W. Klein

发表

Mutations in the calcium-sensing receptor: A new genetic risk factor for chronic pancreatitis?

F. Schmitz, J. Epplen, P. Felderbauer, 2006, Scandinavian journal of gastroenterology.

A Polymorphism in the CD14 Gene is Associated with Crohn Disease

C. Folwaczny, W. Klein, M. Hocke, 2002, Scandinavian journal of gastroenterology.

A case–control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease

W. Schmiegel, W. Klein, T. Griga, 2005, International journal of immunogenetics.

The 14-bp deletion polymorphism in the HLA-G gene displays significant differences between ulcerative colitis and Crohn's disease and is associated with ileocecal resection in Crohn's disease.

T. Mussack, J. Glas, C. Folwaczny, 2007, International immunology.

Association of the ASP299GLY TLR4 polymorphism with COPD.

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

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

B. Müller-Myhsok, S. Ripke, S. Brand, 2009, The American Journal of Gastroenterology.

Association study of Wegener granulomatosis and the functionally relevant A645G polymorphism in the bactericidal/permeability increasing protein (BPI) gene

J. Epplen, W. Klein, W. Gross, 2005, International journal of immunogenetics.

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.

Association of interleukin 8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma

J. Epplen, G. Rohde, G. Schultze-Werninghaus, 2005 .

The polymorphism at position −174 of the IL-6 gene is not associated with inflammatory bowel disease

C. Folwaczny, W. Klein, J. Epplen, 2001, European journal of gastroenterology & hepatology.

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

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

Interleukin-4 and interleukin-4 receptor gene polymorphisms in inflammatory bowel diseases

C. Folwaczny, W. Klein, M. Hocke, 2001, Genes and Immunity.

Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex

D. Horn, R. Siebert, G. Kristiansen, 2021, Journal of Medical Genetics.

A polymorphism in the macrophage migration inhibitory factor gene is involved in the genetic predisposition of Crohn's disease and associated with cumulative steroid doses.

W. Schmiegel, W. Klein, J. Epplen, 2007, Hepato-gastroenterology.

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.

Identification of a novel calcium-sensing receptor gene mutation causing familial hypocalciuric hypercalcemia by single-strand conformation polymorphism analysis.

F. Schmitz, P. Felderbauer, W. Klein, 2005, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The ATG16L1 Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population

B. Müller-Myhsok, T. Mussack, S. Brand, 2008, The American Journal of Gastroenterology.

A polymorphism in the IL11 gene is associated with ulcerative colitis

M Hocke, C. Folwaczny, W. Klein, 2002, Genes and Immunity.

Inhibitors in the NFκB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations

S. Böhringer, J. Epplen, W. Klein, 2002, Genes and Immunity.

Polymorphisms in the interleukin‐8 gene in patients with chronic obstructive pulmonary disease

G. Rohde, G. Schultze-Werninghaus, W. Klein, 2005, Electrophoresis.

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

B. Müller-Myhsok, S. Brand, J. Glas, 2005, Gut.

Complex genetic predisposition in adult and juvenile rheumatoid arthritis

J. Epplen, W. Klein, B. Miterski, 2004, BMC Genetics.

Role of the NFKB1 −94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL‐1RN genes

B. Müller-Myhsok, T. Mussack, S. Brand, 2006, Inflammatory bowel diseases.

rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants

Wolfram Klein, Bertram Müller-Myhsok, Thomas Mussack, 2007, PloS one.

Epistasis Between Toll-Like Receptor-9 Polymorphisms and Variants in NOD2 and IL23R Modulates Susceptibility to Crohn's Disease

B. Müller-Myhsok, S. Brand, J. Glas, 2009, The American Journal of Gastroenterology.

rs224136 on Chromosome 10q21.1 and Variants in PHOX2B, NCF4, and FAM92B Are Not Major Genetic Risk Factors for Susceptibility to Crohn's Disease in the German Population

B. Müller-Myhsok, T. Mussack, S. Brand, 2009, The American Journal of Gastroenterology.

Association of interleukin-8 receptor α polymorphisms with chronic obstructive pulmonary disease and asthma

J. Epplen, G. Rohde, G. Schultze-Werninghaus, 2005, Genes and Immunity.

Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset

B. Müller-Myhsok, S. Brand, J. Glas, 2010, PloS one.

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.

Pancreatitis in primary hyperparathyroidism-related hypercalcaemia is not associated with mutations in the CASR gene.

V. Fendrich, D. Bartsch, P. Felderbauer, 2007, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The IL‐10 gene is not involved in the predisposition to inflammatory bowel disease

J. Epplen, C. Folwaczny, W. Klein, 2000, Electrophoresis.

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

J. Epplen, W. Klein, L. Arning, 2005, Journal of Negative Results in BioMedicine.

POLYMORPHISMS IN THE CANINE ROD TRANSDUCIN GENE AND EXCLUSION AS CAUSE FORGENERALISED PROGRESSIVE RETINAL ATROPHY (GPRA): SHORT COMMUNICATION

J. Epplen, W. Klein, G. Dekomien, 1998 .

The IL‐10 gene is not involved in the predisposition to inflammatory bowel disease

J. Epplen, C. Folwaczny, W. Klein, 2000, Electrophoresis.

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

J. Epplen, W. Klein, L. Arning, 2005, Journal of Negative Results in BioMedicine.

The disease susceptibility risk mediated by gene variants in PHOX2B, NCF4, FAM92B, and in the intergenic region on chromosome 10q21.1 differs between North American and European patients with Crohn's disease

B. Müller-Myhsok, S. Brand, J. Glas, 2008 .