Roselie Jongbloed

1.1k total citations
18 papers, 820 citations indexed

About

Roselie Jongbloed is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Orthopedics and Sports Medicine. According to data from OpenAlex, Roselie Jongbloed has authored 18 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cardiology and Cardiovascular Medicine, 10 papers in Molecular Biology and 4 papers in Orthopedics and Sports Medicine. Recurrent topics in Roselie Jongbloed's work include Cardiac electrophysiology and arrhythmias (11 papers), Ion channel regulation and function (8 papers) and Cardiovascular Effects of Exercise (5 papers). Roselie Jongbloed is often cited by papers focused on Cardiac electrophysiology and arrhythmias (11 papers), Ion channel regulation and function (8 papers) and Cardiovascular Effects of Exercise (5 papers). Roselie Jongbloed collaborates with scholars based in Netherlands, Belgium and Czechia. Roselie Jongbloed's co-authors include Pieter A. Doevendans, J. Peter van Tintelen, Arthur A.M. Wilde, Robert M.W. Hofstra, Marcel M. A. M. Mannens, Richard N.W. Hauer, Ans C.P. Wiesfeld, Luz‐Maria Rodriguez, Joep Geraedts and Zahurul A. Bhuiyan and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and The American Journal of Cardiology.

In The Last Decade

Roselie Jongbloed

18 papers receiving 808 citations

Peers

Countries citing papers authored by Roselie Jongbloed

Since Specialization

Citations

This map shows the geographic impact of Roselie Jongbloed's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Roselie Jongbloed with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roselie Jongbloed more than expected).

Fields of papers citing papers by Roselie Jongbloed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roselie Jongbloed. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Roselie Jongbloed. The network helps show where Roselie Jongbloed may publish in the future.

Co-authorship network of co-authors of Roselie Jongbloed

This figure shows the co-authorship network connecting the top 25 collaborators of Roselie Jongbloed. A scholar is included among the top collaborators of Roselie Jongbloed based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Roselie Jongbloed. Roselie Jongbloed is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation 2014 ·Cardiovascular Research ·Roel L. H. M. G. Spätjens, Markéta Bébarová, Sandrine Seyen, (unknown), Roselie Jongbloed, Yvonne Arens, Jordi Heijman, Paul G.A. Volders	7
2	Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers 2013 ·The American Journal of Cardiology ·Judith A. Groeneweg, Paul A. van der Zwaag, Louise R.A. Olde Nordkamp, Hennie Bikker, Jan D.H. Jongbloed, Roselie Jongbloed, Ans C.P. Wiesfeld, Moniek G.P.J. Cox, Jeroen F. van der Heijden, Douwe E. Atsma, Karin Boer, Pieter A. Doevendans, Aryan Vink, Toon A.B. van Veen, Dennis Dooijes, Maarten P. van den Berg, Arthur A.M. Wilde, J. Peter van Tintelen, Richard N.W. Hauer	39
3	A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy 2009 ·Human Mutation ·Paul A. van der Zwaag, Jan D.H. Jongbloed, Maarten P. van den Berg, Jasper J. van der Smagt, Roselie Jongbloed, Hennie Bikker, Robert M.W. Hofstra, J. Peter van Tintelen	90
4	Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients 2009 ·Circulation Cardiovascular Genetics ·Zahurul A. Bhuiyan, Jan D.H. Jongbloed, Jasper van der Smagt, (unknown), Ans C.P. Wiesfeld, Marcel Nelen, Meyke Schouten, Roselie Jongbloed, Moniek G.P.J. Cox, Marleen van Wolferen, Luz M. Rodriguez, Isabelle C. Van Gelder, Hennie Bikker, Albert J.H. Suurmeijer, Maarten P. van den Berg, Marcel M. A. M. Mannens, Richard N.W. Hauer, Arthur A.M. Wilde, J. Peter van Tintelen	73
5	Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation 2008 ·American Journal of Physiology-Heart and Circulatory Physiology ·Markéta Bébarová, Tom O’Hara, J. L. M. C. Geelen, Roselie Jongbloed, Carl Timmermans, Yvonne Arens, Luz‐Maria Rodriguez, Yoram Rudy, Paul G.A. Volders	27
6	Genetische identificatie van patiënten en families met lange-QT-syndroom: Grote regionale verschillen in de resultaten van 10 jaar 2007 ·Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank ·(unknown), Pieter G. Postema, Irene M. van Langen, Eline A. Nannenberg, Mariëlle Alders, Roselie Jongbloed, H. Smeets, Arthur A.M. Wilde	3
7	Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients 2006 ·Genetics in Medicine ·(unknown), Mike Gerards, Lars Eijssen, Alexandra T.M. Hendrickx, Roselie Jongbloed, John H. J. Wokke, Rogier Q. Hintzen, (unknown), I.F.M. de Coo, Egill Briem, Valeria Tiranti, Hubert J.M. Smeets	28
8	Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21 2006 ·Heart Rhythm ·Paul G.A. Volders, Qian Zhu, Carl Timmermans, Petra M.H. Eurlings, Xiaoyan Su, Yvonne Arens, Li Li, Roselie Jongbloed, Min Xia, Luz‐Maria Rodriguez, (unknown)	37
9	Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies 2006 ·Heart Rhythm ·Tamara T. Koopmann, Mariëlle Alders, Roselie Jongbloed, (unknown), Marcel M. A. M. Mannens, Arthur A.M. Wilde, Connie R. Bezzina	49
10	Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 2006 ·Circulation ·J. Peter van Tintelen, Mark M. Entius, Zahurul A. Bhuiyan, Roselie Jongbloed, Ans C.P. Wiesfeld, Arthur A.M. Wilde, Jasper van der Smagt, Ludolf G. Boven, Marcel M. A. M. Mannens, Irene M. van Langen, Robert M.W. Hofstra, Luuk Otterspoor, Pieter A. Doevendans, Luz‐Maria Rodriguez, Isabelle C. Van Gelder, Richard N.W. Hauer	266
11	Novel Mutation in the Per-Arnt-Sim Domain of KCNH2 Causes a Malignant Form of Long-QT Syndrome 2005 ·Circulation ·Tom Rossenbacker, Kanigula Mubagwa, Roselie Jongbloed, Johan Vereecke, Koenraad Devriendt, Marc Gewillig, Edward Carmeliet, Désiré Collen, Hein Heidbüchel, Peter Carmeliet	33
12	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 2003 ·Human Mutation ·Xander H.T. Wehrens, Tom Rossenbacker, Roselie Jongbloed, Marc Gewillig, Hein Heidbüchel, Pieter A. Doevendans, Marc A. Vos, Hein J.J. Wellens, Robert S. Kass	30
13	Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy 2003 ·Journal of the American College of Cardiology ·Roselie Jongbloed, Carlo Marcelis, Pieter A. Doevendans, (unknown), Willem G. van Dockum, Joep Geraedts, Hubert J.M. Smeets	43
14	DHPLC analysis of potassium ion channel genes in congenital long QT syndrome 2003 ·Human Mutation ·Roselie Jongbloed, Carlo Marcelis, (unknown), Pieter A. Doevendans, (unknown), Hubert Smeets	5
15	DHPLC analysis of potassium ion channel genes in congenital long QT syndrome 2002 ·Human Mutation ·Roselie Jongbloed, Carlo Marcelis, (unknown), Pieter A. Doevendans, Joep Geraedts, Hubert J.M. Smeets	48
16	The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene 1997 ·Human Genetics ·(unknown), Arthur A.M. Wilde, Etienne O. Robles de Medina, (unknown), J. L. M. C. Geelen, Roselie Jongbloed, Hein J.J. Wellens, Joep Geraedts	25
17	RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families 1993 ·Human Genetics ·H. J. DE LIEFDE MEIJER, Roselie Jongbloed, (unknown), L. J. M. Spaapen, Joep Geraedts	5
18	Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping 1989 ·Human Genetics ·H. J. DE LIEFDE MEIJER, Guus Hamers, Roselie Jongbloed, (unknown), René R. W. J. van der Hulst, Joep Geraedts	12

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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