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prof. dr. J.P. (Peter) van Tintelen

prof. dr. J.P. (Peter) van Tintelen

Full Professor
prof. dr. J.P. (Peter) van Tintelen
  • Department of Genetics

Side Activities

board member, Stichting Cardiomyopathie-Onderzoek Nederland

clinical geneticist, Department Veterinary Medicine, Utrecht University

member supervisory board, Stichting LEEFH (Landelijk Expertisecentrum Erfelijkheidsonderzoek, Familiaire Hart- en Vaatziekten)

Chair, Vereniging Stichtingen Klinische Genetica

member Advisory Board, Hartenbank (Cardiac Tissue Repository), Netherlands Heart Institute

medical advisor, Marfan Syndrome Patient Organization Netherlands

Research Output (191)

Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in Arrhythmogenic Right Ventricular Cardiomyopathy:A Multinational Study

Gasperetti Alessio, Carrick Richard T, Costa Sarah, Compagnucci Paolo, Bosman Laurens P, Chivulescu Monica, Tichnell Crystal, Murray Brittney, Tandri Harikrishna, Tadros Rafik, Rivard Lena, van den Berg Maarten P, Zeppenfeld Katja, Wilde Arthur A M, Pompilio Giulio, Carbucicchio Corrado, Dello Russo Antonio, Casella Michela, Svensson Anneli, Brunckhorst Corinna, van Tintelen Peter, Platonov Pyotr G, Haugaa Kristina, Duru Firat, Te Riele Anneline S J M, Khairy Paul, Tondo Claudio, Calkins Hugh, James Cynthia A, Saguner Ardan M, Cadrin-Tourigny Julia 7 Oct 2022, In: Circulation. 146 , p. 1434-1443 10 p.

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

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 1 Jul 2022, In: Animals : an open access journal from MDPI. 12 , p. 1-18

A polymorphism in Histidine-Rich Calcium Binding Protein as second hit in Phospholamban Cardiomyopathy

Van der Voorn S. M., Dimitrova K., Van Drie E., Bourfiss M., Taha K., De Brouwer R., Verstraelen T. E., De Boer R. A., Asselbergs F. W., Van Tintelen J. P., Van Veen T. A. B. 10 Jun 2022, In: Cardiovascular research. 118

Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathy

de Brouwer Remco, Bosman Laurens P, Gripenstedt Sophia, Wilde Arthur A M, van den Berg Maarten P, van Tintelen J Peter, de Boer Rudolf A, Te Riele Anneline S J M, 7 Jun 2022, In: Heart Rhythm. 19 , p. 1659-1665 7 p.

Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members

Mittal Nishka, Dave Jaydev, Harakalova Magdalena, van Tintelen J. Peter, Asselbergs Folkert W., Doevendans Pieter A., Costa Kevin D., Turnbull Irene C., Stillitano Francesca Apr 2022, In: Stem Cell Research. 60 , p. 1-5

Echocardiographic Deformation Imaging for Early Detection of Genetic Cardiomyopathies:JACC Review Topic of the Week

Taha Karim, Kirkels Feddo P., Teske Arco J., Asselbergs Folkert W., van Tintelen J. Peter, Doevendans Pieter A., Kutty Shelby, Haugaa Kristina H., Cramer Maarten J. 15 Feb 2022, In: Journal of the American College of Cardiology. 79 , p. 594-608 15 p.

Integrating Exercise Into Personalized Ventricular Arrhythmia Risk Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy

Bosman Laurens P, Wang Weijia, Lie Øyvind H, van Lint Freyja H M, Rootwelt-Norberg Christine, Murray Brittney A, Tichnell Crystal, Cadrin-Tourigny Julia, van Tintelen J Peter, Asselbergs Folkert W, Calkins Hugh, Te Riele Anneline S J M, Haugaa Kristina H, James Cynthia A 28 Jan 2022, In: Circulation. Arrhythmia and electrophysiology. 15 , p. 85-93

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

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 Dec 2021, In: American Journal of Medical Genetics. Part A. 185 , p. 3814-3820 7 p.

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

Gigli Marta, Stolfo Davide, Graw Sharon L, Merlo Marco, Gregorio Caterina, Nee Chen Suet, Dal Ferro Matteo, PaldinoMD Alessia, De Angelis Giulia, Brun Francesca, Jirikowic Jean, Salcedo Ernesto E, Turja Sylvia, Fatkin Diane, Johnson Renee, van Tintelen J Peter, Te Riele Anneline S J M, Wilde Arthur A M, Lakdawala Neal K, Picard Kermshlise, Miani Daniela, Muser Daniele, Maria Severini Giovanni, Calkins Hugh, James Cynthia A, Murray Brittney, Tichnell Crystal, Parikh Victoria N, Ashley Euan A, Reuter Chloe, Song Jiangping, Judge Daniel P, McKenna William J, Taylor Matthew R G, Sinagra Gianfranco, Mestroni Luisa 16 Nov 2021, In: Circulation. 144 , p. 1600-1611 12 p.

Uptake and patient perspectives on additional testing for novel disease-associated genes:Lessons from a pah cohort

Jansen Samara M.A., van de Heuvel Lieke M., Houweling Arjan C., Peter van Tintelen J., de Man Frances S., Noordegraaf Anton Vonk, Bogaard Harm Jan 28 Sep 2021, In: Genes. 12

All research output

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