Gea Beunders

886 total citations
5 papers, 66 citations indexed

About

Gea Beunders is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gea Beunders has authored 5 papers receiving a total of 66 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pulmonary and Respiratory Medicine. Recurrent topics in Gea Beunders's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Gea Beunders is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Gea Beunders collaborates with scholars based in Netherlands, United Kingdom and Belgium. Gea Beunders's co-authors include Lidewij Henneman, Erik A. Sistermans, Alexander Hoischen, R. Frank Kooy, Els Voorhoeve, Norma Morrison, Tjitske Kleefstra, Willy M. Nillesen, Nathalie Van der Aa and John Tolmie and has published in prestigious journals such as European Journal of Human Genetics, Clinical Genetics and Genes Brain & Behavior.

In The Last Decade

Gea Beunders

5 papers receiving 66 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gea Beunders Netherlands	4	52	34	10	9	5	5	66
Julie McCarrier United States	5	37 0.7×	22 0.6×	6 0.6×	10 1.1×	5 1.0×	10	73
Mathijs Kattenberg Netherlands	4	65 1.3×	41 1.2×	11 1.1×	7 0.8×	6 1.2×	6	126
Nobuhiko Okamoto Japan	4	34 0.7×	35 1.0×	9 0.9×	8 0.9×	12 2.4×	7	68
Abeer Al‐Saegh Oman	5	62 1.2×	23 0.7×	11 1.1×	7 0.8×	3 0.6×	5	78
Nurit Assia Batzir Israel	5	43 0.8×	58 1.7×	8 0.8×	11 1.2×		9	92
Chontelle King New Zealand	6	51 1.0×	48 1.4×	9 0.9×	10 1.1×	3 0.6×	6	109
Shelagh Joss United Kingdom	4	45 0.9×	30 0.9×	8 0.8×	5 0.6×		6	59
Liliana Fernández United States	6	87 1.7×	49 1.4×	10 1.0×	41 4.6×	10 2.0×	8	151
Anaïs Begemann Switzerland	3	47 0.9×	51 1.5×	9 0.9×	9 1.0×		4	108
Tammy Kammin United Kingdom	5	54 1.0×	58 1.7×	6 0.6×	13 1.4×	21 4.2×	5	115

Countries citing papers authored by Gea Beunders

Since Specialization

Citations

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

Fields of papers citing papers by Gea Beunders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gea Beunders

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

All Works

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5 of 5 papers shown

1.

Sikkema‐Raddatz, Birgit, Kristin M. Abbott, Morris A. Swertz, et al.. (2021). Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital. Frontiers in Pediatrics. 9. 600556–600556. 2 indexed citations

2.

Beunders, Gea, et al.. (2017). Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives. European Journal of Medical Genetics. 61(4). 213–218. 14 indexed citations

3.

Beunders, Gea, Sonja A. de Munnik, Nathalie Van der Aa, et al.. (2014). Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. European Journal of Human Genetics. 23(6). 803–807. 22 indexed citations

4.

Rizzi, Thais S., Gea Beunders, Patrizia Rizzu, et al.. (2012). Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25. Genes Brain & Behavior. 11(7). 767–771. 7 indexed citations

5.

Beunders, Gea, Martin Callaghan, Nicole de Leeuw, et al.. (2010). Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions. Clinical Genetics. 80(1). 31–38. 21 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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