K. Schiebel

1.5k citations
32 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

    • 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 81
  • Neurology 243
  • Genetics 469
  • Molecular Biology 853
  • Nutrition and Dietetics 155
  • Reproductive Medicine 66
Replace Delphine Fagegaltier with:
Delphine Fagegaltier United States
I. HARBITZ Norway
Pascale Debey France
Osamu Nakabayashi Japan
Yoshiyuki Sakaki Japan
Nicolas Vinckenbosch Switzerland
Noboru Wakasugi Japan
Wenhao Xu United States
Jeffrey A. Goliger United States
Keith McFarland United States
K. Schiebel relative to Delphine Fagegaltier United States Delphine Fagegaltier's profile →
Citations per field
00.5×5×11×
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 2006139
2 2005110
3 1997106
4 199876
5 199375
6 200774
7 199553
8 198849
9 198942
10 198941
11 199839
12 200738
13 199735
14 199134
15 199832
16 199528
17 200022
18 199722
19 199721
20 199720

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 1.2k 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 (243 citations), Genetics (469 citations), Molecular Biology (853 citations), Nutrition and Dietetics (155 citations) and Reproductive Medicine (66 citations). K. Schiebel has collaborated with scholars based in Germany, Australia and United States. Frequent co-authors include Gudrun Rappold, Vera Hemleben, Tosso Leeb, M. Winkelmann, Cord Drögemüller, Martin H. Groschup, Annelyse Mertz, Doris Wöhrle, Birgit Weiß and H. Hamann. Their work appears in journals such as Human Molecular Genetics, Cytogenetic and Genome Research, Chromosome Research, Human Genetics and Mammalian Genome.

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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