Daniel Schrimpf

14.2k citations
52 papers · 1.7k · h-index 20

Impact in

  • Genetics top 0.5%
    • Glioma Diagnosis and Treatment
    • Cancer Genomics and Diagnostics
    • MicroRNA in disease regulation

Papers in

    • Glioma Diagnosis and Treatment 31
    • Chromatin Remodeling and Cancer 9
    • Epigenetics and DNA Methylation 7
    • Hedgehog Signaling Pathway Studies 5

Daniel Schrimpf

49 papers receiving 1.7k citations

Peers

Daniel Schrimpf
Comparison fields: 5 of 99
  • Genetics 1.2k
  • Cancer Research 467
  • Neurology 365
  • Radiology, Nuclear Medicine and Imaging 293
  • Pulmonary and Respiratory Medicine 399
Replace Julie Lejeune with:
Julie Lejeune France
Andrey Golanov Russia
Arne Christians Germany
Yasuji Miyakita Japan
Felipe Andreiuolo France
Magdalena C. Ƶlatescu Canada
Ralf Ketter Germany
Emmanuelle Crinière France
Dominik Sturm Germany
Sylvia Kocialkowski United Kingdom
Daniel Schrimpf relative to Julie Lejeune France Julie Lejeune's profile →
Citations per field
00.5×10×14×
Julie Lejeune · 1×
Citations per year

Countries citing papers authored by Daniel Schrimpf

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Schrimpf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Daniel Schrimpf, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniel Schrimpf Line = papers co-authored together Daniel Schrimpf links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2014306
2 2015233
3 2018207
4 2017130
5 2019101
6 202198
7 201785
8 201941
9 202237
10 201736
11 202135
12 201834
13 201830
14 202126
15 201824
16 202221
17 201621
18 201820
19 201620
20 201519

About Daniel Schrimpf

Daniel Schrimpf is a scholar working on Genetics, Molecular Biology, Cancer Research, Pulmonary and Respiratory Medicine and Neurology, having authored 52 papers that have together received 1.7k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (31 papers), Chromatin Remodeling and Cancer (9 papers), Epigenetics and DNA Methylation (7 papers), Cancer Genomics and Diagnostics (6 papers), Neuroblastoma Research and Treatments (6 papers), MicroRNA in disease regulation (6 papers), Meningioma and schwannoma management (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). The work is most often cited by research in Genetics (1.2k citations), Cancer Research (467 citations), Neurology (365 citations), Radiology, Nuclear Medicine and Imaging (293 citations) and Pulmonary and Respiratory Medicine (399 citations). Daniel Schrimpf has collaborated with scholars based in Germany, Netherlands and United States. Frequent co-authors include Andreas von Deimling, David Capper, Stefan M. Pfister, Felix Sahm, David Jones, Andrey Korshunov, David Reuß, Damian Stichel, Wolfgang Wick and Christel Herold‐Mende. Their work appears in journals such as Acta Neuropathologica, Neuro-Oncology, Acta Neuropathologica Communications, Inflammation Research and Clinical Cancer Research.

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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