Charles H.C.M. Buys

9.4k citations

155 papers · 7.0k indexed · 2 hit papers · h-index 42

Cancer Research top 1%
- Cancer Genomics and Diagnostics 20
Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer 23
Oncology top 1%
- Cancer-related Molecular Pathways 11
Genetics top 1%
- Genomic variations and chromosomal abnormalities 21
Molecular Biology top 2%
- RNA modifications and cancer 18
- Genomics and Chromatin Dynamics 11
- DNA Repair Mechanisms 10
Pulmonary and Respiratory Medicine
- Cystic Fibrosis Research Advances 11

Co-authors: Robert M.W. Hofstra Jan Osinga Anke van den Berg Rudy M. Landsvater Harry Hollema Rein P. Stulp Klaas Kok Ying Wu
Cited by: Cancer Research Pathology and Forensic Medicine Oncology
Journals: Nature (2 papers)New England Journal of Medicine (2 papers)Proceedings of the National Academy of Sciences (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

Charles H.C.M. Buys

152 papers receiving 6.8k citations

Hit Papers

align trajectories log scale

Peers

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

The 25 scholars most cited alongside Charles 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.

Border = papers with Charles H.C.M. Buys Line = papers co-authored together Charles H.C.M. Buys links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	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 ·Debora Angeloni,Arja ter Elst,Ming Wei,Anneke Y. van der Veen,Э. А. Брага,Е.А. Климов,Tineke Timmer,L. A. Korobeinikova,Michael I. Lerman,Charles H.C.M. Buys	2006	33
2	Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosis Prenatal Diagnosis ·Birgit Sikkema‐Raddatz,Ron F. Suijkerbuijk,Katelijne Bouman,Bauke M. de Jong,Charles H.C.M. Buys,Gerard J. te Meerman	2006	5
3	An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures Prenatal Diagnosis ·Birgit Sikkema‐Raddatz,Ron F. Suijkerbuijk,Johan van der Vlag,Marian Stoepker,Charles H.C.M. Buys,Gerard J. te Meerman	2006	2
4	Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation European Journal of Medical Genetics ·Klaas Kok,Trijnie Dijkhuizen,Yolanthe Swart,Hanny Zorgdrager,Pieter van der Vlies,Rudolf S.N. Fehrmann,Gerard J. te Meerman,Klasien B.J. Gerssen‐Schoorl,Ton van Essen,Birgit Sikkema‐Raddatz,Charles H.C.M. Buys	2005	26
5	Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutations Human Mutation ·Petra H.L. Schuilenga‐Hut,Pieter van der Vlies,Marcel F. Jonkman,Esmé Waanders,Charles H.C.M. Buys,Hans Scheffer	2003	38
6	Partial Revertant Mosaicism of Keratin 14 in a Patient with Recessive Epidermolysis Bullosa Simplex11Part of this paper was presented at the 2nd Scientific Meeting of the Dutch Society for Experimental Dermatology, Lunteren, the Netherlands, February 8, 2001 and on the 30th Annual Meeting of the European Society for Dermatological Research, Berlin, September 22, 2000. Journal of Investigative Dermatology ·Petra H.L. Schuilenga‐Hut,Hans Scheffer,Charles H.C.M. Buys,Hendri H. Pas,Miranda Nijenhuis,Marcel F. Jonkman	2002	48
7	Exempting Homologous Pseudogene Sequences from Polymerase Chain Reaction Amplification Allows Genomic Keratin 14 Hotspot Mutation Analysis Journal of Investigative Dermatology ·Petra H.L. Hut,Pieter van der Vlies,Edwin Verlind,Charles H.C.M. Buys,Hans Scheffer,Marcel F. Jonkman,Hiroshi Shimizu	2000	32
8	SMA carrier testing – validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion European Journal of Human Genetics ·Hans Scheffer,Jan Maarten Cobben,Rob G.J. Mensink,Rein P. Stulp,Gerrit van der Steege,Charles H.C.M. Buys	2000	42
9	Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes Human Mutation ·Jan Peter Rake,Annelies M. ten Berge,Gepke Visser,Edwin Verlind,Klary E. Niezen‐Koning,Charles H.C.M. Buys,G. P. A. Smit,Hans Scheffer	2000	10
10	Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1 Genes Chromosomes and Cancer ·Beatriz Carvalho,Raquel Seruca,Fátima Carneiro,Charles H.C.M. Buys,Klaas Kok	1999	19
11	Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations The American Journal of Human Genetics ·Ying Wu,Maran J.W. Berends,Rob G.J. Mensink,Claudia Kempinga,Rolf H. Sijmons,Ate G.J. van der Zee,Harry Hollema,Jan H. Kleibeuker,Charles H.C.M. Buys,Robert M.W. Hofstra	1999	255
12	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinomabreakdown → Nature ·Robert M.W. Hofstra,Rudy M. Landsvater,Isabella Ceccherini,Rein P. Stulp,Tineke Stelwagen,Yin Luo,Barbara Pasini,Jo W.M. Höppener,Hans Kristian Ploos van Amstel,Giovanni Romeo,Cornells J. M. Lips,Charles H.C.M. Buys	1994	872
13	Linkage and apparent heterogeneity in proximal spinal muscular atrophies Neuromuscular Disorders ·Jan M. Cobben,Hans Scheffer,Marjolein Visser,Jan Osinga,Rune R. Frants,Gerrit van der Steege,Cisca Wijmenga,Leo P. ten Kate,Gert‐Jan B. van Ommen,Charles H.C.M. Buys	1993	8
14	3 ALLELIC ASSOCIATION FOR WILSON DISEASE/D13S31 Journal of Pediatric Gastroenterology and Nutrition ·R. H. J. Houwen,R. Berger,D W Cox,Charles H.C.M. Buys	1992	1
15	Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene Human Genetics ·Hans Scheffer,Roderick H.J. Houwen,Gj Temeerman,J. Loessner,B Bachmann,E. Kunert,Edwin Verlind,Charles H.C.M. Buys	1992	6
16	Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcoma Genes Chromosomes and Cancer ·David N. Shapiro,Marc Valentine,Jack Sublett,A Sinclair,A. Thomas Look,A Tereba,Hans Scheffer,Charles H.C.M. Buys	1992	16
17	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 ·Jan‐Willem Taanman,Anneke Y. van der Veen,Cobi Schrage,H. de Vries,Charles H.C.M. Buys	1991	17
18	Localization of amplified c-myc and n-myc in small cell lung cancer cell lines Cancer Genetics and Cytogenetics ·Annemarie H. van der Hout,Klaas Kok,Anneke Y. van der Veen,Jan Osinga,Lou F. M. H. de Leij,Charles H.C.M. Buys	1989	13
19	The single copy probe pG24E2.4 [D13S21] reveals a Bspl286 RFLP at 13ql4.1–ql4.2 Nucleic Acids Research ·A. Bowcock,Joan M. Hebert,Hans Scheffer,Dirk Penninga,Charles H.C.M. Buys	1989	2
20	Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma Cancer Genetics and Cytogenetics ·Annemarie H. van der Hout,Klaas Kok,Anke van den Berg,J. Wolter Oosterhuis,B. Carritt,Charles H.C.M. Buys	1988	33

About Charles H.C.M. Buys

Charles H.C.M. Buys is a scholar working on Cancer Research, Pathology and Forensic Medicine and Genetics, having authored 155 papers that have together received 7.0k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (23 papers), Genomic variations and chromosomal abnormalities (21 papers), Cancer Genomics and Diagnostics (20 papers), RNA modifications and cancer (18 papers), Cystic Fibrosis Research Advances (11 papers), Cancer-related Molecular Pathways (11 papers), Genomics and Chromatin Dynamics (11 papers) and DNA Repair Mechanisms (10 papers). The work is most often cited by research in Cancer Research (1.3k citations), Pathology and Forensic Medicine (1.5k citations) and Oncology (1.8k citations). Charles H.C.M. Buys has collaborated with scholars based in Netherlands, United States and Germany. Frequent 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 Jan H. Kleibeuker. Their work appears in journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

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.

Explore authors with similar magnitude of impact