A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation

por Otten, Ellen, Birnie, Erwin, Ranchor, Adelita V, van Tintelen, J Peter, van Langen, Irene M
Publicado 2015

A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial

por van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke
Publicado 2019

Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant

por Overwater, Eline, Efrat, Rifka, Barge‐Schaapveld, Daniela Q. C. M., Lakeman, Phillis, Weiss, Marjan M., Maugeri, Alessandra, van Tintelen, J. Peter, Houweling, Arjan C.
Publicado 2018

Uptake and Patient Perspectives on Additional Testing for Novel Disease-Associated Genes: Lessons from a PAH Cohort

por Jansen, Samara M. A., van de Heuvel, Lieke M., Houweling, Arjan C., van Tintelen, J. Peter, de Man, Frances S., Vonk Noordegraaf, Anton, Jan Bogaard, Harm
Publicado 2021

Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac Conditions

por van den Heuvel, Lieke M., van Teijlingen, Maxiem O., van der Roest, Wilma, van Langen, Irene M., Smets, Ellen M.A., van Tintelen, J. Peter, Christiaans, Imke
Publicado 2020

Blood‐based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta‐analysis

por Jansen, Mark, Algül, Sila, Bosman, Laurens P., Michels, Michelle, van der Velden, Jolanda, de Boer, Rudolf A., van Tintelen, J. Peter, Asselbergs, Folkert W., Baas, Annette F.
Publicado 2022

Towards a Better Understanding of Genotype–Phenotype Correlations and Therapeutic Targets for Cardiocutaneous Genes: The Importance of Functional Studies above Prediction

por Vermeer, Mathilde C. S. C., Andrei, Daniela, Marsili, Luisa, van Tintelen, J. Peter, Silljé, Herman H. W., van den Berg, Maarten P., van der Meer, Peter, Bolling, Maria C.
Publicado 2022

Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy

por Wasielewski, Marijke, van Spaendonck-Zwarts, Karin Y, Westerink, Nico-Derk L, Jongbloed, Jan D H, Postma, Aleida, Gietema, Jourik A, van Tintelen, J Peter, van den Berg, Maarten P
Publicado 2014

Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants

por Roudijk, Rob W., Bosman, Laurens P., van der Heijden, Jeroen F., de Bakker, Jacques M. T., Hauer, Richard N. W., van Tintelen, J. Peter, Asselbergs, Folkert W., te Riele, Anneline S. J. M., Loh, Peter
Publicado 2020

Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant

por Rumping, Lynne, Wessels, Marja W., Postma, Alex V., van Schuppen, Joost, van Slegtenhorst, Marjon A., Saris, Jasper J., van Tintelen, J. Peter, Robertson, Stephen P., Alders, Mariëlle, Maas, Saskia M., Deprez, Ronald H. Lekanne
Publicado 2021

High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation

por Klauke, Baerbel, Gaertner-Rommel, Anna, Schulz, Uwe, Kassner, Astrid, zu Knyphausen, Edzard, Laser, Thorsten, Kececioglu, Deniz, Paluszkiewicz, Lech, Blanz, Ute, Sandica, Eugen, van den Bogaerdt, Antoon J., van Tintelen, J. Peter, Gummert, Jan, Milting, Hendrik
Publicado 2017

Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional Model

por Gaar-Humphreys, Karen R., Spanjersberg, Talitha C. F., Santarelli, Giorgia, Grinwis, Guy C. M., Szatmári, Viktor, Roelen, Bernard A. J., Vink, Aryan, van Tintelen, J. Peter, Asselbergs, Folkert W., Fieten, Hille, Harakalova, Magdalena, van Steenbeek, Frank G.
Publicado 2022

Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population

por Bourfiss, Mimount, van Vugt, Marion, Alasiri, Abdulrahman I., Ruijsink, Bram, van Setten, Jessica, Schmidt, A. Floriaan, Dooijes, Dennis, Puyol-Antón, Esther, Velthuis, Birgitta K., van Tintelen, J. Peter, te Riele, Anneline S.J.M., Baas, Annette F., Asselbergs, Folkert W.
Publicado 2022

Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy

por Akinrinade, Oyediran, Heliö, Tiina, Lekanne Deprez, Ronald H., Jongbloed, Jan D. H., Boven, Ludolf G., van den Berg, Maarten P., Pinto, Yigal M., Alastalo, Tero-Pekka, Myllykangas, Samuel, Spaendonck-Zwarts, Karin van, van Tintelen, J. Peter, van der Zwaag, Paul A., Koskenvuo, Juha
Publicado 2019

Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy

por Akinrinade, Oyediran, Heliö, Tiina, Lekanne Deprez, Ronald H., Jongbloed, Jan D. H., Boven, Ludolf G., van den Berg, Maarten P., Pinto, Yigal M., Alastalo, Tero-Pekka, Myllykangas, Samuel, van Spaendonck-Zwarts, Karin, van Tintelen, J. Peter, van der Zwaag, Paul A., Koskenvuo, Juha
Publicado 2020

Genetic Evaluation in a Cohort of 126 Dutch Pulmonary Arterial Hypertension Patients

por van den Heuvel, Lieke M., Jansen, Samara M. A., Alsters, Suzanne I. M., Post, Marco C., van der Smagt, Jasper J., Handoko-De Man, Frances S., van Tintelen, J. Peter, Gille, Hans, Christiaans, Imke, Vonk Noordegraaf, Anton, Bogaard, HarmJan, Houweling, Arjan C.
Publicado 2020

Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies

por van der Voorn, Stephanie M., van Drie, Esmée, Proost, Virginnio, Dimitrova, Kristina, Ernst, Robert F., James, Cynthia A., Tichnell, Crystal, Murray, Brittney, Calkins, Hugh, Saguner, Ardan M., Duru, Firat, Ellinor, Patrick T., Bezzina, Connie R., Jurgens, Sean J., van Tintelen, J. Peter, van Veen, Toon A. B.
Publicado 2023

Inflammation Aggravates Disease Severity in Marfan Syndrome Patients

por Radonic, Teodora, de Witte, Piet, Groenink, Maarten, de Waard, Vivian, Lutter, Rene, van Eijk, Marco, Jansen, Marnix, Timmermans, Janneke, Kempers, Marlies, Scholte, Arthur J., Hilhorst-Hofstee, Yvonne, van den Berg, Maarten P., van Tintelen, J. Peter, Pals, Gerard, Baars, Marieke J. H., Mulder, Barbara J. M., Zwinderman, Aeilko H.
Publicado 2012

Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)

por Murray, Brittney, Hoorntje, Edgar T., te Riele, Anneline S. J. M., Tichnell, Crystal, van der Heijden, Jeroen F., Tandri, Harikrishna, van den Berg, Maarten P., Jongbloed, Jan D. H., Wilde, Arthur A. M., Hauer, Richard N. W., Calkins, Hugh, Judge, Daniel P., James, Cynthia A., van Tintelen, J. Peter, Dooijes, Dennis
Publicado 2018

Exercise does not influence development of phenotype in PLN p.(Arg14del) cardiomyopathy

por van Lint, Freyja H. M., Hassanzada, Fahima, Verstraelen, Tom E., Wang, Weijia, Bosman, Laurens P., van der Zwaag, Paul A., Oomen, Toon, Calkins, Hugh, Murray, Brittney, Tichnell, Crystal, Beuren, Thais M. A., Asselbergs, Folkert W., Houweling, Arjan, van den Berg, Maarten P., Wilde, Arthur A. M., James, Cynthia A., van Tintelen, J. Peter
Publicado 2023