Peter Lohse

8.1k total citations
127 papers, 5.3k citations indexed

About

Peter Lohse is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Peter Lohse has authored 127 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 32 papers in Immunology and 29 papers in Genetics. Recurrent topics in Peter Lohse's work include Inflammasome and immune disorders (24 papers), Inflammatory Bowel Disease (24 papers) and Blood Coagulation and Thrombosis Mechanisms (9 papers). Peter Lohse is often cited by papers focused on Inflammasome and immune disorders (24 papers), Inflammatory Bowel Disease (24 papers) and Blood Coagulation and Thrombosis Mechanisms (9 papers). Peter Lohse collaborates with scholars based in Germany, United States and Canada. Peter Lohse's co-authors include Stephan Brand, Burkhard Göke, Thomas Ochsenkühn, Jack W. Szostak, Jürgen Glas, Astrid Konrad, Simone Pfennig, Julia Seiderer, Christian J. Thaler and Cornelia Tillack and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Peter Lohse

127 papers receiving 5.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Peter Lohse Germany	41	2.3k	1.5k	1.1k	855	747	127	5.3k
Juri Kopolovic Israel	43	1.6k 0.7×	1.5k 1.0×	714 0.6×	1.1k 1.3×	467 0.6×	137	5.5k
Raphael Hirsch United States	37	1.0k 0.4×	1.2k 0.8×	728 0.6×	629 0.7×	400 0.5×	94	3.6k
Michio Nagata Japan	38	2.1k 0.9×	762 0.5×	883 0.8×	885 1.0×	313 0.4×	201	5.7k
Yves Pirson Belgium	44	2.3k 1.0×	1.2k 0.8×	3.0k 2.6×	990 1.2×	557 0.7×	200	7.4k
Ayşı̇n Bakkaloğlu Türkiye	40	3.7k 1.6×	1.3k 0.9×	925 0.8×	896 1.0×	430 0.6×	176	6.5k
Élie Haddad Canada	46	1.4k 0.6×	3.2k 2.2×	1.0k 0.9×	474 0.6×	723 1.0×	179	6.9k
Jeffrey Siegel United States	22	960 0.4×	2.1k 1.4×	668 0.6×	1.1k 1.3×	1.8k 2.4×	41	6.1k
M. Louise Markert United States	32	1.4k 0.6×	2.6k 1.8×	983 0.9×	388 0.5×	929 1.2×	79	4.8k
S Thiru United Kingdom	37	1.2k 0.5×	1.2k 0.8×	664 0.6×	1.7k 2.0×	463 0.6×	112	5.4k
David M. Dorfman United States	41	1.6k 0.7×	2.4k 1.7×	547 0.5×	441 0.5×	539 0.7×	153	6.7k

Countries citing papers authored by Peter Lohse

Since Specialization

Citations

This map shows the geographic impact of Peter 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 Peter Lohse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Lohse more than expected).

Fields of papers citing papers by Peter Lohse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter 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 Peter Lohse. The network helps show where Peter Lohse may publish in the future.

Co-authorship network of co-authors of Peter Lohse

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Lohse. A scholar is included among the top collaborators of Peter 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 Peter Lohse. Peter Lohse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hecht, S, et al.. (2022). Reduced Steroid Synthesis in the Follicular Fluid of MTHFR 677TT Mutation Carriers: Effects of Increased Folic Acid Administration. Geburtshilfe und Frauenheilkunde. 82(10). 1074–1081. 2 indexed citations

Kuemmerle‐Deschner, Jasmin, Assen Koitschev, Pascal N. Tyrrell, et al.. (2015). Early detection of sensorineural hearing loss in Muckle-Wells-syndrome. Pediatric Rheumatology. 13(1). 43–43. 40 indexed citations

Lohse, Peter, et al.. (2012). A Recessive Mutation Resulting in a Disabling Amino Acid Substitution (T194R) in the LHX3 Homeodomain Causes Combined Pituitary Hormone Deficiency. Hormone Research in Paediatrics. 77(1). 41–51. 17 indexed citations

Braun‐Falco, Markus, et al.. (2011). Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH)–a new autoinflammatory syndrome distinct from PAPA syndrome. Journal of the American Academy of Dermatology. 66(3). 409–415. 202 indexed citations

Glas, Jürgen, Julia Seiderer, Cornelia Tillack, et al.. (2011). CEACAM6 Gene Variants in Inflammatory Bowel Disease. PLoS ONE. 6(4). e19319–e19319. 13 indexed citations

Jürgens, Matthias, Rüdiger P. Laubender, Maria Weidinger, et al.. (2010). Disease Activity, ANCA, and IL23R Genotype Status Determine Early Response to Infliximab in Patients With Ulcerative Colitis. The American Journal of Gastroenterology. 105(8). 1811–1819. 142 indexed citations

Glas, Jürgen, Julia Seiderer, Cornelia Tillack, et al.. (2010). The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. PLoS ONE. 5(12). e14466–e14466. 26 indexed citations

Glas, Jürgen, Johannes Stallhofer, Stephan Ripke, et al.. (2009). Novel Genetic Risk Markers for Ulcerative Colitis in the IL2/IL21 Region Are in Epistasis With IL23R and Suggest a Common Genetic Background for Ulcerative Colitis and Celiac Disease. The American Journal of Gastroenterology. 104(7). 1737–1744. 63 indexed citations

Schmechel, Silke, Astrid Konrad, Julia Diegelmann, et al.. (2007). Linking genetic susceptibility to Crohnʼs disease with Th17 cell function: IL-22 serum levels are increased in Crohnʼs disease and correlate with disease activity and IL23R genotype status. Inflammatory Bowel Diseases. 14(2). 204–212. 165 indexed citations

10.

Morgenstern, Eberhard, Susan L. Cuvelier, Davit Manukyan, et al.. (2006). Eosinophils are a major intravascular location for tissue factor storage and exposure. Blood. 109(3). 995–1002. 186 indexed citations

11.

Török, Helga‐Paula, Jürgen Glas, Peter Lohse, & Christian Folwaczny. (2006). Genetic variants and the risk of Crohn’s disease: what does it mean for future disease management?. Expert Opinion on Pharmacotherapy. 7(12). 1591–1602. 3 indexed citations

12.

Thaler, Christian J., et al.. (2006). Effects of the Common 677C>T Mutation of the 5,10‐Methylenetetrahydrofolate Reductase (MTHFR) Gene on Ovarian Responsiveness to Recombinant Follicle‐Stimulating Hormone. American Journal of Reproductive Immunology. 55(4). 251–258. 49 indexed citations

13.

Rack, Anita, S Stojanov, Bernd H. Belohradsky, & Peter Lohse. (2006). A new low‐penetrance TNFRSF1A mutation causing atypical periodic fever. Pediatrics International. 48(2). 169–171. 2 indexed citations

14.

Brand, Stephan, Astrid Konrad, Alexander Crispin, et al.. (2005). The Role of Toll-like Receptor 4 Asp299Gly and Thr399Ile Polymorphisms and CARD15/NOD2 Mutations in the Susceptibility and Phenotype of Crohnʼs Disease. Inflammatory Bowel Diseases. 11(7). 645–652. 130 indexed citations

15.

Novosel, Astrid, et al.. (2004). Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutation. European Journal of Pediatrics. 163(12). 701–703. 10 indexed citations

16.

Peiró, Gloria, Peter Lohse, Doris Mayr, & Joachim Diebold. (2003). Insulin-like Growth Factor-I Receptor and PTEN Protein Expression in Endometrial Carcinoma: Correlation With bax and bcl-2 Expression, Microsatellite Instability Status, and Outcome. American Journal of Clinical Pathology. 120(1). 78–85. 28 indexed citations

17.

Török, Helga‐Paula, Jürgen Glas, Peter Lohse, & Christian Folwaczny. (2003). Alterations of the CARD15/NOD2 Gene and the Impact on Management and Treatment of Crohn’s Disease Patients. Digestive Diseases. 21(4). 339–345. 17 indexed citations

18.

Suga, Hiroaki, Peter Lohse, & Jack W. Szostak. (1998). Structural and Kinetic Characterization of an Acyl Transferase Ribozyme. Journal of the American Chemical Society. 120(6). 1151–1156. 44 indexed citations

19.

Bober, Eva, Barbara Winter, Peter Lohse, et al.. (1988). Alkali myosin light chains in man are encoded by a multigene family that includes the adult skeletal muscle, the embryonic or atrial, and nonsarcomeric isoforms. Gene. 66(1). 135–146. 28 indexed citations

20.

Arnold, Hans-Henning, et al.. (1988). A novel human myosin alkali light chain is developmentally regulated. European Journal of Biochemistry. 178(1). 53–60. 21 indexed citations

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.

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