Charles H.C.M. Buys

9.4k total citations · 2 hit papers
155 papers, 7.0k citations indexed

About

Charles H.C.M. Buys is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Charles H.C.M. Buys has authored 155 papers receiving a total of 7.0k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 32 papers in Oncology and 32 papers in Genetics. Recurrent topics in Charles H.C.M. Buys's work include Genetic factors in colorectal cancer (23 papers), Genomic variations and chromosomal abnormalities (21 papers) and Cancer Genomics and Diagnostics (20 papers). Charles H.C.M. Buys is often cited by papers focused on Genetic factors in colorectal cancer (23 papers), Genomic variations and chromosomal abnormalities (21 papers) and Cancer Genomics and Diagnostics (20 papers). Charles H.C.M. Buys collaborates with scholars based in Netherlands, United States and Germany. Charles H.C.M. Buys's co-authors include Robert M.W. Hofstra, Jan Osinga, Anke van den Berg, Rudy M. Landsvater, Harry Hollema, Rein P. Stulp, Klaas Kok, Ying Wu, Hans Scheffer and Rob G.J. Mensink and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Charles H.C.M. Buys

152 papers receiving 6.8k citations

Hit Papers

A mutation in the RET proto-oncogene associated with mult... 1994 2026 2004 2015 1994 2007 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
    1994 872 citations Robert M.W. Hofstra, Rein P. Stulp et al. profile →
  2. In Vitro Fertilization with Preimplantation Genetic Screening
    2007 476 citations Birgit Sikkema‐Raddatz, Charles H.C.M. Buys et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles H.C.M. Buys Netherlands 42 3.2k 1.8k 1.5k 1.5k 1.3k 155 7.0k
Virginia V. Michels United States 47 3.1k 1.0× 1.2k 0.7× 1.2k 0.8× 2.6k 1.8× 1.2k 0.9× 148 9.1k
Svetlana Pack United States 47 3.1k 1.0× 1.5k 0.9× 690 0.5× 1.1k 0.7× 1.1k 0.8× 130 6.5k
Mitsuru Emi Japan 45 3.1k 1.0× 1.4k 0.8× 879 0.6× 1.4k 1.0× 1.1k 0.8× 192 6.2k
Paul J. Goodfellow United States 51 5.1k 1.6× 2.8k 1.5× 2.7k 1.7× 2.2k 1.5× 3.0k 2.3× 222 11.1k
S B Baylin United States 23 7.7k 2.4× 2.0k 1.1× 972 0.6× 984 0.7× 1.6k 1.2× 32 9.3k
Kristiina Aittomäki Finland 47 3.3k 1.0× 1.3k 0.7× 760 0.5× 2.4k 1.6× 1.1k 0.8× 130 7.3k
Andrew C. Karaplis Canada 50 6.2k 1.9× 4.3k 2.4× 896 0.6× 2.1k 1.4× 570 0.4× 125 10.3k
Charles E. Jackson United States 51 4.8k 1.5× 2.3k 1.3× 1.2k 0.8× 2.2k 1.5× 819 0.6× 139 11.6k
Georgia Chenevix‐Trench Australia 53 5.2k 1.6× 2.2k 1.2× 1.7k 1.1× 3.3k 2.2× 1.8k 1.4× 219 8.7k
Lee S. Weinstein United States 55 5.4k 1.7× 1.6k 0.9× 382 0.2× 3.7k 2.5× 557 0.4× 184 10.4k

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

Since Specialization
Citations

This map shows the geographic impact of Charles 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 Charles 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 Charles H.C.M. Buys more than expected).

Fields of papers citing papers by Charles H.C.M. Buys

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles 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 Charles H.C.M. Buys. The network helps show where Charles H.C.M. Buys may publish in the future.

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

This figure shows the co-authorship network connecting the top 25 collaborators of Charles H.C.M. Buys. A scholar is included among the top collaborators of Charles 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 Charles H.C.M. Buys. Charles 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
1.
Angeloni, Debora, Arja ter Elst, Ming Wei, et al.. (2006). Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes. Genes Chromosomes and Cancer. 45(7). 676–691. 33 indexed citations
2.
Westra, Jantine L., Michael Schaapveld, Harry Hollema, et al.. (2005). Determination of TP53 Mutation Is More Relevant Than Microsatellite Instability Status for the Prediction of Disease-Free Survival in Adjuvant-Treated Stage III Colon Cancer Patients. Journal of Clinical Oncology. 23(24). 5635–5643. 109 indexed citations
3.
Kok, Klaas, Trijnie Dijkhuizen, Pieter van der Vlies, et al.. (2005). Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation. European Journal of Medical Genetics. 48(3). 250–262. 26 indexed citations
4.
Vlies, Pieter van der, et al.. (2003). Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutations. Human Mutation. 21(4). 447–447. 38 indexed citations
5.
6.
Wu, Ying, Maran J.W. Berends, Rolf H. Sijmons, et al.. (2001). A role for MLH3 in hereditary nonpolyposis colorectal cancer. Nature Genetics. 29(2). 137–138. 121 indexed citations
7.
8.
Vlies, Pieter van der, Edwin Verlind, Charles H.C.M. Buys, et al.. (2000). Exempting Homologous Pseudogene Sequences from Polymerase Chain Reaction Amplification Allows Genomic Keratin 14 Hotspot Mutation Analysis. Journal of Investigative Dermatology. 114(4). 616–619. 32 indexed citations
9.
Carvalho, Beatriz, Raquel Seruca, Fátima Carneiro, Charles H.C.M. Buys, & Klaas Kok. (1999). Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1. Genes Chromosomes and Cancer. 26(1). 29–34. 19 indexed citations
10.
Wu, Ying, Maran J.W. Berends, Rob G.J. Mensink, et al.. (1999). Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations. The American Journal of Human Genetics. 65(5). 1291–1298. 255 indexed citations
11.
Xiang, RuiHua, Charles H. Hensel, Dawn Garcia, et al.. (1996). Isolation of the Human Semaphorin III/F Gene (SEMA3F) at Chromosome 3p21, a Region Deleted in Lung Cancer. Genomics. 32(1). 39–48. 135 indexed citations
12.
Angrist, Misha, Stacey Bolk, Bonnie Thiel, et al.. (1995). Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. Human Molecular Genetics. 4(5). 821–830. 180 indexed citations
13.
Cobben, Jan M., Hans Scheffer, Marjolein Visser, et al.. (1993). Linkage and apparent heterogeneity in proximal spinal muscular atrophies. Neuromuscular Disorders. 3(4). 327–333. 8 indexed citations
14.
Houwen, R. H. J., et al.. (1992). 3 ALLELIC ASSOCIATION FOR WILSON DISEASE/D13S31. Journal of Pediatric Gastroenterology and Nutrition. 15(3). 341–341. 1 indexed citations
15.
Scheffer, Hans, et al.. (1992). Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene. Human Genetics. 89(6). 607–11. 6 indexed citations
16.
Taanman, Jan‐Willem, et al.. (1991). Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridisation. Human Genetics. 87(3). 325–327. 17 indexed citations
17.
Hout, Annemarie H. van der, et al.. (1989). Localization of amplified c-myc and n-myc in small cell lung cancer cell lines. Cancer Genetics and Cytogenetics. 38(1). 1–8. 13 indexed citations
18.
19.
Mooibroek, Hans, Jan Osinga, Pieter E. Postmus, B. Carritt, & Charles H.C.M. Buys. (1987). Loss of heterozygosity for a chromosome 3 sequence presumably at 3p21 in small cell lung cancer. Cancer Genetics and Cytogenetics. 27(2). 361–365. 26 indexed citations
20.
Buys, Charles H.C.M., et al.. (1984). Banding of unfixed mitotic chromosomes in suspension after release from human lymphocytes and fibroblasts. Human Genetics. 66(4). 361–364. 7 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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