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Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.
Xu C, Wang F, Wang B, Li X, Li C, Wang D, Xiong X, Wang P, Lu Q, Wang X, Yang Q, Yin D, Huang Y, Ji L, Wang N, Chen S, Cheng X, Liao Y, Ma X, Su D, Chen G, Xia H, Shi L, Tu X, Wang QK. Xu C, et al. Among authors: wang x, wang f, wang p, wang n, wang d, wang b, wang qk. Stroke. 2010 Aug;41(8):1587-92. doi: 10.1161/STROKEAHA.110.583096. Epub 2010 Jun 24. Stroke. 2010. PMID: 20576952
Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease.
Li X, Huang Y, Yin D, Wang D, Xu C, Wang F, Yang Q, Wang X, Li S, Chen S, Xiong X, Huang Y, Zhao Y, Wang L, Zhu X, Su Z, Zhou B, Zhang Y, Wang L, Chang L, Xu C, Li H, Ke T, Ren X, Cheng X, Yang Y, Liao Y, Tu X, Wang QK. Li X, et al. Among authors: wang x, wang f, wang l, wang d, wang qk. Atherosclerosis. 2013 Nov;231(1):136-40. doi: 10.1016/j.atherosclerosis.2013.08.031. Epub 2013 Sep 12. Atherosclerosis. 2013. PMID: 24125424
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population.
Wang P, Xu C, Wang C, Wu Y, Wang D, Chen S, Zhao Y, Wang X, Li S, Yang Q, Zeng Q, Tu X, Liao Y, Wang QK, Cheng X. Wang P, et al. Among authors: wang x, wang d, wang c, wang qk. PLoS One. 2015 May 19;10(5):e0125926. doi: 10.1371/journal.pone.0125926. eCollection 2015. PLoS One. 2015. PMID: 25993436 Free PMC article.
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.
Huang Y, Wang C, Yao Y, Zuo X, Chen S, Xu C, Zhang H, Lu Q, Chang L, Wang F, Wang P, Zhang R, Hu Z, Song Q, Yang X, Li C, Li S, Zhao Y, Yang Q, Yin D, Wang X, Si W, Li X, Xiong X, Wang D, Huang Y, Luo C, Li J, Wang J, Chen J, Wang L, Wang L, Han M, Ye J, Chen F, Liu J, Liu Y, Wu G, Yang B, Cheng X, Liao Y, Wu Y, Ke T, Chen Q, Tu X, Elston R, Rao S, Yang Y, Xia Y, Wang QK. Huang Y, et al. Among authors: wang x, wang f, wang l, wang j, wang p, wang d, wang c, wang qk. PLoS Genet. 2015 Aug 12;11(8):e1005393. doi: 10.1371/journal.pgen.1005393. eCollection 2015 Aug. PLoS Genet. 2015. PMID: 26267381 Free PMC article.
Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.
Chen S, Wang X, Wang J, Zhao Y, Wang D, Tan C, Fa J, Zhang R, Wang F, Xu C, Huang Y, Li S, Yin D, Xiong X, Li X, Chen Q, Tu X, Yang Y, Xia Y, Xu C, Wang QK. Chen S, et al. Among authors: wang x, wang f, wang j, wang d, wang qk. Atherosclerosis. 2016 Mar;246:148-156. doi: 10.1016/j.atherosclerosis.2016.01.008. Epub 2016 Jan 8. Atherosclerosis. 2016. PMID: 26775120 Free PMC article.
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.
Yin D, Naji DH, Xia Y, Li S, Bai Y, Jiang G, Zhao Y, Wang X, Huang Y, Chen S, Fa J, Tan C, Zhou M, Zhou Y, Wang L, Liu Y, Chen F, Liu J, Chen Q, Tu X, Xu C, Wang QK. Yin D, et al. Among authors: wang x, wang l, wang qk. Sci Rep. 2017 Feb 9;7:42175. doi: 10.1038/srep42175. Sci Rep. 2017. PMID: 28181534 Free PMC article.
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.
Wang P, Qin W, Wang P, Huang Y, Liu Y, Zhang R, Li S, Yang Q, Wang X, Chen F, Liu J, Yang B, Cheng X, Liao Y, Wu Y, Ke T, Tu X, Ren X, Yang Y, Xia Y, Luo X, Liu M, Li H, Liu J, Xiao Y, Chen Q, Xu C, Wang QK. Wang P, et al. Among authors: wang x, wang qk. Sci Rep. 2018 Feb 19;8(1):3297. doi: 10.1038/s41598-018-21611-7. Sci Rep. 2018. PMID: 29459676 Free PMC article.
Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke.
Xiong X, Naji DH, Wang B, Zhao Y, Wang J, Wang D, Zhang Y, Li S, Chen S, Huang Y, Yang Q, Wang X, Yin D, Tu X, Chen Q, Ma X, Xu C, Wang QK. Xiong X, et al. Among authors: wang x, wang j, wang d, wang b, wang qk. J Stroke Cerebrovasc Dis. 2018 Jun;27(6):1683-1691. doi: 10.1016/j.jstrokecerebrovasdis.2018.01.029. Epub 2018 Feb 28. J Stroke Cerebrovasc Dis. 2018. PMID: 29501268 Free PMC article.
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation.
Xiong H, Yang Q, Zhang X, Wang P, Chen F, Liu Y, Wang P, Zhao Y, Li S, Huang Y, Chen S, Wang X, Zhang H, Yu D, Tan C, Fang C, Huang Y, Wu G, Wu Y, Cheng X, Liao Y, Zhang R, Yang Y, Ke T, Ren X, Li H, Tu X, Xia Y, Xu C, Chen Q, Wang QK. Xiong H, et al. Among authors: wang x, wang p, wang qk. Ann Hum Genet. 2019 Jul;83(4):239-248. doi: 10.1111/ahg.12305. Epub 2019 Mar 1. Ann Hum Genet. 2019. PMID: 30821358 Free PMC article.
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