R. J. E. Jongbloed

634 total citations
15 papers, 480 citations indexed

About

R. J. E. Jongbloed is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, R. J. E. Jongbloed has authored 15 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 6 papers in Genetics. Recurrent topics in R. J. E. Jongbloed's work include Cardiac electrophysiology and arrhythmias (5 papers), Ion channel regulation and function (4 papers) and Mitochondrial Function and Pathology (2 papers). R. J. E. Jongbloed is often cited by papers focused on Cardiac electrophysiology and arrhythmias (5 papers), Ion channel regulation and function (4 papers) and Mitochondrial Function and Pathology (2 papers). R. J. E. Jongbloed collaborates with scholars based in Netherlands, Belgium and India. R. J. E. Jongbloed's co-authors include Joep Geraedts, Arthur A.M. Wilde, J. Peter van Tintelen, J.J.M. Engelen, Esther de Graaff, Ben A. Oostra, Jean‐Pierre Fryns, Christine de Die‐Smulders, Dennis Dooijes and Hubert J.M. Smeets and has published in prestigious journals such as Human Molecular Genetics, Cardiovascular Research and Journal of Molecular and Cellular Cardiology.

In The Last Decade

R. J. E. Jongbloed

15 papers receiving 474 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
R. J. E. Jongbloed Netherlands	11	309	202	167	48	45	15	480
K Lindblad Sweden	11	185 0.6×	18 0.1×	129 0.8×	19 0.4×	9 0.2×	16	407
Daniel Amsallem France	10	173 0.6×	16 0.1×	222 1.3×	19 0.4×	11 0.2×	21	335
Cha Gon Lee South Korea	12	117 0.4×	15 0.1×	126 0.8×	25 0.5×	66 1.5×	35	353
Anita Shanmugham United States	4	82 0.3×	13 0.1×	275 1.6×	8 0.2×	15 0.3×	4	357
Viola Doccini Italy	9	109 0.4×	17 0.1×	182 1.1×	25 0.5×	8 0.2×	10	317
Eve Õiglane‐Shlik Estonia	10	177 0.6×	6 0.0×	185 1.1×	16 0.3×	37 0.8×	17	320
Ian Andrews Australia	7	72 0.2×	48 0.2×	181 1.1×	7 0.1×	21 0.5×	8	312
Huanzheng Li China	8	158 0.5×	12 0.1×	63 0.4×	8 0.2×	26 0.6×	29	248
Valeria Messina Italy	9	254 0.8×	7 0.0×	37 0.2×	5 0.1×	18 0.4×	22	323
R. Desai United States	2	234 0.8×	30 0.1×	141 0.8×	5 0.1×	27 0.6×	5	430

Countries citing papers authored by R. J. E. Jongbloed

Since Specialization

Citations

This map shows the geographic impact of R. J. E. 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 R. J. E. Jongbloed with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. J. E. Jongbloed more than expected).

Fields of papers citing papers by R. J. E. Jongbloed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. J. E. 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 R. J. E. Jongbloed. The network helps show where R. J. E. Jongbloed may publish in the future.

Co-authorship network of co-authors of R. J. E. Jongbloed

This figure shows the co-authorship network connecting the top 25 collaborators of R. J. E. Jongbloed. A scholar is included among the top collaborators of R. J. E. 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 R. J. E. Jongbloed. R. J. E. 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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15 of 15 papers shown

Wijngaard, Arthur van den, Paul G.A. Volders, J. Peter van Tintelen, et al.. (2011). Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy. Netherlands Heart Journal. 19(7-8). 344–351. 45 indexed citations

Zwaag, Paul A. van der, Moniek G.P.J. Cox, Christian van der Werf, et al.. (2010). Recurrent and founder mutations in the Netherlands. Netherlands Heart Journal. 18(12). 583–591. 21 indexed citations

Hofman, Nynke, R. J. E. Jongbloed, Pieter G. Postema, et al.. (2010). Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome. Netherlands Heart Journal. 19(1). 10–16. 5 indexed citations

Christiaans, Imke, Eline A. Nannenberg, Dennis Dooijes, et al.. (2010). Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. Netherlands Heart Journal. 18(5). 248–254. 53 indexed citations

Gerards, Mike, Wim J. Sluiter, B.J.C. van den Bosch, et al.. (2009). Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. Journal of Medical Genetics. 47(8). 507–512. 59 indexed citations

Saenen, Johan, R. J. E. Jongbloed, Carlo Marcelis, et al.. (2007). A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes. Journal of Molecular and Cellular Cardiology. 43(1). 63–72. 14 indexed citations

Hofman, Nynke, et al.. (2007). [Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years].. PubMed. 151(11). 644–8. 3 indexed citations

Paulussen, Aimée, Ann Raes, R. J. E. Jongbloed, et al.. (2005). HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency. Cardiovascular Research. 67(3). 467–475. 18 indexed citations

Jacobs, L.J.A.M., R. J. E. Jongbloed, Frits A. Wijburg, et al.. (2004). Pearson syndrome and the role of deletion dimers and duplications in the mtDNA. Journal of Inherited Metabolic Disease. 27(1). 47–55. 22 indexed citations

10.

Jongbloed, R. J. E., Arthur A.M. Wilde, J. L. M. C. Geelen, et al.. (1999). Novel KCNQ1 and HERG missense mutations in Dutch long-QT families. Human Mutation. 13(4). 301–310. 51 indexed citations

11.

Graaff, Esther de, R. J. E. Jongbloed, Christine de Die‐Smulders, et al.. (1994). A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome. Human Molecular Genetics. 3(4). 615–620. 97 indexed citations

12.

Hamers, A.J.H., Hans‐Peter Meyer, R. J. E. Jongbloed, René R. W. J. van der Hulst, & Joep Geraedts. (1990). Rate of recombination of chromosomes 21 in parents of children with Down syndrome. Clinical Genetics. 37(6). 463–469. 3 indexed citations

13.

Pieters, M.H.E.C., Joep Geraedts, John C.M. Dumoulin, et al.. (1990). Human gametes and zygotes studied by nonradioactive in situ hybridization. Cytogenetic and Genome Research. 53(1). 15–19. 53 indexed citations

14.

Hamers, A.J.H., et al.. (1987). On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms. Clinical Genetics. 32(6). 409–413. 10 indexed citations

15.

Dunnen, Johan T. den, R. J. E. Jongbloed, A.H.M. Geurts van Kessel, & J.G.G. Schoenmakers. (1985). Human lens γ-crystallin sequences are located in the p12-qter region of chromosome 2. Human Genetics. 70(3). 217–221. 26 indexed citations

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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