Christel Herold‐Mende

79.2k citations
313 papers · 14.4k indexed · 3 hit papers · h-index 63
Topics
Glioma Diagnosis and Treatment (114 papers)Cancer, Hypoxia, and Metabolism (33 papers)Meningioma and schwannoma management (25 papers)

In The Last Decade

Christel Herold‐Mende

300 papers receiving 14.2k citations

Hit Papers

Type and frequency of IDH1 and IDH2 mutations are related...2009202620142020200920112015250500750

Peers

Christel Herold‐Mende
Comparison fields: 5 of 146
  • Molecular Biology 6.3k
  • Genetics 5.6k
  • Oncology 4.3k
  • Cancer Research 3.6k
  • Immunology 2.0k
Replace Jann N. Sarkaria with:
Jann N. Sarkaria United States
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Citations per field
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Jann N. Sarkaria · 1×
Citations per year

Countries citing papers authored by Christel Herold‐Mende

Since Specialization
Citations

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

Fields of papers citing papers by Christel Herold‐Mende

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christel Herold‐Mende. 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 Christel Herold‐Mende. The network helps show where Christel Herold‐Mende may publish in the future.

Co-authorship network of co-authors of Christel Herold‐Mende

This figure shows the co-authorship network connecting the top 25 collaborators of Christel Herold‐Mende. A scholar is included among the top collaborators of Christel Herold‐Mende 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 Christel Herold‐Mende. Christel Herold‐Mende 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 9
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5 7
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8 9
9 23
10 27
11 26
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13 22
14 10
15 45
16 100
17 272
18 251
19 150
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[Significance of aberrant p53 protein in head-neck tumors and its effect on proliferation and differentiation].
4

About Christel Herold‐Mende

Christel Herold‐Mende is a scholar working on Genetics, Cancer Research and Oncology, having authored 313 papers that have together received 14.4k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (114 papers), Cancer, Hypoxia, and Metabolism (33 papers) and Meningioma and schwannoma management (25 papers). The work is most often cited by research in Genetics (5.6k citations), Cancer Research (3.6k citations) and Oncology (4.3k citations). Christel Herold‐Mende has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Andreas von Deimling, Andreas Unterberg, David Capper, Benito Campos, Christian Hartmann, Wolfgang Wick, Rezvan Ahmadi, Guido Reifenberger, Bernhard Radlwimmer and Gerhard Dyckhoff. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Angewandte Chemie International Edition.

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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