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ir. O. (Jasper) van der Bast

ir. O. (Jasper) van der Bast

Assistant Professor - medical
  • Section Clinical Genetics

Research Programs

Circulatory Health

Research Output (126)

Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations

van der Vis Joanne J., van der Smagt Jasper J., van Batenburg Aernoud A., Goldschmeding Roel, van Es H. Wouter, Grutters Jan C., van Moorsel Coline H.M. Dec 2021, In: Respirology. 26 , p. 1160-1170 11 p.

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

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 13 Oct 2020, In: Genes. 11 , p. 1-12 12 p.

PULMONARY FIBROSIS AND A TERT FOUNDER MUTATION WITH A LATENCY PERIOD OF 300 YEARS

van der Vis Joanne J, van der Smagt Jasper J, Hennekam Frederic A M, Grutters Jan C, van Moorsel Coline H M 18 Apr 2020, In: Chest. 158 , p. 612-619 8 p.

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome

Kummeling Joost, Stremmelaar Diante E., Raun Nicholas, Reijnders Margot R.F., Willemsen Marjolein H., Ruiterkamp-Versteeg Martina, Schepens Marga, Man Calvin C.O., Gilissen Christian, Cho Megan T., McWalter Kirsty, Sinnema Margje, Wheless James W., Simon Marleen E.H., Genetti Casie A., Casey Alicia M., Terhal Paulien A., van der Smagt Jasper J., van Gassen Koen L.I., Joset Pascal, Bahr Angela, Steindl Katharina, Rauch Anita, Keller Elmar, Raas-Rothschild Annick, Koolen David A., Agrawal Pankaj B., Hoffman Trevor L., Powell-Hamilton Nina N., Thiffault Isabelle, Engleman Kendra, Zhou Dihong, Bodamer Olaf, Hoefele Julia, Riedhammer Korbinian M., Schwaibold Eva M.C., Tasic Velibor, Schubert Dirk, Top Deniz, Pfundt Rolph, Higgs Martin R., Kramer Jamie M., Kleefstra Tjitske 1 Jan 2020, In: Molecular Psychiatry. 26 , p. 2013-2024 12 p.

Pulmonary fibrosis linked to variants in the ACD gene, encoding the telomere protein TPP1

Hoffman Thijs W., Van Der Vis Joanne J., Van Der Smagt Jasper J., Massink Maarten P.G., Grutters Jan C., Van Moorsel Coline H.M. 1 Dec 2019, In: European Respiratory Journal. 54

Spectrum of K(V)2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders

Kang Seok Kyu, Vanoye Carlos G., Misra Sunita N., Echevarria Dennis M., Calhoun Jeffrey D., O'Connor John B., Fabre Katarina L., McKnight Dianalee, Demmer Laurie, Goldenberg Paula, Grote Lauren E., Thiffault Isabelle, Saunders Carol, Strauss Kevin A., Torkamani Ali, van der Smagt Jasper, van Gassen Koen, Carson Robert P., Diaz Jullianne, Leon Eyby, Jacher Joseph E., Hannibal Mark C., Litwin Jessica, Friedman Neil R., Schreiber Allison, Lynch Bryan, Poduri Annapurna, Marsh Eric D., Goldberg Ethan M., Millichap John J., George Alfred L., Jr., Kearney Jennifer A. 1 Dec 2019, In: Annals of Neurology. 86 , p. 899-912 14 p.

The Netherlands Arrhythmogenic Cardiomyopathy Registry:design and status update

Bosman L. P., Verstraelen T. E., van Lint F. H.M., Cox M. G.P.J., Groeneweg J. A., Mast T. P., van der Zwaag P. A., Volders P. G.A., Evertz R., Wong L., de Groot N. M.S., Zeppenfeld K., van der Heijden J. F., van den Berg M. P., Wilde A. A.M., Asselbergs F. W., Hauer R. N.W., te Riele A. S.J.M., van Tintelen J. P., Baas A. F., Barge-Schaapveld D. Q.C.M., Boekholdt S. M., Cramer M. J.M., Dooijes D., Jongbloed J. D.H., Loh P., Planken R. N., Prakken N. H.J., van der Smagt J. J., van der Wal A. C., Teske A. J., van Veen T. A.B., Velthuis B. K., Vink A., Yap S. C., 1 Oct 2019, In: Netherlands Heart Journal. 27 , p. 480-486 7 p.

Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo:Segregation and Haplotype Analysis of a Multinational Cohort

van Lint Freyja H M, Murray Brittney, Tichnell Crystal, Zwart Rob, Amat Nuria, Lekanne Deprez Ronald H, Dittmann Sven, Stallmeyer Birgit, Calkins Hugh, van der Smagt Jasper J, van den Wijngaard Arthur, Dooijes Dennis, van der Zwaag Paul A, Schulze-Bahr Eric, Judge Daniel P, Jongbloed Jan D H, van Tintelen J Peter, James Cynthia A 6 Aug 2019, In: Circulation. Genomic and precision medicine. 12

Lack of genotype-phenotype correlation in basal cell nevus syndrome:A Dutch multicenter retrospective cohort study

Cosgun Betül, Reinders Marie G.H.C., van Geel Michel, Steijlen Peter M., van Hout Antonius F.W., Leter Edward M., van der Smagt Jasper J., van Hagen Johanna M., Berger Lieke P.V., Kets C. Marleen, Wagner Anja, Aalfs Cora M., Hes Frederik J., van der Kolk Lizet E., Gille Johan J.P., Mosterd Klara 30 Jul 2019, In: Journal of the American Academy of Dermatology. 83 , p. 604-607 4 p.

Heritability in genetic heart disease:The role of genetic background

Jansweijer Joeri A., Van Spaendonck-Zwarts Karin Y., Tanck Michael W.T., Peter Van Tintelen J., Christiaans Imke, Van Der Smagt Jasper, Vermeer Alexa, Bos J. Martijn, Moss Arthur J., Swan Heikki, Priori Sylvia, Rydberg Annika, Tfelt-Hansen Jacob, Ackerman Michael, Olivotto Iacopo, Charron Philippe, Gimeno Juan R., Van Den Berg Maarten, Wilde Arthur, Pinto Yigal M. 1 May 2019, In: Open Heart. 6 7 p.

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