Stefan U. Kass

5.1k citations
23 papers · 4.0k indexed · 1 hit paper · h-index 18
Topics
Epigenetics and DNA Methylation (10 papers)Genetic Syndromes and Imprinting (5 papers)Genetics and Neurodevelopmental Disorders (5 papers)

In The Last Decade

Stefan U. Kass

23 papers receiving 3.9k citations

Hit Papers

Methylated DNA and MeCP2 recruit histone deacetylase to r...1998202620072016199850010001.5k2.0k

Peers

Stefan U. Kass
Comparison fields: 5 of 118
  • Molecular Biology 3.3k
  • Genetics 1.2k
  • Cellular and Molecular Neuroscience 289
  • Oncology 287
  • Cognitive Neuroscience 273
Replace Armin Schumacher with:
Armin Schumacher United States
Christopher J. Phiel United States
Roland P.S. Kwok United States
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Stefan U. Kass relative to Armin Schumacher United States Armin Schumacher's profile →
Citations per field
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Citations per year

Countries citing papers authored by Stefan U. Kass

Since Specialization
Citations

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

Fields of papers citing papers by Stefan U. Kass

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefan U. Kass. 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 Stefan U. Kass. The network helps show where Stefan U. Kass may publish in the future.

Co-authorship network of co-authors of Stefan U. Kass

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan U. Kass. A scholar is included among the top collaborators of Stefan U. Kass 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 Stefan U. Kass. Stefan U. Kass 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 6
2 59
3 52
4 91
5 172
6 133
7 27
8 20
9 22
10 50
11 1
12 108
13
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcriptionbreakdown →
2139
14 42
15 308
16 436
17 79
18 1
19 15
20 24

About Stefan U. Kass

Stefan U. Kass is a scholar working on Aging, Behavioral Neuroscience and Genetics, having authored 23 papers that have together received 4.0k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (10 papers), Genetic Syndromes and Imprinting (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Molecular Biology (3.3k citations), Genetics (1.2k citations) and Endocrine and Autonomic Systems (141 citations). Stefan U. Kass has collaborated with scholars based in United States, Belgium and United Kingdom. Frequent co-authors include Alan P. Wolffe, Nicoletta Landsberger, Peter Lloyd Jones, Danielle Vermaak, Gert Jan C. Veenstra, Paul A. Wade, John Strouboulis, Dmitry Pruss, Ilse Van den Wyngaert and R.L.P. Adams. Their work appears in journals such as Science, Journal of Biological Chemistry and Nature Genetics.

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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