Gea Beunders
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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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
- Alexander Hoischen (1 shared paper)John Tolmie (1 shared paper)Martin Callaghan (1 shared paper)Norma Morrison (1 shared paper)Nicole de Leeuw (1 shared paper)Erik A. Sistermans (2 shared papers)Lidewij Henneman (1 shared paper)HG Brunner (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)European Journal of Human Genetics (1 paper)Clinical Genetics (1 paper)Frontiers in Pediatrics (1 paper)Genes Brain & Behavior (1 paper)
- Partner nations
- NetherlandsBelgiumUnited Kingdom
In The Last Decade
Gea Beunders
5 papers receiving 68 citations
Peers
Comparison fields: 5 of 22
- Genetics 55
- Pediatrics, Perinatology and Child Health 15
- Molecular Biology 32
- Cognitive Neuroscience 8
- Speech and Hearing 2
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 | 2010 | 38 | |
| 2 | 2014 | 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 83 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 (55 citations), Pediatrics, Perinatology and Child Health (15 citations), Molecular Biology (32 citations), Cognitive Neuroscience (8 citations) and Speech and Hearing (2 citations). Gea Beunders has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Alexander Hoischen, John Tolmie, Martin Callaghan, Norma Morrison, Nicole de Leeuw, Erik A. Sistermans, Lidewij Henneman, HG Brunner, Tjitske Kleefstra and R. Frank Kooy. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, Frontiers in Pediatrics and Genes Brain & Behavior.
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.