Jasper van der Smagt

1.5k total citations
11 papers, 658 citations indexed

About

Jasper van der Smagt is a scholar working on Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Jasper van der Smagt has authored 11 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cardiology and Cardiovascular Medicine, 4 papers in Pulmonary and Respiratory Medicine and 4 papers in Genetics. Recurrent topics in Jasper van der Smagt's work include Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (2 papers). Jasper van der Smagt is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers) and Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (2 papers). Jasper van der Smagt collaborates with scholars based in Netherlands, France and Germany. Jasper van der Smagt's co-authors include Marcel M. A. M. Mannens, J. Peter van Tintelen, Richard N.W. Hauer, Pieter A. Doevendans, Arthur A.M. Wilde, Ans C.P. Wiesfeld, Roselie Jongbloed, Isabelle C. Van Gelder, Zahurul A. Bhuiyan and Luuk Otterspoor and has published in prestigious journals such as Circulation, The American Journal of Human Genetics and European Respiratory Journal.

In The Last Decade

Jasper van der Smagt

11 papers receiving 636 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jasper van der Smagt Netherlands 9 376 221 198 156 132 11 658
Yvonne Arens Netherlands 14 206 0.5× 122 0.6× 110 0.6× 38 0.2× 127 1.0× 22 428
Jason Cowan United States 12 378 1.0× 299 1.4× 79 0.4× 8 0.1× 30 0.2× 16 625
Nuria Amat‐Alarcon United States 7 555 1.5× 100 0.5× 47 0.2× 261 1.7× 3 0.0× 9 638
Shozo Oku Japan 10 176 0.5× 101 0.5× 40 0.2× 22 0.1× 10 0.1× 20 391
Adam Mitchell United States 10 26 0.1× 240 1.1× 42 0.2× 65 0.4× 24 0.2× 20 435
Eva-Lena Stattin Sweden 5 71 0.2× 71 0.3× 142 0.7× 10 0.1× 12 0.1× 6 301
Alessandra Lorenzon Italy 16 1.3k 3.3× 245 1.1× 69 0.3× 559 3.6× 2 0.0× 20 1.4k
Siv Fokstuen Switzerland 15 177 0.5× 250 1.1× 238 1.2× 2 0.0× 106 0.8× 33 573
Benjamin M. Helm United States 13 110 0.3× 176 0.8× 207 1.0× 2 0.0× 87 0.7× 49 445
Emile Hendriks United Kingdom 13 23 0.1× 142 0.6× 125 0.6× 7 0.0× 43 0.3× 23 313

Countries citing papers authored by Jasper van der Smagt

Since Specialization
Citations

This map shows the geographic impact of Jasper van der Smagt'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 Jasper van der Smagt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jasper van der Smagt more than expected).

Fields of papers citing papers by Jasper van der Smagt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jasper van der Smagt. 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 Jasper van der Smagt. The network helps show where Jasper van der Smagt may publish in the future.

Co-authorship network of co-authors of Jasper van der Smagt

This figure shows the co-authorship network connecting the top 25 collaborators of Jasper van der Smagt. A scholar is included among the top collaborators of Jasper van der Smagt 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 Jasper van der Smagt. Jasper van der Smagt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Borie, Raphaël, Bruno Crestani, Liam Galvin, et al.. (2022). Genetic testing in interstitial lung disease: An international survey. Respirology. 27(9). 747–757. 10 indexed citations
2.
Picard, Jean‐Yves, G Morin, Mojgan Devouassoux‐Shisheboran, et al.. (2022). Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphatase. Human Reproduction. 37(12). 2952–2959. 5 indexed citations
3.
Borie, Raphaël, Caroline Kannengiesser, Κατερίνα Αντωνίου, et al.. (2022). European Respiratory Society statement on familial pulmonary fibrosis. European Respiratory Journal. 61(3). 2201383–2201383. 43 indexed citations
4.
Smagt, Jasper van der, et al.. (2021). Pulmonary fibrosis in non-mutation carriers of families with short telomere syndrome gene mutations. OA4330–OA4330. 1 indexed citations
5.
Harakaľová, Magdaléna, Arjan Sammani, Marijke Linschoten, et al.. (2015). A Systematic Analysis of Genetic Dilated Cardiomyopathy Reveals Numerous Ubiquitously Expressed and Muscle-Specific Genes. European Journal of Heart Failure. 17(5). 484–493. 45 indexed citations
6.
Hochstenbach, Ron, Pieter-Jaap Krijtenburg, Lars T. van der Veken, et al.. (2014). Monosomy 20 Mosaicism Revealed by Extensive Karyotyping in Blood and Skin Cells: Case Report and Review of the Literature. Cytogenetic and Genome Research. 144(3). 155–162. 19 indexed citations
7.
Harakaľová, Magdaléna, Jasper van der Smagt, Carolien G. F. de Kovel, et al.. (2012). Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus. European Journal of Human Genetics. 21(5). 487–493. 32 indexed citations
8.
Bhuiyan, Zahurul A., Jan D.H. Jongbloed, Jasper van der Smagt, et al.. (2009). Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients. Circulation Cardiovascular Genetics. 2(5). 418–427. 73 indexed citations
9.
Cramer, Maarten‐Jan M., et al.. (2006). Familial Occurrence of Isolated Non-Compaction Cardiomyopathy. European Journal of Heart Failure. 8(8). 826–831. 13 indexed citations
10.
Bliek, Jet, Pauline Terhal, Saskia M. Maas, et al.. (2006). Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype. The American Journal of Human Genetics. 78(4). 604–614. 151 indexed citations
11.
Tintelen, J. Peter van, Mark M. Entius, Zahurul A. Bhuiyan, et al.. (2006). Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Circulation. 113(13). 1650–1658. 266 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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