P.M. Grootscholten
- Molecular Biology top 10%
- Genetics top 2%
- Cardiology and Cardiovascular Medicine top 10%
- Genetics top 10%
- Surgery
- Co-authors
- Johan T. den DunnenP. PearsonEgbert BakkerG J van OmmenChristine Van BroeckhovenMartin C. WapenaarLau A.J. BlondenH.B. Ginjaar
- Topics
- Muscle Physiology and Disorders (8 papers)Neurogenetic and Muscular Disorders Research (7 papers)RNA modifications and cancer (5 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
P.M. Grootscholten
15 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 1.2k
- Genetics 517
- Cardiology and Cardiovascular Medicine 272
- Genetics 268
- Surgery 222
Countries citing papers authored by P.M. Grootscholten
This map shows the geographic impact of P.M. Grootscholten'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 P.M. Grootscholten with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P.M. Grootscholten more than expected).
Fields of papers citing papers by P.M. Grootscholten
This network shows the impact of papers produced by P.M. Grootscholten. 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 P.M. Grootscholten. The network helps show where P.M. Grootscholten may publish in the future.
Co-authorship network of co-authors of P.M. Grootscholten
This figure shows the co-authorship network connecting the top 25 collaborators of P.M. Grootscholten. A scholar is included among the top collaborators of P.M. Grootscholten 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 P.M. Grootscholten. P.M. Grootscholten is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 14 | |
| 3 | Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5. | 86 |
| 4 | 9 | |
| 5 | 25 | |
| 6 | The physical map of the human RET proto-oncogene. | 76 |
| 7 | Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. | 174 |
| 8 | 66 | |
| 9 | 62 | |
| 10 | 52 | |
| 11 | 115 | |
| 12 | 16 | |
| 13 | Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. | 438 |
| 14 | 153 | |
| 15 | 99 |
About P.M. Grootscholten
P.M. Grootscholten is a scholar working on Genetics, Aging and Molecular Biology, having authored 15 papers that have together received 1.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Genetics (517 citations), Molecular Biology (1.2k citations) and Cardiology and Cardiovascular Medicine (272 citations). P.M. Grootscholten has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Johan T. den Dunnen, P. Pearson, Egbert Bakker, G J van Ommen, Christine Van Broeckhoven, Martin C. Wapenaar, Lau A.J. Blonden, H.B. Ginjaar, C.H.C.M. Buys and Hans Scheffer. Their work appears in journals such as Nucleic Acids Research, Neurology and International Journal of Molecular Sciences.
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.