Gunnar Schotta

11.2k citations
77 papers · 6.3k indexed · 2 hit papers · h-index 39

Impact in

    • Epigenetics and DNA Methylation
    • Genomics and Chromatin Dynamics
    • Cancer-related gene regulation
    • RNA modifications and cancer
    • RNA Research and Splicing
    • CRISPR and Genetic Engineering
    • DNA Repair Mechanisms
  • Aging top 2%

Papers in

    • Genomics and Chromatin Dynamics 39
    • Epigenetics and DNA Methylation 35
    • Cancer-related gene regulation 13
    • RNA modifications and cancer 11
    • CRISPR and Genetic Engineering 7
    • RNA Research and Splicing 7
    • Histone Deacetylase Inhibitors Research 5

Gunnar Schotta

76 papers receiving 6.2k citations

Hit Papers

A silencing pathway to induce H3-K9 and H4-K20 trimethylation at constitutive heterochromatin 2004 · 850 citations
8502002202620102018250500750

Peers

Gunnar Schotta
Comparison fields: 5 of 112
  • Molecular Biology 5.6k
  • Aging 108
  • Plant Science 1.1k
  • Genetics 829
  • Cancer Research 400
Replace Monika Lachner with:
Monika Lachner Austria
Susanne Opravil Austria
Judd C. Rice United States
Devon Ryan Germany
Stephen Rea Germany
Sharon Dent United States
Juan M. Vaquerizas Germany
Matthew C. Lorincz Canada
Janet F. Partridge United States
Dana J. Huebert United States
Gunnar Schotta relative to Monika Lachner Austria Monika Lachner's profile →
Citations per field
00.5×
Monika Lachner · 1×
Citations per year

Countries citing papers authored by Gunnar Schotta

Since Specialization
Citations

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

Fields of papers citing papers by Gunnar Schotta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gunnar Schotta, 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 Gunnar Schotta Line = papers co-authored together Gunnar Schotta links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20231
2 202210
3 202223
4 2021148
5 20211
6 202120
7 202153
8 202030
9 201954
10 201935
11 201751
12 20168
13 201514
14 2014127
15 201469
16 201379
17 201246
18 201112
19 2004218
20 2003158

About Gunnar Schotta

Gunnar Schotta is a scholar working on Molecular Biology, Aging, Virology, Hematology and Genetics, having authored 77 papers that have together received 6.3k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (39 papers), Epigenetics and DNA Methylation (35 papers), Cancer-related gene regulation (13 papers), Chromosomal and Genetic Variations (13 papers), RNA modifications and cancer (11 papers), CRISPR and Genetic Engineering (7 papers), RNA Research and Splicing (7 papers) and Histone Deacetylase Inhibitors Research (5 papers). The work is most often cited by research in Molecular Biology (5.6k citations), Aging (108 citations), Plant Science (1.1k citations), Genetics (829 citations) and Cancer Research (400 citations). Gunnar Schotta has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Günter Reuter, Thomas Jenuwein, Anja Ebert, Roopsha Sengupta, Monika Lachner, Danny Reinberg, Kavitha Sarma, S. Jorgensen, Claus Storgaard Sørensen and Stefan Kubicek. Their work appears in journals such as Nucleic Acids Research, Cell Reports, Genes & Development, Nature Communications and Nature Cell Biology.

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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