Jiang Q - Search Results

1

Laparoscopic-Assisted Anorectal Pull-Through for Currarino Syndrome.

Li Q, Zhang Z, Jiang Q, Yan Y, Xiao P, Ma Y, Li L. Li Q, et al. Among authors: jiang q. J Laparoendosc Adv Surg Tech A. 2020 Jul;30(7):826-833. doi: 10.1089/lap.2019.0779. Epub 2020 Apr 17. J Laparoendosc Adv Surg Tech A. 2020. PMID: 32302513

2

Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients.

Zhang Z, Jiang Q, Li Q, Cheng W, Qiao G, Xiao P, Gan L, Su L, Miao C, Li L. Zhang Z, et al. Among authors: jiang q. Int J Clin Exp Pathol. 2015 May 1;8(5):5528-34. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 26191260 Free PMC article.

3

Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion.

Li Q, Zhang Z, Yan Y, Xiao P, Gao Z, Cheng W, Su L, Yu K, Xie H, Chen X, Jiang Q, Li L. Li Q, et al. Among authors: jiang q. Mol Cytogenet. 2015 Dec 15;8:95. doi: 10.1186/s13039-015-0201-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 26673557 Free PMC article.

4

The mid-term outcomes of TRM-PIAS, proctocolectomy and ileoanal anastomosis for total colonic aganglionosis.

Li Q, Li L, Jiang Q, Zhang Z, Xiao P. Li Q, et al. Among authors: jiang q. Pediatr Surg Int. 2016 May;32(5):477-82. doi: 10.1007/s00383-016-3870-9. Epub 2016 Feb 1. Pediatr Surg Int. 2016. PMID: 26833313

5

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. Li Q, et al. Among authors: jiang q. J Pediatr Gastroenterol Nutr. 2017 Mar;64(3):385-390. doi: 10.1097/MPG.0000000000001263. J Pediatr Gastroenterol Nutr. 2017. PMID: 27203398

6

Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease.

Su L, Zhang Z, Gan L, Jiang Q, Xiao P, Zou J, Li Q, Jiang H. Su L, et al. Among authors: jiang q, jiang h. Exp Mol Pathol. 2016 Oct;101(2):241-248. doi: 10.1016/j.yexmp.2016.09.003. Epub 2016 Sep 13. Exp Mol Pathol. 2016. PMID: 27619161

7

Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese family.

Jiang Q, Zhang X, Ma Y, Li Q, Zheng C, Yan Y, Zhang Z, Xiao P, Su L, Cheng W, Pan H, Li L. Jiang Q, et al. Clin Case Rep. 2016 Nov 17;5(1):9-13. doi: 10.1002/ccr3.741. eCollection 2017 Jan. Clin Case Rep. 2016. PMID: 28096981 Free PMC article.

8

Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing.

Zhang Z, Li Q, Diao M, Liu N, Cheng W, Xiao P, Zou J, Su L, Yu K, Wu J, Li L, Jiang Q. Zhang Z, et al. Among authors: jiang q. Sci Rep. 2017 Nov 1;7(1):14796. doi: 10.1038/s41598-017-14835-6. Sci Rep. 2017. PMID: 29093530 Free PMC article. Clinical Trial.

9

RET somatic mutations are underrecognized in Hirschsprung disease.

Jiang Q, Liu F, Miao C, Li Q, Zhang Z, Xiao P, Su L, Yu K, Chen X, Zhang F, Chakravarti A, Li L. Jiang Q, et al. Genet Med. 2018 Jul;20(7):770-777. doi: 10.1038/gim.2017.178. Epub 2017 Oct 26. Genet Med. 2018. PMID: 29261189 Free PMC article.

10

Response to Brosens et al.

Jiang Q, Chen X, Zhang F, Chakravarti A, Li L. Jiang Q, et al. Genet Med. 2018 Nov;20(11):1479-1480. doi: 10.1038/gim.2018.7. Genet Med. 2018. PMID: 29493585 Free article. No abstract available.

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