Qiu X - Search Results

1

A Tool for Early Prediction of Severe Coronavirus Disease 2019 (COVID-19): A Multicenter Study Using the Risk Nomogram in Wuhan and Guangdong, China.

Gong J, Ou J, Qiu X, Jie Y, Chen Y, Yuan L, Cao J, Tan M, Xu W, Zheng F, Shi Y, Hu B. Gong J, et al. Among authors: qiu x. Clin Infect Dis. 2020 Jul 28;71(15):833-840. doi: 10.1093/cid/ciaa443. Clin Infect Dis. 2020. PMID: 32296824 Free PMC article.

2

ChREBP gene polymorphisms are associated with coronary artery disease in Han population of Hubei province.

Guo S, Zheng F, Qiu X, Yang N. Guo S, et al. Among authors: qiu x. Clin Chim Acta. 2011 Sep 18;412(19-20):1854-60. doi: 10.1016/j.cca.2011.06.024. Epub 2011 Jun 25. Clin Chim Acta. 2011. PMID: 21726544

3

Common rs7138803 variant of FAIM2 and obesity in Han Chinese.

Li C, Qiu X, Yang N, Gao J, Rong Y, Xiong C, Zheng F. Li C, et al. Among authors: qiu x. BMC Cardiovasc Disord. 2013 Aug 8;13:56. doi: 10.1186/1471-2261-13-56. BMC Cardiovasc Disord. 2013. PMID: 23924573 Free PMC article.

4

SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis.

Wang XB, Cui NH, Gao JJ, Qiu XP, Zheng F. Wang XB, et al. J Neurol Sci. 2014 May 15;340(1-2):63-8. doi: 10.1016/j.jns.2014.02.026. Epub 2014 Feb 28. J Neurol Sci. 2014. PMID: 24630593

5

Angiotensin-converting enzyme gene polymorphisms and risk for sporadic Alzheimer's disease: a meta-analysis.

Wang XB, Cui NH, Gao JJ, Qiu XP, Yang N, Zheng F. Wang XB, et al. J Neural Transm (Vienna). 2015 Feb;122(2):211-24. doi: 10.1007/s00702-014-1235-x. Epub 2014 May 23. J Neural Transm (Vienna). 2015. PMID: 24851853

6

Angiotensin-converting enzyme insertion/deletion polymorphism is not a major determining factor in the development of sporadic Alzheimer disease: evidence from an updated meta-analysis.

Wang XB, Cui NH, Yang J, Qiu XP, Gao JJ, Yang N, Zheng F. Wang XB, et al. PLoS One. 2014 Oct 31;9(10):e111406. doi: 10.1371/journal.pone.0111406. eCollection 2014. PLoS One. 2014. PMID: 25360660 Free PMC article.

7

Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.

Qiao C, Wei T, Hu B, Peng C, Qiu X, Wei L, Yan M. Qiao C, et al. Among authors: qiu x. Mol Med Rep. 2015 Aug;12(2):3067-72. doi: 10.3892/mmr.2015.3714. Epub 2015 May 4. Mol Med Rep. 2015. PMID: 25936877

8

Hypermethylation of ACP1, BMP4, and TSPYL5 in Hepatocellular Carcinoma and Their Potential Clinical Significance.

Qiu X, Hu B, Huang Y, Deng Y, Wang X, Zheng F. Qiu X, et al. Dig Dis Sci. 2016 Jan;61(1):149-57. doi: 10.1007/s10620-015-3878-3. Epub 2015 Sep 19. Dig Dis Sci. 2016. PMID: 26386860

9

Novel keratin 5 mutation in a family with epidermolysis bullosa simplex.

Gao J, Wang X, Zheng F, Dong S, Qiu X. Gao J, et al. Among authors: qiu x. Exp Ther Med. 2015 Dec;10(6):2432-2436. doi: 10.3892/etm.2015.2811. Epub 2015 Oct 16. Exp Ther Med. 2015. PMID: 26668653 Free PMC article.

10

Associations of ChREBP and Global DNA Methylation with Genetic and Environmental Factors in Chinese Healthy Adults.

Gao J, Qiu X, Wang X, Peng C, Zheng F. Gao J, et al. Among authors: qiu x. PLoS One. 2016 Jun 9;11(6):e0157128. doi: 10.1371/journal.pone.0157128. eCollection 2016. PLoS One. 2016. PMID: 27281235 Free PMC article.

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