Michael Mueller
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Spectroscopy top 2%
- Advanced Proteomics Techniques and Applications
Papers in
- Genetics 25
- Genomics and Rare Diseases 14
- Genetic Associations and Epidemiology 4
- Genetics and Neurodevelopmental Disorders 3
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- Advanced Proteomics Techniques and Applications 7
- Co-authors
- Lennart Martens (7 shared papers)Elien Vandermarliere (1 shared paper)Juan Antonio Vizcaíno (3 shared papers)Henning Hermjakob (3 shared papers)Timothy J. Aitman (8 shared papers)Rick Cote (1 shared paper)Jonathan Rameseder (1 shared paper)Florian Reisinger (1 shared paper)
- Journals
- Genetics in Medicine (9 papers)PROTEOMICS (5 papers)Scientific Reports (4 papers)Nature Communications (4 papers)Nature Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Michael Mueller
55 papers receiving 3.1k citations
Michael Mueller's Hit Papers
Peers
Comparison fields: 5 of 123
- Genetics 911
- Spectroscopy 394
- Cancer Research 274
- Molecular Biology 889
- Aging 14
Countries citing papers authored by Michael Mueller
This map shows the geographic impact of Michael Mueller'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 Michael Mueller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael Mueller more than expected).
Fields of papers citing papers by Michael Mueller
This network shows the impact of papers produced by Michael Mueller. 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 Michael Mueller. The network helps show where Michael Mueller may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael Mueller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 420 | |
| 2 | The 100 000 Genomes Project: bringing whole genome sequencing to the NHS Hit paper breakdown → | 2018 | 339 |
| 3 | 2009 | 205 | |
| 4 | 2008 | 198 | |
| 5 | Substitution mutational signatures in whole-genome–sequenced cancers in the UK population Hit paper breakdown → | 2022 | 195 |
| 6 | 2013 | 191 | |
| 7 | 2017 | 122 | |
| 8 | 2021 | 106 | |
| 9 | 2008 | 86 | |
| 10 | 2020 | 83 | |
| 11 | 2015 | 71 | |
| 12 | 2013 | 66 | |
| 13 | 2012 | 57 | |
| 14 | 2021 | 55 | |
| 15 | 2022 | 54 | |
| 16 | 2008 | 51 | |
| 17 | 2023 | 51 | |
| 18 | 2016 | 50 | |
| 19 | 2022 | 48 | |
| 20 | 2021 | 44 |
About Michael Mueller
Michael Mueller is a scholar working on Genetics, Spectroscopy, Cancer Research, Cellular and Molecular Neuroscience and Molecular Biology, having authored 55 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Advanced Proteomics Techniques and Applications (7 papers), Cancer Genomics and Diagnostics (6 papers), Genetic Associations and Epidemiology (4 papers), Hereditary Neurological Disorders (3 papers), Bioinformatics and Genomic Networks (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Genetics (911 citations), Spectroscopy (394 citations), Cancer Research (274 citations), Molecular Biology (889 citations) and Aging (14 citations). Michael Mueller has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Lennart Martens, Elien Vandermarliere, Juan Antonio Vizcaíno, Henning Hermjakob, Timothy J. Aitman, Rick Cote, Jonathan Rameseder, Florian Reisinger, Joseph M. Foster and Rolf Apweiler. Their work appears in journals such as Genetics in Medicine, PROTEOMICS, Scientific Reports, Nature Communications and Nature 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.