P Lohse

685 total citations
25 papers, 419 citations indexed

About

P Lohse is a scholar working on Molecular Biology, Surgery and Oncology. According to data from OpenAlex, P Lohse has authored 25 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Surgery and 4 papers in Oncology. Recurrent topics in P Lohse's work include Inflammasome and immune disorders (7 papers), IL-33, ST2, and ILC Pathways (2 papers) and Lipoproteins and Cardiovascular Health (2 papers). P Lohse is often cited by papers focused on Inflammasome and immune disorders (7 papers), IL-33, ST2, and ILC Pathways (2 papers) and Lipoproteins and Cardiovascular Health (2 papers). P Lohse collaborates with scholars based in Germany, United States and Switzerland. P Lohse's 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 and has published in prestigious journals such as Journal of Clinical Investigation, Gastroenterology and FEBS Letters.

In The Last Decade

P Lohse

25 papers receiving 403 citations

Peers

P Lohse
Osamu Takase Japan
Zahra Ghiassi–Nejad United States
Ilka Edenhofer Switzerland
Sı́lvia Casas Spain
Jisu Oh South Korea
Striker Lj United States
Fumiaki Urase Japan
Javier Varona Santos United States
Attila Pethö‐Schramm Switzerland
Masashi Kitahara Japan
Osamu Takase Japan
P Lohse
Citations per year, relative to P Lohse P Lohse (= 1×) peers Osamu Takase

Countries citing papers authored by P Lohse

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

20 of 20 papers shown
1.
Endres, Theresa, Raphaela Goldbach‐Mansky, Norbert Blank, et al.. (2013). PW02-040 - Low-penetrance NLRP3 variants. Pediatric Rheumatology. 11(S1). 1 indexed citations
2.
Endres, Theresa, Raphaela Goldbach‐Mansky, Norbert Blank, et al.. (2013). PReS-FINAL-2331: Low-penetrance NLRP3 variants. Pediatric Rheumatology. 11(S2). 2 indexed citations
3.
Lohse, P, et al.. (2012). A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency. 15th International & 14th European Congress of Endocrinology. 29. 7 indexed citations
4.
Ebrahimi‐Fakhari, Darius, Stefan Schönland, Ute Hegenbart, et al.. (2012). Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk. Scandinavian Journal of Rheumatology. 42(1). 52–58. 19 indexed citations
5.
Wittkowski, Helmut, J. B. Kuemmerle‐Deschner, Judith Austermann, et al.. (2011). MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes. Annals of the Rheumatic Diseases. 70(12). 2075–2081. 45 indexed citations
6.
Faßbender, Klaus, et al.. (2011). Neurologische Manifestationen der AGel-Amyloidose (Meretoja-Syndrom) bei einer deutschen Familie. Fortschritte der Neurologie · Psychiatrie. 79(4). 238–241. 4 indexed citations
7.
Griese, Matthias, Jan Ripper, P Lohse, et al.. (2011). Long-term follow-up and treatment of congenital alveolar proteinosis. BMC Pediatrics. 11(1). 72–72. 25 indexed citations
8.
Morbach, Henner, et al.. (2009). Tumor necrosis factor receptor 1-associated periodic syndrome without fever: cytokine profile before and during etanercept treatment. Rheumatology International. 30(2). 207–212. 13 indexed citations
9.
Hecht, S, et al.. (2008). Anti-Müller-Hormon (AMH) als prognostischer Faktor der kontrollierten ovariellen Hyperstimulation. Geburtshilfe und Frauenheilkunde. 68(S 01). 1 indexed citations
10.
11.
Stanojević, Boban, et al.. (2007). Germline VHL gene mutations in three Serbian families with von Hippel-Lindau disease.. PubMed. 54(5). 402–6. 3 indexed citations
12.
Hospach, Toni, P Lohse, H. Heilbronner, Guenther E. Dannecker, & Peter Lohse. (2005). Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins. Arthritis & Rheumatism. 52(11). 3606–3610. 9 indexed citations
13.
14.
Peiró, Gloria, Joachim Diebold, Peter Lohse, et al.. (2002). Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinoma. Human Pathology. 33(3). 347–354. 51 indexed citations
15.
16.
Lohse, Peter, P Lohse, M. Elleder, et al.. (2000). Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease. Journal of Lipid Research. 41(1). 23–31. 38 indexed citations
17.
Lohse, Peter, et al.. (1999). Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease. Journal of Lipid Research. 40(2). 221–228. 22 indexed citations
18.
Mann, W. Alexander, P Lohse, Richard E. Gregg, et al.. (1995). Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu).. Journal of Clinical Investigation. 96(2). 1100–1107. 26 indexed citations
19.
Lohse, P, et al.. (1993). [The genetics of factor XII deficiency].. PubMed. 31. 174–8. 1 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Osamu Takase Breakdown of academic impact, for papers by Zahra Ghiassi–Nejad Breakdown of academic impact, for papers by Ilka Edenhofer Breakdown of academic impact, for papers by Sı́lvia Casas Breakdown of academic impact, for papers by Jisu Oh Breakdown of academic impact, for papers by Striker Lj Breakdown of academic impact, for papers by Fumiaki Urase Breakdown of academic impact, for papers by Javier Varona Santos Breakdown of academic impact, for papers by Attila Pethö‐Schramm Breakdown of academic impact, for papers by Masashi Kitahara
Rankless by CCL
2026