Angiotensin and its AT₂ receptor : new insights into an old systemSTOLL, Monika; UNGER, Thomas.Regulatory peptides. 2001, Vol 99, Num 2-3, pp 175-182, issn 0167-0115Article

Inherited Risk Factors for Thrombotic Diseases in Children: The Genome-Wide PerspectivePREUSS, Christoph; STOLL, Monika.Seminars in thrombosis and hemostasis. 2011, Vol 37, Num 7, pp 848-855, issn 0094-6176, 8 p.Article

Platelet reactivity and clopidogrel resistance are associated with the H2 haplotype of the P2Y₁₂-ADP receptor geneSTARITZ, Peter; KURZ, Kerstin; STOLL, Monika et al.International journal of cardiology. 2009, Vol 133, Num 3, pp 341-345, issn 0167-5273, 5 p.Article

The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studiesBERGER, Klaus; STÖGBAUER, Florian; FUNKE, Harald et al.Human genetics. 2007, Vol 121, Num 2, pp 169-178, issn 0340-6717, 10 p.Article

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsCROUCHER, Peter J. P; MASCHERETTI, Silvia; WON HO KIM et al.European journal of human genetics. 2003, Vol 11, Num 1, pp 6-16, issn 1018-4813, 11 p.Article

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor bindingSCHOOFS, Till; ROHDE, Christian; STOLL, Monika et al.Blood. 2013, Vol 121, Num 1, pp 178-187, issn 0006-4971, 10 p.Article

Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational studyHOLZHAUER, Susanne; GOLDENBERG, Neil A; JUNKER, Ralf et al.Blood. 2012, Vol 120, Num 7, pp 1510-1515, issn 0006-4971, 6 p.Article

Extreme heterogeneity in CARD15 and DLG5 crohn disease-associated polymorphisms between German and Norwegian populationsMEDICI, Valentina; MASCHERETTI, Silvia; SCHREIBER, Stefan et al.European journal of human genetics. 2006, Vol 14, Num 4, pp 459-468, issn 1018-4813, 10 p.Article

Promotor polymorphisms of plasminogen activator inhibitor-1 and other thrombophilic genotypes in cerebral venous thrombosis: a case-control study in adultsRINGELSTEIN, Marius; JUNG, Alexander; BERGER, Klaus et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2287-2292, issn 0340-5354, 6 p.Article

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric strokeARNING, Astrid; HIERSCHE, Milan; WITTEN, Anika et al.Blood. 2012, Vol 120, Num 26, pp 5231-5236, issn 0006-4971, 6 p.Article

Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control StudiesASSIMES, Themistocles L; HOLM, Hilma; PATTERSON, Chris C et al.Journal of the American College of Cardiology. 2010, Vol 56, Num 19, pp 1552-1563, issn 0735-1097, 12 p.Article

A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczemaSCHULZ, Florian; MARENHOLZ, Ingo; STOLL, Monika et al.Journal of allergy and clinical immunology. 2007, Vol 120, Num 5, pp 1097-1102, issn 0091-6749, 6 p.Article

IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitisGIALLOURAKIS, Cosmas; STOLL, Monika; MILLER, Katie et al.American journal of human genetics. 2003, Vol 73, Num 1, pp 205-211, issn 0002-9297, 7 p.Article

Differential regulation of thrombospondin-1 and fibronectin by angiotensin II receptor subtypes in cultured endothelial cellsFISCHER, Jens W; STOLL, Monika; HAHN, Alfred W. A et al.Cardiovascular research. 2001, Vol 51, Num 4, pp 784-791, issn 0008-6363Article

DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target GenesHASCHER, Antje; HAASE, Ann-Kristin; OGAWA, Seishi et al.Clinical cancer research (Print). 2014, Vol 20, Num 4, pp 814-826, issn 1078-0432, 13 p.Article

Genetic variants implicated in telomere length associated with left ventricular function in patients with hypertension and cardiac organ damageHUBER, Matthias; TRESZL, Andras; VÖLLER, Heinz et al.Journal of molecular medicine (Berlin. Print). 2012, Vol 90, Num 9, pp 1059-1067, issn 0946-2716, 9 p.Article

The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's diseaseDÄBRITZ, Jan; FRIEDRICHS, Frauke; FOELL, Dirk et al.American journal of physiology. Gastrointestinal and liver physiology. 2011, Vol 63, Num 5, issn 0193-1857, G823-G832Article

Fibrinogen α and γ genes and factor V^Leiden in children with thromboembolism: results from 2 family-based association studiesNOWAK-GÖTTL, Ulrike; WEILER, Hartmut; HERNANDEZ, Irene et al.Blood. 2009, Vol 114, Num 9, pp 1947-1953, issn 0006-4971, 7 p.Article

Genetic analysis of salt-sensitive hypertension in Dahl rats reveals a link between cardiac fibrosis and high cholesterolWENDT, Norbert; SCHULZ, Angela; QADRI, Fatimunnisa et al.Cardiovascular research. 2009, Vol 81, Num 3, pp 618-626, issn 0008-6363, 9 p.Article

The Crohn's disease susceptibility gene DLG5 as a member of the CARD interaction networkFRIEDRICHS, Frauke; HENCKAERTS, Liesbet; VERMEIRE, Severine et al.Journal of molecular medicine (Berlin. Print). 2008, Vol 86, Num 4, pp 423-432, issn 0946-2716, 10 p.Article

Familial elevated factor VIII in children with symptomatic venous thrombosis and post-thrombotic syndrome : Results of a multicenter studyKREUZ, Wolfhart; STOLL, Monika; JUNKER, Ralf et al.Arteriosclerosis, thrombosis, and vascular biology. 2006, Vol 26, Num 8, pp 1901-1906, issn 1079-5642, 6 p.Article