Liu W - Search Results

1

A Novel CD40L Mutation Associated with X-Linked Hyper IgM Syndrome in a Chinese Family.

Li L, Ji J, Han M, Xu Y, Zhang X, Liu W, Liu S. Li L, et al. Among authors: liu s, liu w. Immunol Invest. 2020 Apr;49(3):307-316. doi: 10.1080/08820139.2019.1638397. Epub 2019 Aug 12. Immunol Invest. 2020. PMID: 31401902

2

A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family.

Li L, Liu WM, Liu MX, Zheng SQ, Zhang JX, Che FY, Liu SG. Li L, et al. Asian J Androl. 2017 Mar-Apr;19(2):260-261. doi: 10.4103/1008-682X.172647. Asian J Androl. 2017. PMID: 26806084 Free PMC article. No abstract available.

3

Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based Study.

Dong H, Liu W, Liu M, Xu L, Li Q, Zhang R, Zhang X, Liu S. Dong H, et al. Among authors: liu m, liu s, liu w. PLoS One. 2016 Aug 16;11(8):e0160265. doi: 10.1371/journal.pone.0160265. eCollection 2016. PLoS One. 2016. PMID: 27529419 Free PMC article.

4

Choline acetyltransferase may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.

Yang X, Liu W, Yi M, Zhang R, Xu Y, Huang Z, Liu S, Li T. Yang X, et al. Among authors: liu s, liu w. World J Biol Psychiatry. 2018 Oct;19(7):521-526. doi: 10.1080/15622975.2017.1282176. Epub 2017 Feb 14. World J Biol Psychiatry. 2018. PMID: 28090804

5

Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population.

Liu W, Qiu S, Gao C, Wang G, Liu S, Guan H. Liu W, et al. Among authors: liu s. Neurosci Lett. 2017 Sep 29;658:161-164. doi: 10.1016/j.neulet.2017.08.041. Epub 2017 Aug 19. Neurosci Lett. 2017. PMID: 28830823

6

Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.

Guan H, Liang X, Zhang R, Wang H, Liu W, Zhang R, Yang J, Liu S. Guan H, et al. Among authors: liu s, liu w. Hematology. 2018 Jul;23(6):357-361. doi: 10.1080/10245332.2017.1398210. Epub 2017 Nov 3. Hematology. 2018. PMID: 29099659 Free article.

7

Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis.

Zhou Z, Yang C, Lv F, Liu W, Yan S, Zang H, Li M, Wang F, Zang Y, Liu S. Zhou Z, et al. Among authors: liu s, liu w. J Cell Biochem. 2018 Nov;119(11):9474-9482. doi: 10.1002/jcb.27264. Epub 2018 Aug 3. J Cell Biochem. 2018. PMID: 30074255

8

Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report.

Li X, Li L, Sun Y, Lv F, Zhang G, Liu W, Zhang M, Jiang H, Liu S. Li X, et al. Among authors: liu s, liu w. BMC Med Genet. 2019 Aug 27;20(1):146. doi: 10.1186/s12881-019-0875-y. BMC Med Genet. 2019. PMID: 31455269 Free PMC article.

9

Value of ABCG2 Q141K and Q126X genotyping in predicting risk of preeclampsia in Chinese Han women population.

Hou H, Geng M, Zhang R, Liu W, Wang J, Li J, Lin Y, Liu S, Wang Z, Guo H, Guan H, Tan P. Hou H, et al. Among authors: liu s, liu w. Pregnancy Hypertens. 2019 Jul;17:197-202. doi: 10.1016/j.preghy.2019.06.006. Epub 2019 Jun 26. Pregnancy Hypertens. 2019. PMID: 31487640

10

Next-generation sequencing identifies a novel frameshift variant in FRMD7 in a Chinese family with idiopathic infantile nystagmus.

Wang F, Guan H, Liu W, Zhao G, Liu S. Wang F, et al. Among authors: liu s, liu w. J Clin Lab Anal. 2020 Jan;34(1):e23012. doi: 10.1002/jcla.23012. Epub 2019 Sep 8. J Clin Lab Anal. 2020. PMID: 31495972 Free PMC article.

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