P Lohse
- Co-authors
- Peter LohseD. SeidelH. Bryan BrewerD BojanovskiHanns‐Georg KleinP. Haydn PritchardGustavo BarettonGloria Peiró
- Topics
- Inflammasome and immune disorders (7 papers)IL-33, ST2, and ILC Pathways (2 papers)Lipoproteins and Cardiovascular Health (2 papers)
- Cited by
- PhysiologyHematologyImmunology
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
P Lohse
25 papers receiving 403 citations
Peers
Comparison fields: 5 of 55
- Molecular Biology 218
- Surgery 132
- Immunology 80
- Physiology 62
- Endocrinology, Diabetes and Metabolism 53
Countries citing papers authored by P Lohse
This map shows the geographic impact of P Lohse'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 P Lohse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Lohse more than expected).
Fields of papers citing papers by P Lohse
This network shows the impact of papers produced by P Lohse. 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 P Lohse. The network helps show where P Lohse may publish in the future.
Co-authorship network of co-authors of P Lohse
This figure shows the co-authorship network connecting the top 25 collaborators of P Lohse. A scholar is included among the top collaborators of P Lohse 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 P Lohse. P Lohse 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 | 2 | |
| 3 | A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency | 7 |
| 4 | 19 | |
| 5 | 45 | |
| 6 | 4 | |
| 7 | 25 | |
| 8 | 13 | |
| 9 | 1 | |
| 10 | 3 | |
| 11 | Germline VHL gene mutations in three Serbian families with von Hippel-Lindau disease. | 3 |
| 12 | 9 | |
| 13 | 36 | |
| 14 | 51 | |
| 15 | 23 | |
| 16 | 38 | |
| 17 | 22 | |
| 18 | 26 | |
| 19 | [The genetics of factor XII deficiency]. | 1 |
| 20 | 50 |
About P Lohse
P Lohse is a scholar working on Hematology, Molecular Biology and Cancer Research, having authored 25 papers that have together received 419 indexed citations. Recurring topics across this work include Inflammasome and immune disorders (7 papers), IL-33, ST2, and ILC Pathways (2 papers) and Lipoproteins and Cardiovascular Health (2 papers). The work is most often cited by research in Physiology (30 citations), Hematology (49 citations) and Immunology (80 citations). P Lohse has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Peter Lohse, D. Seidel, H. Bryan Brewer, D Bojanovski, Hanns‐Georg Klein, P. Haydn Pritchard, Gustavo Baretton, Gloria Peiró, U. Löhrs and Joachim Diebold. Their work appears in journals such as Journal of Clinical Investigation, Gastroenterology and FEBS Letters.
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.