BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 24937328)

  • 1. Exome sequencing identifies DLG1 as a novel gene for potential susceptibility to Crohn's disease in a Chinese family study.
    Xu S; Zhou F; Tao J; Song L; Ng SC; Wang X; Chen L; Yi F; Ran Z; Zhou R; Xia B
    PLoS One; 2014; 9(6):e99807. PubMed ID: 24937328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
    Ellinghaus D; Zhang H; Zeissig S; Lipinski S; Till A; Jiang T; Stade B; Bromberg Y; Ellinghaus E; Keller A; Rivas MA; Skieceviciene J; Doncheva NT; Liu X; Liu Q; Jiang F; Forster M; Mayr G; Albrecht M; Häsler R; Boehm BO; Goodall J; Berzuini CR; Lee J; Andersen V; Vogel U; Kupcinskas L; Kayser M; Krawczak M; Nikolaus S; Weersma RK; Ponsioen CY; Sans M; Wijmenga C; Strachan DP; McArdle WL; Vermeire S; Rutgeerts P; Sanderson JD; Mathew CG; Vatn MH; Wang J; Nöthen MM; Duerr RH; Büning C; Brand S; Glas J; Winkelmann J; Illig T; Latiano A; Annese V; Halfvarson J; D'Amato M; Daly MJ; Nothnagel M; Karlsen TH; Subramani S; Rosenstiel P; Schreiber S; Parkes M; Franke A
    Gastroenterology; 2013 Aug; 145(2):339-47. PubMed ID: 23624108
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.
    Onoufriadis A; Stone K; Katsiamides A; Amar A; Omar Y; de Lange KM; Taylor K; Barrett JC; Pollok R; Hayee B; Mansfield JC; Sanderson JD; Simpson MA; Mathew CG; Prescott NJ
    J Crohns Colitis; 2018 Feb; 12(3):321-326. PubMed ID: 29211899
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
    Christodoulou K; Wiskin AE; Gibson J; Tapper W; Willis C; Afzal NA; Upstill-Goddard R; Holloway JW; Simpson MA; Beattie RM; Collins A; Ennis S
    Gut; 2013 Jul; 62(7):977-84. PubMed ID: 22543157
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.
    Petersen BS; Spehlmann ME; Raedler A; Stade B; Thomsen I; Rabionet R; Rosenstiel P; Schreiber S; Franke A
    BMC Genomics; 2014 Jul; 15(1):564. PubMed ID: 24996980
    [TBL] [Abstract][Full Text] [Related]  

  • 6. rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
    Glas J; Seiderer J; Wetzke M; Konrad A; Török HP; Schmechel S; Tonenchi L; Grassl C; Dambacher J; Pfennig S; Maier K; Griga T; Klein W; Epplen JT; Schiemann U; Folwaczny C; Lohse P; Göke B; Ochsenkühn T; Müller-Myhsok B; Folwaczny M; Mussack T; Brand S
    PLoS One; 2007 Sep; 2(9):e819. PubMed ID: 17786191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.
    Seiderer J; Elben I; Diegelmann J; Glas J; Stallhofer J; Tillack C; Pfennig S; Jürgens M; Schmechel S; Konrad A; Göke B; Ochsenkühn T; Müller-Myhsok B; Lohse P; Brand S
    Inflamm Bowel Dis; 2008 Apr; 14(4):437-45. PubMed ID: 18088064
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of T Helper 1 Cytokine Gene Single Nucleotide Polymorphisms with Ulcerative Colitis and Crohn's Disease.
    Ebrahimi Daryani N; Sadr M; Soltani S; Saghazadeh A; Moossavi S; Shahkarami S; Farhadi E; Rezaei N
    Dig Dis; 2019; 37(1):21-32. PubMed ID: 30134230
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Single nucleotide polymorphisms in C-type lectin genes, clustered in the IBD2 and IBD6 susceptibility loci, may play a role in the pathogenesis of inflammatory bowel diseases.
    Wolfkamp SC; Verstege MI; Vogels EW; Meisner S; Verseijden C; Stokkers PC; te Velde AA
    Eur J Gastroenterol Hepatol; 2012 Aug; 24(8):965-70. PubMed ID: 22664939
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome sequencing identifies novel compound heterozygous IFNA4 and IFNA10 mutations as a cause of impaired function in Crohn's disease patients.
    Xiao CX; Xiao JJ; Xu HZ; Wang HH; Chen X; Liu YS; Li P; Shi Y; Nie YZ; Li S; Wu KC; Liu ZJ; Ren JL; Guleng B
    Sci Rep; 2015 May; 5():10514. PubMed ID: 26000985
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.
    Beaudoin M; Goyette P; Boucher G; Lo KS; Rivas MA; Stevens C; Alikashani A; Ladouceur M; Ellinghaus D; Törkvist L; Goel G; Lagacé C; Annese V; Bitton A; Begun J; Brant SR; Bresso F; Cho JH; Duerr RH; Halfvarson J; McGovern DP; Radford-Smith G; Schreiber S; Schumm PL; Sharma Y; Silverberg MS; Weersma RK; ; ; ; D'Amato M; Vermeire S; Franke A; Lettre G; Xavier RJ; Daly MJ; Rioux JD
    PLoS Genet; 2013; 9(9):e1003723. PubMed ID: 24068945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
    Yang SK; Hong M; Zhao W; Jung Y; Baek J; Tayebi N; Kim KM; Ye BD; Kim KJ; Park SH; Lee I; Lee EJ; Kim WH; Cheon JH; Kim YH; Jang BI; Kim HS; Choi JH; Koo JS; Lee JH; Jung SA; Lee YJ; Jang JY; Shin HD; Kang D; Youn HS; Liu J; Song K
    Gut; 2014 Jan; 63(1):80-7. PubMed ID: 23850713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn's Disease Patients.
    Kevans D; Silverberg MS; Borowski K; Griffiths A; Xu W; Onay V; Paterson AD; Knight J; Croitoru K;
    J Crohns Colitis; 2016 Feb; 10(2):209-15. PubMed ID: 26512135
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.
    Onodera K; Arimura Y; Isshiki H; Kawakami K; Nagaishi K; Yamashita K; Yamamoto E; Niinuma T; Naishiro Y; Suzuki H; Imai K; Shinomura Y
    PLoS One; 2015; 10(9):e0137801. PubMed ID: 26375822
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Variants at the 3p21 locus influence susceptibility and phenotype both in adults and early-onset patients with inflammatory bowel disease.
    Latiano A; Palmieri O; Corritore G; Valvano MR; Bossa F; Cucchiara S; Castro M; Riegler G; De Venuto D; D'Incà R; Andriulli A; Annese V
    Inflamm Bowel Dis; 2010 Jul; 16(7):1108-17. PubMed ID: 20024904
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2.
    Diegelmann J; Czamara D; Le Bras E; Zimmermann E; Olszak T; Bedynek A; Göke B; Franke A; Glas J; Brand S
    PLoS One; 2013; 8(11):e77773. PubMed ID: 24223725
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NLRP3 gene is associated with ulcerative colitis (UC), but not Crohn's disease (CD), in Chinese Han population.
    Zhang HX; Wang ZT; Lu XX; Wang YG; Zhong J; Liu J
    Inflamm Res; 2014 Dec; 63(12):979-85. PubMed ID: 25297810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families.
    Levine AP; Pontikos N; Schiff ER; Jostins L; Speed D; ; Lovat LB; Barrett JC; Grasberger H; Plagnol V; Segal AW
    Gastroenterology; 2016 Oct; 151(4):698-709. PubMed ID: 27373512
    [TBL] [Abstract][Full Text] [Related]  

  • 20. PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background.
    Glas J; Wagner J; Seiderer J; Olszak T; Wetzke M; Beigel F; Tillack C; Stallhofer J; Friedrich M; Steib C; Göke B; Ochsenkühn T; Karbalai N; Diegelmann J; Czamara D; Brand S
    PLoS One; 2012; 7(3):e33682. PubMed ID: 22457781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.