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

J Diegelmann; J Glas; J Seiderer; G Pasciuto; C Tillack; A Konrad; HP Török; S Pfennig; U Schiemann; W Klein; JT Epplen; T Griga; P Lohse; B Göke; T Ochsenkühn; M Folwaczny; B Müller-Myhsok; S Brand

doi:10.1055/s-0028-1089404

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

Zeitschrift für Gastroenterologie ◽

10.1055/s-0028-1089404 ◽

2008 ◽

Vol 46 (09) ◽

Author(s):

J Diegelmann ◽

J Glas ◽

J Seiderer ◽

G Pasciuto ◽

C Tillack ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

North American ◽

Intergenic Region ◽

Disease Susceptibility ◽

Gene Variants

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M2046 Significant Differences in the Genetic Susceptibility to Crohn's Disease Between North American and European Populations Regarding Gene Variants in Phox2b, Ncf4, Fam92b, and in the Intergenic Region On Chromosome 10q21.1

Gastroenterology ◽

10.1016/s0016-5085(08)62139-3 ◽

2008 ◽

Vol 134 (4) ◽

pp. A-458

Author(s):

Julia Diegelmann ◽

Jürgen Glas ◽

Julia Seiderer ◽

Giulia Pasciuto ◽

Cornelia Tillack ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Genetic Susceptibility ◽

North American ◽

Intergenic Region ◽

Gene Variants ◽

European Populations

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The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

Zeitschrift für Gastroenterologie ◽

10.1055/s-0028-1089401 ◽

2008 ◽

Vol 46 (09) ◽

Author(s):

J Seiderer ◽

J Glas ◽

J Diegelmann ◽

G Pasciuto ◽

C Tillack ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Susceptibility ◽

Susceptibility Gene ◽

Gene Variants ◽

Disease Phenotype ◽

Disease Susceptibility Gene

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P220 - The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

Journal of Crohn s and Colitis ◽

10.1016/s1873-9946(09)60247-6 ◽

2009 ◽

Vol 3 (1) ◽

pp. S97

Author(s):

J. Seiderer ◽

J. Glas ◽

J. Diegelmann ◽

G. Pasciuto ◽

C. Tillack ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Susceptibility ◽

Susceptibility Gene ◽

Gene Variants ◽

Disease Phenotype ◽

Disease Susceptibility Gene

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The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants

PLoS ONE ◽

10.1371/journal.pone.0014466 ◽

2010 ◽

Vol 5 (12) ◽

pp. e14466 ◽

Cited By ~ 24

Author(s):

Jürgen Glas ◽

Julia Seiderer ◽

Cornelia Tillack ◽

Simone Pfennig ◽

Florian Beigel ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Single Nucleotide Polymorphisms ◽

Disease Susceptibility ◽

Susceptibility Gene ◽

Gene Variants ◽

Nucleotide Polymorphisms ◽

Single Nucleotide ◽

Disease Susceptibility Gene

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First evidence for strong epistasis between two Crohn's disease susceptibility loci: PTGER4-expression-modulating polymorphisms in the 5p13.1 region enhance ATG16L1-associated susceptibility to Crohn's disease

Zeitschrift für Gastroenterologie ◽

10.1055/s-0028-1089398 ◽

2008 ◽

Vol 46 (09) ◽

Author(s):

J Seiderer ◽

J Glas ◽

G Pasciuto ◽

J Diegelmann ◽

C Tillack ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Susceptibility ◽

Susceptibility Loci

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NOD1 gene E266K (G796A) polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease

Zeitschrift für Gastroenterologie ◽

10.1055/s-2007-982693 ◽

2007 ◽

Vol 45 (05) ◽

Author(s):

T Molnár ◽

P Hofner ◽

F Nagy ◽

PL Lakatos ◽

S Fischer ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Susceptibility ◽

Disease Phenotype

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Faculty Opinions recommendation of Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1087155.540141 ◽

2007 ◽

Author(s):

Jonathan Howard

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Susceptibility ◽

Sequence Variants ◽

Autophagy Gene

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Su1988 ENVIRONMENTAL EFFECT OF RESOLVED HUMAN CMV INFECTION AND NK RECEPTOR GENETICS IN PEDIATRIC CROHN'S DISEASE SUSCEPTIBILITY AND PHENOTYPE.

Gastroenterology ◽

10.1016/s0016-5085(20)32514-2 ◽

2020 ◽

Vol 158 (6) ◽

pp. S-735

Author(s):

Terri Shih ◽

Susy Yusung ◽

Dalin Li ◽

Rivkah Gonsky ◽

Gregory J. Botwin ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Environmental Effect ◽

Disease Susceptibility ◽

Cmv Infection ◽

Human Cmv ◽

Nk Receptor

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Interaction between STAT3 gene polymorphisms and smoking on Crohn’s disease susceptibility: a case–control study in a Chinese Han population

Inflammation Research ◽

10.1007/s00011-016-0941-2 ◽

2016 ◽

Vol 65 (7) ◽

pp. 573-578 ◽

Cited By ~ 1

Author(s):

Jun-hong Li ◽

Ning Wu ◽

Hong-mei Yang ◽

Hong-bing Tang ◽

Dong-ping Bao ◽

...

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Gene Polymorphisms ◽

Disease Susceptibility ◽

Case Control Study ◽

Case Control ◽

Chinese Han Population ◽

Chinese Han ◽

Han Population ◽

Control Study

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Erratum to The Unsolved Link of Genetic Markers and Crohn’s Disease Progression: A North American Cohort Experience

Inflammatory Bowel Diseases ◽

10.1093/ibd/izz136 ◽

2019 ◽

Vol 25 (12) ◽

pp. e170-e170

Keyword(s):

Crohn’S Disease ◽

Crohn's Disease ◽

Disease Progression ◽

Genetic Markers ◽

North American ◽

North American Cohort

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