Eline Overwater

475 total citations
13 papers, 167 citations indexed

About

Eline Overwater is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eline Overwater has authored 13 papers receiving a total of 167 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pulmonary and Respiratory Medicine, 7 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eline Overwater's work include Aortic Disease and Treatment Approaches (6 papers), Connective tissue disorders research (6 papers) and Aortic aneurysm repair treatments (4 papers). Eline Overwater is often cited by papers focused on Aortic Disease and Treatment Approaches (6 papers), Connective tissue disorders research (6 papers) and Aortic aneurysm repair treatments (4 papers). Eline Overwater collaborates with scholars based in Netherlands, United States and Belgium. Eline Overwater's co-authors include Gerard Pals, Arjan C. Houweling, Dimitra Micha, Marjan M. Weiss, Yvonne Hilhorst‐Hofstee, Alessandra Maugeri, Fop van Kooten, Ferdy Kurniawan Cayami, Erik A. Sistermans and Pieternel van Exter and has published in prestigious journals such as SHILAP Revista de lepidopterología, Ophthalmology and Human Mutation.

In The Last Decade

Eline Overwater

12 papers receiving 163 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eline Overwater Netherlands 7 76 76 40 31 23 13 167
Juan Alberto Piñero‐Fernández Spain 7 22 0.3× 125 1.6× 132 3.3× 18 0.6× 29 1.3× 13 271
Shiho Makabe Japan 10 51 0.7× 107 1.4× 59 1.5× 23 0.7× 20 0.9× 33 218
Laura Gigante Italy 8 51 0.7× 33 0.4× 23 0.6× 36 1.2× 26 1.1× 17 186
Yannis Lombardi France 6 40 0.5× 14 0.2× 47 1.2× 15 0.5× 8 0.3× 14 208
M. De Arce Ireland 7 45 0.6× 38 0.5× 36 0.9× 25 0.8× 6 0.3× 7 181
Tomasz Gawlik Poland 11 30 0.4× 107 1.4× 71 1.8× 61 2.0× 3 0.1× 20 269
Nilüfer Alpay Kanıtez Türkiye 7 34 0.4× 58 0.8× 37 0.9× 9 0.3× 12 0.5× 23 159
C. Thuillier France 9 44 0.6× 20 0.3× 42 1.1× 159 5.1× 7 0.3× 40 264
Engela Honey South Africa 9 18 0.2× 38 0.5× 65 1.6× 33 1.1× 11 0.5× 25 168
Abheha Satkunaratnam Canada 9 26 0.3× 31 0.4× 64 1.6× 77 2.5× 9 0.4× 17 331

Countries citing papers authored by Eline Overwater

Since Specialization
Citations

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

Fields of papers citing papers by Eline Overwater

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eline Overwater. 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 Eline Overwater. The network helps show where Eline Overwater may publish in the future.

Co-authorship network of co-authors of Eline Overwater

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

All Works

13 of 13 papers shown
1.
Verhagen, Judith M.A., Jos A. Bekkers, Marlies Kempers, et al.. (2022). Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort. Genetics in Medicine. 24(10). 2112–2122. 3 indexed citations
2.
Bos, J. Martijn, et al.. (2021). Spontaneous Coronary Artery Dissection as Presenting Feature of Vascular Ehlers-Danlos Syndrome. SHILAP Revista de lepidopterología. 11(3). 129–131.
3.
Barrie, Elizabeth S., Eline Overwater, Mieke M. van Haelst, et al.. (2020). Expanding the spectrum of CEP55‐associated disease to viable phenotypes. American Journal of Medical Genetics Part A. 182(5). 1201–1208. 7 indexed citations
4.
Overwater, Eline, et al.. (2019). Hereditary thoracic aortic disease associated with cysteine substitution c.937T > G p.(Cys313Gly) in FBN1. Netherlands Heart Journal. 27(12). 637–638. 2 indexed citations
5.
Overwater, Eline, Daniela Q.C.M. Barge‐Schaapveld, Phillis Lakeman, et al.. (2018). Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant. Molecular Genetics & Genomic Medicine. 7(2). e00518–e00518. 4 indexed citations
6.
Overwater, Eline & Arjan C. Houweling. (2017). Iris Flocculi and Type B Aortic Dissection. Ophthalmology. 124(11). 1711–1711. 1 indexed citations
7.
Yeung, Kak Khee, Natalija Bogunovic, Eline Overwater, et al.. (2017). Transdifferentiation of Human Dermal Fibroblasts to Smooth Muscle-Like Cells to Study the Effect ofMYH11andACTA2Mutations in Aortic Aneurysms. Human Mutation. 38(4). 439–450. 18 indexed citations
8.
Satchwell, Timothy J., Andrew Bell, Stéphanie Pellegrin, et al.. (2016). Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts. Haematologica. 101(9). 1018–1027. 22 indexed citations
9.
Škorić‐Milosavljević, Doris, Eline Overwater, Karin Boer, et al.. (2016). Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature. American Journal of Medical Genetics Part A. 170(7). 1874–1880. 19 indexed citations
10.
Baars, Hubert F., Eline Overwater, Marieke J.H. Baars, et al.. (2015). Clinical and Genetic Aspects of Bicuspid Aortic Valve: A Proposed Model for Family Screening Based on a Review of Literature. SHILAP Revista de lepidopterología. 5(1). 4842–4842. 1 indexed citations
11.
Micha, Dimitra, Dongchuan Guo, Yvonne Hilhorst‐Hofstee, et al.. (2015). SMAD2Mutations Are Associated with Arterial Aneurysms and Dissections. Human Mutation. 36(12). 1145–1149. 61 indexed citations
12.
Overwater, Eline, Yvo M. Smulders, M. van der Burg, et al.. (2014). The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation. European Journal of Pediatrics. 173(12). 1695–1698. 6 indexed citations
13.
Overwater, Eline, Teun Peter Saltzherr, Peng Jin, et al.. (2010). The Association of Mobile Medical Team Involvement on On-Scene Times and Mortality in Trauma Patients. The Journal of Trauma: Injury, Infection, and Critical Care. 69(3). 589–594. 23 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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