Implantable loop recorders in patients with heart disease: comparison between patients with and without syncope

por Assaf, Amira, Sakhi, Rafi, Michels, Michelle, Roos-Hesselink, Jolien W, Verhagen, Judith M A, Bhagwandien, Rohit E, Szili-Torok, Tamas, Theuns, Dominic, Yap, Sing-Chien
Publicado 2021

Novel Morphological Features on CMR for the Prediction of Pathogenic Sarcomere Gene Variants in Subjects Without Hypertrophic Cardiomyopathy

por van der Velde, Nikki, Huurman, Roy, Hassing, H. Carlijne, Budde, Ricardo P. J., van Slegtenhorst, Marjon A., Verhagen, Judith M. A., Schinkel, Arend F. L., Michels, Michelle, Hirsch, Alexander
Publicado 2021

Contemporary family screening in hypertrophic cardiomyopathy: the role of cardiovascular magnetic resonance( )

por Huurman, Roy, van der Velde, Nikki, Schinkel, Arend F L, Hassing, H Carlijne, Budde, Ricardo P J, van Slegtenhorst, Marjon A, Verhagen, Judith M A, Hirsch, Alexander, Michels, Michelle
Publicado 2022

Prognostic significance of left atrial strain in sarcomere gene variant carriers without hypertrophic cardiomyopathy

por Huurman, Roy, Bowen, Daniel J., Mutluer, Ferit O., Loff Barreto, Bernardo, van Slegtenhorst, Marjon A., Verhagen, Judith M. A., Hirsch, Alexander, van den Bosch, Annemien E., Michels, Michelle, Schinkel, Arend F. L.
Publicado 2022

Abnormal Aortic Wall Properties in Women with Turner Syndrome

por Bons, Lidia R., Van Den Hoven, Allard T., Malik, Maira, Van Den Bosch, Annemien E., McGhie, Jacky S., Duijnhouwer, Anthonie L., Siebelink, Hans-Marc J., Hirsch, Alexander, Devos, Daniel H., Rietzschel, Ernst, von der Thüsen, Jan H., van de Laar, Ingrid M.B.H., Verhagen, Judith M.A., van der Pluijm, Ingrid, Budde, Ricardo P.J., Roos-Hesselink, Jolien W.
Publicado 2020

Biallelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organization

por Ruijmbeek, Claudine W.B., Housley, Filomena, Idrees, Hafiza, Housley, Michael P., Pestel, Jenny, Keller, Leonie, Lai, Jason K.H., van der Linde, Herma C., Willemsen, Rob, Piesker, Janett, Al-Hassnan, Zuhair N., Almesned, Abdulrahman, Dalinghaus, Michiel, van den Bersselaar, Lisa M., van Slegtenhorst, Marjon A., Tessadori, Federico, Bakkers, Jeroen, van Ham, Tjakko J., Stainier, Didier Y.R., Verhagen, Judith M.A., Reischauer, Sven
Publicado 2023

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

por 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
Publicado 2018

Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic Disease

por Verhagen, Judith M. A., Burger, Joyce, Bekkers, Jos A., den Dekker, Alexander T., von der Thüsen, Jan H., Zajec, Marina, Brüggenwirth, Hennie T., van der Sterre, Marianne L. T., van den Born, Myrthe, Luider, Theo M., van IJcken, Wilfred F. J., Wessels, Marja W., Essers, Jeroen, Roos-Hesselink, Jolien W., van der Pluijm, Ingrid, van de Laar, Ingrid M. B. H., Brosens, Erwin
Publicado 2021

Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy

por 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.
Publicado 2018

Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification

por van der Meulen, Marijke H., Herkert, Johanna C., den Boer, Susanna L., du Marchie Sarvaas, Gideon J., Blom, Nico A., ten Harkel, Arend D.J., Breur, Hans M.P.J., Rammeloo, Lukas A.J., Tanke, Ronald B., Marcelis, Carlo, van de Laar, Ingrid M.B.H., Verhagen, Judith M.A., Lekanne dit Deprez, Ronald H., Barge-Schaapveld, Daniela Q.C.M., Baas, Annette F., Sammani, Arjan, Christiaans, Imke, van Tintelen, J. Peter, Dalinghaus, Michiel
Publicado 2022

Biallelic Variants in ASNA1, Encoding a Cytosolic Targeting Factor of Tail-Anchored Proteins, Cause Rapidly Progressive Pediatric Cardiomyopathy

por Verhagen, Judith M.A., van den Born, Myrthe, van der Linde, Herma C., G.J. Nikkels, Peter, Verdijk, Rob M., Kivlen, Maryann H., van Unen, Leontine M.A., Baas, Annette F., ter Heide, Henriette, van Osch-Gevers, Lennie, Hoogeveen-Westerveld, Marianne, Herkert, Johanna C., Bertoli-Avella, Aida M., van Slegtenhorst, Marjon A., Wessels, Marja W., Verheijen, Frans W., Hassel, David, Hofstra, Robert M.W., Hegde, Ramanujan S., van Hasselt, Peter M., van Ham, Tjakko J., van de Laar, Ingrid M.B.H.
Publicado 2019

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor

por Gillis, Elisabeth, Kumar, Ajay A., Luyckx, Ilse, Preuss, Christoph, Cannaerts, Elyssa, van de Beek, Gerarda, Wieschendorf, Björn, Alaerts, Maaike, Bolar, Nikhita, Vandeweyer, Geert, Meester, Josephina, Wünnemann, Florian, Gould, Russell A., Zhurayev, Rustam, Zerbino, Dmytro, Mohamed, Salah A., Mital, Seema, Mertens, Luc, Björck, Hanna M., Franco-Cereceda, Anders, McCallion, Andrew S., Van Laer, Lut, Verhagen, Judith M. A., van de Laar, Ingrid M. B. H., Wessels, Marja W., Messas, Emmanuel, Goudot, Guillaume, Nemcikova, Michaela, Krebsova, Alice, Kempers, Marlies, Salemink, Simone, Duijnhouwer, Toon, Jeunemaitre, Xavier, Albuisson, Juliette, Eriksson, Per, Andelfinger, Gregor, Dietz, Harry C., Verstraeten, Aline, Loeys, Bart L.
Publicado 2017

Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor

por Gillis, Elisabeth, Kumar, Ajay A., Luyckx, Ilse, Preuss, Christoph, Cannaerts, Elyssa, van de Beek, Gerarda, Wieschendorf, Björn, Alaerts, Maaike, Bolar, Nikhita, Vandeweyer, Geert, Meester, Josephina, Wünnemann, Florian, Gould, Russell A., Zhurayev, Rustam, Zerbino, Dmytro, Mohamed, Salah A., Mital, Seema, Mertens, Luc, Björck, Hanna M., Franco-Cereceda, Anders, McCallion, Andrew S., Van Laer, Lut, Verhagen, Judith M. A., van de Laar, Ingrid M. B. H., Wessels, Marja W., Messas, Emmanuel, Goudot, Guillaume, Nemcikova, Michaela, Krebsova, Alice, Kempers, Marlies, Salemink, Simone, Duijnhouwer, Toon, Jeunemaitre, Xavier, Albuisson, Juliette, Eriksson, Per, Andelfinger, Gregor, Dietz, Harry C., Verstraeten, Aline, Loeys, Bart L.
Publicado 2017

Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

por Bertoli-Avella, Aida M., Gillis, Elisabeth, Morisaki, Hiroko, Verhagen, Judith M.A., de Graaf, Bianca M., van de Beek, Gerarda, Gallo, Elena, Kruithof, Boudewijn P.T., Venselaar, Hanka, Myers, Loretha A., Laga, Steven, Doyle, Alexander J., Oswald, Gretchen, van Cappellen, Gert W.A., Yamanaka, Itaru, van der Helm, Robert M., Beverloo, Berna, de Klein, Annelies, Pardo, Luba, Lammens, Martin, Evers, Christina, Devriendt, Koenraad, Dumoulein, Michiel, Timmermans, Janneke, Bruggenwirth, Hennie T., Verheijen, Frans, Rodrigus, Inez, Baynam, Gareth, Kempers, Marlies, Saenen, Johan, Van Craenenbroeck, Emeline M., Minatoya, Kenji, Matsukawa, Ritsu, Tsukube, Takuro, Kubo, Noriaki, Hofstra, Robert, Goumans, Marie Jose, Bekkers, Jos A., Roos-Hesselink, Jolien W., van de Laar, Ingrid M.B.H., Dietz, Harry C., Van Laer, Lut, Morisaki, Takayuki, Wessels, Marja W., Loeys, Bart L.
Publicado 2015