Mark A. van de Wiel

10.5k citations
165 papers · 7.3k indexed · 2 hit papers · h-index 41
Topics
Gene expression and cancer classification (41 papers)Genomic variations and chromosomal abnormalities (21 papers)Statistical Methods and Inference (20 papers)

In The Last Decade

Mark A. van de Wiel

159 papers receiving 7.1k citations

Hit Papers

Implementing a Class of Permutation Tests: ThecoinPackage2006202620122019200820062505007501000

Peers

Mark A. van de Wiel
Comparison fields: 5 of 208
  • Molecular Biology 2.9k
  • Cancer Research 1.8k
  • Oncology 1.1k
  • Genetics 971
  • Pathology and Forensic Medicine 762
Replace Natacha Turck with:
Natacha Turck Switzerland
Frédérique Lisacek Switzerland
Alexandre Hainard Switzerland
Daniel Zelterman United States
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Natalia Tiberti Italy
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W. Evan Johnson United States
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Mark A. van de Wiel relative to Natacha Turck Switzerland Natacha Turck's profile →
Citations per field
00.5×1.5×1.8×
Natacha Turck · 1×
Citations per year

Countries citing papers authored by Mark A. van de Wiel

Since Specialization
Citations

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

Fields of papers citing papers by Mark A. van de Wiel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark A. van de Wiel. 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 Mark A. van de Wiel. The network helps show where Mark A. van de Wiel may publish in the future.

Co-authorship network of co-authors of Mark A. van de Wiel

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. van de Wiel. A scholar is included among the top collaborators of Mark A. van de Wiel 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 Mark A. van de Wiel. Mark A. van de Wiel 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
#WorkIndexed citations
1 0
2 0
3 2
4 7
5 17
6 1
7 24
8 17
9 45
10 57
11 30
12 2
13 9
14 26
15 108
16 6
17 3
18 7
19 154
20 24

About Mark A. van de Wiel

Mark A. van de Wiel is a scholar working on Statistics and Probability, Cancer Research and Otorhinolaryngology, having authored 165 papers that have together received 7.3k indexed citations. Recurring topics across this work include Gene expression and cancer classification (41 papers), Genomic variations and chromosomal abnormalities (21 papers) and Statistical Methods and Inference (20 papers). The work is most often cited by research in Cancer Research (1.8k citations), Otorhinolaryngology (310 citations) and Statistics and Probability (383 citations). Mark A. van de Wiel has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Achim Zeileis, Kurt Hornik, Torsten Hothorn, Wessel N. van Wieringen, Bauke Ylstra, Gerrit A. Meijer, Saskia M. Wilting, Beatriz Carvalho, Ruud H. Brakenhoff and Peter J.F. Snijders. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

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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