Katrin Schiebel

1.5k citations
33 papers · 1.2k · h-index 20

Impact in

  • Neurology top 5%
    • Neurological diseases and metabolism
  • Genetics top 5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Animal Genetics and Reproduction

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 13
    • Genomics and Chromatin Dynamics 6
    • Prion Diseases and Protein Misfolding 6
    • Sexual Differentiation and Disorders 5

Katrin Schiebel

33 papers receiving 1.2k citations

Peers

Katrin Schiebel
Comparison fields: 5 of 79
  • Neurology 259
  • Genetics 479
  • Molecular Biology 890
  • Nutrition and Dietetics 167
  • Reproductive Medicine 71
Replace INGRID HARBITZ with:
INGRID HARBITZ Norway
Michael C. Summers United States
Zuzanna Tymowska‐Lalanne United Kingdom
Hester P. M. Pratt United Kingdom
Yoshiyuki Sakaki Japan
Wenhao Xu United States
Y Shibata Japan
Noboru Wakasugi Japan
Jeffrey A. Goliger United States
Keith McFarland United States
Katrin Schiebel relative to INGRID HARBITZ Norway INGRID HARBITZ's profile →
Citations per field
00.5×5×10×12.5×
INGRID HARBITZ · 1×
Citations per year

Countries citing papers authored by Katrin Schiebel

Since Specialization
Citations

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

Fields of papers citing papers by Katrin Schiebel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2006142
2 1997117
3 2005111
4 199881
5 200774
6 199373
7 199550
8 198849
9 198942
10 198941
11 200739
12 199838
13 199134
14 199833
15 199731
16 199528
17 200225
18 199723
19 200022
20 199721

About Katrin Schiebel

Katrin Schiebel is a scholar working on Genetics, Molecular Biology, Neurology, Plant Science and Cancer Research, having authored 33 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Genomics and Chromatin Dynamics (6 papers), Prion Diseases and Protein Misfolding (6 papers), Chromosomal and Genetic Variations (6 papers), Neurological diseases and metabolism (5 papers), Sexual Differentiation and Disorders (5 papers), Genetic and Environmental Crop Studies (3 papers) and Plant Disease Resistance and Genetics (3 papers). The work is most often cited by research in Neurology (259 citations), Genetics (479 citations), Molecular Biology (890 citations), Nutrition and Dietetics (167 citations) and Reproductive Medicine (71 citations). Katrin Schiebel has collaborated with scholars based in Germany, Australia and Poland. Frequent co-authors include Gudrun Rappold, Vera Hemleben, Tosso Leeb, M. Winkelmann, Martin H. Groschup, Cord Drögemüller, Annelyse Mertz, Andreas Humeny, H. Hamann and Doris Wöhrle. Their work appears in journals such as Chromosome Research, Cytogenetic and Genome Research, Human Molecular Genetics, Human Genetics and Clinical Chemistry.

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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