C Höweler
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- Mitochondrial Function and Pathology 7
- Muscle Physiology and Disorders 4
- DNA Repair Mechanisms 2
-
- Genetic Neurodegenerative Diseases 11
- Co-authors
- H. F. M. Busch (3 shared papers)Joep Geraedts (1 shared paper)A. Staal (1 shared paper)Martinus F. Niermeijer (1 shared paper)Axel R. Wintzen (6 shared papers)Gert Jansen (2 shared papers)Bé Wieringa (2 shared papers)Baziel G.M. van Engelen (4 shared papers)
- Journals
- Journal of Medical Genetics (4 papers)Brain (3 papers)Neuromuscular Disorders (3 papers)Neurology (2 papers)Clinical Neurology and Neurosurgery (1 paper)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
C Höweler
22 papers receiving 942 citations
Peers
Comparison fields: 5 of 61
- Cellular and Molecular Neuroscience 469
- Neurology 185
- Epidemiology 259
- Molecular Biology 555
- Genetics 77
Countries citing papers authored by C Höweler
This map shows the geographic impact of C Höweler'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 C Höweler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Höweler more than expected).
Fields of papers citing papers by C Höweler
This network shows the impact of papers produced by C Höweler. 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 C Höweler. The network helps show where C Höweler may publish in the future.
Co-authors
The 25 scholars most cited alongside C Höweler, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 180 | |
| 2 | 2000 | 161 | |
| 3 | Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. | 1994 | 134 |
| 4 | 2002 | 106 | |
| 5 | 1996 | 67 | |
| 6 | 1993 | 64 | |
| 7 | 1995 | 45 | |
| 8 | 2007 | 43 | |
| 9 | 1997 | 34 | |
| 10 | 1992 | 33 | |
| 11 | 1979 | 30 | |
| 12 | 1997 | 26 | |
| 13 | 1993 | 20 | |
| 14 | 1994 | 9 | |
| 15 | 1983 | 8 | |
| 16 | A clinical and genetic study in myotonic dystrophy | 1986 | 7 |
| 17 | 1980 | 4 | |
| 18 | X-linked mental retardation and neurological symptoms: a nosological approach. | 1995 | 3 |
| 19 | 1997 | 2 | |
| 20 | X-linked mental retardation and neurological symptoms: A nosological approach | 1995 | 1 |
About C Höweler
C Höweler is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Surgery and Epidemiology, having authored 22 papers that have together received 979 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (7 papers), Inflammatory Myopathies and Dermatomyositis (4 papers), Muscle Physiology and Disorders (4 papers), Parkinson's Disease Mechanisms and Treatments (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), DNA Repair Mechanisms (2 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (469 citations), Neurology (185 citations), Epidemiology (259 citations), Molecular Biology (555 citations) and Genetics (77 citations). C Höweler has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include H. F. M. Busch, Joep Geraedts, A. Staal, Martinus F. Niermeijer, Axel R. Wintzen, Gert Jansen, Bé Wieringa, Baziel G.M. van Engelen, Marion L. C. Maat–Schieman and Jessica E. Hoogendijk. Their work appears in journals such as Journal of Medical Genetics, Brain, Neuromuscular Disorders, Neurology and Clinical Neurology and Neurosurgery.
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.