Multistage Complexation of Fluoride Ions by a Fluorescent Triphenylamine Bearing Three Dimesitylboryl Groups: Controlling Intramolecular Charge Transfer von Schmidt, Hauke C, Reuter, Luisa G, Hamacek, Josef, Wenger, Oliver S

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Charge Delocalization in a Homologous Series of α,α′-Bis(dianisylamino)-Substituted Thiophene Monocations von Reuter, Luisa G, Bonn, Annabell G, Stückl, A. Claudia, He, Bice, Pati, Palas Baran, Zade, Sanjio S, Wenger, Oliver S

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Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants von Gigli, Marta, Stolfo, Davide, Graw, Sharon L., Merlo, Marco, Gregorio, Caterina, Nee Chen, Suet, Dal Ferro, Matteo, PaldinoMD, Alessia, De Angelis, Giulia, Brun, Francesca, Jirikowic, Jean, Salcedo, Ernesto E., Turja, Sylvia, Fatkin, Diane, Johnson, Renee, van Tintelen, J. Peter, Te Riele, Anneline S.J.M., Wilde, Arthur A.M., Lakdawala, Neal K., Picard, Kermshlise, Miani, Daniela, Muser, Daniele, Maria Severini, Giovanni, Calkins, Hugh, James, Cynthia A., Murray, Brittney, Tichnell, Crystal, Parikh, Victoria N., Ashley, Euan A., Reuter, Chloe, Song, Jiangping, Judge, Daniel P., McKenna, William J., Taylor, Matthew R.G., Sinagra, Gianfranco, Mestroni, Luisa

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Phase 3 Trial of Selpercatinib in Advanced RET-Mutant Medullary Thyroid Cancer von Hadoux, Julien, Elisei, Rossella, Brose, Marcia S., Hoff, Ana O., Robinson, Bruce G., Gao, Ming, Jarzab, Barbara, Isaev, Pavel, Kopeckova, Katerina, Wadsley, Jonathan, Führer, Dagmar, Keam, Bhumsuk, Bardet, Stéphane, Sherman, Eric J., Tahara, Makoto, Hu, Mimi I., Singh, Ravinder, Lin, Yan, Soldatenkova, Victoria, Wright, Jennifer, Lin, Boris, Maeda, Patricia, Capdevila, Jaume, Wirth, Lori J.

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Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy von Parikh, Victoria N, Caleshu, Colleen, Reuter, Chloe, Lazzeroni, Laura C, Ingles, Jodie, Garcia, John, McCaleb, Kristen, Adesiyun, Tolulope, Sedaghat-Hamedani, Farbod, Kumar, Saurabh, Graw, Sharon, Gigli, Marta, Stolfo, Davide, Dal Ferro, Matteo, Ing, Alexander Y, Nussbaum, Robert, Funke, Birgit, Wheeler, Matthew T, Hershberger, Ray E, Cook, Stuart, Steinmetz, Lars M, Lakdawala, Neal K, Taylor, Matthew R G, Mestroni, Luisa, Merlo, Marco, Sinagra, Gianfranco, Semsarian, Christopher, Meder, Benjamin, Judge, Daniel P, Ashley, Euan

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The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M., Kirillova, Anna, Reuter, Chloe M., Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A., Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D.H., Nussbaum, Robert L., Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R.G., Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M., Elliott, Perry M., Syrris, Petros, van Tintelen, J. Peter, James, Cynthia A., Haggerty, Christopher M., Parikh, Victoria N.

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Emery–Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure von Cannie, Douglas E, Syrris, Petros, Protonotarios, Alexandros, Bakalakos, Athanasios, Pruny, Jean-François, Ditaranto, Raffaello, Martinez-Veira, Cristina, Larrañaga-Moreira, Jose M, Medo, Kristen, Bermúdez-Jiménez, Francisco José, Ben Yaou, Rabah, Leturcq, France, Mezcua, Ainhoa Robles, Marini-Bettolo, Chiara, Cabrera, Eva, Reuter, Chloe, Limeres Freire, Javier, Rodríguez-Palomares, José F, Mestroni, Luisa, Taylor, Matthew R G, Parikh, Victoria N, Ashley, Euan A, Barriales-Villa, Roberto, Jiménez-Jáimez, Juan, Garcia-Pavia, Pablo, Charron, Philippe, Biagini, Elena, García Pinilla, José M, Bourke, John, Savvatis, Konstantinos, Wahbi, Karim, Elliott, Perry M

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Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M., Kirillova, Anna, Reuter, Chloe M., Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A., Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D.H., Nussbaum, Robert L., Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R.G., Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M., Elliott, Perry M., Syrris, Petros, van Tintelen, J. Peter, James, Cynthia A., Haggerty, Christopher M., Parikh, Victoria N.

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The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M, Kirillova, Anna, Reuter, Chloe M, Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A, Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D H, Nussbaum, Robert L, Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R G, Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M, Elliott, Perry M, Syrris, Petros, van Tintelen, J Peter

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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant von Hoorntje, Edgar T., Burns, Charlotte, Marsili, Luisa, Corden, Ben, Parikh, Victoria N., te Meerman, Gerard J., Gray, Belinda, Adiyaman, Ahmet, Bagnall, Richard D., Barge-Schaapveld, Daniela Q.C.M., van den Berg, Maarten P., Bootsma, Marianne, Bosman, Laurens P., Correnti, Gemma, Duflou, Johan, Eppinga, Ruben N., Fatkin, Diane, Fietz, Michael, Haan, Eric, Jongbloed, Jan D.H., Hauer, Arnaud D., Lam, Lien, van Lint, Freyja H.M., Lota, Amrit, Marcelis, Carlo, McCarthy, Hugh J., van Mil, Anneke M., Oldenburg, Rogier A., Pachter, Nicholas, Planken, R. Nils, Reuter, Chloe, Semsarian, Christopher, van der Smagt, Jasper J., Thompson, Tina, Vohra, Jitendra, Volders, Paul G.A., van Waning, Jaap I., Whiffin, Nicola, van den Wijngaard, Arthur, Amin, Ahmad S., Wilde, Arthur A.M., van Woerden, Gijs, Yeates, Laura, Zentner, Dominica, Ashley, Euan A., Wheeler, Matthew T., Ware, James S., van Tintelen, J. Peter, Ingles, Jodie

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Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure von Cannie, Douglas E, Syrris, Petros, Protonotarios, Alexandros, Bakalakos, Athanasios, Pruny, Jean-Francois, Ditaranto, Raffaello, Martinez-Veira, Cristina, Larranaga-Moreira, Jose M, Medo, Kristen, Bermudez-Jimenez, Francisco Jose, Ben Yaou, Rabah, Leturcq, France, Mezcua, Ainhoa Robles, Marini-Bettolo, Chiara, Cabrera, Eva, Reuter, Chloe, Freire, Javier Limeres, Rodriguez-Palomares, Jose F, Mestroni, Luisa, Taylor, Matthew RG, Parikh, Victoria N, Ashley, Euan A, Barriales-Villa, Roberto, Jimenez-Jaimez, Juan, Garcia-Pavia, Pablo, Charron, Philippe, Biagini, Elena, Pinilla, Jose M Garcia, Bourke, John, Savvatis, Konstantinos, Wahbi, Karim, Elliott, Perry M

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