Literature DB >> 17440194

Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population.

Xiaoping Miao, Maria-Mercè Garcia-Barceló, Man-ting So, Thomas Yuk-yu Leon, Danny Ko-chun Lau, Ting-Ting Liu, Edwin Kin-Wai Chan, Lawrence Chuen-Leung Lan, Kenneth Kak-yuen Wong, Vincent Chi-hang Lui, Paul Kwong-hang Tam.   

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Year:  2007        PMID： 17440194      PMCID： PMC1942142          DOI： 10.1136/gut.2006.116145

Source DB:  PubMed          Journal:  Gut        ISSN： 0017-5749            Impact factor:   23.059


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  10 in total

1.  The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives.

Authors:  A Pattyn; X Morin; H Cremer; C Goridis; J F Brunet
Journal:  Nature       Date:  1999-05-27       Impact factor: 49.962

Review 2.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

3.  Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.

Authors:  M-M Garcia-Barceló; M-H Sham; V C-H Lui; B L-S Chen; Y-Q Song; W-S Lee; S-K Yung; G Romeo; P K-H Tam
Journal:  J Med Genet       Date:  2003-11       Impact factor: 6.318

4.  Association study of PHOX2B as a candidate gene for Hirschsprung's disease.

Authors:  M Garcia-Barceló; M H Sham; V C H Lui; B L S Chen; J Ott; P K H Tam
Journal:  Gut       Date:  2003-04       Impact factor: 23.059

5.  Epidemiologic methods: the "art" in the state of the art.

Authors:  David G Kleinbaum
Journal:  J Clin Epidemiol       Date:  2002-12       Impact factor: 6.437

6.  Hirschsprung disease is linked to defects in neural crest stem cell function.

Authors:  Toshihide Iwashita; Genevieve M Kruger; Ricardo Pardal; Mark J Kiel; Sean J Morrison
Journal:  Science       Date:  2003-08-15       Impact factor: 47.728

Review 7.  Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorder.

Authors:  A S Brooks; B A Oostra; R M W Hofstra
Journal:  Clin Genet       Date:  2005-01       Impact factor: 4.438

8.  A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

Authors:  M Angrist; E Kauffman; S A Slaugenhaupt; T C Matise; E G Puffenberger; S S Washington; A Lipson; D T Cass; T Reyna; D E Weeks
Journal:  Nat Genet       Date:  1993-08       Impact factor: 38.330

9.  An in vitro approach to test the possible role of candidate factors in the transcriptional regulation of the RET proto-oncogene.

Authors:  Tiziana Bachetti; Silvia Borghini; Roberto Ravazzolo; Isabella Ceccherini
Journal:  Gene Expr       Date:  2005

10.  TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease.

Authors:  Mercè Garcia-Barcelo; Raymond W Ganster; Vincent C H Lui; Thomas Y Y Leon; Man-Ting So; Anson M F Lau; Ming Fu; Mai-Har Sham; Joanne Knight; Maria Stella Zannini; Pak C Sham; Paul K H Tam
Journal:  Hum Mol Genet       Date:  2004-11-17       Impact factor: 6.150
  10 in total
  10 in total

Review 1.  Genetic basis of Hirschsprung's disease.

Authors:  Paul K H Tam; Mercè Garcia-Barceló
Journal:  Pediatr Surg Int       Date:  2009-06-12       Impact factor: 1.827

2.  Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population.

Authors:  Jun Yang; Shengyu Duan; Rong Zhong; Jieyun Yin; Jiarui Pu; Juntao Ke; Xuzai Lu; Li Zou; Hongmei Zhang; Zhidong Zhu; Depeng Wang; Huasheng Xiao; Anyuan Guo; Jiahong Xia; Xiaoping Miao; Shaotao Tang; Guobin Wang
Journal:  Mol Neurobiol       Date:  2013-01-12       Impact factor: 5.590

3.  RET and NRG1 interplay in Hirschsprung disease.

Authors:  Hongsheng Gui; Wai-Kiu Tang; Man-Ting So; Petroola Proitsi; Pak C Sham; Paul K Tam; Elly Sau-Wai Ngan; Elly Sau-Wai Ngan; Stacey S Cherny; Maria-Mercè Garcia-Barceló
Journal:  Hum Genet       Date:  2013-02-12       Impact factor: 4.132

4.  Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.

Authors:  Jinfa Tou; Li Wang; Li Liu; Ying Wang; Rong Zhong; Shengyu Duan; Weiguang Liu; Qixing Xiong; Qinglong Gu; Hong Yang; Hui Li
Journal:  BMC Med Genet       Date:  2011-02-25       Impact factor: 2.103

5.  Common genetic variations in Patched1 (PTCH1) gene and risk of hirschsprung disease in the Han Chinese population.

Authors:  Yang Wang; Jun Wang; Weihua Pan; Ying Zhou; Yongtao Xiao; Kejun Zhou; Jie Wen; Tingxi Yu; Wei Cai
Journal:  PLoS One       Date:  2013-09-20       Impact factor: 3.240

6.  Effects of NRG1 Polymorphisms on Hirschsprung's Disease Susceptibility: A Meta-analysis.

Authors:  Meng Jiang; Changli Li; Guoqing Cao; Dehua Yang; Xi Zhang; Li Yang; Shuai Li; Shao-Tao Tang
Journal:  Sci Rep       Date:  2017-08-30       Impact factor: 4.379

7.  Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

Authors:  Dehua Yang; Jun Yang; Shuai Li; Meng Jiang; Guoqing Cao; Li Yang; Xi Zhang; Ying Zhou; Kang Li; Shao-Tao Tang
Journal:  Sci Rep       Date:  2017-03-03       Impact factor: 4.379

8.  Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.

Authors:  Yang Wang; Weihui Yan; Jun Wang; Ying Zhou; Jie Chen; Beilin Gu; Wei Cai
Journal:  J Cell Mol Med       Date:  2018-04-14       Impact factor: 5.310

9.  Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.

Authors:  Yang Wang; Qian Jiang; Hao Cai; Ze Xu; Wenjie Wu; Beilin Gu; Long Li; Wei Cai
Journal:  Aging (Albany NY)       Date:  2020-03-06       Impact factor: 5.682

10.  Characterization of interstitial Cajal progenitors cells and their changes in Hirschsprung's disease.

Authors:  Zhi-Hua Chen; Yong-Chang Zhang; Wei-Fang Jiang; Cissy Yang; Gang-Ming Zou; Yu Kong; Wei Cai
Journal:  PLoS One       Date:  2014-01-24       Impact factor: 3.240
  10 in total

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