C.H.C.M. Buys

2.7k total citations
53 papers, 1.8k citations indexed

About

C.H.C.M. Buys is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, C.H.C.M. Buys has authored 53 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 12 papers in Oncology and 11 papers in Genetics. Recurrent topics in C.H.C.M. Buys's work include RNA modifications and cancer (8 papers), Genomics and Chromatin Dynamics (6 papers) and Genetic factors in colorectal cancer (6 papers). C.H.C.M. Buys is often cited by papers focused on RNA modifications and cancer (8 papers), Genomics and Chromatin Dynamics (6 papers) and Genetic factors in colorectal cancer (6 papers). C.H.C.M. Buys collaborates with scholars based in Netherlands, United States and United Kingdom. C.H.C.M. Buys's 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, Anke van den Berg and Marianne de Visser and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Gut.

In The Last Decade

C.H.C.M. Buys

52 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
C.H.C.M. Buys Netherlands 22 1.1k 466 436 320 294 53 1.8k
Jan Osinga Netherlands 23 754 0.7× 342 0.7× 384 0.9× 365 1.1× 288 1.0× 34 1.5k
P Cairns United States 17 1.7k 1.6× 599 1.3× 496 1.1× 168 0.5× 536 1.8× 18 2.5k
A L Børresen Norway 21 834 0.8× 667 1.4× 255 0.6× 401 1.3× 443 1.5× 45 1.6k
David Cappellen France 21 1.6k 1.4× 545 1.2× 403 0.9× 165 0.5× 277 0.9× 50 2.3k
Xiaobing He United States 12 1.3k 1.2× 685 1.5× 202 0.5× 443 1.4× 498 1.7× 22 1.9k
Maria F. Paz Spain 16 1.8k 1.6× 358 0.8× 157 0.4× 297 0.9× 390 1.3× 22 2.3k
H L Moses United States 14 1.0k 0.9× 597 1.3× 243 0.6× 114 0.4× 242 0.8× 18 1.7k
Patrick W. Heiser United States 13 2.0k 1.8× 873 1.9× 664 1.5× 411 1.3× 325 1.1× 32 2.8k
Annie S.Y. Chan China 19 1.1k 1.0× 581 1.2× 197 0.5× 184 0.6× 465 1.6× 20 1.8k
Shiuh-Ming Luoh United States 13 1.2k 1.1× 476 1.0× 115 0.3× 308 1.0× 138 0.5× 14 2.0k

Countries citing papers authored by C.H.C.M. Buys

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of C.H.C.M. Buys

This figure shows the co-authorship network connecting the top 25 collaborators of C.H.C.M. Buys. A scholar is included among the top collaborators of C.H.C.M. Buys 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 C.H.C.M. Buys. C.H.C.M. Buys is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Hofstra, Robert M.W., Ying Wu, Rein P. Stulp, et al.. (2000). RET andGDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems. Human Mutation. 15(5). 418–429. 70 indexed citations
3.
Verheij, Joanne, K. Bouman, Richard A. van Lingen, et al.. (1999). Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22. American Journal of Medical Genetics. 86(2). 168–173. 15 indexed citations
4.
Sijmons, Rolf H., Robert M.W. Hofstra, Frits A. Wijburg, et al.. (1998). Oncological implications of RET gene mutations in Hirschsprung’s disease. Gut. 43(4). 542–547. 49 indexed citations
5.
Scheffer, Hans, E. R. Brunt, Pieter van der Vlies, et al.. (1998). Three novel KCNA1 mutations in episodic ataxia type I families. Human Genetics. 102(4). 464–466. 48 indexed citations
6.
Dørum, Anne, Pål Møller, Erik-Jan Kamsteeg, et al.. (1997). A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing. European Journal of Cancer. 33(14). 2390–2392. 21 indexed citations
7.
Kok, Klaas, Susan L. Naylor, & C.H.C.M. Buys. (1997). Deletions of the Short Arm of Chromosome 3 in Solid Tumors and the Search for Suppressor Genes. Advances in cancer research. 71. 27–92. 295 indexed citations
8.
Berg, Anke van den, Miriam Hulsbeek, Debora de Jong, et al.. (1996). Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis. Genes Chromosomes and Cancer. 15(1). 64–72. 56 indexed citations
9.
10.
Steege, Gerrit van der, Jan-Maarten Cobben, Jan Osinga, et al.. (1995). A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis. Human Genetics. 96(5). 589–591. 2 indexed citations
11.
Pasini, Barbara, Robert M.W. Hofstra, Ling Yin, et al.. (1995). The physical map of the human RET proto-oncogene.. PubMed. 11(9). 1737–43. 76 indexed citations
12.
Kok, Klaas, Robert M.W. Hofstra, Alison Pilz, et al.. (1993). A gene in the chromosomal region 3p21 with greatly reduced expression in lung cancer is similar to the gene for ubiquitin-activating enzyme.. Proceedings of the National Academy of Sciences. 90(13). 6071–6075. 83 indexed citations
13.
Dijkhuizen, Trijnie, et al.. (1993). Loss of heterozygosity at the short arm of chromosome 3 in renal‐cell cancer correlates with the cytological tumour type. International Journal of Cancer. 53(3). 353–357. 46 indexed citations
14.
Mao, Fan, et al.. (1991). A new RFLP identified at the D3S48 locus. Nucleic Acids Research. 19(17). 4797–4797. 11 indexed citations
15.
16.
Bowcock, A., Joan M. Hebert, Hans Scheffer, Dirk Penninga, & C.H.C.M. Buys. (1989). The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with Sspl. Nucleic Acids Research. 17(20). 8399–8399. 1 indexed citations
17.
Smith, Barbara A., H. Telenius, Rudy M. Landsvater, et al.. (1988). BcII RFLP for the human vimentin gene. Nucleic Acids Research. 16(18). 9068–9068. 3 indexed citations
18.
Scheffer, Hans, et al.. (1986). A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus. Human Genetics. 74(3). 249–255. 17 indexed citations
19.
Buys, C.H.C.M., et al.. (1984). Isolated metaphase chromosomes stabilized by DNA-intercalation or polyamine additon: A comparison. Cell Biology International Reports. 8(4). 273–273. 5 indexed citations
20.
Buys, C.H.C.M., et al.. (1965). A new blood group locus in cattle. Genetica. 36(1). 1–10. 5 indexed citations

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.

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