P Lohse

2.1k citations

57 papers · 1.4k indexed · h-index 27

Impact in

Endocrinology, Diabetes and Metabolism top 5%
- Diabetes, Cardiovascular Risks, and Lipoproteins
Hematology top 5%
- Autoimmune and Inflammatory Disorders Research

Papers in

Immunology 15
- IL-33, ST2, and ILC Pathways 5
- Immune Response and Inflammation 5
Hematology 6

Co-authors: H. Bryan Brewer D J Rader M. R. Kindt D. Seidel Hans-Henning Arnold S Stojanov Thomas Ochsenkühn H Bryan Brewer
Journals: Journal of Biological Chemistry (7 papers)Journal of Lipid Research (5 papers)Journal of Clinical Investigation (2 papers)Neurology (2 papers)Alimentary Pharmacology & Therapeutics (2 papers)
Partner nations: Germany United States France

In The Last Decade

P Lohse

56 papers receiving 1.4k citations

Peers

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-authors

The 25 scholars most cited alongside P Lohse, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P Lohse Line = papers co-authored together P Lohse links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine Journal of Perinatology ·F. Schr�der, Matthias Griese, P Lohse, Mitsuhiro Fukao, Lars Lange	2013	14
2	Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population European Journal of Pediatrics ·Elke Lainka, Fatouh Hikal, P Lohse, Christian Timmann, S Stojanov, Rüdiger von Kries, Tim Niehues, Ulrich Neudorf	2012	19
3	Respiratory distress syndrome due to a novel homozygousABCA3mutation in a term neonate BMJ Case Reports ·Fred Johnston, Alexis Mussachio, Sadeeq ur Rahman, Rusaczonek, Peter Ruef, Matthias Griese, P Lohse, Charalampos Aslanidis, Gerd Schmitz, Lutz Koch, Sommaye Hamzei Taj	2011	2
4	Genetic polymorphisms of TP53 and FAS promoter modulate the progression of coronary artery disease after coronary artery bypass grafting: a gender-specific view Inflammation Research ·Dyan Paramitha, Martin K. Angele, Yinghong Ying, P Lohse, Bruno Reichart, Ling Rui	2011	7
5	38-jähriger Patient mit Verdacht auf eine angeborene hormonelle Störung Der Internist ·S Berezin Alexey, E. G. Hahn, P Lohse, Igor Alexander Harsch	2010	0
6	Association of the interleukin‐23 receptor gene variant rs11209026 with Crohn’s disease in German children Acta Paediatrica ·Martin Lacher, Sebastian Schroepf, Robert J. Ziarnik, Dietrich von Schweinitz, Antje Ballauff, Ina Koch, P Lohse, HanMei Choi, Roland Kappler, Sibylle Koletzko	2010	13
7	Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis Archives of Disease in Childhood Fetal & Neonatal ·Denny Lumban Raja, 塩野谷恵彦, Gerhard Liebisch, Heiko Krude, P Lohse, Charalampos Aslanidis, Gerd Schmitz, Jochen Peters, Andreas Holzinger	2010	32
8	Respiratory disease in Niemann‐Pick type C2 is caused by pulmonary alveolar proteinosis Clinical Genetics ·Matthias Griese, Frank Brasch, Nancy Holder, S. Seif El Nasr-storey, Nihed Bahria El Asghar, Elina Ikonen, J.F. Morar, Gerhard Liebisch, P. Merville, P Lohse, Wolfgang Meyer, Gerd Schmitz, G. F. Streib, Jan Ripper, A. Rolfs, Andrea Schams, hafitatul aini	2009	63
9	Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics Lara D. Veeken ·Elke Lainka, Ulrich Neudorf, P Lohse, Christian Timmann, S Stojanov, Xiao Zhang, Rüdiger von Kries, Tim Niehues	2009	34
10	Children with absent surfactant protein D in bronchoalveolar lavage have more frequently pneumonia Pediatric Allergy and Immunology ·Matthias Griese, Liette St-Pierre, Shiyu Fang, Annika Braun, P Lohse, D. Saur	2008	19
11	Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment Annals of the Rheumatic Diseases ·S Stojanov, Christian Dejaco, P Lohse, Karen Huss, Belma Doğan-Güngen, B. H. Belohradsky, Manfred Herold, Michael Schirmer	2008	38
12	The role of fatty acid hydrolase gene variants in inflammatory bowel disease Alimentary Pharmacology & Therapeutics ·Martin Storr, Tosca Hernández, Julia Diegelmann, B Yüce, Simone Pfennig, Thomas Ochsenkühn, Burkhard Göke, P Lohse, Stephan Brand	2008	24
13	Substitution of cyclophosphamide and busulfan by fludarabine, treosulfan and melphalan in a preparative regimen for children and adolescents with Shwachman–Diamond syndrome Bone Marrow Transplantation ·Martin G. Sauer, Cornelia Zeidler, Barbara Meissner, Klaus Rehe, Alexander Hanke, Karl Welte, P Lohse, K-W Sykora	2007	31
14	The +1059G/C polymorphism in the C‐reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn's disease Alimentary Pharmacology & Therapeutics ·D. THALMAIER, Julia Dambacher, Julia Seiderer, Astrid Konrad, J.J. Fry, Simone Pfennig, J.‐M. Otte, Alexander Crispin, Burkhard Göke, Thomas Ochsenkühn, P Lohse, Stephan Brand	2006	33
15	Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease Gut ·Helga‐Paula Török, Jürgen Glas, Luis Alberto Osorio Guerrero, P Lohse, Cristel Gervais, Luis Alberto Polo García Rosell, Elizabeth Chris Aylas-Florez, Fabian Schnitzler, Julia Seiderer, Cai Li, Stephan Brand, Gui Chen Zhang, Peter Jagiello, Jörg T. Epplen, Thomas Griga, Wolfram Klein, U Schiemann, Matthias Folwaczny, Thomas Ochsenkühn, C Folwaczny	2005	114
16	Genetic Analyses Permit the Differentiation Between Reactive Malfunctions (‘Promyelocyte Arrest’) and Arising Promyelocyte Leukemia in a Pregnant Patient With a History of a Medulloblastoma Leukemia & lymphoma ·Andrei Sakai, Thomas Duell, R. Bartl, P Lohse, V. A. Dahate, J Diébold, Peter Köhl, M Sharon Stack, Helga Schmetzer	2004	3
17	Extended Microsatellite Analysis in Microsatellite Stable, MSH2 and MLH1 Mutation-Negative HNPCC Patients: Genetic Reclassification and Correlation with Clinical Features Digestion ·U Schiemann, С.С. Абрамчук, Khadija Asif, V. A. Bobko, P Lohse, Gustavo Baretton, Michael H. Muders, Thomas Mussack, R. Kopp, Elke Holinski‐Feder	2004	25
18	Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms? PubMed ·С.С. Абрамчук, R. Kopp, P Lohse, Ni Jian, David Biron, Daniela E. Aust, V. A. Bobko, Firman Gustina, Khadija Asif, G Shibi, Elke Holinski‐Feder	2001	22
19	Rapid in vivo transport and catabolism of human apolipoprotein A-IV-1 and slower catabolism of the apoA-IV-2 isoprotein. Journal of Clinical Investigation ·D J Rader, 小尾口邦彦, P Lohse, Bruno Vergès, M. R. Kindt, Loren A. Zech, Armin Steinmetz, H. Bryan Brewer	1993	32
20	A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiency. Journal of Clinical Investigation ·S S Fojo, P Lohse, Catherine L. Parrott, Giovannella Baggio, Carlo Gabelli, F. Thomas, John L. Hoffman, H. Bryan Brewer	1989	47

About P Lohse

P Lohse is a scholar working on Immunology, Hematology, Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics, having authored 57 papers that have together received 1.4k indexed citations. Recurring topics across this work include Inflammasome and immune disorders (14 papers), Inflammatory Bowel Disease (6 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (6 papers), Lipoproteins and Cardiovascular Health (5 papers), Peroxisome Proliferator-Activated Receptors (5 papers), IL-33, ST2, and ILC Pathways (5 papers), Immune Response and Inflammation (5 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (295 citations), Hematology (156 citations), Immunology (270 citations), Surgery (450 citations) and Cancer Research (147 citations). P Lohse has collaborated with scholars based in Germany, United States and France. Frequent co-authors include H. Bryan Brewer, D J Rader, M. R. Kindt, D. Seidel, Hans-Henning Arnold, S Stojanov, Thomas Ochsenkühn, H Bryan Brewer, Stephan Brand and Christian Timmann. Their work appears in journals such as Journal of Biological Chemistry, Journal of Lipid Research, Journal of Clinical Investigation, Neurology and Alimentary Pharmacology & Therapeutics.

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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