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 22
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 5
- BRCA gene mutations in cancer 4
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- Metabolomics and Mass Spectrometry Studies 4
- Co-authors
- Oliver Kohlbacher (12 shared papers)Knut Reinert (5 shared papers)Eva Lange (4 shared papers)Clemens Gröpl (4 shared papers)Nico Pfeifer (3 shared papers)Ole Schulz-Trieglaff (3 shared papers)Benjamin Schubert (1 shared paper)Christopher Mohr (1 shared paper)
- Journals
- Bioinformatics (4 papers)European Journal of Human Genetics (4 papers)Journal of Proteome Research (4 papers)Movement Disorders (3 papers)Human Genetics (2 papers)
- Partner nations
- GermanyUnited StatesIndia
In The Last Decade
Marc Sturm
49 papers receiving 2.8k citations
Marc Sturm's Hit Papers
Peers
Comparison fields: 5 of 135
- Spectroscopy 1.0k
- Molecular Biology 1.6k
- Genetics 379
- Cancer Research 189
- Immunology 269
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-authors
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
Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | mzML—a Community Standard for Mass Spectrometry Data Hit paper breakdown → | 2010 | 515 |
| 2 | OpenMS – An open-source software framework for mass spectrometry Hit paper breakdown → | 2008 | 501 |
| 3 | 2014 | 426 | |
| 4 | 2015 | 342 | |
| 5 | 2007 | 218 | |
| 6 | 2013 | 124 | |
| 7 | 2016 | 87 | |
| 8 | 2009 | 66 | |
| 9 | 2005 | 62 | |
| 10 | 2012 | 38 | |
| 11 | 2015 | 35 | |
| 12 | 2015 | 35 | |
| 13 | 2018 | 33 | |
| 14 | 2018 | 28 | |
| 15 | 2013 | 25 | |
| 16 | 2007 | 22 | |
| 17 | 2006 | 21 | |
| 18 | 2020 | 20 | |
| 19 | 2015 | 20 | |
| 20 | 2018 | 16 |
About Marc Sturm
Marc Sturm is a scholar working on Genetics, Molecular Biology, Spectroscopy, Cancer Research and Pathology and Forensic Medicine, having authored 53 papers that have together received 2.8k 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), Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Metabolomics and Mass Spectrometry Studies (4 papers), BRCA gene mutations in cancer (4 papers) and Mass Spectrometry Techniques and Applications (4 papers). The work is most often cited by research in Spectroscopy (1.0k citations), Molecular Biology (1.6k citations), Genetics (379 citations), Cancer Research (189 citations) and Immunology (269 citations). Marc Sturm has collaborated with scholars based in Germany, United States and India. Frequent co-authors include Oliver Kohlbacher, Knut Reinert, Eva Lange, Clemens Gröpl, Nico Pfeifer, Ole Schulz-Trieglaff, Benjamin Schubert, Christopher Mohr, Magdalena Feldhahn and András Szolek. Their work appears in journals such as Bioinformatics, European Journal of Human Genetics, Journal of Proteome Research, Movement Disorders and Human 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.