J. Spranger
Impact in
- Genetics top 5%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Developmental Biology top 10%
- Congenital limb and hand anomalies
Papers in
- Genetics 19
- Connective tissue disorders research 16
- Genomic variations and chromosomal abnormalities 1
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- Human Health and Disease 2
- Prenatal Substance Exposure Effects 1
- Co-authors
- Bernhard Zabel (9 shared papers)Andreas Winterpacht (5 shared papers)Stefan Mundlos (6 shared papers)Bryan D. Hall (1 shared paper)Ulrike Schwarze (3 shared papers)Eberhard Straub (2 shared papers)Thomas Braulke (1 shared paper)Stephan Tiede (1 shared paper)
- Journals
- European Journal of Pediatrics (6 papers)Human Mutation (2 papers)The Journal of Pediatrics (2 papers)The American Journal of Human Genetics (2 papers)The Lancet (1 paper)
- Partner nations
- GermanyUnited StatesJapan
In The Last Decade
J. Spranger
50 papers receiving 949 citations
Peers
Comparison fields: 5 of 55
- Genetics 393
- Developmental Biology 16
- Pediatrics, Perinatology and Child Health 54
- Urology 11
- Physiology 37
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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 144 | |
| 2 | 2005 | 116 | |
| 3 | 1979 | 78 | |
| 4 | 2000 | 57 | |
| 5 | 2006 | 43 | |
| 6 | 2001 | 40 | |
| 7 | 1981 | 39 | |
| 8 | 1980 | 38 | |
| 9 | 1970 | 31 | |
| 10 | 1987 | 31 | |
| 11 | 2006 | 30 | |
| 12 | Skeletal complications in osteogenesis imperfecta. A review of 153 South African patients. | 1983 | 29 |
| 13 | 1993 | 29 | |
| 14 | 1994 | 26 | |
| 15 | 1976 | 25 | |
| 16 | 1984 | 24 | |
| 17 | 2015 | 24 | |
| 18 | 1965 | 23 | |
| 19 | 1999 | 23 | |
| 20 | [A new (brachymelic) type of primordial dwarfism (author's transl)]. | 1976 | 20 |
About J. Spranger
J. Spranger is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Complementary and alternative medicine, Physiology and Developmental Biology, having authored 54 papers that have together received 1.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (16 papers), Lysosomal Storage Disorders Research (3 papers), Complementary and Alternative Medicine Studies (2 papers), Human Health and Disease (2 papers), Bone Tumor Diagnosis and Treatments (1 paper), Prenatal Substance Exposure Effects (1 paper), Congenital limb and hand anomalies (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Genetics (393 citations), Developmental Biology (16 citations), Pediatrics, Perinatology and Child Health (54 citations), Urology (11 citations) and Physiology (37 citations). J. Spranger has collaborated with scholars based in Germany, United States and Japan. Frequent co-authors include Bernhard Zabel, Andreas Winterpacht, Stefan Mundlos, Bryan D. Hall, Ulrike Schwarze, Eberhard Straub, Thomas Braulke, Stephan Tiede, Michael Cantz and K. Brühl. Their work appears in journals such as European Journal of Pediatrics, Human Mutation, The Journal of Pediatrics, The American Journal of Human Genetics and The Lancet.
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.