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Anzahl der Publikationen: 29
Zeitschriftenartikel
Pavlik, Roman; Hecht, Stephanie; Noss, Ulrich; Soldin, Offie P.; Mendu, Rao D.; Soldin, Steven J.; Lohse, Peter und Thaler, Christian J.
(2022):
Reduced Steroid Synthesis in the Follicular Fluid of MTHFR 677TT Mutation Carriers: Effects of Increased Folic Acid Administration.
In: Geburtshilfe und Frauenheilkunde, Bd. 82, Nr. 10: S. 1074-1081
Schnitzler, Fabian; Friedrich, Matthias; Angelberger, Marianne; Diegelmann, Julia; Stallhofer, Johannes; Wolf, Christiane; Dütschler, Joel; Truniger, Samuel; Olszak, Torsten; Beigel, Florian; Tillack, Cornelia; Lohse, Peter und Brand, Stephan
(2020):
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery.
In: PLOS One 15(7), e0236421 [PDF, 881kB]
In: PLOS One 15(7), e0236421 [PDF, 881kB]
Blaschek, Astrid; Kries, Rüdiger V.; Lohse, Peter; Huss, Kristina; Vill, Katharina; Belohradsky, Bernd H.; Heinen, Florian; Müller-Felber, Wolfgang und Kuempfel, Tania
(2018):
TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.
In: European Journal of Paediatric Neurology, Bd. 22, Nr. 1: S. 72-81
Kröner, Carolin; Wittmann, Thomas; Reu, Simone; Teusch, Veronika; Klemme, Mathias; Rauch, Daniela; Hengst, Meike; Kappler, Matthias; Cobanoglu, Nazan; Sismanlar, Tugba; Aslan, Ayse T.; Campo, Ilaria; Prösmans, Marijke; Schaible, Thomas; Terheggen-Lagro, Susanne; Regamey, Nicolas; Eber, Ernst; Seidenberg, Jürgen; Schwerk, Nicolaus; Aslanidis, Charalampos; Lohse, Peter; Brasch, Frank; Zarbock, Ralf und Griese, Matthias
(2017):
Lung disease caused by ABCA3 mutations.
In: Thorax, Bd. 72, Nr. 3: S. 213-220
[PDF, 538kB]
Sadovnick, A. Dessa; Traboulsee, Anthony L.; Bernales, Cecily Q.; Ross, Jay P.; Forwell, Amanda L.; Yee, Irene M.; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Benedicte; Goris, An; Astobiza, Ianire; Alloza, Iraide; Antigüedad, Alfredo; Vandenbroeck, Koen; Akkad, Denis A.; Aktas, Orhan; Blaschke, Paul; Buttmann, Mathias; Chan, Andrew; Epplen, Joerg T.; Gerdes, Lisa-Ann; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Lohse, Peter; Rieckmann, Peter; Zettl, Uwe K.; Zipp, Frauke; Bertram, Lars; Lill, Christina M.; Fernandez, Oscar; Urbaneja, Patricia; Leyva, Laura; Carlos Alvarez-Cermeno, Jose; Arroyo, Rafael; Garagorri, Aroa M.; Garcia-Martinez, Angel; Villar, Luisa M.; Urcelay, Elena; Malhotra, Sunny; Montalban, Xavier; Comabella, Manuel; Berger, Thomas; Fazekas, Franz; Reindl, Markus; Schmied, Mascha C.; Zimprich, Alexander und Vilarino-Güell, Carles
(2016):
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
In: G3 - Genes Genomes Genetics, Bd. 6, Nr. 7: S. 2073-2079
[PDF, 1MB]
Wittmann, Thomas; Frixel, Sabrina; Höppner, Stefanie; Schindlbeck, Ulrike; Schams, Andrea; Kappler, Matthias; Hegermann, Jan; Wrede, Christoph; Liebisch, Gerhard; Vierzig, Anne; Zacharasiewicz, Angela; Kopp, Matthias Volkmar; Poets, Christian F.; Baden, Winfried; Hartl, Dominik; Kaam, Anton H. van; Lohse, Peter; Aslanidis, Charalampos; Zarbock, Ralf und Griese, Matthias
(2016):
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
In: Molecular Medicine, Bd. 22
[PDF, 1MB]
Griese, Matthias; Lorenz, Elke; Hengst, Meike; Schams, Andrea; Wesselak, Traudl; Rauch, Daniela; Wittmann, Thomas; Kirchberger, Valerie; Escribano, Amparo; Schaible, Thomas; Baden, Winfried; Schulze, Johannes; Krude, Heiko; Aslanidis, Charalampos; Schwerk, Nicolaus; Kappler, Matthias; Hartl, Dominik; Lohse, Peter und Zarbock, Ralf
(2016):
Surfactant proteins in pediatric interstitial lung disease.
In: Pediatric Research, Bd. 79, Nr. 1: S. 34-41
Schnitzler, Fabian; Friedrich, Matthias; Wolf, Christiane; Stallhofer, Johannes; Angelberger, Marianne; Diegelmann, Julia; Olszak, Torsten; Tillack, Cornelia; Beigel, Florian; Goeke, Burkhard; Glas, Jürgen; Lohse, Peter und Brand, Stephan
(2015):
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A > C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations.
In: PLOS ONE 10(7), e0116044 [PDF, 233kB]
In: PLOS ONE 10(7), e0116044 [PDF, 233kB]
Lill, Christina M.; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A.; Ugidos, Nerea; La Hera, Belen de; Guillot-Noel, Lena; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M.; Mescheriakova, Julia Y.; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A.; Aktas, Orhan; Alloza, Iraide; Antigüedad, Alfredo; Arroyo, Rafa; Astobiza, Ianire; Blaschke, Paul; Boyko, Alexei N.; Buttmann, Mathias; Chan, Andrew; Dörner, Thomas; Epplen, Joerg T.; Favorova, Olga O.; Fedetz, Maria; Fernandez, Oscar; Garcia-Martinez, Angel; Gerdes, Lisa-Ann; Graetz, Christiane; Hartung, Hans-Peter; Hoffjan, Sabine; Izquierdo, Guillermo; Korobko, Denis S.; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Leyva, Laura; Lohse, Peter; Malkova, Nadezhda A.; Montalban, Xavier; Popova, Ekaterina V.; Rieckmann, Peter; Rozhdestvenskii, Alexei S.; Schmied, Christiane; Smagina, Inna V.; Tsareva, Ekaterina Y.; Winkelmann, Alexander; Zettl, Uwe K.; Binder, Harald; Cournu-Rebeix, Isabelle; Hintzen, Rogier; Zimprich, Alexander; Comabella, Manuel; Fontaine, Bertrand; Urcelay, Elena; Vandenbroeck, Koen; Filipenko, Maxim; Matesanz, Fuencisla; Zipp, Frauke und Bertram, Lars
(2015):
Genome-wide significant association with seven novel multiple sclerosis risk loci.
In: Journal of medical genetics, Bd. 52, Nr. 12: S. 848-855
[PDF, 524kB]
Griese, Matthias; Irnstetter, Armin; Hengst, Meike; Burmester, Helen; Nagel, Felicitas; Ripper, Jan; Feilcke, Maria; Pawlita, Ingo; Gothe, Florian; Kappler, Matthias; Schams, Andrea; Wesselak, Traudl; Rauch, Daniela; Wittmann, Thomas; Lohse, Peter; Brasch, Frank und Kröner, Carolin
(2015):
Categorizing diffuse parenchymal lung disease in children.
In: Orphanet Journal of Rare Diseases
10:122
[PDF, 988kB]
Hildebrandt, Jenna; Yalcin, Ebru; Bresser, Hans-Georg; Cinel, Guzin; Gappa, Monika; Haghighi, Alireza; Kiper, Nural; Khalilzadeh, Soheila; Reiter, Karl; Sayer, John; Schwerk, Nicolaus; Sibbersen, Anke; Daele, Sabine van; Nübling, Georg; Lohse, Peter und Griese, Matthias
(26. November 2014):
Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.
In: Orphanet Journal of Rare Diseases
9:171
[PDF, 961kB]
Schnitzler, Fabian; Friedrich, Matthias; Wolf, Christiane; Angelberger, Marianne; Diegelmann, Julia; Olszak, Torsten; Beigel, Florian; Tillack, Cornelia; Stallhofer, Johannes; Göke, Burkhard; Glas, Jürgen; Lohse, Peter und Brand, Stephan
(2014):
The NOD2 p.Leu1007fsX1008 Mutation (rs2066847) Is a Stronger Predictor of the Clinical Course of Crohn's Disease than the FOXO3A Intron Variant rs12212067.
In: PLOS ONE 9(11), e108503 [PDF, 220kB]
In: PLOS ONE 9(11), e108503 [PDF, 220kB]
Lill, Christina M.; Schjeide, Brit-Maren M.; Graetz, Christiane; Liu, Tian; Damotte, Vincent; Akkad, Denis A.; Blaschke, Paul; Gerdes, Lisa-Ann; Kroner, Antje; Luessi, Felix; Cournu-Rebeix, Isabelle; Hoffjan, Sabine; Winkelmann, Alexander; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Otaegui, David; Antigueedad, Alfredo; Alcina, Antonio; Comabella, Manuel; Montalban, Xavier; Olascoaga, Javier; Matesanz, Fuencisla; Dörner, Thomas; Li, Shu-Chen; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Rieckmann, Peter; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Buttmann, Mathias; Kümpfel, Tania; Kubisch, Christian; Zettl, Uwe K.; Epplen, Joerg T.; Fontaine, Bertrand; Zipp, Frauke; Vandenbroeck, Koen und Bertram, Lars
(März 2013):
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
In: Journal of Medical Genetics, Bd. 50, Nr. 3: S. 140-143
[PDF, 127kB]
Lill, Christina M.; Liu, Tian; Schjeide, Brit-Maren M.; Roehr, Johannes T.; Akkad, Denis A.; Damotte, Vincent; Alcina, Antonio; Ortiz, Miguel A.; Arroyo, Rafa; Lopez de Lapuente, Aitzkoa; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Luessi, Felix; Fernadez, Oscar; Izquierdo, Guillermo; Antigüedad, Alfredo; Hoffjan, Sabine; Cournu-Rebeix, Isabelle; Gromöller, Silvana; Faber, Hans; Liebsch, Maria; Meissner, Esther; Chanvillard, Coralie; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Dörner, Thomas; Steinhagen-Thiessen, Elisabeth; Baeckman, Lars; Heekeren, Hauke R.; Li, Shu-Chen; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Kümpfel, Tania; Kubisch, Christian; Epplen, Jörg T.; Zettl, Uwe K.; Fontaine, Bertrand; Vandenbroeck, Koen; Matesanz, Fuencisla; Urcelay, Elena; Bertram, Lars und Zipp, Frauke
(September 2012):
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.
In: Journal of medical genetics, Bd. 49, Nr. 9: S. 558-562
[PDF, 217kB]
Bechtold-Dalla Pozza, Susanne; Hiedl, Stefan; Roeb, Julia; Lohse, Peter; Malik, Raleigh E.; Park, Soyoung; Duran-Prado, Mario und Rhodes, Simon J.
(2012):
A Recessive Mutation Resulting in a Disabling Amino Acid Substitution (T194R) in the LHX3 Homeodomain Causes Combined Pituitary Hormone Deficiency.
In: Hormone Research in Paediatrics, Nr. 1: S. 41-51
[PDF, 1MB]
Wittkowski, Helmut; Kuemmerle-Deschner, Jasmin B.; Austermann, Judith; Holzinger, Dirk; Goldbach-Mansky, Raphaela; Gramlich, Katharina; Lohse, Peter; Jung, Thomas; Roth, Johannes; Benseler, Susanne M. und Foell, Dirk
(Dezember 2011):
MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes.
In: Annals of the rheumatic diseases, Bd. 70, Nr. 12: S. 2075-2081
[PDF, 280kB]
Kleinlein, Barbara; Griese, Matthias; Liebisch, Gerhard; Krude, Heiko; Lohse, Peter; Aslanidis, Charalampos; Schmitz, Gerd; Peters, Jochen und Holzinger, Andreas
(November 2011):
Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis.
In: Archives of disease in childhood. Fetal and neonatal edition, Bd. 96, Nr. 6:
F453-F456
[PDF, 196kB]
Griese, Matthias; Ripper, Jan; Sibbersen, Anke; Lohse, Pia; Lohse, Peter; Brasch, Frank; Schams, Andrea; Pamir, Asli; Schaub, Bianca; Muensterer, Oliver J.; Schoen, Carola; Gloeckner-Pagel, Judith; Nicolai, Thomas; Reiter, Karl und Hector, Andreas
(2011):
Long-term follow-up and treatment of congenital alveolar proteinosis.
In: BMC Pediatrics
11:72
[PDF, 2MB]
Glas, Jürgen; Seiderer, Julia; Fries, Christoph; Tillack, Cornelia; Pfennig, Simone; Weidinger, Maria; Beigel, Florian; Olszak, Torsten; Lass, Ulrich; Göke, Burkhard; Ochsenkühn, Thomas; Wolf, Christiane; Lohse, Peter; Müller-Myhsok, Bertram; Diegelmann, Julia; Czamara, Darina und Brand, Stephan
(2011):
CEACAM6 gene variants in inflammatory bowel disease.
In: PLOS ONE 6(4), e19319 [PDF, 214kB]
In: PLOS ONE 6(4), e19319 [PDF, 214kB]
Storr, Martin; Emmerdinger, Dominik; Diegelmann, Julia; Pfennig, Simone; Ochsenkühn, Thomas; Göke, Burkhard; Lohse, Peter und Brand, Stephan
(2010):
The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.
In: PLOS ONE 5(2), e9453 [PDF, 106kB]
In: PLOS ONE 5(2), e9453 [PDF, 106kB]
Jürgens, Matthias; Laubender, Rüdiger P.; Hartl, F.; Weidinger, M.; Seiderer, Julia; Wagner, J.; Wetzke, M.; Beigel, Florian; Pfennig, S.; Stallhofer, J.; Schnitzler, Fabian; Tillack, Cornelia; Lohse, Peter; Göke, Burkhard; Glas, Jürgen; Ochsenkühn, Thomas und Brand, Stephan
(2010):
Disease Activity, ANCA, and IL23R Genotype Status Determine Early Response to Infliximab in Patients With Ulcerative Colitis.
In: American Journal of Gastroenterology, Bd. 105, Nr. 8: S. 1811-1819
Glas, Jürgen; Seiderer, Julia; Nagy, Melinda; Fries, Christoph; Beigel, Florian; Weidinger, Maria; Pfennig, Simone; Klein, Wolfram; Epplen, Jörg T.; Lohse, Peter; Folwaczny, Matthias; Göke, Burkhard; Ochsenkühn, Thomas; Diegelmann, Julia; Müller-Myhsok, Bertram; Roeske, Darina und Brand, Stephan
(2010):
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
In: PLOS ONE 5(4), e10373 [PDF, 128kB]
In: PLOS ONE 5(4), e10373 [PDF, 128kB]
Glas, Jürgen; Seiderer, Julia; Tillack, Cornelia; Pfennig, Simone; Beigel, Florian; Jürgens, Matthias; Olszak, Torsten; Laubender, Rüdiger P.; Weidinger, Maria; Müller-Myhsok, Bertram; Göke, Burkhard; Ochsenkühn, Thomas; Lohse, Peter; Diegelmann, Julia; Czamara, Darina und Brand, Stephan
(2010):
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.
In: PLOS ONE 5(12), e14466 [PDF, 125kB]
In: PLOS ONE 5(12), e14466 [PDF, 125kB]
Eifert, Sandra; Rasch, Astrid; Beiras-Fernandez, Andres; Nollert, Georg; Reichart, Bruno und Lohse, Peter
(2009):
Gene polymorphisms in APOE, NOS3, and LIPC genes may be risk factors for cardiac adverse events after primary CABG.
In: Journal of Cardiothoracic Surgery
4:46
[PDF, 294kB]
Griese, Matthias; Haug, Melanie; Brasch, Frank; Freihorst, Achim; Lohse, Peter; Kries, Rüdiger von; Zimmermann, Theodor und Hartl, Dominik
(2009):
Incidence and classification of pediatric diffuse parenchymal lung diseases in Germany.
In: Orphanet Journal of Rare Diseases
4:26
[PDF, 347kB]
Stojanov, S.; Dejaco, C.; Lohse, Peter; Huss, Kristina; Duftner, C. und Belohradsky, B.H.
(2008):
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.
In: Annals of the Rheumatic Diseases, Bd. 67: S. 1292-1298
[PDF, 380kB]
Glas, Jürgen; Seiderer, Julia; Wetzke, Martin; Konrad, Astrid; Török, Helga-Paula; Schmechel, Silke; Tonenchi, Laurian; Grassl, Christine; Dambacher, Julia; Pfennig, Simone; Maier, Kerstin; Griga, Thomas; Klein, Wolfram; Epplen, Jörg T.; Schiemann, Uwe; Folwaczny, Christian; Lohse, Peter; Göke, Burkhard; Ochsenkühn, Thomas; Müller-Myhsok, Bertram; Folwaczny, Matthias; Mussack, Thomas und Brand, Stephan
(2007):
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
In: PLOS ONE (9), e819 [PDF, 133kB]
In: PLOS ONE (9), e819 [PDF, 133kB]
Broedl, Uli C.; Lehrke, Michael; Fleischer-Brielmaier, Elisabeth; Tietz, Anne B.; Nagel, Jutta M.; Göke, Burkhard; Lohse, Peter und Parhofer, Klaus G.
(2006):
Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome.
In: Cardiovascular Diabetology
5:11
[PDF, 284kB]
Svaldi, Mirija; Lanthaler, Andrea Judith; Dugas, Martin; Lohse, Peter; Pescosta, Norbert; Straka, Christian und Mitterer, Manfred
(2003):
T-cell receptor excision circles: A novel prognostic parameter for the outcome of transplantation in multiple myeloma patients.
In: British Journal of Haematology, Bd. 122, Nr. 5: S. 795-801