221 related articles for article (PubMed ID: 19953089)
1. Differences in genetic background between active smokers, passive smokers, and non-smokers with Crohn's disease.
van der Heide F; Nolte IM; Kleibeuker JH; Wijmenga C; Dijkstra G; Weersma RK
Am J Gastroenterol; 2010 May; 105(5):1165-72. PubMed ID: 19953089
[TBL] [Abstract][Full Text] [Related]
2. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
Török HP; Glas J; Endres I; Tonenchi L; Teshome MY; Wetzke M; Klein W; Lohse P; Ochsenkühn T; Folwaczny M; Göke B; Folwaczny C; Müller-Myhsok B; Brand S
Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129
[TBL] [Abstract][Full Text] [Related]
3. PTPN2 but not PTPN22 is associated with Crohn's disease in a New Zealand population.
Morgan AR; Han DY; Huebner C; Lam WJ; Fraser AG; Ferguson LR
Tissue Antigens; 2010 Aug; 76(2):119-25. PubMed ID: 20403149
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 19623168
[TBL] [Abstract][Full Text] [Related]
5. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort.
Weersma RK; Stokkers PC; van Bodegraven AA; van Hogezand RA; Verspaget HW; de Jong DJ; van der Woude CJ; Oldenburg B; Linskens RK; Festen EA; van der Steege G; Hommes DW; Crusius JB; Wijmenga C; Nolte IM; Dijkstra G;
Gut; 2009 Mar; 58(3):388-95. PubMed ID: 18824555
[TBL] [Abstract][Full Text] [Related]
6. 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.
Glas J; Seiderer J; Pasciuto G; Tillack C; Diegelmann J; Pfennig S; Konrad A; Schmechel S; Wetzke M; Török HP; Stallhofer J; Jürgens M; Griga T; Klein W; Epplen JT; Schiemann U; Mussack T; Lohse P; Göke B; Ochsenkühn T; Folwaczny M; Müller-Myhsok B; Brand S
Am J Gastroenterol; 2009 Mar; 104(3):665-72. PubMed ID: 19262523
[TBL] [Abstract][Full Text] [Related]
7. Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort.
Weersma RK; Stokkers PC; Cleynen I; Wolfkamp SC; Henckaerts L; Schreiber S; Dijkstra G; Franke A; Nolte IM; Rutgeerts P; Wijmenga C; Vermeire S
Am J Gastroenterol; 2009 Mar; 104(3):630-8. PubMed ID: 19174780
[TBL] [Abstract][Full Text] [Related]
8. Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations.
Medici V; Mascheretti S; Croucher PJ; Stoll M; Hampe J; Grebe J; Sturniolo GC; Solberg C; Jahnsen J; Moum B; Schreiber S; Vatn MH
Eur J Hum Genet; 2006 Apr; 14(4):459-68. PubMed ID: 16493449
[TBL] [Abstract][Full Text] [Related]
9. Polymorphism of the IRGM gene might predispose to fistulizing behavior in Crohn's disease.
Latiano A; Palmieri O; Cucchiara S; Castro M; D'Incà R; Guariso G; Dallapiccola B; Valvano MR; Latiano T; Andriulli A; Annese V
Am J Gastroenterol; 2009 Jan; 104(1):110-6. PubMed ID: 19098858
[TBL] [Abstract][Full Text] [Related]
10. The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
Glas J; Konrad A; Schmechel S; Dambacher J; Seiderer J; Schroff F; Wetzke M; Roeske D; Török HP; Tonenchi L; Pfennig S; Haller D; Griga T; Klein W; Epplen JT; Folwaczny C; Lohse P; Göke B; Ochsenkühn T; Mussack T; Folwaczny M; Müller-Myhsok B; Brand S
Am J Gastroenterol; 2008 Mar; 103(3):682-91. PubMed ID: 18162085
[TBL] [Abstract][Full Text] [Related]
11. DLG5 variants contribute to Crohn disease risk in a Canadian population.
Newman WG; Gu X; Wintle RF; Liu X; van Oene M; Amos CI; Siminovitch KA
Hum Mutat; 2006 Apr; 27(4):353-8. PubMed ID: 16450402
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 18047539
[TBL] [Abstract][Full Text] [Related]
13. TUCAN (CARD8) genetic variants and inflammatory bowel disease.
McGovern DP; Butler H; Ahmad T; Paolucci M; van Heel DA; Negoro K; Hysi P; Ragoussis J; Travis SP; Cardon LR; Jewell DP
Gastroenterology; 2006 Oct; 131(4):1190-6. PubMed ID: 17030188
[TBL] [Abstract][Full Text] [Related]
14. DLG5 variants in inflammatory bowel disease.
Büning C; Geerdts L; Fiedler T; Gentz E; Pitre G; Reuter W; Luck W; Buhner S; Molnar T; Nagy F; Lonovics J; Dignass A; Landt O; Nickel R; Genschel J; Lochs H; Schmidt HH; Witt H
Am J Gastroenterol; 2006 Apr; 101(4):786-92. PubMed ID: 16494592
[TBL] [Abstract][Full Text] [Related]
15. Intestinal permeability and genetic determinants in patients, first-degree relatives, and controls in a high-incidence area of Crohn's disease in Southern Italy.
Fries W; Renda MC; Lo Presti MA; Raso A; Orlando A; Oliva L; Giofré MR; Maggio A; Mattaliano A; Macaluso A; Cottone M
Am J Gastroenterol; 2005 Dec; 100(12):2730-6. PubMed ID: 16393227
[TBL] [Abstract][Full Text] [Related]
16. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.
Tomer G; Ceballos C; Concepcion E; Benkov KJ
Am J Gastroenterol; 2003 Nov; 98(11):2479-84. PubMed ID: 14638352
[TBL] [Abstract][Full Text] [Related]
17. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases.
Weersma RK; Oostenbrug LE; Nolte IM; Van Der Steege G; Oosterom E; Van Dullemen HM; Kleibeuker JH; Dijkstra G
Scand J Gastroenterol; 2007 Jul; 42(7):827-33. PubMed ID: 17558906
[TBL] [Abstract][Full Text] [Related]
18. Identification of DLG5 and SLC22A5 gene polymorphisms in Malaysian patients with Crohn's disease.
Chua KH; Lian LH; Kee BP; Thum CM; Lee WS; Hilmi I; Goh KL
J Dig Dis; 2011 Dec; 12(6):459-66. PubMed ID: 22118696
[TBL] [Abstract][Full Text] [Related]
19. A distinct pattern of disease-associated single nucleotide polymorphisms in IBD risk genes in a family with Crohn's disease.
Barthel C; Spalinger MR; Brunner J; Lang S; Fried M; Rogler G; Scharl M
Eur J Gastroenterol Hepatol; 2014 Jul; 26(7):803-6. PubMed ID: 24901824
[TBL] [Abstract][Full Text] [Related]
20. [NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study].
Lakatos L; Lakatos PL; Willheim-Polli C; Reinisch W; Ferenci P; Tulassay Z; Molnár T; Kovács A; Papp J; Szalay F;
Orv Hetil; 2004 Jul; 145(27):1403-11. PubMed ID: 15320482
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
