R.F. Suijkerbuijk

620 total citations
14 papers, 465 citations indexed

About

R.F. Suijkerbuijk is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, R.F. Suijkerbuijk has authored 14 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in R.F. Suijkerbuijk's work include Genomic variations and chromosomal abnormalities (5 papers), Testicular diseases and treatments (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). R.F. Suijkerbuijk is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Testicular diseases and treatments (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). R.F. Suijkerbuijk collaborates with scholars based in Netherlands, United Kingdom and Germany. R.F. Suijkerbuijk's co-authors include Ad Geurts van Kessel, Bauke M. de Jong, A. Stewart, David Iles, Arnold Schwartz, L.-C. Tsui, Thomas Deufel, B. Wieringa, F. Lehmann‐Horn and Luc Heytens and has published in prestigious journals such as Journal of Biological Chemistry, Human Molecular Genetics and European Urology.

In The Last Decade

R.F. Suijkerbuijk

14 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R.F. Suijkerbuijk Netherlands	12	274	139	94	75	68	14	465
Annette Düwel Spain	10	397 1.4×	92 0.7×	39 0.4×	43 0.6×	52 0.8×	13	575
Kouji Narahara Japan	18	509 1.9×	500 3.6×	50 0.5×	19 0.3×	54 0.8×	52	877
Michael Marble United States	13	370 1.4×	234 1.7×	62 0.7×	21 0.3×	63 0.9×	33	636
Giuseppina Marseglia Italy	8	199 0.7×	98 0.7×	60 0.6×	59 0.8×	26 0.4×	12	392
Petra Muschke Germany	10	204 0.7×	214 1.5×	45 0.5×	17 0.2×	64 0.9×	19	433
Esther Kinning United Kingdom	13	321 1.2×	256 1.8×	110 1.2×	14 0.2×	42 0.6×	28	556
Gail D. Wenger United States	11	187 0.7×	60 0.4×	31 0.3×	16 0.2×	147 2.2×	14	406
Suna Önengüt United States	11	396 1.4×	120 0.9×	30 0.3×	31 0.4×	21 0.3×	11	551
Patrizia Amati France	15	691 2.5×	253 1.8×	75 0.8×	15 0.2×	24 0.4×	22	1.1k
Paige K. Bradley United States	6	187 0.7×	128 0.9×	95 1.0×	11 0.1×	54 0.8×	8	510

Countries citing papers authored by R.F. Suijkerbuijk

Since Specialization

Citations

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

Fields of papers citing papers by R.F. Suijkerbuijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R.F. Suijkerbuijk. 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 R.F. Suijkerbuijk. The network helps show where R.F. Suijkerbuijk may publish in the future.

Co-authorship network of co-authors of R.F. Suijkerbuijk

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

All Works

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14 of 14 papers shown

Criado, Maria Begoña, Alberto Barros, R.F. Suijkerbuijk, et al.. (1995). Detection of numerical alterations for chromosomes 7 and 12 in benign thyroid lesions by in situ hybridization. Histological implications.. PubMed. 147(1). 136–44. 27 indexed citations

Suijkerbuijk, R.F., et al.. (1994). Chromosomal localization of the rat N-<i>ras</i> protooncogene by fluorescence in situ hybridization. Cytogenetic and Genome Research. 67(1). 23–26. 11 indexed citations

Iles, David, F. Lehmann‐Horn, Stephen W. Scherer, et al.. (1994). Localization of the gene encoding the α₂/δ-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families. Human Molecular Genetics. 3(6). 969–975. 126 indexed citations

Hoebee, Barbara, et al.. (1994). Isolation of rat chromosome-specific paint probes by bivariate flow sorting followed by degenerate oligonucleotide primed-PCR. Cytogenetic and Genome Research. 66(4). 277–282. 33 indexed citations

Suijkerbuijk, R.F., et al.. (1994). Comparative genomic hybridization as a tool to define two distinct chromosome 12‐derived amplification units in well‐differentiated liposarcomas. Genes Chromosomes and Cancer. 9(4). 292–295. 57 indexed citations

Kessel, Ad Geurts van, R.F. Suijkerbuijk, Richard J. Sinke, et al.. (1993). Molecular cytogenetics of human germ cell tumours. European Urology. 23(1). 4 indexed citations

Speleman, Frank, et al.. (1993). Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12. Clinical Genetics. 44(3). 156–163. 12 indexed citations

Kessel, Ad Geurts van, R.F. Suijkerbuijk, Richard J. Sinke, et al.. (1993). Molecular Cytogenetics of HumanGerm Cell Tumours: i(12p) andRelated Chromosomal Anomalies. European Urology. 23(1). 23–29. 36 indexed citations

Suijkerbuijk, R.F., et al.. (1993). Assignment of three human high-affinity Fcγ receptor I genes to chromosome 1, band q21.1. Immunogenetics. 38(1). 57–59. 13 indexed citations

10.

Suijkerbuijk, R.F., et al.. (1993). Identification of a yeast artificial chromosome (YAC) that spans the papiliary renal cell carcinoma-associated t(X;1)(p11;q21) breakpoint. Cancer Genetics and Cytogenetics. 66(2). 167–167. 1 indexed citations

11.

Wetering, Marc van de, Mariëtte A. Oosterwegel, Frank C. P. Holstege, et al.. (1992). The human T cell transcription factor-1 gene. Structure, localization, and promoter characterization.. Journal of Biological Chemistry. 267(12). 8530–8536. 40 indexed citations

12.

Merkx, Gerard, et al.. (1992). Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.. Journal of Medical Genetics. 29(10). 739–741. 28 indexed citations

13.

Hamers, A.J.H., Bauke M. de Jong, R.F. Suijkerbuijk, et al.. (1991). A 46,XY female with mixed gonadal dysgenesis and a 48,XY,+7,+i(12p) chromosome pattern in a primary gonadal tumor. Cancer Genetics and Cytogenetics. 57(2). 219–224. 15 indexed citations

14.

Suijkerbuijk, R.F., et al.. (1991). Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization.. PubMed. 48(2). 269–73. 62 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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