HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy von Milano, Annalisa, MSc, Vermeer, Alexa M.C., MD, Lodder, Elisabeth M., PhD, Barc, Julien, PhD, Verkerk, Arie O., PhD, Postma, Alex V., PhD, van der Bilt, Ivo A.C., MD, Baars, Marieke J.H., MD, PhD, van Haelst, Paul L., MD, PhD, Caliskan, Kadir, MD, Hoedemaekers, Yvonne M., MD, PhD, Le Scouarnec, Solena, PhD, Redon, Richard, PhD, Pinto, Yigal M., MD, PhD, Christiaans, Imke, MD, PhD, Wilde, Arthur A., MD, PhD, Bezzina, Connie R., PhD

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Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations von Vermeer, Alexa M.C., MD, Lodder, Elisabeth M., PhD, Thomas, Dierk, MD, Duijkers, Floor A.M., MD, PhD, Marcelis, Carlo, MD, PhD, van Gorselen, Edwin O.F., MD, Fortner, Philipp, MD, Buss, Sebastian J., MD, Mereles, Derliz, MD, Katus, Hugo A., MD, Wilde, Arthur A.M., MD, PhD, Bezzina, Connie R., PhD, Boekholdt, S. Matthijs, MD, PhD, Schweizer, Patrick A., MD, Christiaans, Imke, MD, PhD

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MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset von Marsili, Luisa, van Lint, Freyja H. M., Russo, Francesco, van Spaendonck-Zwarts, Karin Y., Ader, Flavie, Bichon, Marie-Line, Faivre, Laurence, Houweling, Arjan C., Isidor, Bertrand, Lekanne Deprez, Ronald H., Cox, Moniek G. P. J., Wilde, Arthur A. M., Mazel, Benoit, Mercier, Sandra, Dooijes, Dennis, Millat, Gilles, Nguyen, Karine, Post, Jan G., Richard, Pascale, van de Beek, Irma, Vermeer, Alexa M. C., Boven, Ludolf, Jongbloed, Jan D. H., van Tintelen, J. Peter

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Letter by Vermeer et al Regarding Article, "Phenotypic Spectrum of HCN4 Mutations: A Clinical Case" von Vermeer, Alexa M C, Christiaans, Imke, Lodder, Elisabeth M

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Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive von Vermeer, Alexa M.C., MD, Clur, Sally-Ann B., MD, PhD, Blom, Nico A., MD, PhD, Wilde, Arthur A.M., MD, PhD, Christiaans, Imke, MD, PhD

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Tropomyosin–troponin complex in inherited cardiomyopathies von Juárez, Christian Krijger, Sequeira, Vasco, van den Boogaard, Malou, Veerman, Christiaan C., Hoetjes, Nicola J., Poel, Edwin, Tanck, Michael W.T., Lekanne Deprez, Ronald H., Vermeer, Alexa M.C., van der Velden, Jolanda, Amin, Ahmad S.

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Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations von Witjas-Paalberends, E Rosalie, Güçlü, Ahmet, Germans, Tjeerd, Knaapen, Paul, Harms, Hendrik J, Vermeer, Alexa M C, Christiaans, Imke, Wilde, Arthur A M, Dos Remedios, Cris, Lammertsma, Adriaan A, van Rossum, Albert C, Stienen, Ger J M, van Slegtenhorst, Marjon, Schinkel, Arend F, Michels, Michelle, Ho, Carolyn Y, Poggesi, Corrado, van der Velden, Jolanda

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Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias von Pham, Caroline, Andrzejczyk, Karolina, Jurgens, Sean J., Deprez, Ronald Lekanne, Palm, Kaylin C.A., Vermeer, Alexa M.C., Nijman, Janneke, Christiaans, Imke, van Dessel, Pascal F.H.M., Beekman, Leander, Choi, Seung Hoan, Lubitz, Steven A., Skoric-Milosavljevic, Doris, van den Bersselaar, Lisa, Jansen, Philip R., Copier, Jaël S., Ellinor, Patrick T., Wilde, Arthur A.M., Bezzina, Connie R., Lodder, Elisabeth M.

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Heritability in genetic heart disease: the role of genetic background von Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Tanck, Michael W T, van Tintelen, J Peter, Christiaans, Imke, van der Smagt, Jasper J, Vermeer, Alexa M C, Bos, J Martijn, Moss, Arthur J, Swan, Heikki, Priori, Sylvia G, Rydberg, Annika, Tfelt-Hansen, Jacob, Ackerman, Michael J, Olivotto, Iacopo, Charron, Philippe, Gimeno, Juan R, van den Berg, Maarten P, Wilde, Arthur AM, Pinto, Yigal M

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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies von Jansen, Mark, de Brouwer, Remco, Hassanzada, Fahima, Schoemaker, Angela E., Schmidt, Amand F., Kooijman-Reumerman, Maria D., Bracun, Valentina, Slieker, Martijn G., Dooijes, Dennis, Vermeer, Alexa M.C., Wilde, Arthur A.M., Amin, Ahmad S., Lekanne Deprez, Ronald H., Herkert, Johanna C., Christiaans, Imke, de Boer, Rudolf A., Jongbloed, Jan D.H., van Tintelen, J. Peter, Asselbergs, Folkert W., Baas, Annette F.

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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study von Jansen, Mark, de Brouwer, Remco, Hassanzada, Fahima, Schoemaker, Angela E, Schmidt, Amand F, Kooijman-Reumerman, Maria D, Bracun, Valentina, Slieker, Martijn G, Dooijes, Dennis, Vermeer, Alexa M C, Wilde, Arthur A M, Amin, Ahmad S, Lekanne Deprez, Ronald H, Herkert, Johanna C, Christiaans, Imke, de Boer, Rudolf A, Jongbloed, Jan D H, van Tintelen, J Peter, Asselbergs, Folkert W, Baas, Annette F

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HCN4Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy von Milano, Annalisa, Vermeer, Alexa MC, Lodder, Elisabeth M, Barc, Julien, Verkerk, Arie O, Postma, Alex V, van der Bilt, Ivo AC, Baars, Marieke JH, van Haelst, Paul L, Caliskan, Kadir, Hoedemaekers, Yvonne M, Le Scouarnec, Solena, Redon, Richard, Pinto, Yigal M, Christiaans, Imke, Wilde, Arthur A, Bezzina, Connie R

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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study von Jansen, Mark, de Brouwer, Remco, Hassanzada, Fahima, Schoemaker, Angela E, Schmidt, Amand F, Kooijman-Reumerman, Maria D, Bracun, Valentina, Slieker, Martijn G, Dooijes, Dennis, Vermeer, Alexa MC, Wilde, Arthur AM, Amin, Ahmad S, Lekanne Deprez, Ronald H, Herkert, Johanna C, Christiaans, Imke, de Boer, Rudolf A, Jongbloed, Jan DH, van Tintelen, J Peter, Asselbergs, Folkert W, Baas, Annette F

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International External Validation Study of the 2014 European Society of Cardiology Guidelines on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (EVIDENCE-HCM) von O’Mahony, Constantinos, Jichi, Fatima, Ommen, Steve R, Christiaans, Imke, Arbustini, Eloisa, Garcia-Pavia, Pablo, Cecchi, Franco, Olivotto, Iacopo, Kitaoka, Hiroaki, Gotsman, Israel, Carr-White, Gerald, Mogensen, Jens, Antoniades, Loizos, Mohiddin, Saidi A, Maurer, Mathew S, Tang, Hak Chiaw, Geske, Jeffrey B, Siontis, Konstantinos C, Mahmoud, Karim D, Vermeer, Alexa, Wilde, Arthur, Favalli, Valentina, Guttmann, Oliver P, Gallego-Delgado, Maria, Dominguez, Fernando, Tanini, Ilaria, Kubo, Toru, Keren, Andre, Bueser, Teofila, Waters, Sarah, Issa, Issa F, Malcolmson, James, Burns, Tom, Sekhri, Neha, Hoeger, Christopher W, Omar, Rumana Z, Elliott, Perry M

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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect von Tadros, Rafik, Francis, Catherine, Xu, Xiao, Vermeer, Alexa M. C., Harper, Andrew R., Huurman, Roy, Kelu Bisabu, Ken, Walsh, Roddy, Hoorntje, Edgar T., te Rijdt, Wouter P., Buchan, Rachel J., van Velzen, Hannah G., van Slegtenhorst, Marjon A., Vermeulen, Jentien M., Offerhaus, Joost Allard, Bai, Wenjia, de Marvao, Antonio, Lahrouchi, Najim, Beekman, Leander, Karper, Jacco C., Veldink, Jan H., Kayvanpour, Elham, Pantazis, Antonis, Baksi, A. John, Whiffin, Nicola, Mazzarotto, Francesco, Sloane, Geraldine, Suzuki, Hideaki, Schneider-Luftman, Deborah, Elliott, Paul, Richard, Pascale, Ader, Flavie, Villard, Eric, Lichtner, Peter, Meitinger, Thomas, Tanck, Michael W. T., van Tintelen, J. Peter, Thain, Andrew, McCarty, David, Hegele, Robert A., Roberts, Jason D., Amyot, Julie, Dubé, Marie-Pierre, Cadrin-Tourigny, Julia, Giraldeau, Geneviève, L’Allier, Philippe L., Garceau, Patrick, Tardif, Jean-Claude, Boekholdt, S. Matthijs, Lumbers, R. Thomas, Asselbergs, Folkert W., Barton, Paul J. R., Cook, Stuart A., Prasad, Sanjay K., O’Regan, Declan P., van der Velden, Jolanda, Verweij, Karin J. H., Talajic, Mario, Lettre, Guillaume, Pinto, Yigal M., Meder, Benjamin, Charron, Philippe, de Boer, Rudolf A., Christiaans, Imke, Michels, Michelle, Wilde, Arthur A. M., Watkins, Hugh, Matthews, Paul M., Ware, James S., Bezzina, Connie R.

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