(Q54542312)

31 May 2018

title

Association of IL23R, TNFRSF1A, and HLA-DRB1*0103 allele variants with inflammatory bowel disease phenotypes in the Finnish population. (English)

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31 May 2018

inflammatory bowel diseases

main subject

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6

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31 May 2018

Elisabet Einarsdottir

object named as

Elisabet Einarsdottir

5

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author name string

Maarit Lappalainen

1

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31 May 2018

Leena Halme

2

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31 May 2018

Ulla Turunen

3

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31 May 2018

Päivi Saavalainen

4

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31 May 2018

Kimmo Kontula

7

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31 May 2018

Paulina Paavola-Sakki

8

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31 May 2018

publication date

1 August 2008

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31 May 2018

Inflammatory Bowel Diseases

published in

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31 May 2018

volume

14

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31 May 2018

issue

8

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31 May 2018

page(s)

1118-1124

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31 May 2018

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

cites work

1 reference

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

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Functional variants of OCTN cation transporter genes are associated with Crohn disease

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Genetic variation in DLG5 is associated with inflammatory bowel disease

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Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study.

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

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Association of Organic Cation Transporter Risk Haplotype With Perianal Penetrating Crohn’s Disease but Not With Susceptibility to IBD

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DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population

21 January 2018

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

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Deficient host-bacteria interactions in inflammatory bowel disease? The toll-like receptor (TLR)-4 Asp299gly polymorphism is associated with Crohn's disease and ulcerative colitis

21 January 2018

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Polymorphisms of the lipopolysaccharide-signaling complex in inflammatory bowel disease: association of a mutation in the Toll-like receptor 4 gene with ulcerative colitis

21 January 2018

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The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases

21 January 2018

1 reference

Tumor necrosis factor receptor gene polymorphisms in Crohn's disease: association with clinical phenotypes

21 January 2018

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Tumour necrosis factor-alpha receptor 1 and 2 polymorphisms in inflammatory bowel disease and their association with response to infliximab

21 January 2018

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Linkage of inflammatory bowel disease to human chromosome 6p

21 January 2018

1 reference

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

21 January 2018

1 reference

A population- and family-based study of Canadian families reveals association of HLA DRB1*0103 with colonic involvement in inflammatory bowel disease

21 January 2018

1 reference

CARD15 and HLA DRB1 alleles influence susceptibility and disease localization in Crohn's disease

21 January 2018

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IBD1 and IBD3 determine location of Crohn's disease in the Spanish population.

21 January 2018

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The contribution of human leucocyte antigen complex genes to disease phenotype in ulcerative colitis

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Clinical and genetic heterogeneity in Mexican patients with ulcerative colitis.

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

21 January 2018

1 reference

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

21 January 2018

1 reference

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

21 January 2018

1 reference

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

21 January 2018

1 reference

IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease

21 January 2018

1 reference

IL23R Arg381Gln is associated with childhood onset inflammatory bowel disease in Scotland

21 January 2018

1 reference

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients

21 January 2018

1 reference

IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease

21 January 2018

1 reference

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease

21 January 2018

1 reference

IL23R R381Q and ATG16L1 T300A Are Strongly Associated With Crohn's Disease in a Study of New Zealand Caucasians With Inflammatory Bowel Disease

21 January 2018

1 reference

Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population

21 January 2018

1 reference

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

21 January 2018

1 reference

Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype

21 January 2018

1 reference

A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5

21 January 2018

1 reference

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

21 January 2018

1 reference

Confirmation of the role of ATG16l1 as a Crohnʼs disease susceptibility gene

21 January 2018

1 reference

Positional cloning of disease genes: advantages of genetic isolates

21 January 2018

1 reference

Molecular genetics of the Finnish disease heritage.

21 January 2018

1 reference

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.

21 January 2018

1 reference

Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease.

21 January 2018

1 reference

HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish caucasian populations

21 January 2018

1 reference

Genetic markers may predict disease behavior in patients with ulcerative colitis

21 January 2018

1 reference

NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

21 January 2018

1 reference

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

21 January 2018

1 reference

Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31

21 January 2018

1 reference

Direct or indirect association in a complex disease: the role ofSLC22A4 andSLC22A5 functional variants in Crohn disease

21 January 2018

1 reference

Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease

21 January 2018

1 reference

Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men

21 January 2018

1 reference

ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach

21 January 2018

1 reference

Polymorphisms in the TNF-alpha and TNF-receptor genes in patients with coronary artery disease

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/IBD.20431

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31 May 2018

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31 May 2018