Jochen Weile

4.0k citations
29 papers · 681 · h-index 13

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • RNA and protein synthesis mechanisms
    • Bioinformatics and Genomic Networks
    • CRISPR and Genetic Engineering
    • Genomics and Phylogenetic Studies

Papers in

    • Bioinformatics and Genomic Networks 5
    • Genomics and Phylogenetic Studies 4
    • CRISPR and Genetic Engineering 3
    • DNA Repair Mechanisms 2
    • Ubiquitin and proteasome pathways 2
    • Genomics and Rare Diseases 10
    • Evolution and Genetic Dynamics 2

Jochen Weile

28 papers receiving 677 citations

Peers

Jochen Weile
Comparison fields: 5 of 73
  • Genetics 281
  • Molecular Biology 434
  • Cancer Research 67
  • Computational Theory and Mathematics 45
  • Clinical Biochemistry 10
Replace Minghong Ward with:
Minghong Ward United States
Vijaya Parthiban Germany
Gabriel Musso United States
Tiziana Sanavia Italy
Anwesha Bohler Netherlands
Alok Jaiswal Finland
Jagannath Misra United States
Victoria Petri United States
Graham K. Bilter United States
Jane McPheat United Kingdom
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Citations per field
00.5×2.6×
Minghong Ward · 1×
Citations per year

Countries citing papers authored by Jochen Weile

Since Specialization
Citations

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

Fields of papers citing papers by Jochen Weile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2019136
2 201896
3 202180
4 201349
5 202040
6 202038
7 201134
8 202330
9 201024
10 201022
11 202116
12 202413
13 202312
14 200711
15 201711
16 201910
17 20129
18 20208
19 20197
20 20116

About Jochen Weile

Jochen Weile is a scholar working on Molecular Biology, Genetics, Surgery, Economics and Econometrics and Cardiology and Cardiovascular Medicine, having authored 29 papers that have together received 681 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Bioinformatics and Genomic Networks (5 papers), Genomics and Phylogenetic Studies (4 papers), CRISPR and Genetic Engineering (3 papers), DNA Repair Mechanisms (2 papers), Ubiquitin and proteasome pathways (2 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers) and Evolution and Genetic Dynamics (2 papers). The work is most often cited by research in Genetics (281 citations), Molecular Biology (434 citations), Cancer Research (67 citations), Computational Theory and Mathematics (45 citations) and Clinical Biochemistry (10 citations). Jochen Weile has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Frederick P. Roth, Song Sun, Alan F. Rubin, Douglas M. Fowler, Roujia Li, Lea M. Starita, Jay Shendure, Anthony T. Papenfuss, Anil Wipat and Hanqing Liu. Their work appears in journals such as Bioinformatics, Genome biology, The American Journal of Human Genetics, Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics and Human Mutation.

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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