Roselie Jongbloed - Concepedia

Concepedia

Author

Roselie Jongbloed

Maastricht University

Also Known As

Roselie J Jongbloed, Roselie J. E. Jongbloed, Roselie J. Jongbloed, Roselie J.E. Jongbloed, Roselie Jongbloed

28

Publications

1.1K

Citations

14

H-Index

41

Concepts

All Affiliations

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

RJ

About

Roselie Jongbloed is an author at Maastricht University specializing in medicine, genetics, and cardiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	542
2	Engineering	1	1	32
3	Natural Sciences	1	1	70
4	Cellular Physiology	1	1	40
5	Molecular Biology	1	1	70

Roselie Jongbloed

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14

Publications

1.1K

Citations

14

H-Index

	Year	Citations
Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy J. Peter van Tintelen, Mark M. Entius, Zahurul A. Bhuiyan, Circulation	2006	353
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy Paul A. van der Zwaag, Jan D.H. Jongbloed, Maarten P. van den Berg, Human Mutation CardiomyopathyFunctional GenomicsHereditary CardiomyopathyGeneticsGenetic Variants Database	2009	119
Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients Zahurul A. Bhuiyan, Jan D.H. Jongbloed, Jasper van der Smagt, Circulation Cardiovascular Genetics	2009	91
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies Tamara T. Koopmann, Mariëlle Alders, Roselie Jongbloed, Heart Rhythm Mendelian DisorderGenetic DisorderNatural SciencesGeneticsMolecular Biology	2006	70
Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21 Paul G.A. Volders, Qian Zhu, Carl Timmermans, Heart Rhythm Mendelian DisorderCytogeneticsGenetic DisorderGeneticsFamilial Atrial Fibrillation	2006	63
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome Roselie Jongbloed, Carlo Marcelis, Crool Velter, Human Mutation Cardiac MuscleHeart FailureGeneticsCongenital Heart AnomalyCongenital Heart Defect	2002	61
Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy Roselie Jongbloed, Carlo Marcelis, Pieter A. Doevendans, Journal of the American College of Cardiology CardiomyopathyFamilial Hypertrophic CardiomyopathyGeneticsPathologyCongenital Heart Anomaly	2003	59
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers Judith A. Groeneweg, Paul A. van der Zwaag, Louise R.A. Olde Nordkamp, The American Journal of Cardiology CardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular DiseaseTask Force Criteria	2013	54
A Novel mutation L619F in the cardiac Na channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating Xander H.T. Wehrens, Tom Rossenbacker, Roselie Jongbloed, Human Mutation Steady State InactivationCardiac MuscleGeneticsCellular PhysiologyDefective Inactivation	2003	40
Novel Mutation in the Per-Arnt-Sim Domain of KCNH2 Causes a Malignant Form of Long-QT Syndrome Tom Rossenbacker, Kanigula Mubagwa, Roselie Jongbloed, Circulation	2005	39

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