Astrid S. Plomp
Impact in
- Genetics top 1%
- Dermatological and Skeletal Disorders
- Connective tissue disorders research
- Cell Biology top 5%
- Skin and Cellular Biology Research
Papers in
- Genetics 30
- Dermatological and Skeletal Disorders 15
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 4
- Genetics and Neurodevelopmental Disorders 3
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- Retinal Development and Disorders 9
- Mitochondrial Function and Pathology 5
- Co-authors
- Arthur A. Bergen (20 shared papers)Paulus T.V.M. de Jong (11 shared papers)Frank Baas (4 shared papers)S. van Soest (4 shared papers)Ruud A. Wolterman (1 shared paper)Els C. Robanus-Maandag (1 shared paper)Theo J.M. Hulsebos (1 shared paper)Pieter Wesseling (1 shared paper)
- Journals
- Investigative Ophthalmology & Visual Science (5 papers)Human Molecular Genetics (2 papers)International Journal of Molecular Sciences (2 papers)Human Mutation (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- NetherlandsBelgiumGermany
In The Last Decade
Astrid S. Plomp
46 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 78
- Genetics 1.3k
- Cell Biology 421
- Rheumatology 260
- Molecular Biology 1.0k
- Nephrology 91
Countries citing papers authored by Astrid S. Plomp
This map shows the geographic impact of Astrid S. Plomp'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 Astrid S. Plomp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Astrid S. Plomp more than expected).
Fields of papers citing papers by Astrid S. Plomp
This network shows the impact of papers produced by Astrid S. Plomp. 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 Astrid S. Plomp. The network helps show where Astrid S. Plomp may publish in the future.
Co-authors
The 25 scholars most cited alongside Astrid S. Plomp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 437 | |
| 2 | 2007 | 255 | |
| 3 | 2014 | 228 | |
| 4 | 2003 | 187 | |
| 5 | 2007 | 148 | |
| 6 | 2010 | 112 | |
| 7 | 2003 | 109 | |
| 8 | 2006 | 91 | |
| 9 | 2018 | 66 | |
| 10 | 2023 | 62 | |
| 11 | 2017 | 57 | |
| 12 | 2003 | 44 | |
| 13 | 2003 | 43 | |
| 14 | 2016 | 39 | |
| 15 | 2010 | 34 | |
| 16 | 1998 | 33 | |
| 17 | 2006 | 32 | |
| 18 | 2003 | 32 | |
| 19 | 2017 | 31 | |
| 20 | 1998 | 29 |
About Astrid S. Plomp
Astrid S. Plomp is a scholar working on Genetics, Molecular Biology, Cell Biology, Plant Science and Ophthalmology, having authored 52 papers that have together received 2.3k indexed citations. Recurring topics across this work include Dermatological and Skeletal Disorders (15 papers), Retinal Development and Disorders (9 papers), Skin and Cellular Biology Research (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Mitochondrial Function and Pathology (5 papers), Chromosomal and Genetic Variations (5 papers), Connective tissue disorders research (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (1.3k citations), Cell Biology (421 citations), Rheumatology (260 citations), Molecular Biology (1.0k citations) and Nephrology (91 citations). Astrid S. Plomp has collaborated with scholars based in Netherlands, Belgium and Germany. Frequent co-authors include Arthur A. Bergen, Paulus T.V.M. de Jong, Frank Baas, S. van Soest, Ruud A. Wolterman, Els C. Robanus-Maandag, Theo J.M. Hulsebos, Pieter Wesseling, Jacoline B. ten Brink and Sharon F. Terry. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Human Molecular Genetics, International Journal of Molecular Sciences, Human Mutation 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.