Gea Beunders
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Developmental Neuroscience top 10%
- Neurogenesis and neuroplasticity mechanisms
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
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- Williams Syndrome Research 1
- Co-authors
- Erik A. Sistermans (3 shared papers)Aggie W. M. Nieuwint (2 shared papers)Johanna M. van Hagen (2 shared papers)Jiddeke M. van de Kamp (2 shared papers)Reinier H. Veenhoven (1 shared paper)Helger G. Yntema (2 shared papers)Willy M. Nillesen (2 shared papers)Hanne E.J. Meijers-Heijboer (2 shared papers)
- Journals
- Genetics in Medicine (4 papers)The American Journal of Human Genetics (3 papers)Clinical Genetics (2 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Gea Beunders
17 papers receiving 531 citations
Peers
Comparison fields: 5 of 49
- Genetics 397
- Developmental Neuroscience 30
- Pediatrics, Perinatology and Child Health 41
- Cognitive Neuroscience 59
- Developmental 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 | 2013 | 140 | |
| 2 | 2015 | 114 | |
| 3 | 2009 | 56 | |
| 4 | 2016 | 54 | |
| 5 | 2010 | 41 | |
| 6 | 2019 | 38 | |
| 7 | 2021 | 36 | |
| 8 | 2014 | 30 | |
| 9 | 2022 | 19 | |
| 10 | 2017 | 15 | |
| 11 | 2024 | 12 | |
| 12 | 2010 | 11 | |
| 13 | 2023 | 8 | |
| 14 | 2012 | 6 | |
| 15 | 2021 | 5 | |
| 16 | 2023 | 3 | |
| 17 | 2025 | 1 |
About Gea Beunders
Gea Beunders is a scholar working on Genetics, Developmental Neuroscience, Public Health, Environmental and Occupational Health, Molecular Biology and Nuclear Energy and Engineering, having authored 17 papers that have together received 589 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Down syndrome and intellectual disability research (1 paper), Williams Syndrome Research (1 paper) and Prion Diseases and Protein Misfolding (1 paper). The work is most often cited by research in Genetics (397 citations), Developmental Neuroscience (30 citations), Pediatrics, Perinatology and Child Health (41 citations), Cognitive Neuroscience (59 citations) and Developmental Biology (5 citations). Gea Beunders has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Erik A. Sistermans, Aggie W. M. Nieuwint, Johanna M. van Hagen, Jiddeke M. van de Kamp, Reinier H. Veenhoven, Helger G. Yntema, Willy M. Nillesen, Hanne E.J. Meijers-Heijboer, Nicole de Leeuw and Han G. Brunner. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Clinical Genetics, European Journal of Human Genetics and Journal of Medical 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.