213 related articles for article (PubMed ID: 26887379)
1. Exome-Wide Association Study Identified New Risk Loci for Hirschsprung's Disease.
Tang W; Tang J; Zhao Y; Qin Y; Jin G; Xu X; Zhu H; Shen H; Wang X; Hu Z; Xia Y
Mol Neurobiol; 2017 Apr; 54(3):1777-1785. PubMed ID: 26887379
[TBL] [Abstract][Full Text] [Related]
2. Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population.
Yu XX; Chu X; Wu WJ; Wei ZL; Song HL; Bai MR; Lu YJ; Gu BL; Gong YM; Cai W
Pediatr Res; 2021 Feb; 89(3):694-700. PubMed ID: 32380506
[TBL] [Abstract][Full Text] [Related]
3. Fine mapping of the NRG1 Hirschsprung's disease locus.
Tang CS; Tang WK; So MT; Miao XP; Leung BM; Yip BH; Leon TY; Ngan ES; Lui VC; Chen Y; Chan IH; Chung PH; Liu XL; Wu XZ; Wong KK; Sham PC; Cherny SS; Tam PK; Garcia-Barceló MM
PLoS One; 2011 Jan; 6(1):e16181. PubMed ID: 21283760
[TBL] [Abstract][Full Text] [Related]
4. Advances in molecular genetics of Hirschsprung's disease.
Pan ZW; Li JC
Anat Rec (Hoboken); 2012 Oct; 295(10):1628-38. PubMed ID: 22815266
[TBL] [Abstract][Full Text] [Related]
5. Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population.
Yang J; Duan S; Zhong R; Yin J; Pu J; Ke J; Lu X; Zou L; Zhang H; Zhu Z; Wang D; Xiao H; Guo A; Xia J; Miao X; Tang S; Wang G
Mol Neurobiol; 2013 Jun; 47(3):957-66. PubMed ID: 23315268
[TBL] [Abstract][Full Text] [Related]
6. Genetic Background of Hirschsprung Disease: A Bridge Between Basic Science and Clinical Application.
Bahrami A; Joodi M; Moetamani-Ahmadi M; Maftouh M; Hassanian SM; Ferns GA; Avan A
J Cell Biochem; 2018 Jan; 119(1):28-33. PubMed ID: 28543993
[TBL] [Abstract][Full Text] [Related]
7. Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease.
Kim JY; Seo JM; Kim DY; Oh JT; Park KW; Kim HY; Jung K; Park BL; Kim JH; Shin HD
Neonatology; 2015; 108(3):164-71. PubMed ID: 26183064
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
Moore SW; Zaahl M
J Pediatr Surg; 2009 Oct; 44(10):1899-903. PubMed ID: 19853744
[TBL] [Abstract][Full Text] [Related]
9. GT-repeat extension in the IL11 promoter is associated with Hirschsprung's disease (HSCR).
Haase MG; Schulze A; Grover S; Kemnitz I; König IR; Fitze G
Gene; 2018 Nov; 677():163-168. PubMed ID: 30056070
[TBL] [Abstract][Full Text] [Related]
10. Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease.
Gunadi ; Kalim AS; Iskandar K; Marcellus ; Puspitarani DA; Diposarosa R; Makhmudi A; Astuti GDN
J Pediatr Surg; 2023 Apr; 58(4):723-728. PubMed ID: 36586783
[TBL] [Abstract][Full Text] [Related]
11. Sotos syndrome associated with Hirschsprung's disease: a new case and exome-sequencing analysis.
Sio CA; Jung K; Kim JH; Cheong HS; Shin E; Jang H; Yoon M; Jang H; Shin HD
Pediatr Res; 2017 Jul; 82(1):87-92. PubMed ID: 28399120
[TBL] [Abstract][Full Text] [Related]
12. The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease.
Zhang S; Jiang K; Yuan Z; Wang W
Exp Mol Pathol; 2014 Apr; 96(2):219-24. PubMed ID: 24576558
[TBL] [Abstract][Full Text] [Related]
13. Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
Luzón-Toro B; Gui H; Ruiz-Ferrer M; Sze-Man Tang C; Fernández RM; Sham PC; Torroglosa A; Kwong-Hang Tam P; Espino-Paisán L; Cherny SS; Bleda M; Enguix-Riego Mdel V; Dopazo J; Antiñolo G; García-Barceló MM; Borrego S
Sci Rep; 2015 Nov; 5():16473. PubMed ID: 26559152
[TBL] [Abstract][Full Text] [Related]
14. The ITGB2 immunomodulatory gene (CD18), enterocolitis, and Hirschsprung's disease.
Moore SW; Sidler D; Zaahl MG
J Pediatr Surg; 2008 Aug; 43(8):1439-44. PubMed ID: 18675632
[TBL] [Abstract][Full Text] [Related]
15. Hirschsprung's disease as a model of complex genetic etiology.
Borrego S; Ruiz-Ferrer M; Fernández RM; Antiñolo G
Histol Histopathol; 2013 Sep; 28(9):1117-36. PubMed ID: 23605783
[TBL] [Abstract][Full Text] [Related]
16. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.
Gui H; Schriemer D; Cheng WW; Chauhan RK; Antiňolo G; Berrios C; Bleda M; Brooks AS; Brouwer RW; Burns AJ; Cherny SS; Dopazo J; Eggen BJ; Griseri P; Jalloh B; Le TL; Lui VC; Luzón-Toro B; Matera I; Ngan ES; Pelet A; Ruiz-Ferrer M; Sham PC; Shepherd IT; So MT; Sribudiani Y; Tang CS; van den Hout MC; van der Linde HC; van Ham TJ; van IJcken WF; Verheij JB; Amiel J; Borrego S; Ceccherini I; Chakravarti A; Lyonnet S; Tam PK; Garcia-Barceló MM; Hofstra RM
Genome Biol; 2017 Mar; 18(1):48. PubMed ID: 28274275
[TBL] [Abstract][Full Text] [Related]
17. Correlation between genetic variations in Hox clusters and Hirschsprung's disease.
Garcia-Barceló MM; Miao X; Lui VC; So MT; Ngan ES; Leon TY; Lau DK; Liu TT; Lao X; Guo W; Holden WT; Moore J; Tam PK
Ann Hum Genet; 2007 Jul; 71(Pt 4):526-36. PubMed ID: 17274802
[TBL] [Abstract][Full Text] [Related]
18. Potential association of VAMP5 polymorphisms with total colonic aganglionosis in Hirschsprung disease.
Shin JG; Kim DY; Seo JM; Oh JT; Park KW; Kim HY; Park BL; Kim JH; Shin HD
Neurogastroenterol Motil; 2016 Jul; 28(7):1055-63. PubMed ID: 26970437
[TBL] [Abstract][Full Text] [Related]
19. Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children.
Wu Q; Zhao J; Zheng Y; Xie X; He Q; Zhu Y; Wang N; Huang L; Lu L; Hu T; Zeng J; Xia H; Zhang Y; Zhong W
J Gene Med; 2021 Feb; 23(2):e3301. PubMed ID: 33294994
[TBL] [Abstract][Full Text] [Related]
20. Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis.
Huang J; Dang R; Torigoe D; Lei C; Lan X; Chen H; Sasaki N; Wang J; Agui T
PLoS One; 2015; 10(3):e0122068. PubMed ID: 25790447
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
