Beat Steinmann
Impact in
- Genetics top 0.2%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
- Rheumatology top 0.5%
- Bone and Dental Protein Studies
Papers in
- Genetics 71
- Connective tissue disorders research 67
- Dermatological and Skeletal Disorders 25
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- Protein Tyrosine Phosphatases 7
- Co-authors
- Anne De Paepe (5 shared papers)Richard Wenstrup (3 shared papers)Peter Beighton (2 shared papers)Petros Tsipouras (2 shared papers)Peter M. Royce (6 shared papers)Andrea Superti‐Furga (20 shared papers)Cecilia Giunta (19 shared papers)Michael Raghunath (12 shared papers)
- Journals
- Human Mutation (8 papers)European Journal of Pediatrics (6 papers)Pediatric Research (6 papers)Human Genetics (6 papers)Molecular Genetics and Metabolism (6 papers)
- Partner nations
- SwitzerlandUnited StatesGermany
In The Last Decade
Beat Steinmann
121 papers receiving 6.1k citations
Beat Steinmann's Hit Papers
Peers
Comparison fields: 5 of 140
- Genetics 3.1k
- Rheumatology 964
- Clinical Biochemistry 429
- Cell Biology 784
- Immunology and Allergy 237
Countries citing papers authored by Beat Steinmann
This map shows the geographic impact of Beat Steinmann'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 Beat Steinmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beat Steinmann more than expected).
Fields of papers citing papers by Beat Steinmann
This network shows the impact of papers produced by Beat Steinmann. 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 Beat Steinmann. The network helps show where Beat Steinmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Beat Steinmann, 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 123 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 Hit paper breakdown → | 1998 | 1201 |
| 2 | Connective tissue and its heritable disorders : molecular, genetic, and medical aspects | 1993 | 380 |
| 3 | 1997 | 209 | |
| 4 | 1996 | 169 | |
| 5 | 2012 | 166 | |
| 6 | 2008 | 150 | |
| 7 | 2009 | 111 | |
| 8 | 1994 | 110 | |
| 9 | 2006 | 107 | |
| 10 | 1993 | 104 | |
| 11 | 2001 | 99 | |
| 12 | 2012 | 93 | |
| 13 | 2001 | 92 | |
| 14 | 2000 | 92 | |
| 15 | 2006 | 90 | |
| 16 | 1992 | 84 | |
| 17 | 2002 | 83 | |
| 18 | 2006 | 82 | |
| 19 | 1996 | 82 | |
| 20 | 1979 | 78 |
About Beat Steinmann
Beat Steinmann is a scholar working on Genetics, Molecular Biology, Rheumatology, Cell Biology and Oncology, having authored 123 papers that have together received 6.4k indexed citations. Recurring topics across this work include Connective tissue disorders research (67 papers), Dermatological and Skeletal Disorders (25 papers), Metabolism and Genetic Disorders (13 papers), Proteoglycans and glycosaminoglycans research (8 papers), Skin and Cellular Biology Research (8 papers), Protein Tyrosine Phosphatases (7 papers), Lysosomal Storage Disorders Research (7 papers) and Dupuytren's Contracture and Treatments (7 papers). The work is most often cited by research in Genetics (3.1k citations), Rheumatology (964 citations), Clinical Biochemistry (429 citations), Cell Biology (784 citations) and Immunology and Allergy (237 citations). Beat Steinmann has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Anne De Paepe, Richard Wenstrup, Peter Beighton, Petros Tsipouras, Peter M. Royce, Andrea Superti‐Furga, Cecilia Giunta, Michael Raghunath, René Santer and R Gitzelmann. Their work appears in journals such as Human Mutation, European Journal of Pediatrics, Pediatric Research, Human Genetics and Molecular Genetics and Metabolism.
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.