Zwaag, Paul A, Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Winkel, Bo G, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A, Lubitz, Steven A, Antzelevitch, Charles, Platonov, Pyotr G, Odening, Katja E, Roden, Dan M, Roberts, Jason D, Skinner, Jonathan R, Tfelt-Hansen, Jacob, van den Berg, Maarten P, Olesen, Morten S, Lambiase, Pier D, Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B, Kaeaeb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F

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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility von Tadros, Rafik, Chiang, David Y., Jouni, Mariam, Potet, Franck, Offerhaus, Joost A., Walsh, Roddy, Choi, Seung Hoan, Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Castelletti, Silvia, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F., Cerrato, Natascia, Van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Rowe, Matthew K., Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Steinfurt, Johannes, Jabbari, Reza, Bikker, Hennie, Manevy, Federico, Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Veldink, Jan H., van den Berg, Leonard H., Cusi, Daniele, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Bézieau, Stéphane, London, Barry, Roden, Dan, Odening, Katja E., Cerrone, Marina, Chinitz, Larry A., Volders, Paul G., van de Berg, Maarten P., Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D., Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D., Mansourati, Jacques, Loeys, Bart, Leenhardt, Antoine, Maury, Philippe, Schulze-Bahr, Eric, Breckpot, Jeroen, Babuty, Dominique, Priori, Silvia G., Napolitano, Carlo, de Asmundis, Carlo, Brugada, Pedro, Brugada, Ramon, Arbelo, Elena, Mabo, Philippe, Behar, Nathalie, Molina, Maria Sabater, Gimeno, Juan R., Hasdemir, Can, Schwartz, Peter J., Behr, Elijah R., Haissaguerre, Michel, Sacher, Frédéric, Rooryck, Caroline, Tan, Hanno L., Postema, Pieter G., Delmar, Mario, Ellinor, Patrick T., Lubitz, Steven A., George, Alfred L., MacRae, Calum A., Burridge, Paul W., Dina, Christian, Probst, Vincent, Wilde, Arthur A.

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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility von Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y, Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J, Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A, Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O, Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D, Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F, Cerrato, Natascia, Martins, Raphaël P, Campuzano, Oscar, van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Clémenty, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noël, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K, Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P, Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B, Boukens, Bas J, Škorić-Milosavljević, Doris, Bikker, Hennie, Manevy, Federico, Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Müller-Nurasyid, Martina, Strauch, Konstantin, Peters, Annette, Schulz, Holger, Schwettmann, Lars, Leidl, Reiner, Heier, Margit, Veldink, Jan H, van den Berg, Leonard H, van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Hervé, Chatel, Stéphanie, Karakachoff, Matilde, Bézieau, Stéphane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E, Cerrone, Marina, Chinitz, Larry A, Volders, Paul G, van de Berg, Maarten P, Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kääb, Stefan, Arnaout, Alain Al, Dupuis, Jean-Marc, Pasquie, Jean-Luc

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Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility von Tadros, Rafik, Chiang, David Y., Jouni, Mariam, Potet, Franck, Offerhaus, Joost A., Walsh, Roddy, Choi, Seung Hoan, Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Castelletti, Silvia, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F., Cerrato, Natascia, Van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Rowe, Matthew K., Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Steinfurt, Johannes, Jabbari, Reza, Bikker, Hennie, Manevy, Federico, Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Veldink, Jan H., van den Berg, Leonard H., Cusi, Daniele, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Bézieau, Stéphane, London, Barry, Roden, Dan, Odening, Katja E., Cerrone, Marina, Chinitz, Larry A., Volders, Paul G., van de Berg, Maarten P., Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D., Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D., Mansourati, Jacques, Loeys, Bart, Leenhardt, Antoine, Maury, Philippe, Schulze-Bahr, Eric, Breckpot, Jeroen, Babuty, Dominique, Priori, Silvia G., Napolitano, Carlo, de Asmundis, Carlo, Brugada, Pedro, Brugada, Ramon, Arbelo, Elena, Mabo, Philippe, Behar, Nathalie, Molina, Maria Sabater, Gimeno, Juan R., Hasdemir, Can, Schwartz, Peter J., Behr, Elijah R., Haissaguerre, Michel, Sacher, Frédéric, Rooryck, Caroline, Tan, Hanno L., Postema, Pieter G., Delmar, Mario, Ellinor, Patrick T., Lubitz, Steven A., George, Alfred L., MacRae, Calum A., Burridge, Paul W., Dina, Christian, Probst, Vincent, Wilde, Arthur A.

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Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility von Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y., Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J., Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A., Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O., Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D., Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F., Cerrato, Natascia, Martins, Raphaël P., Campuzano, Oscar, Van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Clémenty, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noël, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K., Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P., Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B., Boukens, Bas J., Škorić-Milosavljević, Doris, Bikker, Hennie, Manevy, Federico C., Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Müller-Nurasyid, Martina, Veldink, Jan H., van den Berg, Leonard H., Van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Hervé, Chatel, Stéphanie, Karakachoff, Matilde, Bézieau, Stéphane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E., Cerrone, Marina, Chinitz, Larry A., Volders, Paul G., van de Berg, Maarten P., Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kääb, Stefan, Al Arnaout, Alain, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D., Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D.

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter, Amin, Ahmad, Nannenberg, Eline, Ware, James, Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt, Bézieau, Stéphane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick, Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen, Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P.C., Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart, Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël, Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary, Shimamoto, Keiko, Shoemaker, M.Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David, Usuda, Keisuke, van der Zwaag, Paul, van Dooren, Sonia, van Laer, Lut, Winbo, Annika, Winkel, Bo, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G.A., Lubitz, Steven, Antzelevitch, Charles, Platonov, Pyotr, Odening, Katja, Roden, Dan, Roberts, Jason, Skinner, Jonathan, Tfelt-Hansen, Jacob, van den Berg, Maarten, Olesen, Morten, Lambiase, Pier, Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan, Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter, Amin, Ahmad, Nannenberg, Eline, Ware, James, Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt, Bézieau, Stéphane, Bos, J Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick, Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen, Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid, Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart, Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël, Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary, Shimamoto, Keiko, Shoemaker, M Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David, Usuda, Keisuke, van Der Zwaag, Paul, van Dooren, Sonia, van Laer, Lut, Winbo, Annika, Winkel, Bo, Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul, Lubitz, Steven, Antzelevitch, Charles, Platonov, Pyotr, Odening, Katja, Roden, Dan, Roberts, Jason, Skinner, Jonathan, Tfelt-Hansen, Jacob, van den Berg, Maarten, Olesen, Morten, Lambiase, Pier, Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan, Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela

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Inappropriate doses of direct oral anticoagulants in real-world clinical practice: prevalence and associated factors. A subanalysis of the FANTASIIA Registry von Ruiz Ortiz, Martín, Muñiz, Javier, Raña Míguez, Paula, Roldán, Inmaculada, Marín, Francisco, Asunción Esteve-Pastor, María, Cequier, Angel, Martínez-Sellés, Manuel, Bertomeu, Vicente, Anguita, Manuel

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Safety Evaluation of an Oak-Flavored Milk Powder Containing Ellagitannins upon Oral Administration in the Rat von Azorín-Ortuño, María, Urbán, Cristina, Cerón, José J, Tecles, Fernando, Gil-Izquierdo, Angel, Pallarés, Francisco J, Tomás-Barberán, Francisco A, Espín, Juan Carlos

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Passive smoking in babies: the BIBE study (Brief Intervention in babies. Effectiveness) von Ortega, Guadalupe, Castellà, Cristina, Martín-Cantera, Carlos, Ballvé, Jose L, Díaz, Estela, Saez, Marc, Lozano, Juan, Rofes, Lourdes, Morera, Concepció, Barceló, Antònia, Cabezas, Carmen, Pascual, Jose A, Pérez-Ortuño, Raúl, Saltó, Esteve, Valverde, Araceli, Jané, Mireia

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