Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy von van Waning, Jaap I., Caliskan, Kadir, Michels, Michelle, Schinkel, Arend F.L., Hirsch, Alexander, Dalinghaus, Michiel, Hoedemaekers, Yvonne M., Wessels, Marja W., IJpma, Arne S., Hofstra, Robert M.W., van Slegtenhorst, Marjon A., Majoor-Krakauer, Danielle

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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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Untargeted Metabolomics Identifies Potential Hypertrophic Cardiomyopathy Biomarkers in Carriers of MYBPC3 Founder Variants von Jansen, Mark, Schuldt, Maike, van Driel, Beau O, Schmidt, Amand F, Christiaans, Imke, van der Crabben, Saskia N, Hoedemaekers, Yvonne M, Dooijes, Dennis, Jongbloed, Jan D H, Boven, Ludolf G, Deprez, Ronald H Lekanne, Wilde, Arthur A M, Jans, Judith J M, van der Velden, Jolanda, de Boer, Rudolf A, van Tintelen, J Peter, Asselbergs, Folkert W, Baas, Annette F

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The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction Cardiomyopathy von Hoedemaekers, Yvonne M, Caliskan, Kadir, Michels, Michelle, Frohn-Mulder, Ingrid, van der Smagt, Jasper J, Phefferkorn, Judith E, Wessels, Marja W, ten Cate, Folkert J, Sijbrands, Eric J.G, Dooijes, Dennis, Majoor-Krakauer, Danielle F

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Diastolic Abnormalities as the First Feature of Hypertrophic Cardiomyopathy in Dutch Myosin-Binding Protein C Founder Mutations von Michels, Michelle, MD, Soliman, Osama I.I., MD, PhD, Kofflard, Marcel J., MD, PhD, Hoedemaekers, Yvonne M., MD, Dooijes, Dennis, PhD, Majoor-Krakauer, Danielle, MD, PhD, ten Cate, Folkert J., MD, PhD

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A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial von van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke

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Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers von Michels, Michelle, Soliman, Osama I.I., Phefferkorn, Judith, Hoedemaekers, Yvonne M., Kofflard, Marcel J., Dooijes, Dennis, Majoor-Krakauer, Danielle, Ten Cate, Folkert J.

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Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy von van Waning, Jaap I., Caliskan, Kadir, Hoedemaekers, Yvonne M., van Spaendonck-Zwarts, Karin Y., Baas, Annette F., Boekholdt, S. Matthijs, van Melle, Joost P., Teske, Arco J., Asselbergs, Folkert W., Backx, Ad P.C.M., du Marchie Sarvaas, Gideon J., Dalinghaus, Michiel, Breur, Johannes M.P.J., Linschoten, Marijke P.M., Verlooij, Laura A., Kardys, Isabella, Dooijes, Dennis, Lekanne Deprez, Ronald H., IJpma, Arne S., van den Berg, Maarten P., Hofstra, Robert M.W., van Slegtenhorst, Marjon A., Jongbloed, Jan D.H., Majoor-Krakauer, Danielle

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Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis von Bertoli-Avella, Aida M, van de Laar, Ingrid M B H, Oldenburg, Rogier A, Pals, Gerard, Roos-Hesselink, Jolien W, de Graaf, Bianca M, Verhagen, Judith M A, Hoedemaekers, Yvonne M, Willemsen, Rob, Severijnen, Lies-Anne, Venselaar, Hanka, Vriend, Gert, Pattynama, Peter M, Collée, Margriet, Majoor-Krakauer, Danielle, Poldermans, Don, Frohn-Mulder, Ingrid M E, Micha, Dimitra, Timmermans, Janneke, Hilhorst-Hofstee, Yvonne, Bierma-Zeinstra, Sita M, Willems, Patrick J, Kros, Johan M, Oei, Edwin H G, Oostra, Ben A, Wessels, Marja W

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FLNC Missense Variants in Familial Noncompaction Cardiomyopathy von van Waning, Jaap, Hoedemaekers, Yvonne, te Rijdt, Wouter, Jpma, Arne, Heijsman, Daphne, Caliskan, Kadir, Hoendermis, Elke, Willems, Tineke, van den Wijngaard, Arthur, Suurmeijer, Albert, van Slegtenhorst, Marjon, Jongbloed, Jan, Majoor-Krakauer, Danielle, van der Zwaag, Paul

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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial von van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, Baars, Marieke J H, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke

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Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects von Wessels, Marja W, Herkert, Johanna C, Frohn-Mulder, Ingrid M, Dalinghaus, Michiel, van den Wijngaard, Arthur, de Krijger, Ronald R, Michels, Michelle, de Coo, Irenaeus Fm, Hoedemaekers, Yvonne M, Dooijes, Dennis

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SEPT–GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnostics von Alimohamed, Mohamed Z., Boven, Ludolf G., van Dijk, Krista K., Vos, Yvonne J., Hoedemaekers, Yvonne M., van der Zwaag, Paul A., Sijmons, Rolf H., Jongbloed, Jan D.H., Sikkema-Raddatz, Birgit, Westers, Helga

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Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patients von Alimohamed, Mohamed Z., Johansson, Lennart F., Posafalvi, Anna, Boven, Ludolf G., van Dijk, Krista K., Walters, Lisa, Vos, Yvonne J., Westers, Helga, Hoedemaekers, Yvonne M., Sinke, Richard J., Sijmons, Rolf H., Sikkema-Raddatz, Birgit, Jongbloed, Jan D.H., van der Zwaag, Paul A.

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Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees von van den Heuvel, Lieke M, Huisinga, Mette J, Hoedemaekers, Yvonne M, Baas, Annette F, Plantinga, Mirjam, Henneman, Lidewij, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke

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Functional investigation of two simultaneous or separately segregating DSP variants within a single family supports the theory of a dose‐dependent disease severity von Vermeer, Mathilde C. S. C., Andrei, Daniela, Kramer, Duco, Nijenhuis, Albertine M., Hoedemaekers, Yvonne M., Westers, Helga, Jongbloed, Jan D. H., Pas, Hendri H., Berg, Maarten P., Silljé, Herman H. W., Meer, Peter, Bolling, Maria C.

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Cardiac β-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies von Hoedemaekers, Yvonne M., Caliskan, Kadir, Majoor-Krakauer, Danielle, van de Laar, Ingrid, Michels, Michelle, Witsenburg, Maarten, ten Cate, Folkert J., Simoons, Maarten L., Dooijes, Dennis

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Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy von Nannenberg, Eline A., MD, Michels, Michelle, MD, PhD, Christiaans, Imke, MD, PhD, Majoor-Krakauer, Danielle, MD, PhD, Hoedemaekers, Yvonne M., MD, PhD, van Tintelen, J. Peter, MD, PhD, Lombardi, M. Paola, PhD, ten Cate, Folkert J., MD, PhD, Schinkel, Arend F.L., MD, PhD, Tijssen, Jan G.P., PhD, van Langen, Irene M., MD, PhD, Wilde, Arthur A.M., MD, PhD, Sijbrands, Eric J.G., MD, PhD

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The first titin (c.59926 + 1G > A) founder mutation associated with dilated cardiomyopathy von Hoorntje, Edgar T., van Spaendonck‐Zwarts, Karin Y., te Rijdt, Wouter P., Boven, Ludolf, Vink, Aryan, van der Smagt, Jasper J., Asselbergs, Folkert W., van Wijngaarden, Jan, Hennekam, Eric A., Pinto, Yigal M., Lekanne Deprez, Ronald H., Barge‐Schaapveld, Daniela Q.C.M., Bootsma, Marianne, Regieli, Jakub, Hoedemaekers, Yvonne M., Jongbloed, Jan D.H., van den Berg, Maarten P., van Tintelen, J. Peter

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The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant von Bos, Thomas A., Piers, Sebastiaan R. D., Wessels, Marja W., Houweling, Arjan C., Bökenkamp, Regina, Bootsma, Marianne, Bosman, Laurens P., Evertz, Reinder, Hellebrekers, Debby M. E. I., Hoedemaekers, Yvonne M., Knijnenburg, Jeroen, Lekanne Deprez, Ronald, van Mil, Anneke M., te Riele, Anneline S. J. M., van Slegtenhorst, Marjon A., Wilde, Arthur A. M., Yap, Sing-Chien, Dooijes, Dennis, Koopmann, Tamara T., van Tintelen, J. Peter, Barge-Schaapveld, Daniela Q. C. M.

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