K. Schiebel

1.5k citations
32 papers · 1.1k · 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

    • Genomics and Chromatin Dynamics 6
    • Sexual Differentiation and Disorders 5
    • Prion Diseases and Protein Misfolding 5
    • Ubiquitin and proteasome pathways 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 13

K. Schiebel

32 papers receiving 1.1k citations

Peers

K. Schiebel
Comparison fields: 5 of 77
  • Neurology 231
  • Genetics 439
  • Molecular Biology 801
  • Nutrition and Dietetics 149
  • Reproductive Medicine 62
Replace Delphine Fagegaltier with:
Delphine Fagegaltier United States
Pascale Debey France
I. HARBITZ Norway
Osamu Nakabayashi Japan
Yoshiyuki Sakaki Japan
Noboru Wakasugi Japan
Wenhao Xu United States
Dietrich Simon Germany
Keith McFarland United States
Susan M. Uptain United States
K. Schiebel relative to Delphine Fagegaltier United States Delphine Fagegaltier's profile →
Citations per field
00.5×10.3×
Delphine Fagegaltier · 1×
Citations per year

Countries citing papers authored by K. Schiebel

Since Specialization
Citations

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

Fields of papers citing papers by K. Schiebel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2006128
2 2005109
3 199795
4 200773
5 199869
6 199368
7 199552
8 198845
9 198941
10 198938
11 200737
12 199735
13 199831
14 199831
15 199131
16 199527
17 200022
18 199721
19 199720
20 199719

About K. Schiebel

K. Schiebel is a scholar working on Molecular Biology, Genetics, Plant Science, Neurology and Nutrition and Dietetics, having authored 32 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Chromosomal and Genetic Variations (6 papers), Genomics and Chromatin Dynamics (6 papers), Sexual Differentiation and Disorders (5 papers), Prion Diseases and Protein Misfolding (5 papers), Neurological diseases and metabolism (4 papers), Ubiquitin and proteasome pathways (3 papers) and Genetic and Environmental Crop Studies (3 papers). The work is most often cited by research in Neurology (231 citations), Genetics (439 citations), Molecular Biology (801 citations), Nutrition and Dietetics (149 citations) and Reproductive Medicine (62 citations). K. Schiebel has collaborated with scholars based in Germany, Australia and United States. Frequent co-authors include Gudrun Rappold, Vera Hemleben, Tosso Leeb, Cord Drögemüller, Martin H. Groschup, M. Winkelmann, Annelyse Mertz, H. Hamann, Doris Wöhrle and W. Schempp. Their work appears in journals such as Cytogenetic and Genome Research, Human Molecular Genetics, Chromosome Research, Human Genetics and Gene.

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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