G.C. Beverstock

938 total citations
30 papers, 634 citations indexed

About

G.C. Beverstock is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, G.C. Beverstock has authored 30 papers receiving a total of 634 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Hematology. Recurrent topics in G.C. Beverstock's work include Acute Myeloid Leukemia Research (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (6 papers). G.C. Beverstock is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (6 papers). G.C. Beverstock collaborates with scholars based in Netherlands, Germany and United Kingdom. G.C. Beverstock's co-authors include P.M. Kluin, Hanneke C. Kluin‐Nelemans, W.E. Fibbe, G. J. den Ottolander, GJ van Ommen, J Jansen, J.W. Wessels, Daphne de Jong, M.H. Breuning and Jacqueline Limpens and has published in prestigious journals such as Blood, British Journal of Cancer and Leukemia.

In The Last Decade

G.C. Beverstock

30 papers receiving 615 citations

Peers

G.C. Beverstock
T. W. J. Hustinx Netherlands
Fiorella Shabtai Israel
M. Leversha United Kingdom
Kavita S. Reddy United States
Klasien B.J. Gerssen‐Schoorl Netherlands
Anita S. Kulharya United States
R. A. Pfeiffer Germany
Marie‐France Portnoï France
Herman E. Wyandt United States
James Tepperberg United States
T. W. J. Hustinx Netherlands
G.C. Beverstock
Citations per year, relative to G.C. Beverstock G.C. Beverstock (= 1×) peers T. W. J. Hustinx

Countries citing papers authored by G.C. Beverstock

Since Specialization
Citations

This map shows the geographic impact of G.C. Beverstock'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 G.C. Beverstock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G.C. Beverstock more than expected).

Fields of papers citing papers by G.C. Beverstock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G.C. Beverstock. 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 G.C. Beverstock. The network helps show where G.C. Beverstock may publish in the future.

Co-authorship network of co-authors of G.C. Beverstock

This figure shows the co-authorship network connecting the top 25 collaborators of G.C. Beverstock. A scholar is included among the top collaborators of G.C. Beverstock 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 G.C. Beverstock. G.C. Beverstock 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.
Giles, Rachel H., Fred Petrij, J. Wessels, et al.. (1997). Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16). Leukemia. 11(12). 2087–2096. 55 indexed citations
2.
3.
Horsthemke, Bernhard, Anneke Maat‐Kievit, A. van den Ouweland, et al.. (1996). Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.. Journal of Medical Genetics. 33(10). 848–851. 28 indexed citations
4.
5.
Maaswinkel‐Mooij, P. D., P. de Jong, & G.C. Beverstock. (1993). 46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q— syndrome. Clinical Genetics. 43(2). 76–78. 4 indexed citations
6.
Wessels, J.W., W.E. Fibbe, J. E. Landegent, et al.. (1993). t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia. Cancer Genetics and Cytogenetics. 65(1). 7–11. 50 indexed citations
7.
Beverstock, G.C., et al.. (1993). A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo. Blood. 82(10). 2948–2952. 17 indexed citations
8.
Dreef, EJ, H van Kamp, W.E. Fibbe, et al.. (1993). Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization. Blood. 82(3). 904–913. 3 indexed citations
9.
Wessels, J., et al.. (1993). A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo. Blood. 82(10). 2948–2952. 26 indexed citations
10.
11.
Kibbelaar, R.E., H van Kamp, EJ Dreef, et al.. (1991). Detection of trisomy 8 in hematological disorders by in situ hybridization. Cytogenetic and Genome Research. 56(3-4). 132–136. 53 indexed citations
12.
Kluin‐Nelemans, Hanneke C., Jacqueline Limpens, G.C. Beverstock, et al.. (1991). A new non-Hodgkin's B-cell line (DoHH2) with a chromosomal translocation t(14;18)(q32;q21).. PubMed. 5(3). 221–4. 84 indexed citations
13.
Beverstock, G.C., et al.. (1989). Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.. Journal of Medical Genetics. 26(5). 330–333. 10 indexed citations
14.
Beverstock, G.C., et al.. (1988). A patient with an interstitial deletion of the short arm of chromosome 6. Clinical Genetics. 33(2). 95–101. 21 indexed citations
15.
Veenema, H, et al.. (1988). The fragile X‐chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981–1986. Clinical Genetics. 33(6). 410–417. 3 indexed citations
16.
Kluin‐Nelemans, Hanneke C., Henk W. J. Hakvoort, Jaap T. van Dissel, et al.. (1987). Hairy cell leukemia: In-vitro proliferation and pseudo-colony formation. Leukemia Research. 11(10). 911–921. 6 indexed citations
17.
Beverstock, G.C., et al.. (1986). Reciprocal translocation, t(11;17)(q23–25;q21), in a patient with an immature ALL. Cancer Genetics and Cytogenetics. 22(1). 83–87. 4 indexed citations
18.
Bröcker-Vriends, A, et al.. (1986). Monosomy 8p: an easily overlooked syndrome.. Journal of Medical Genetics. 23(2). 153–154. 21 indexed citations
19.
Beverstock, G.C., et al.. (1985). Absence of significant autosomal lesions in Huntington's disease. Annals of Human Genetics. 49(4). 283–290. 1 indexed citations
20.

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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