Gea Beunders
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 5
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 2
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- Congenital heart defects research 1
- Co-authors
- Lidewij Henneman (1 shared paper)Erik A. Sistermans (2 shared papers)Berten Ceulemans (1 shared paper)Norma Morrison (1 shared paper)Martin Callaghan (1 shared paper)R. Frank Kooy (1 shared paper)Alexander Hoischen (1 shared paper)Nicole de Leeuw (1 shared paper)
- Journals
- Frontiers in Pediatrics (1 paper)European Journal of Medical Genetics (1 paper)Genes Brain & Behavior (1 paper)Clinical Genetics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- NetherlandsBelgiumUnited Kingdom
In The Last Decade
Gea Beunders
5 papers receiving 67 citations
Peers
Comparison fields: 5 of 21
- Genetics 47
- Pediatrics, Perinatology and Child Health 9
- Molecular Biology 30
- Cognitive Neuroscience 8
- Cell Biology 5
Countries citing papers authored by Gea Beunders
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
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-authors
The 25 scholars most cited alongside Gea Beunders, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 22 | |
| 2 | 2010 | 22 | |
| 3 | 2017 | 14 | |
| 4 | 2012 | 7 | |
| 5 | 2021 | 2 |
About Gea Beunders
Gea Beunders is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cognitive Neuroscience and Cell Biology, having authored 5 papers that have together received 67 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Autism Spectrum Disorder Research (1 paper), Neonatal Respiratory Health Research (1 paper), Cystic Fibrosis Research Advances (1 paper), Cellular transport and secretion (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (47 citations), Pediatrics, Perinatology and Child Health (9 citations), Molecular Biology (30 citations), Cognitive Neuroscience (8 citations) and Cell Biology (5 citations). Gea Beunders has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Lidewij Henneman, Erik A. Sistermans, Berten Ceulemans, Norma Morrison, Martin Callaghan, R. Frank Kooy, Alexander Hoischen, Nicole de Leeuw, Helger G. Yntema and Nathalie Van der Aa. Their work appears in journals such as Frontiers in Pediatrics, European Journal of Medical Genetics, Genes Brain & Behavior, Clinical Genetics and European Journal of Human Genetics.
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.