The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening by Christiaans, Imke, Birnie, Erwin, van Langen, Irene M., van Spaendonck-Zwarts, Karin Y., van Tintelen, J. Peter, van den Berg, Maarten P., Atsma, Douwe E., Helderman-van den Enden, Apollonia T.J.M., Pinto, Yigal M., Hermans-van Ast, J.F., Bonsel, Gouke J., Wilde, Arthur A.M.

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Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN) by van de Laar, Ingrid M.B.H., Baas, Annette F., De Backer, Julie, Blankenstein, Jan D., Dulfer, Eelco, Helderman-van den Enden, Apollonia T.J.M., Houweling, Arjan C., Kempers, Marlies JE, Loeys, Bart, Malfait, Fransiska, Robert, Leema, Tanteles, George, Frank, Michael

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Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A: sentinel event for evolving dilated cardiomyopathy—a case... by ter Bekke, Rachel M A, de Schouwer, Koen, Conti, Sergio, Claes, Godelieve R F, Vanoevelen, Jo, Gommers, Suzanne, Helderman-van den Enden, Apollonia T J M, Brunner-LaRocca, Hans-Peter

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Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy by Verhagen, Judith M A, Veldman, Job H, van der Zwaag, Paul A, von der Thüsen, Jan H, Brosens, Erwin, Christiaans, Imke, Dooijes, Dennis, Helderman-van den Enden, Apollonia T J M, Lekanne Deprez, Ronald H, Michels, Michelle, van Mil, Anneke M, Oldenburg, Rogier A, van der Smagt, Jasper J, van den Wijngaard, Arthur, Wessels, Marja W, Hofstra, Robert M W, van Slegtenhorst, Marjon A, Jongbloed, Jan D H, van de Laar, Ingrid M B H

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An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy by Helderman-van den Enden, Apollonia T J M, Madan, Kamlesh, Breuning, Martijn H, van der Hout, Annemieke H, Bakker, Egbert, de Die-Smulders, Christine E M, Ginjaar, Hendrika B

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Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms: A family report by Liem, M. K., Lesnik Oberstein, S. A. J., Vollebregt, M. J., Middelkoop, H. A. M., van der Grond, J., Helderman-van den Enden, A. T. J. M.

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An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy by Helderman-van den Enden, Apollonia T J M, Madan, Kamlesh, Breuning, Martijn H, van der Hout, Annemieke H, Bakker, Egbert, de Die-Smulders, Christine E M, Ginjaar, Hendrika B

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Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers by Claes, Godelieve R F, van Tienen, Florence H J, Lindsey, Patrick, Krapels, Ingrid P C, Helderman-van den Enden, Apollonia T J M, Hoos, Marije B, Barrois, Yvette E G, Janssen, Johanna W H, Paulussen, Aimée D C, Sels, Jan-Willem E M, Kuijpers, Simone H H, van Tintelen, J Peter, van den Berg, Maarten P, Heesen, Wilfred F, Garcia-Pavia, Pablo, Perrot, Andreas, Christiaans, Imke, Salemink, Simone, Marcelis, Carlo L M, Smeets, Hubert J M, Brunner, Han G, Volders, Paul G A, van den Wijngaard, Arthur

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Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: deter... by Christiaans, Imke, Birnie, Erwin, Bonsel, Gouke J, Mannens, Marcel M A M, Michels, Michelle, Majoor-Krakauer, Daniëlle, Dooijes, Dennis, van Tintelen, J Peter, van den Berg, Maarten P, Volders, Paul G A, Arens, Yvonne H, van den Wijngaard, Arthur, Atsma, Douwe E, Helderman-van den Enden, Apollonia T J M, Houweling, Arjan C, de Boer, Karin, van der Smagt, Jasper J, Hauer, Richard N W, Marcelis, Carlo L M, Timmermans, Janneke, van Langen, Irene M, Wilde, Arthur A M

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A near false-negative finding of mosaic trisomy 21-a cautionary tale by Beverstock, G. C., Hansson, Kerstin, Helderman-Van Den Enden, Apollonia T. J. M., Bröcker-Vriends, Annette, Klumper, F., Bartelings, Margot, Dobbe-Van Meerendonk, Willemijn, Roosmalen, J. V., Kolkman, P. H., Kanhai, H. H. H.

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Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A: sentinel event for evolving dilated cardiomyopathy-a case... by Ter Bekke, Rachel M A, de Schouwer, Koen, Conti, Sergio, Claes, Godelieve R F, Vanoevelen, Jo, Gommers, Suzanne, Helderman-van den Enden, Apollonia T J M, Brunner-LaRocca, Hans-Peter

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Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms: a family report by Liem, Michael K, Lesnik Oberstein, Saskia A J, Vollebregt, Magdalena J, Middelkoop, Huub A M, van der Grond, Jeroen, Helderman-van den Enden, Apollonia T J M

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Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study by Bancroft, Elizabeth K, Page, Elizabeth C, Castro, Elena, Lilja, Hans, Vickers, Andrew, Sjoberg, Daniel, Assel, Melissa, Foster, Christopher S, Drew, Kate, Mæhle, Lovise, Axcrona, Karol, Evans, D. Gareth, Bulman, Barbara, Eccles, Diana, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A, Ringelberg, Janneke, Cybulski, Cezary, Wokolorczyk, Dominika, Selkirk, Christina, Hulick, Peter J, Bojesen, Anders, Skytte, Anne-Bine, Lam, Jimmy, Taylor, Louise, Oldenburg, Rogier, Verhaegh, Gerald, van Zelst-Stams, Wendy A, Oosterwijk, Jan C, Blanco, Ignacio, Salinas, Monica, Cook, Jackie, Rosario, Derek J, Buys, Saundra, Conner, Tom, Ausems, Margreet G, Ong, Kai-ren, Hoffman, Jonathan, Domchek, Susan, Teixeira, Manuel R, Maia, Sofia, Foulkes, William D, Taherian, Nassim, Ruijs, Marielle, den Enden, Apollonia T. Helderman-van, Izatt, Louise, Davidson, Rosemarie, Adank, Muriel A, Walker, Lisa, Schmutzler, Rita, Tucker, Kathy, Kirk, Judy, Hodgson, Shirley, Harris, Marion, Douglas, Fiona, Lindeman, Geoffrey J, Zgajnar, Janez, Tischkowitz, Marc, Susman, Rachel, Ramón y Cajal, Teresa, Patcher, Nicholas, Spigelman, Allan, Liljegren, Annelie, Side, Lucy, Brewer, Carole, Donaldson, Alan, Stefansdottir, Vigdis, Chen-Shtoyerman, Rakefet, Amor, David J, Barwell, Julian, Giri, Veda N, Murthy, Vedang, Nicolai, Nicola, Teo, Soo-Hwang, Greenhalgh, Lynn, Strom, Sara, Henderson, Alex, McGrath, John, Gallagher, David, Aaronson, Neil, Ardern-Jones, Audrey, Bangma, Chris, Dearnaley, David, Eyfjord, Jorunn, Rothwell, Jeanette, Falconer, Alison, Gronberg, Henrik, Johannsson, Oskar, Kote-Jarai, Zsofia, Axcrona, Ulrika, Melia, Jane, McKinley, Joanne, Mitra, Anita V, Moynihan, Clare, Rennert, Gad, Suri, Mohnish, Wilson, Penny, Killick, Emma, Moss, Sue

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Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers by Page, Elizabeth C., Bancroft, Elizabeth K., Brook, Mark N., Assel, Melissa, Hassan Al Battat, Mona, Thomas, Sarah, Taylor, Natalie, Raghallaigh, Holly Ni, Evans, D. Gareth, Maehle, Lovise, Grindedal, Eli Marie, James, Paul, Mascarenhas, Lyon, McKinley, Joanne, Thomas, Tessy, van Asperen, Christi, Vasen, Hans, Kiemeney, Lambertus A., Ringelberg, Janneke, Jensen, Thomas Dyrsø, Osther, Palle J.S., Helfand, Brian T., Genova, Elena, Oldenburg, Rogier A., Cybulski, Cezary, Ong, Kai-Ren, Lam, Jimmy, Taylor, Louise, Feliubadaló, Lidia, van Zelst-Stams, Wendy, Rosario, Derek J., Domchek, Susan, Powers, Jacquelyn, Buys, Saundra, O'Toole, Karen, Ausems, Margreet G.E.M., Schmutzler, Rita K., Rhiem, Kerstin, Izatt, Louise, Cardoso, Marta, Aprikian, Armen, van Randeraad, Heleen, Davidson, Rosemarie, Longmuir, Mark, Helderman van den Enden, Apollonia T.J.M., Adank, Muriel, Williams, Rachel, Andrews, Lesley, Murphy, Declan G., Halliday, Dorothy, Walker, Lisa, Liljegren, Annelie, Carlsson, Stefan, Morton, Catherine, Snape, Katie, Hanson, Helen, Tischkowitz, Marc, Taylor, Amy, Kirk, Judy, Susman, Rachel, Chen-Shtoyerman, Rakefet, Spigelman, Allan, Pachter, Nicholas, Ahmed, Munaza, Ramon y Cajal, Teresa, Brewer, Carole, Gadea, Neus, van Os, Theo, Gallagher, David, Johannsson, Oskar, Barwell, Julian, Nicolai, Nicola, Friedman, Eitan, Greenhalgh, Lynn, Murthy, Vedang, Saya, Sibel, McGrath, John, Rønlund, Karina, Teo, Soo H., Kast, Karin, Aaronson, Neil K., Ardern-Jones, Audrey, Bangma, Chris H., Dearnaley, David, Tricker, Karen, Eyfjord, Jorunn, Falconer, Alison, Foster, Christopher, Gronberg, Henrik, Hamdy, Freddie C., Stefansdottir, Vigdis, Khoo, Vincent, Lindeman, Geoffrey J., Lubinski, Jan, Mikropoulos, Christos, Mitra, Anita, Moynihan, Clare, Wilson, Penny, Dudderidge, Tim, Offman, Judith

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Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy by Stroeks, Sophie L V M, Hellebrekers, Debby, Claes, Godelieve R F, Krapels, Ingrid P C, Henkens, Michiel H T M, Sikking, Maurits, Vanhoutte, Els K, Helderman-van den Enden, Apollonia, Brunner, Han G, van den Wijngaard, Arthur, Verdonschot, Job A J

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