Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 93

Related Citations for PubMed (Select 22914433)

1.

Association between genetic variants in the HNF4A gene and childhood-onset Crohn's disease.

Marcil V, Sinnett D, Seidman E, Boudreau F, Gendron FP, Beaulieu JF, Menard D, Lambert M, Bitton A, Sanchez R, Amre D, Levy E.

Genes Immun. 2012 Oct;13(7):556-65. doi: 10.1038/gene.2012.37. Epub 2012 Aug 23.

PMID:
22914433
2.

Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.

Amre DK, Mack DR, Morgan K, Fujiwara M, Israel D, Deslandres C, Seidman EG, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Levy E.

Am J Gastroenterol. 2009 Nov;104(11):2824-8. doi: 10.1038/ajg.2009.430. Epub 2009 Jul 21.

PMID:
19623168
3.

Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease.

Glas J, Seiderer J, Fischer D, Tengler B, Pfennig S, Wetzke M, Beigel F, Olszak T, Weidinger M, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Diegelmann J, Czamara D, Brand S.

Inflamm Bowel Dis. 2011 Sep;17(9):1917-24. doi: 10.1002/ibd.21562. Epub 2010 Dec 3.

PMID:
21830270
4.

Investigation of associations between the pregnane-X receptor gene (NR1I2) and Crohn's disease in Canadian children using a gene-wide haplotype-based approach.

Amre DK, Mack DR, Israel D, Morgan K, Krupoves A, Costea I, Lambrette P, Grimard G, Deslandres C, Levy E, Seidman EG.

Inflamm Bowel Dis. 2008 Sep;14(9):1214-8. doi: 10.1002/ibd.20461.

PMID:
18381611
5.

Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.

Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.

Am J Gastroenterol. 2008 Mar;103(3):615-20. Epub 2007 Nov 28.

PMID:
18047539
6.

Association of FCGR2A, JAK2 or HNF4A variants with ulcerative colitis in Koreans.

Yang SK, Jung Y, Kim H, Hong M, Ye BD, Song K.

Dig Liver Dis. 2011 Nov;43(11):856-61. doi: 10.1016/j.dld.2011.07.006. Epub 2011 Aug 9.

PMID:
21831733
7.

Hepatocyte nuclear factor-4alpha P2 promoter haplotypes are associated with type 2 diabetes in the Japanese population.

Hara K, Horikoshi M, Kitazato H, Ito C, Noda M, Ohashi J, Froguel P, Tokunaga K, Tobe K, Nagai R, Kadowaki T.

Diabetes. 2006 May;55(5):1260-4.

8.

Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease.

Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG.

Aliment Pharmacol Ther. 2009 May 1;29(9):1025-31. doi: 10.1111/j.1365-2036.2009.03953.x. Epub 2009 Feb 7. Erratum in: Aliment Pharmacol Ther. 2009 Aug 15;30(4):422.

PMID:
19210299
9.

Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population.

Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Duricova D, Nevoral J, Vitek L, Lukas M, Cinek O.

Inflamm Bowel Dis. 2011 Jul;17(7):1523-9. doi: 10.1002/ibd.21532. Epub 2010 Nov 8.

PMID:
21674708
10.

NELL1, NCF4, and FAM92B genes are not major susceptibility genes for Crohn's disease in Canadian children and young adults.

Amre DK, Mack DR, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Levy E.

Inflamm Bowel Dis. 2012 Mar;18(3):529-35. doi: 10.1002/ibd.21708. Epub 2011 Apr 6.

PMID:
21472827
11.

Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians.

Johansson S, Raeder H, Eide SA, Midthjell K, Hveem K, Søvik O, Molven A, Njølstad PR.

Diabetes. 2007 Dec;56(12):3112-7. Epub 2007 Sep 7.

12.

Associations between ABCB1/MDR1 gene polymorphisms and Crohn's disease: a gene-wide study in a pediatric population.

Krupoves A, Seidman EG, Mack D, Israel D, Morgan K, Lambrette P, Costea I, Deslandres C, Grimard G, Law L, Levy E, Amre DK.

Inflamm Bowel Dis. 2009 Jun;15(6):900-8. doi: 10.1002/ibd.20849.

PMID:
19107781
13.

Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes.

Anuradha S, Radha V, Mohan V.

Clin Genet. 2011 Dec;80(6):541-9. doi: 10.1111/j.1399-0004.2010.01577.x. Epub 2010 Nov 10.

PMID:
21062274
14.

Evidence for common genetic control in pathways of inflammation for Crohn's disease and psoriatic arthritis.

Ho P, Bruce IN, Silman A, Symmons D, Newman B, Young H, Griffiths CE, John S, Worthington J, Barton A.

Arthritis Rheum. 2005 Nov;52(11):3596-602.

15.

HNF4α and CDH1 are associated with ulcerative colitis in a Dutch cohort.

van Sommeren S, Visschedijk MC, Festen EA, de Jong DJ, Ponsioen CY, Wijmenga C, Weersma RK.

Inflamm Bowel Dis. 2011 Aug;17(8):1714-8. doi: 10.1002/ibd.21541. Epub 2010 Nov 28.

PMID:
21744425
16.

Genetic variants in IL-23R and ATG16L1 independently predispose to increased susceptibility to Crohn's disease in a Canadian population.

Newman WG, Zhang Q, Liu X, Amos CI, Siminovitch KA.

J Clin Gastroenterol. 2009 May-Jun;43(5):444-7. doi: 10.1097/MCG.0b013e318168bdf0.

PMID:
19276991
17.

The association of MYO9B gene in Italian patients with inflammatory bowel diseases.

Latiano A, Palmieri O, Valvano MR, D'Incà R, Caprilli R, Cucchiara S, Sturniolo GC, Bossa F, Andriulli A, Annese V.

Aliment Pharmacol Ther. 2008 Feb 1;27(3):241-8. Epub 2007 Oct 15.

18.

Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children.

Amre DK, Mack DR, Morgan K, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Feguery H, Bucionis V, Deslandres C, Levy E, Seidman EG.

Inflamm Bowel Dis. 2009 Apr;15(4):501-7. doi: 10.1002/ibd.20785.

PMID:
18985712
19.

Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease.

Beckly JB, Hancock L, Geremia A, Cummings JR, Morris A, Cooney R, Pathan S, Guo C, Jewell DP.

Inflamm Bowel Dis. 2008 Apr;14(4):500-7. doi: 10.1002/ibd.20365.

PMID:
18200509
20.

Association between genetic variants in myosin IXB and Crohn's disease.

Cooney R, Cummings JR, Pathan S, Beckly J, Geremia A, Hancock L, Guo C, Morris A, Jewell DP.

Inflamm Bowel Dis. 2009 Jul;15(7):1014-21. doi: 10.1002/ibd.20885.

PMID:
19235913
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk