Michael Baudis
Impact in
- Genetics top 1%
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 44
- Genomic variations and chromosomal abnormalities 34
- Genomics and Rare Diseases 8
- Glioma Diagnosis and Treatment 7
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- Cancer Genomics and Diagnostics 19
- Co-authors
- Peter Lichter (7 shared papers)Michael L. Cleary (1 shared paper)Reiner Siebert (6 shared papers)Ruthild G. Weber (3 shared papers)Guido Reifenberger (1 shared paper)Vincent Peter Collins (1 shared paper)Jan Patrick Boström (1 shared paper)Marietta Wolter (1 shared paper)
- Journals
- Genes Chromosomes and Cancer (4 papers)PLoS ONE (4 papers)Bioinformatics (4 papers)Neuro-Oncology (4 papers)BMC Cancer (3 papers)
- Partner nations
- SwitzerlandGermanyUnited States
In The Last Decade
Michael Baudis
92 papers receiving 4.3k citations
Michael Baudis's Hit Papers
Peers
Comparison fields: 5 of 99
- Genetics 889
- Cancer Research 573
- Pathology and Forensic Medicine 688
- Health Informatics 73
- Genetics 788
Countries citing papers authored by Michael Baudis
This map shows the geographic impact of Michael Baudis'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 Baudis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael Baudis more than expected).
Fields of papers citing papers by Michael Baudis
This network shows the impact of papers produced by Michael Baudis. 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 Baudis. The network helps show where Michael Baudis may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael Baudis, 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 96 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma Hit paper breakdown → | 2017 | 851 |
| 2 | 1997 | 348 | |
| 3 | GA4GH: International policies and standards for data sharing across genomic research and healthcare Hit paper breakdown → | 2021 | 203 |
| 4 | 2008 | 170 | |
| 5 | 2001 | 154 | |
| 6 | 2005 | 145 | |
| 7 | 2000 | 128 | |
| 8 | 2001 | 120 | |
| 9 | 2020 | 120 | |
| 10 | 2007 | 119 | |
| 11 | 2002 | 114 | |
| 12 | 2020 | 98 | |
| 13 | 2014 | 91 | |
| 14 | 2009 | 85 | |
| 15 | 2007 | 76 | |
| 16 | 2019 | 72 | |
| 17 | 2019 | 71 | |
| 18 | 1997 | 70 | |
| 19 | 2005 | 70 | |
| 20 | 2013 | 68 |
About Michael Baudis
Michael Baudis is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Genetics and Health Information Management, having authored 96 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (34 papers), Cancer Genomics and Diagnostics (19 papers), Lymphoma Diagnosis and Treatment (15 papers), Genomics and Rare Diseases (8 papers), Electronic Health Records Systems (8 papers), Research Data Management Practices (8 papers), Glioma Diagnosis and Treatment (7 papers) and Biomedical Text Mining and Ontologies (5 papers). The work is most often cited by research in Genetics (889 citations), Cancer Research (573 citations), Pathology and Forensic Medicine (688 citations), Health Informatics (73 citations) and Genetics (788 citations). Michael Baudis has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include Peter Lichter, Michael L. Cleary, Reiner Siebert, Ruthild G. Weber, Guido Reifenberger, Vincent Peter Collins, Jan Patrick Boström, Marietta Wolter, Evert-Jan Gijsbert Boerma and Philip M. Kluin. Their work appears in journals such as Genes Chromosomes and Cancer, PLoS ONE, Bioinformatics, Neuro-Oncology and BMC Cancer.
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.