Beauty and the beat: A complicated case of multifocal ectopic Purkinje-related premature contractions

by ter Bekke, Rachel M.A., David, Miren, Krapels, Ingrid P.C., Crijns, Harry J.G.M., Volders, Paul G.A.
Published 2018

A global longitudinal strain cut‐off value to predict adverse outcomes in individuals with a normal ejection fraction

by Verdonschot, Job A.J., Henkens, Michiel T.H.M., Wang, Ping, Schummers, Georg, Raafs, Anne G., Krapels, Ingrid P.C., van Empel, Vanessa, Heymans, Stephane R.B., Brunner‐La Rocca, Hans‐Peter, Knackstedt, Christian
Published 2021

The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification

by Becker, Lena-Luise, Dafsari, Hormos Salimi, Schallner, Jens, Abdin, Dalia, Seifert, Michael, Petit, Florence, Smol, Thomas, Bok, Levinus, Rodan, Lance, Krapels, Ingrid, Spranger, Stephanie, Weschke, Bernhard, Johnson, Katherine, Straub, Volker, Kaindl, Angela M., Di Donato, Nataliya, von der Hagen, Maja, Cirak, Sebahattin
Published 2020

Clustering of Cardiac Transcriptome Profiles Reveals Unique: Subgroups of Dilated Cardiomyopathy Patients

by Verdonschot, Job A.J., Wang, Ping, Derks, Kasper W.J., Adriaens, Michiel E., Stroeks, Sophie L.V.M., Henkens, Michiel T.H.M., Raafs, Anne G., Sikking, Maurits, de Koning, Bart, van den Wijngaard, Arthur, Krapels, Ingrid P.C., Nabben, Miranda, Brunner, Han G., Heymans, Stephane R.B.
Published 2023

Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers

by Verdonschot, Job A. J., Robinson, Emma L., James, Kiely N., Mohamed, Mohamed W., Claes, Godelieve R. F., Casas, Kari, Vanhoutte, Els K., Hazebroek, Mark R., Kringlen, Gabriel, Pasierb, Michele M., van den Wijngaard, Arthur, Glatz, Jan F. C., Heymans, Stephane R. B., Krapels, Ingrid P. C., Nahas, Shareef, Brunner, Han G., Szklarczyk, Radek
Published 2019

Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

by Verdonschot, Job A J, Merlo, Marco, Dominguez, Fernando, Wang, Ping, Henkens, Michiel T H M, Adriaens, Michiel E, Hazebroek, Mark R, Masè, Marco, Escobar, Luis E, Cobas-Paz, Rafael, Derks, Kasper W J, van den Wijngaard, Arthur, Krapels, Ingrid P C, Brunner, Han G, Sinagra, Gianfranco, Garcia-Pavia, Pablo, Heymans, Stephane R B
Published 2020

Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships

by Lauffer, Peter, Pals, Gerard, Zwinderman, Aeilko H., Postema, Floor A. M., Baars, Marieke J. H., Dulfer, Eelco, Hilhorst‐Hofstee, Yvonne, Houweling, Arjan C., Kempers, Marlies, Krapels, Ingrid P. C., van de Laar, Ingrid M. B. H., Loeys, Bart, Spaans, Alexander M. J., Warnink‐Kavelaars, Jessica, de Waard, Vivian, Wit, Jan M., Menke, Leonie A.
Published 2022

The Maastricht Acquisition Platform for Studying Mechanisms of Cell–Matrix Crosstalk (MAPEX): An Interdisciplinary and Systems Approach towards Understanding Thoracic Aortic Diseas...

by Ganizada, Berta H., Reesink, Koen D., Parikh, Shaiv, Ramaekers, Mitch J. F. G., Akbulut, Asim C., Saraber, Pepijn J. M. H., Debeij, Gijs P., Jaminon, Armand M., Natour, Ehsan, Lorusso, Roberto, Wildberger, Joachim E., Mees, Barend, Schurink, Geert Willem, Jacobs, Michael J., Cleutjens, Jack, Krapels, Ingrid, Gombert, Alexander, Maessen, Jos G., Accord, Ryan, Delhaas, Tammo, Schalla, Simon, Schurgers, Leon J., Bidar, Elham
Published 2023

Results of next‐generation sequencing gene panel diagnostics including copy‐number variation analysis in 810 patients suspected of heritable thoracic aortic disorders

by Overwater, Eline, Marsili, Luisa, Baars, Marieke J.H., Baas, Annette F., van de Beek, Irma, Dulfer, Eelco, van Hagen, Johanna M., Hilhorst‐Hofstee, Yvonne, Kempers, Marlies, Krapels, Ingrid P., Menke, Leonie A., Verhagen, Judith M.A., Yeung, Kak K., Zwijnenburg, Petra J.G., Groenink, Maarten, van Rijn, Peter, Weiss, Marjan M., Voorhoeve, Els, van Tintelen, J. Peter, Houweling, Arjan C., Maugeri, Alessandra
Published 2018

The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview

by Verheul, Lisa M, van der Ree, Martijn H, Groeneveld, Sanne A, Mulder, Bart A, Christiaans, Imke, Kapel, Gijs F L, Alings, Marco, Bootsma, Marianne, Barge-Schaapveld, Daniela Q C M, Balt, Jippe C, Yap, Sing-Chien, Krapels, Ingrid P C, Ter Bekke, Rachel M A, Volders, Paul G A, van der Crabben, Saskia N, Postema, Pieter G, Wilde, Arthur A M, Dooijes, Dennis, Baas, Annette F, Hassink, Rutger J
Published 2023

Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR

by Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Christel, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric
Published 2012

A mutation update for the FLNC gene in myopathies and cardiomyopathies

by Verdonschot, Job A. J., Vanhoutte, Els K., Claes, Godelieve R. F., Helderman‐van den Enden, Apollonia T. J. M., Hoeijmakers, Janneke G. J., Hellebrekers, Debby M. E. I., de Haan, Amber, Christiaans, Imke, Lekanne Deprez, Ronald H., Boen, Hanne M., van Craenenbroeck, Emeline M., Loeys, Bart L., Hoedemaekers, Yvonne M., Marcelis, Carlo, Kempers, Marlies, Brusse, Esther, van Waning, Jaap I., Baas, Annette F., Dooijes, Dennis, Asselbergs, Folkert W., Barge‐Schaapveld, Daniela Q. C. M., Koopman, Pieter, van den Wijngaard, Arthur, Heymans, Stephane R. B., Krapels, Ingrid P. C., Brunner, Han G.
Published 2020

Improving diagnosis and risk stratification across the ejection fraction spectrum: the Maastricht Cardiomyopathy registry

by Henkens, Michiel T.H.M., Weerts, Jerremy, Verdonschot, Job A.J., Raafs, Anne G., Stroeks, Sophia, Sikking, Maurits A., Amin, Hesam, Mourmans, Sanne G.J., Geraeds, Chrit B.G., Sanders‐van Wijk, Sandra, Barandiarán Aizpurua, Arantxa, Uszko‐Lencer, Nicole H.M.K., Krapels, Ingrid P.C., Wolffs, Petra F.G., Brunner, Han G., van Leeuwen, Rick E.W., Verhesen, Wouter, Schalla, Simon M., van Stipdonk, Antonius W.M., Knackstedt, Christian, Li, Xiaofei, Abdul Hamid, Myrurgia A., van Paassen, Pieter, Hazebroek, Mark R., Vernooy, Kevin, Brunner‐La Rocca, Hans‐Peter, van Empel, Vanessa P.M., Heymans, Stephane R.B.
Published 2022

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

by 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, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M., 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 T., Ortuño, Cristina Gil, 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, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël P., 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 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., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Ackerman, Michael J., Brugada, Ramon, 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, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.
Published 2020