C.H.C.M. Buys
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
-
- RNA modifications and cancer 8
- Genomics and Chromatin Dynamics 6
- Oncology 12
- Cancer-related Molecular Pathways 5
- Co-authors
- Klaas Kok (7 shared papers)Susan L. Naylor (2 shared papers)Robert M.W. Hofstra (15 shared papers)Hans Scheffer (13 shared papers)P.M. Grootscholten (4 shared papers)J. M. Cobben (2 shared papers)J. Osinga (6 shared papers)Gerrit van der Steege (3 shared papers)
- Journals
- Human Genetics (7 papers)Nucleic Acids Research (4 papers)European Journal of Human Genetics (2 papers)Gut (2 papers)Genetica (2 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
C.H.C.M. Buys
52 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 78
- Genetics 285
- Cancer Research 294
- Oncology 466
- Molecular Biology 1.1k
- Pathology and Forensic Medicine 273
Countries citing papers authored by C.H.C.M. Buys
This map shows the geographic impact of C.H.C.M. Buys'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.H.C.M. Buys with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C.H.C.M. Buys more than expected).
Fields of papers citing papers by C.H.C.M. Buys
This network shows the impact of papers produced by C.H.C.M. Buys. 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.H.C.M. Buys. The network helps show where C.H.C.M. Buys may publish in the future.
Co-authors
The 25 scholars most cited alongside C.H.C.M. Buys, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 295 | |
| 2 | Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy. | 1995 | 174 |
| 3 | p53 mutations in human lung tumors. | 1992 | 154 |
| 4 | Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5. | 1996 | 86 |
| 5 | 2006 | 83 | |
| 6 | 1993 | 83 | |
| 7 | The physical map of the human RET proto-oncogene. | 1995 | 76 |
| 8 | 2000 | 70 | |
| 9 | 1996 | 56 | |
| 10 | 1998 | 55 | |
| 11 | 1998 | 49 | |
| 12 | 1998 | 48 | |
| 13 | 2005 | 47 | |
| 14 | 1993 | 46 | |
| 15 | 1999 | 44 | |
| 16 | 1996 | 39 | |
| 17 | 1975 | 39 | |
| 18 | Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene. | 1989 | 35 |
| 19 | The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred. | 1993 | 25 |
| 20 | 1978 | 25 |
About C.H.C.M. Buys
C.H.C.M. Buys is a scholar working on Molecular Biology, Oncology, Genetics, Surgery and Cancer Research, having authored 53 papers that have together received 1.8k indexed citations. Recurring topics across this work include RNA modifications and cancer (8 papers), Genetic factors in colorectal cancer (6 papers), Genomics and Chromatin Dynamics (6 papers), Cancer Genomics and Diagnostics (5 papers), Cancer-related Molecular Pathways (5 papers), Congenital gastrointestinal and neural anomalies (5 papers), Genetic and phenotypic traits in livestock (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (285 citations), Cancer Research (294 citations), Oncology (466 citations), Molecular Biology (1.1k citations) and Pathology and Forensic Medicine (273 citations). C.H.C.M. Buys has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Klaas Kok, Susan L. Naylor, Robert M.W. Hofstra, Hans Scheffer, P.M. Grootscholten, J. M. Cobben, J. Osinga, Gerrit van der Steege, Marianne de Visser and Anke van den Berg. Their work appears in journals such as Human Genetics, Nucleic Acids Research, European Journal of Human Genetics, Gut and Genetica.
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.