Udo Koehler

1.6k citations
44 papers · 985 indexed · h-index 18
Topics
Genomic variations and chromosomal abnormalities (16 papers)Chromosomal and Genetic Variations (10 papers)Genetic factors in colorectal cancer (6 papers)

In The Last Decade

Udo Koehler

43 papers receiving 974 citations

Peers

Udo Koehler
Comparison fields: 5 of 95
  • Genetics 487
  • Molecular Biology 474
  • Plant Science 387
  • Pathology and Forensic Medicine 106
  • Cancer Research 106
Replace Michaela Neusser with:
Michaela Neusser Germany
H. G. Schwarzacher Austria
Ram S. Verma United States
Matthieu Gérard France
Shintaroh Ueda Japan
I. Patel United Kingdom
B. J. Trask United States
Joel K. Yisraeli Israel
Friedrich Weber Germany
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Udo Koehler relative to Michaela Neusser Germany Michaela Neusser's profile →
Citations per field
00.5×6.6×
Michaela Neusser · 1×
Citations per year

Countries citing papers authored by Udo Koehler

Since Specialization
Citations

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

Fields of papers citing papers by Udo Koehler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Udo Koehler

This figure shows the co-authorship network connecting the top 25 collaborators of Udo Koehler. A scholar is included among the top collaborators of Udo Koehler 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 Udo Koehler. Udo Koehler 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 10
2 5
3 12
4 7
5 9
6
Preimplantation Genetic Diagnosis for Monogenic Disorders and Chromosomal Rearrangements – The German Perspective
3
7 17
8 35
9 5
10 54
11 44
12 4
13 33
14 39
15 34
16 21
17 39
18 45
19 10
20 62

About Udo Koehler

Udo Koehler is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 44 papers that have together received 985 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Chromosomal and Genetic Variations (10 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Genetics (487 citations), Plant Science (387 citations) and Cancer Research (106 citations). Udo Koehler has collaborated with scholars based in Germany, Italy and United States. Frequent co-authors include Roscoe Stanyon, Johannes Wienberg, F. Bigoni, Stefania Consigliere, Norbert Arnold, Robert J. Hamers, J. E. Demuth, Elke Holinski‐Feder, Govindasamy Agoramoorthy and Peter D. Kaplan. Their work appears in journals such as Physical Review Letters, Nucleic Acids Research and Human Molecular 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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