Peter Bauer
Impact in
- Nephrology top 0.5%
- Acute Kidney Injury Research
Papers in
- Genetics 78
- Genomics and Rare Diseases 42
- Genetics and Neurodevelopmental Disorders 36
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- Hereditary Neurological Disorders 22
- Genetic Neurodegenerative Diseases 21
- Co-authors
- Philipp Metnitz (21 shared papers)Rui Paulo Moreno (13 shared papers)Wilfred Druml (5 shared papers)Maurizia Capuzzo (5 shared papers)B Dragosics (2 shared papers)T Radaszkiewicz (2 shared papers)Barbara Jordan (4 shared papers)Daniel Schmidlin (2 shared papers)
- Journals
- Brain (19 papers)Movement Disorders (17 papers)European Journal of Human Genetics (17 papers)Clinical Genetics (16 papers)Intensive Care Medicine (11 papers)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Peter Bauer
347 papers receiving 15.5k citations
Peter Bauer's Hit Papers
Peers
Comparison fields: 5 of 202
- Nephrology 1.4k
- Critical Care and Intensive Care Medicine 576
- Cellular and Molecular Neuroscience 1.9k
- Neurology 832
- Genetics 2.6k
Countries citing papers authored by Peter Bauer
This map shows the geographic impact of Peter Bauer'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 Peter Bauer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Bauer more than expected).
Fields of papers citing papers by Peter Bauer
This network shows the impact of papers produced by Peter Bauer. 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 Peter Bauer. The network helps show where Peter Bauer may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Bauer, 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 357 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Minimal Changes of Serum Creatinine Predict Prognosis in Patients after Cardiothoracic Surgery Hit paper breakdown → | 2004 | 1128 |
| 2 | SAPS 3—From evaluation of the patient to evaluation of the intensive care unit. Part 2: Development of a prognostic model for hospital mortality at ICU admission Hit paper breakdown → | 2005 | 1096 |
| 3 | Mortality after surgery in Europe: a 7 day cohort study Hit paper breakdown → | 2012 | 999 |
| 4 | A draft genome of Yersinia pestis from victims of the Black Death Hit paper breakdown → | 2011 | 535 |
| 5 | 2005 | 529 | |
| 6 | A Revised Timescale for Human Evolution Based on Ancient Mitochondrial Genomes Hit paper breakdown → | 2013 | 509 |
| 7 | 1997 | 434 | |
| 8 | 2015 | 401 | |
| 9 | 1992 | 391 | |
| 10 | 2009 | 316 | |
| 11 | 2013 | 268 | |
| 12 | 2007 | 256 | |
| 13 | 2008 | 250 | |
| 14 | 2009 | 243 | |
| 15 | 1985 | 224 | |
| 16 | 2016 | 211 | |
| 17 | 2006 | 200 | |
| 18 | 1991 | 179 | |
| 19 | 1996 | 171 | |
| 20 | 2010 | 167 |
About Peter Bauer
Peter Bauer is a scholar working on Genetics, Cellular and Molecular Neuroscience, Neurology, Physiology and Molecular Biology, having authored 357 papers that have together received 16.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (42 papers), Lysosomal Storage Disorders Research (36 papers), Genetics and Neurodevelopmental Disorders (36 papers), Parkinson's Disease Mechanisms and Treatments (29 papers), Hereditary Neurological Disorders (22 papers), Genetic Neurodegenerative Diseases (21 papers), Neurological diseases and metabolism (21 papers) and Cellular transport and secretion (17 papers). The work is most often cited by research in Nephrology (1.4k citations), Critical Care and Intensive Care Medicine (576 citations), Cellular and Molecular Neuroscience (1.9k citations), Neurology (832 citations) and Genetics (2.6k citations). Peter Bauer has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Philipp Metnitz, Rui Paulo Moreno, Wilfred Druml, Maurizia Capuzzo, B Dragosics, T Radaszkiewicz, Barbara Jordan, Daniel Schmidlin, Andrea M. Lassnigg and Michael Joerg Hiesmayr. Their work appears in journals such as Brain, Movement Disorders, European Journal of Human Genetics, Clinical Genetics and Intensive Care Medicine.
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.