Karin Y. van Spaendonck‐Zwarts

Author

Also Known As

Alexa M. C. Vermeer, Jacqueline Eason, K Y Van Spaendonck-Zwarts, K Y van Spaendonck-Zwarts, K. Y. Van Spaendonck-Zwarts, K. Y. van Spaendonck-Zwarts, K. Y. van Spaendonck‐Zwarts, K.Y. VAN SPAENDONCK‐ZWARTS, K.Y. van Spaendonck-Zwarts, KARIN Y. VAN SPAENDONCK‐ZWARTS

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Groningen University of Groningen Amsterdam UMC Location University of Amsterdam University Medical Center Utrecht University of Amsterdam

About

Karin Y. van Spaendonck‐Zwarts is an author at University Medical Center Groningen specializing in medicine, pathology, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.1K
2	Public Health	3	3	762
3	Biochemistry	1	1	31
4	Biostatistics	1	1	294
5	Genetic Medicine	1	1	294

Karin Y. van Spaendonck‐Zwarts

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Phospholamban R14del Mutation in Patients Diagnosed with Dilated Cardiomyopathy or Arrhythmogenic Right Ventricular Cardiomyopathy: Evidence Supporting the Concept of Arrhythmogenic Cardiomyopathy Paul A. van der Zwaag, Ingrid A.W. van Rijsingen, Angeliki Asimaki, European Journal of Heart Failure	2012	452
Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy Jaap I. van Waning, Kadir Çalişkan, Yvonne M. Hoedemaekers, Journal of the American College of Cardiology CardiomyopathyHeart FailureCardiovascular DiseaseNoncompaction CardiomyopathyGenetic Epidemiology	2018	304
Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics Birgit Sikkema‐Raddatz, Lennart Johansson, Eddy N. de Boer, Human Mutation Exome SequencingGeneticsMutation DetectionGenetic EpidemiologyPathology	2013	294
Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Dirk J. van Veldhuisen, Circulation	2010	243
RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling Maarten M.G. van den Hoogenhof, Abdelaziz Beqqali, Ahmad S. Amin, Circulation	2018	241
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy Karin Y. van Spaendonck‐Zwarts, Anna Pósafalvi, Maarten P. van den Berg, European Heart Journal	2014	216
Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy Joeri A. Jansweijer, Karin Nieuwhof, Francesco Paolo Russo, European Journal of Heart Failure	2016	170
Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene J. Peter van Tintelen, Isabelle C Van Gelder, Angeliki Asimaki, Heart Rhythm CardiomyopathyHeart FailureCardiovascular DiseaseGeneticsGenetic Epidemiology	2009	164
Genetic Analysis in 418 Index Patients with Idiopathic Dilated Cardiomyopathy: Overview of 10 Years’ Experience Karin Y. van Spaendonck‐Zwarts, Ingrid A.W. van Rijsingen, Maarten P. van den Berg, European Journal of Heart Failure	2013	162
Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families Arjan C. Houweling, Lieke Gijezen, Marianne A. Jonker, British Journal of Cancer	2011	162

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