M. Wilbrink

418 total citations
9 papers, 327 citations indexed

About

M. Wilbrink is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, M. Wilbrink has authored 9 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 5 papers in Cancer Research. Recurrent topics in M. Wilbrink's work include Renal and related cancers (6 papers), Cancer Genomics and Diagnostics (5 papers) and Renal cell carcinoma treatment (5 papers). M. Wilbrink is often cited by papers focused on Renal and related cancers (6 papers), Cancer Genomics and Diagnostics (5 papers) and Renal cell carcinoma treatment (5 papers). M. Wilbrink collaborates with scholars based in Netherlands, Germany and United States. M. Wilbrink's co-authors include Ad Geurts van Kessel, Marian A. J. Weterman, Anke van den Berg, Trijnie Dijkhuizen, Stephan Störkel, Bauke M. de Jong, Anneke Y. van der Veen, Bart de Vries, Hilde Janssen and Ian Craig and has published in prestigious journals such as Proceedings of the National Academy of Sciences, International Journal of Cancer and Journal of Molecular Evolution.

In The Last Decade

M. Wilbrink

9 papers receiving 322 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Wilbrink Netherlands 7 273 211 112 36 32 9 327
Takahiro Narimatsu Japan 9 350 1.3× 123 0.6× 251 2.2× 22 0.6× 50 1.6× 16 442
M. Behn Germany 9 277 1.0× 62 0.3× 82 0.7× 31 0.9× 117 3.7× 14 374
Sara E. Khalil United States 6 139 0.5× 134 0.6× 39 0.3× 51 1.4× 37 1.2× 7 317
Sabine Harlander Switzerland 7 260 1.0× 128 0.6× 171 1.5× 42 1.2× 31 1.0× 8 342
Matthew Tanner United States 7 200 0.7× 90 0.4× 129 1.2× 27 0.8× 75 2.3× 8 342
Helena Nord Sweden 13 212 0.8× 47 0.2× 102 0.9× 80 2.2× 58 1.8× 19 364
Yanjing Guo China 10 209 0.8× 81 0.4× 102 0.9× 16 0.4× 94 2.9× 16 321
Désirée Schönenberger Switzerland 4 223 0.8× 111 0.5× 164 1.5× 36 1.0× 28 0.9× 4 290
Fei Lin China 11 159 0.6× 91 0.4× 121 1.1× 10 0.3× 41 1.3× 33 290
Norman Zambrano United States 6 299 1.1× 263 1.2× 124 1.1× 32 0.9× 47 1.5× 11 356

Countries citing papers authored by M. Wilbrink

Since Specialization
Citations

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

Fields of papers citing papers by M. Wilbrink

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Wilbrink. 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 M. Wilbrink. The network helps show where M. Wilbrink may publish in the future.

Co-authorship network of co-authors of M. Wilbrink

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

All Works

9 of 9 papers shown
1.
Weterman, Marian A. J., M. Wilbrink, Marc J. Eleveld, et al.. (2001). Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma. Cytogenetic and Genome Research. 92(3-4). 326–332. 4 indexed citations
2.
Dijkhuizen, Trijnie, Anke van den Berg, Stephan Störkel, et al.. (1997). Renal oncocytoma with t(5;12;11), der(1)t(1;8) and add(19): “true” oncocytoma or chromophobe adenoma?. International Journal of Cancer. 73(4). 521–524. 29 indexed citations
3.
Weterman, Marian A. J., M. Wilbrink, Trijnie Dijkhuizen, Anke van den Berg, & Ad Geurts van Kessel. (1996). Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation. Human Genetics. 98(1). 16–21. 26 indexed citations
4.
Weterman, Marian A. J., M. Wilbrink, Irene M. Janssen, et al.. (1996). Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint. Cytogenetic and Genome Research. 75(1). 2–6. 26 indexed citations
5.
Weterman, Marian A. J., M. Wilbrink, & Ad Geurts van Kessel. (1996). Fusion of the transcription factor TFE3 gene to a novel gene, PRCC , in t(X;1)(p11;q21)-positive papillary renal cell carcinomas. Proceedings of the National Academy of Sciences. 93(26). 15294–15298. 163 indexed citations
6.
Dijkhuizen, Trijnie, Anke van den Berg, M. Wilbrink, et al.. (1995). Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocations. Genes Chromosomes and Cancer. 14(1). 43–50. 56 indexed citations
7.
Harhangi, Harry R., et al.. (1994). Interspecific sequence comparison of the muscle-myosin heavy-chain genes from Drosophila hydei and Drosophila melanogaster. Journal of Molecular Evolution. 39(4). 357–368. 9 indexed citations
8.
Suijkerbuijk, Ron F., Alessandra Meloni, Richard J. Sinke, et al.. (1993). Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2. Cancer Genetics and Cytogenetics. 71(2). 164–169. 6 indexed citations
9.
Hochstenbach, Ron, M. Wilbrink, Ron F. Suijkerbuijk, & Wolfgang Hennig. (1993). Localization of the lampbrush loop pair Nooses on the Y chromosome of Drosophila hydei by fluorescence in situ hybridization. Chromosoma. 102(8). 546–552. 8 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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