J. Spranger
Impact in
- Genetics top 5%
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
Papers in
- Genetics 19
- Connective tissue disorders research 16
- Neurogenetic and Muscular Disorders Research 4
-
- Fibroblast Growth Factor Research 3
- Ubiquitin and proteasome pathways 2
- Co-authors
- Bernhard Zabel (8 shared papers)Andreas Winterpacht (5 shared papers)Stefan Mundlos (6 shared papers)Bryan D. Hall (1 shared paper)Ulrike Schwarze (3 shared papers)É Straub (1 shared paper)Thomas Braulke (1 shared paper)John M. Opitz (3 shared papers)
- Journals
- European Journal of Pediatrics (6 papers)Human Mutation (2 papers)Current Opinion in Rheumatology (1 paper)Journal of Medical Genetics (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
J. Spranger
49 papers receiving 886 citations
Peers
Comparison fields: 5 of 84
- Genetics 493
- Immunology and Allergy 71
- Rheumatology 145
- Developmental Biology 16
- Genetics 55
Countries citing papers authored by J. Spranger
This map shows the geographic impact of J. Spranger'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 J. Spranger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Spranger more than expected).
Fields of papers citing papers by J. Spranger
This network shows the impact of papers produced by J. Spranger. 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 J. Spranger. The network helps show where J. Spranger may publish in the future.
Co-authors
The 25 scholars most cited alongside J. Spranger, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 122 | |
| 2 | 2005 | 101 | |
| 3 | 1979 | 63 | |
| 4 | 2000 | 55 | |
| 5 | 2006 | 41 | |
| 6 | 1980 | 36 | |
| 7 | 2001 | 36 | |
| 8 | 1981 | 35 | |
| 9 | 1993 | 29 | |
| 10 | 1970 | 28 | |
| 11 | 1987 | 25 | |
| 12 | Skeletal complications in osteogenesis imperfecta. A review of 153 South African patients. | 1983 | 25 |
| 13 | 1994 | 24 | |
| 14 | 1976 | 24 | |
| 15 | 2006 | 24 | |
| 16 | 1984 | 22 | |
| 17 | 1999 | 21 | |
| 18 | 2015 | 19 | |
| 19 | [Vater or Vacterl syndrome (author's transl)]. | 1976 | 19 |
| 20 | 1965 | 18 |
About J. Spranger
J. Spranger is a scholar working on Genetics, Molecular Biology, Rheumatology, Pulmonary and Respiratory Medicine and Surgery, having authored 55 papers that have together received 930 indexed citations. Recurring topics across this work include Connective tissue disorders research (16 papers), Bone health and treatments (5 papers), Neurogenetic and Muscular Disorders Research (4 papers), Congenital limb and hand anomalies (4 papers), Child and Adolescent Health (4 papers), Neonatal Respiratory Health Research (4 papers), Fibroblast Growth Factor Research (3 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Genetics (493 citations), Immunology and Allergy (71 citations), Rheumatology (145 citations), Developmental Biology (16 citations) and Genetics (55 citations). J. Spranger has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Bernhard Zabel, Andreas Winterpacht, Stefan Mundlos, Bryan D. Hall, Ulrike Schwarze, É Straub, Thomas Braulke, John M. Opitz, Stephan Tiede and Michael Cantz. Their work appears in journals such as European Journal of Pediatrics, Human Mutation, Current Opinion in Rheumatology, Journal of Medical Genetics and European Journal of Medical 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.