M. Hagedorn

Association of the ASP299GLY TLR4 polymorphism with COPD.

A. Gillissen, G. Rohde, G. Schultze-Werninghaus, 2006, Respiratory medicine.

A Polymorphism of the Bactericidal/Permeability Increasing Protein (BPI) Gene Is Associated With Crohn's Disease

W. Schmiegel, C. Folwaczny, W. Klein, 2005, Journal of clinical gastroenterology.

A polymorphism of the NFKBIA gene is associated with Crohn's disease patients lacking a predisposing allele of the CARD15 gene

W. Schmiegel, C. Folwaczny, W. Klein, 2004, International Journal of Colorectal Disease.

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

M. Vorgerd, J. Epplen, M. Meins, 2006, BMC Medical Genetics.

A promotor polymorphism in the Interleukin 11 gene is associated with chronic obstructive pulmonary disease

J. Epplen, G. Rohde, G. Schultze-Werninghaus, 2004, Electrophoresis.

Association between the promoter polymorphism T/C at position -159 of the CD14 gene and anti-inflammatory therapy in patients with inflammatory bowel disease.

W. Schmiegel, C. Folwaczny, W. Klein, 2005, European journal of medical research.

Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

K. Hameister, J. Epplen, M. Meins, 2005, Journal of Medical Genetics.

The G2964A polymorphism of the STAT6 gene in inflammatory bowel disease.

W. Schmiegel, J. Epplen, C. Folwaczny, 2005, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Novel Mutations in Exon 6 of the GFAP Gene Affect a Highly Conserved IF Motif in the Rod Domain 2B and are Associated with Early Onset Infantile Alexander Disease

U. Stephani, F. Donnerstag, P. Ledaal, 2007, Neuropediatrics.