Marc Sturm
Impact in
- Spectroscopy top 0.5%
- Advanced Proteomics Techniques and Applications
- Mass Spectrometry Techniques and Applications
- Analytical Chemistry and Chromatography
- Molecular Biology top 5%
- Metabolomics and Mass Spectrometry Studies
- Genomics and Phylogenetic Studies
Papers in
- Genetics 21
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- BRCA gene mutations in cancer 4
- Spectroscopy 10
- Advanced Proteomics Techniques and Applications 8
- Mass Spectrometry Techniques and Applications 6
- Co-authors
- Oliver KohlbacherKnut ReinertEva LangeClemens GröplOle Schulz-TrieglaffNico PfeiferAndrás SzolekMagdalena Feldhahn
- Journals
- European Journal of Human Genetics (4 papers)Bioinformatics (4 papers)Journal of Proteome Research (4 papers)Movement Disorders (3 papers)BMC Bioinformatics (2 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Marc Sturm
48 papers receiving 2.7k citations
Hit Papers
Peers
Comparison fields: 5 of 137
- Spectroscopy 1.1k
- Molecular Biology 1.8k
- Immunology 319
- Cancer Research 226
- Genetics 418
Countries citing papers authored by Marc Sturm
This map shows the geographic impact of Marc Sturm'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 Marc Sturm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc Sturm more than expected).
Fields of papers citing papers by Marc Sturm
This network shows the impact of papers produced by Marc Sturm. 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 Marc Sturm. The network helps show where Marc Sturm may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Marc Sturm, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2025 | 0 | |
| 3 | 2024 | 1 | |
| 4 | 2024 | 11 | |
| 5 | 2024 | 1 | |
| 6 | 2024 | 3 | |
| 7 | 2023 | 1 | |
| 8 | 2023 | 2 | |
| 9 | 2023 | 3 | |
| 10 | 2022 | 9 | |
| 11 | 2022 | 3 | |
| 12 | 2021 | 1 | |
| 13 | 2020 | 5 | |
| 14 | 2019 | 7 | |
| 15 | 2018 | 6 | |
| 16 | 2018 | 16 | |
| 17 | 2018 | 8 | |
| 18 | EuroGentest guidelines for diagnostic next generation sequencing | 2014 | 3 |
| 19 | 2014 | 4 | |
| 20 | OpenMS – An open-source software framework for mass spectrometry Hit paper breakdown → | 2008 | 500 |
About Marc Sturm
Marc Sturm is a scholar working on Genetics, Spectroscopy, Cancer Research, Neurology and Molecular Biology, having authored 52 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Cancer Genomics and Diagnostics (8 papers), Advanced Proteomics Techniques and Applications (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Metabolomics and Mass Spectrometry Studies (6 papers), Mass Spectrometry Techniques and Applications (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and BRCA gene mutations in cancer (4 papers). The work is most often cited by research in Spectroscopy (1.1k citations), Molecular Biology (1.8k citations), Immunology (319 citations), Cancer Research (226 citations) and Genetics (418 citations). Marc Sturm has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Oliver Kohlbacher, Knut Reinert, Eva Lange, Clemens Gröpl, Ole Schulz-Trieglaff, Nico Pfeifer, András Szolek, Magdalena Feldhahn, Christopher Mohr and Benjamin Schubert. Their work appears in journals such as European Journal of Human Genetics, Bioinformatics, Journal of Proteome Research, Movement Disorders and BMC Bioinformatics.
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.