190 related articles for article (PubMed ID: 29379196)
1. Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
Fadista J; Lund M; Skotte L; Geller F; Nandakumar P; Chatterjee S; Matsson H; Granström AL; Wester T; Salo P; Virtanen V; Carstensen L; Bybjerg-Grauholm J; Hougaard DM; Pakarinen M; Perola M; Nordenskjöld A; Chakravarti A; Melbye M; Feenstra B
Eur J Hum Genet; 2018 Apr; 26(4):561-569. PubMed ID: 29379196
[TBL] [Abstract][Full Text] [Related]
2. RET 3'UTR polymorphisms and its protective role in Hirschsprung disease in southeastern Chinese.
Pan ZW; Luo CF; Liu ZJ; Li JC
J Pediatr Surg; 2012 Sep; 47(9):1699-705. PubMed ID: 22974609
[TBL] [Abstract][Full Text] [Related]
3. Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Tang CS; Gui H; Kapoor A; Kim JH; Luzón-Toro B; Pelet A; Burzynski G; Lantieri F; So MT; Berrios C; Shin HD; Fernández RM; Le TL; Verheij JB; Matera I; Cherny SS; Nandakumar P; Cheong HS; Antiñolo G; Amiel J; Seo JM; Kim DY; Oh JT; Lyonnet S; Borrego S; Ceccherini I; Hofstra RM; Chakravarti A; Kim HY; Sham PC; Tam PK; Garcia-Barceló MM
Hum Mol Genet; 2016 Dec; 25(23):5265-5275. PubMed ID: 27702942
[TBL] [Abstract][Full Text] [Related]
4. Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients.
Phusantisampan T; Sangkhathat S; Phongdara A; Chiengkriwate P; Patrapinyokul S; Mahasirimongkol S
J Hum Genet; 2012 May; 57(5):286-93. PubMed ID: 22377709
[TBL] [Abstract][Full Text] [Related]
5. Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.
Virtanen VB; Salo PP; Cao J; Löf-Granström A; Milani L; Metspalu A; Rintala RJ; Saarenpää-Heikkilä O; Paunio T; Wester T; Nordenskjöld A; Perola M; Pakarinen MP
Eur J Med Genet; 2019 Apr; 62(4):229-234. PubMed ID: 30031151
[TBL] [Abstract][Full Text] [Related]
6. Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease.
Gunadi ; Kapoor A; Ling AY; Rochadi ; Makhmudi A; Herini ES; Sosa MX; Chatterjee S; Chakravarti A
J Pediatr Surg; 2014 Nov; 49(11):1614-8. PubMed ID: 25475805
[TBL] [Abstract][Full Text] [Related]
7. A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
Griseri P; Bachetti T; Puppo F; Lantieri F; Ravazzolo R; Devoto M; Ceccherini I
Hum Mutat; 2005 Feb; 25(2):189-95. PubMed ID: 15643606
[TBL] [Abstract][Full Text] [Related]
8. Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.
Yang D; Yang J; Li S; Jiang M; Cao G; Yang L; Zhang X; Zhou Y; Li K; Tang ST
Sci Rep; 2017 Mar; 7():43222. PubMed ID: 28256518
[TBL] [Abstract][Full Text] [Related]
9. RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.
Borrego S; Ruiz A; Saez ME; Gimm O; Gao X; López-Alonso M; Hernández A; Wright FA; Antiñolo G; Eng C
J Med Genet; 2000 Aug; 37(8):572-8. PubMed ID: 10922382
[TBL] [Abstract][Full Text] [Related]
10. Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease.
Sribudiani Y; Chauhan RK; Alves MM; Petrova L; Brosens E; Harrison C; Wabbersen T; de Graaf BM; Rügenbrink T; Burzynski G; Brouwer RWW; van IJcken WFJ; Maas SM; de Klein A; Osinga J; Eggen BJL; Burns AJ; Brooks AS; Shepherd IT; Hofstra RMW
Gastroenterology; 2018 Jul; 155(1):118-129.e6. PubMed ID: 29601828
[TBL] [Abstract][Full Text] [Related]
11. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
Fitze G; Appelt H; König IR; Görgens H; Stein U; Walther W; Gossen M; Schreiber M; Ziegler A; Roesner D; Schackert HK
Hum Mol Genet; 2003 Dec; 12(24):3207-14. PubMed ID: 14600022
[TBL] [Abstract][Full Text] [Related]
12. RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
Vaclavikova E; Dvorakova S; Skaba R; Pos L; Sykorova V; Halkova T; Vcelak J; Bendlova B
PLoS One; 2014; 9(6):e98957. PubMed ID: 24897126
[TBL] [Abstract][Full Text] [Related]
13. Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
Burzynski GM; Nolte IM; Osinga J; Ceccherini I; Twigt B; Maas S; Brooks A; Verheij J; Plaza Menacho I; Buys CH; Hofstra RM
Eur J Hum Genet; 2004 Aug; 12(8):604-12. PubMed ID: 15138456
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
Garcia-Barcelo MM; Tang CS; Ngan ES; Lui VC; Chen Y; So MT; Leon TY; Miao XP; Shum CK; Liu FQ; Yeung MY; Yuan ZW; Guo WH; Liu L; Sun XB; Huang LM; Tou JF; Song YQ; Chan D; Cheung KM; Wong KK; Cherny SS; Sham PC; Tam PK
Proc Natl Acad Sci U S A; 2009 Feb; 106(8):2694-9. PubMed ID: 19196962
[TBL] [Abstract][Full Text] [Related]
15. Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia.
Gunadi ; Iskandar K; Makhmudi A; Kapoor A
J Surg Res; 2019 Jan; 233():96-99. PubMed ID: 30502294
[TBL] [Abstract][Full Text] [Related]
16. RET polymorphisms and the risk of Hirschsprung's disease in a Chinese population.
Liu C; Jin L; Li H; Lou J; Luo C; Zhou X; Li JC
J Hum Genet; 2008; 53(9):825-833. PubMed ID: 18612588
[TBL] [Abstract][Full Text] [Related]
17. Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese.
Li Q; Zhang Z; Diao M; Gan L; Cheng W; Xiao P; Su L; Shangguan S; Jiang Q; Li L
J Pediatr Gastroenterol Nutr; 2017 Mar; 64(3):385-390. PubMed ID: 27203398
[TBL] [Abstract][Full Text] [Related]
18. Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.
Liu CP; Tang QQ; Lou JT; Luo CF; Zhou XW; Li DM; Chen F; Li X; Li JC
Biochem Genet; 2010 Jun; 48(5-6):496-503. PubMed ID: 20454948
[TBL] [Abstract][Full Text] [Related]
19. RET and NRG1 interplay in Hirschsprung disease.
Gui H; Tang WK; So MT; Proitsi P; Sham PC; Tam PK; Ngan ES; Cherny SS; Garcia-Barceló MM
Hum Genet; 2013 May; 132(5):591-600. PubMed ID: 23400839
[TBL] [Abstract][Full Text] [Related]
20. Fine mapping of the 9q31 Hirschsprung's disease locus.
Tang CS; Sribudiani Y; Miao XP; de Vries AR; Burzynski G; So MT; Leon YY; Yip BH; Osinga J; Hui KJ; Verheij JB; Cherny SS; Tam PK; Sham PC; Hofstra RM; Garcia-Barceló MM
Hum Genet; 2010 Jun; 127(6):675-83. PubMed ID: 20361209
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]