Beate Schlierf

516 citations
11 papers · 444 · h-index 9

Impact in

Papers in

    • RNA regulation and disease 2
    • RNA Research and Splicing 2
    • Heat shock proteins research 1
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetics and Neurodevelopmental Disorders 1

Beate Schlierf

11 papers receiving 440 citations

Peers

Beate Schlierf
Comparison fields: 5 of 73
  • Developmental Neuroscience 39
  • Cancer Research 91
  • Cell Biology 69
  • Molecular Biology 267
  • Immunology 63
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Citations per field
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Citations per year

Countries citing papers authored by Beate Schlierf

Since Specialization
Citations

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

Fields of papers citing papers by Beate Schlierf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 200084
2
A recombinant CD7-specific single-chain immunotoxin is a potent inducer of apoptosis in acute leukemic T cells.
200263
3 200254
4 200746
5 200646
6 200542
7 200440
8 200534
9 200627
10 19986
11 19982

About Beate Schlierf

Beate Schlierf is a scholar working on Molecular Biology, Genetics, Cancer Research, Cell Biology and Cellular and Molecular Neuroscience, having authored 11 papers that have together received 444 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), RNA regulation and disease (2 papers), Cancer-related molecular mechanisms research (2 papers), RNA Research and Splicing (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Folate and B Vitamins Research (1 paper), Heat shock proteins research (1 paper) and NF-κB Signaling Pathways (1 paper). The work is most often cited by research in Developmental Neuroscience (39 citations), Cancer Research (91 citations), Cell Biology (69 citations), Molecular Biology (267 citations) and Immunology (63 citations). Beate Schlierf has collaborated with scholars based in Germany. Frequent co-authors include Michael Wegner, Georg H. Fey, Gertrud M. Hocke, T. Werner, Olaf Rosorius, Joachim Hauber, Ralf P. Friedrich, G. Glaser, Anke Schardt and Martin Gramatzki. Their work appears in journals such as Journal of Molecular Biology, Experimental Cell Research, Neuropathology and Applied Neurobiology, Biochemical and Biophysical Research Communications and BioTechniques.

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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