Harald Jüppner
- Molecular Biology top 2%
- Genetics top 0.5%
- Nephrology top 0.2%
- Oncology top 2%
- Surgery top 5%
- Co-authors
- Murat BastepeErnestina SchipaniK. KruseMichael MannstadtAndrew ArnoldJoan RudermanTheodora BloomToru Motokura
- Topics
- Genetic Syndromes and Imprinting (41 papers)Genomics and Rare Diseases (24 papers)Congenital heart defects research (20 papers)
- Cited by
- NephrologyGeneticsOncology
- Partner nations
- United StatesGermanyJapan
In The Last Decade
Harald Jüppner
63 papers receiving 6.3k citations
Hit Papers
Peers
Comparison fields: 5 of 121
- Molecular Biology 3.5k
- Genetics 2.4k
- Nephrology 2.1k
- Oncology 1.6k
- Surgery 1.0k
Countries citing papers authored by Harald Jüppner
This map shows the geographic impact of Harald Jüppner'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 Harald Jüppner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harald Jüppner more than expected).
Fields of papers citing papers by Harald Jüppner
This network shows the impact of papers produced by Harald Jüppner. 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 Harald Jüppner. The network helps show where Harald Jüppner may publish in the future.
Co-authorship network of co-authors of Harald Jüppner
This figure shows the co-authorship network connecting the top 25 collaborators of Harald Jüppner. A scholar is included among the top collaborators of Harald Jüppner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Harald Jüppner. Harald Jüppner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 3 | |
| 3 | 0 | |
| 4 | 24 | |
| 5 | 4 | |
| 6 | 18 | |
| 7 | 46 | |
| 8 | 38 | |
| 9 | 7 | |
| 10 | 56 | |
| 11 | 48 | |
| 12 | 45 | |
| 13 | 18 | |
| 14 | 101 | |
| 15 | 31 | |
| 16 | 103 | |
| 17 | 7 | |
| 18 | 34 | |
| 19 | 2 | |
| 20 | A novel cyclin encoded by a bcl1-linked candidate oncogenebreakdown → | 1061 |
About Harald Jüppner
Harald Jüppner is a scholar working on Nephrology, Genetics and Molecular Biology, having authored 65 papers that have together received 6.4k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (41 papers), Genomics and Rare Diseases (24 papers) and Congenital heart defects research (20 papers). The work is most often cited by research in Nephrology (2.1k citations), Genetics (2.4k citations) and Oncology (1.6k citations). Harald Jüppner has collaborated with scholars based in United States, Germany and Japan. Frequent co-authors include Murat Bastepe, Ernestina Schipani, K. Kruse, Michael Mannstadt, Andrew Arnold, Joan Ruderman, Theodora Bloom, Toru Motokura, Myles Wolf and Ravi Thadhani. Their work appears in journals such as Nature, Science and New England Journal of 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.