M. Coerwinkel
- Molecular Biology
- Cellular and Molecular Neuroscience top 5%
- Neurology top 10%
- Cardiology and Cardiovascular Medicine
- Genetics
- Co-authors
- Gert JansenBé WieringaH. HameisterFrank OerlemansH. SmeetsCees J. A. van EchteldMarleen DekkerLieve Vits
- Topics
- Genetic Neurodegenerative Diseases (6 papers)DNA Repair Mechanisms (2 papers)CRISPR and Genetic Engineering (2 papers)
- Partner nations
- NetherlandsGermanyCanada
In The Last Decade
M. Coerwinkel
12 papers receiving 640 citations
Peers
Comparison fields: 5 of 46
- Molecular Biology 565
- Cellular and Molecular Neuroscience 522
- Neurology 141
- Cardiology and Cardiovascular Medicine 110
- Genetics 79
Countries citing papers authored by M. Coerwinkel
This map shows the geographic impact of M. Coerwinkel'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 M. Coerwinkel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Coerwinkel more than expected).
Fields of papers citing papers by M. Coerwinkel
This network shows the impact of papers produced by M. Coerwinkel. 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 M. Coerwinkel. The network helps show where M. Coerwinkel may publish in the future.
Co-authorship network of co-authors of M. Coerwinkel
This figure shows the co-authorship network connecting the top 25 collaborators of M. Coerwinkel. A scholar is included among the top collaborators of M. Coerwinkel 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 M. Coerwinkel. M. Coerwinkel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 250 | |
| 2 | 47 | |
| 3 | Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. | 134 |
| 4 | 121 | |
| 5 | 6 | |
| 6 | 3 | |
| 7 | A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. | 38 |
| 8 | 3 | |
| 9 | 5 | |
| 10 | 22 | |
| 11 | 17 | |
| 12 | 5 |
About M. Coerwinkel
M. Coerwinkel is a scholar working on Cellular and Molecular Neuroscience, Genetics and Clinical Biochemistry, having authored 12 papers that have together received 651 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), DNA Repair Mechanisms (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (522 citations), Neurology (141 citations) and Molecular Biology (565 citations). M. Coerwinkel has collaborated with scholars based in Netherlands, Germany and Canada. Frequent co-authors include Gert Jansen, Bé Wieringa, H. Hameister, Frank Oerlemans, H. Smeets, Cees J. A. van Echteld, Marleen Dekker, Lieve Vits, Anton Berns and Patrick J. Willems. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and Human Molecular 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.