R Gitzelmann
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Rheumatology top 1%
- Glycogen Storage Diseases and Myoclonus
Papers in
-
- Metabolism and Genetic Disorders 53
- Co-authors
- B Steinmann (29 shared papers)Andrea Superti‐Furga (13 shared papers)N. U. Bosshard (13 shared papers)B Steinmann (11 shared papers)Beat Steinmann (10 shared papers)Peter H. Byers (2 shared papers)Salvatore Auricchio (1 shared paper)Antonio Rossi (5 shared papers)
- Journals
- European Journal of Pediatrics (15 papers)Pediatric Research (11 papers)Clinica Chimica Acta (6 papers)Human Genetics (5 papers)Journal of Inherited Metabolic Disease (5 papers)
- Partner nations
- SwitzerlandUnited StatesItaly
In The Last Decade
R Gitzelmann
139 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 117
- Clinical Biochemistry 1.0k
- Rheumatology 701
- Biochemistry 317
- Genetics 1.1k
- Cell Biology 446
Countries citing papers authored by R Gitzelmann
This map shows the geographic impact of R Gitzelmann'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 R Gitzelmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R Gitzelmann more than expected).
Fields of papers citing papers by R Gitzelmann
This network shows the impact of papers produced by R Gitzelmann. 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 R Gitzelmann. The network helps show where R Gitzelmann may publish in the future.
Co-authors
The 25 scholars most cited alongside R Gitzelmann, 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 141 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 172 | |
| 2 | 1996 | 169 | |
| 3 | 1988 | 151 | |
| 4 | Abnormal collagen fibril structure in the gravis form (type I) of Ehlers-Danlos syndrome. | 1979 | 136 |
| 5 | 1967 | 113 | |
| 6 | 1965 | 106 | |
| 7 | 1995 | 98 | |
| 8 | 1965 | 97 | |
| 9 | 1990 | 82 | |
| 10 | 1996 | 82 | |
| 11 | 1993 | 80 | |
| 12 | 1995 | 79 | |
| 13 | 1998 | 77 | |
| 14 | Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase gene. | 1990 | 75 |
| 15 | 1993 | 64 | |
| 16 | 1998 | 62 | |
| 17 | 1992 | 61 | |
| 18 | Ehlers-Danlos syndrome in two siblings with deficient lysyl hydroxylase activity in cultured skin fibroblasts but only mild hydroxylysine deficit in skin. | 1975 | 57 |
| 19 | 1999 | 55 | |
| 20 | 1994 | 53 |
About R Gitzelmann
R Gitzelmann is a scholar working on Clinical Biochemistry, Molecular Biology, Rheumatology, Genetics and Physiology, having authored 141 papers that have together received 3.7k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (53 papers), Neonatal Health and Biochemistry (24 papers), Glycogen Storage Diseases and Myoclonus (22 papers), Diet, Metabolism, and Disease (20 papers), Lysosomal Storage Disorders Research (18 papers), Connective tissue disorders research (14 papers), Digestive system and related health (13 papers) and Amino Acid Enzymes and Metabolism (13 papers). The work is most often cited by research in Clinical Biochemistry (1.0k citations), Rheumatology (701 citations), Biochemistry (317 citations), Genetics (1.1k citations) and Cell Biology (446 citations). R Gitzelmann has collaborated with scholars based in Switzerland, United States and Italy. Frequent co-authors include B Steinmann, Andrea Superti‐Furga, N. U. Bosshard, B Steinmann, Beat Steinmann, Peter H. Byers, Salvatore Auricchio, Antonio Rossi, M. A. Spycher and E Gugler. Their work appears in journals such as European Journal of Pediatrics, Pediatric Research, Clinica Chimica Acta, Human Genetics and Journal of Inherited Metabolic Disease.
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.