Qi M - Search Results

1

Whole-exome sequencing predicted cancer epitope trees of 23 early cervical cancers in Chinese women.

Li X, Huang H, Guan Y, Gong Y, He CY, Yi X, Qi M, Chen ZY. Li X, et al. Among authors: qi m. Cancer Med. 2017 Jan;6(1):207-219. doi: 10.1002/cam4.953. Epub 2016 Dec 20. Cancer Med. 2017. PMID: 27998038 Free PMC article.

2

Identification of a novel SBF2 frameshift mutation in charcot-marie-tooth disease type 4B2 using whole-exome sequencing.

Chen M, Wu J, Liang N, Tang L, Chen Y, Chen H, Wei W, Wei T, Huang H, Yi X, Qi M. Chen M, et al. Among authors: qi m. Genomics Proteomics Bioinformatics. 2014 Oct;12(5):221-7. doi: 10.1016/j.gpb.2014.09.003. Epub 2014 Oct 28. Genomics Proteomics Bioinformatics. 2014. PMID: 25462154 Free PMC article.

3

The R900S mutation in CACNA1S associated with hypokalemic periodic paralysis.

Ke Q, He F, Lu L, Yu P, Jiang Y, Weng C, Huang H, Yi X, Qi M. Ke Q, et al. Among authors: qi m. Neuromuscul Disord. 2015 Dec;25(12):955-8. doi: 10.1016/j.nmd.2015.09.006. Epub 2015 Sep 9. Neuromuscul Disord. 2015. PMID: 26433613

4

Identification of sequence variants in genetic disease-causing genes using targeted next-generation sequencing.

Wei X, Ju X, Yi X, Zhu Q, Qu N, Liu T, Chen Y, Jiang H, Yang G, Zhen R, Lan Z, Qi M, Wang J, Yang Y, Chu Y, Li X, Guang Y, Huang J. Wei X, et al. Among authors: qi m. PLoS One. 2011;6(12):e29500. doi: 10.1371/journal.pone.0029500. Epub 2011 Dec 21. PLoS One. 2011. PMID: 22216297 Free PMC article.

5

Systematic evaluation of a targeted gene capture sequencing panel for molecular diagnosis of retinitis pigmentosa.

Huang H, Chen Y, Chen H, Ma Y, Chiang PW, Zhong J, Liu X, Asan, Wu J, Su Y, Li X, Deng J, Huang Y, Zhang X, Li Y, Fan N, Wang Y, Tang L, Shen J, Chen M, Zhang X, Te D, Banerjee S, Liu H, Qi M, Yi X. Huang H, et al. Among authors: qi m. PLoS One. 2018 Apr 11;13(4):e0185237. doi: 10.1371/journal.pone.0185237. eCollection 2018. PLoS One. 2018. PMID: 29641573 Free PMC article.

6

Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study.

Wei X, Dai Y, Yu P, Qu N, Lan Z, Hong X, Sun Y, Yang G, Xie S, Shi Q, Zhou H, Zhu Q, Chu Y, Yao F, Wang J, He J, Yang Y, Liang Y, Yang Y, Qi M, Yang L, Wang W, Wu H, Duan J, Shen C, Wang J, Cui L, Yi X. Wei X, et al. Among authors: qi m. Eur J Hum Genet. 2014 Jan;22(1):110-8. doi: 10.1038/ejhg.2013.82. Epub 2013 Jun 12. Eur J Hum Genet. 2014. PMID: 23756440 Free PMC article.

7

[A comprehensive repository of mutation data and a clinical assistant decision system for hemoglobinopathy in the Chinese population].

Zhang QQ, Zhang L, Tang YH, Li XR, Xu XP, Qi M, Xu XM. Zhang QQ, et al. Among authors: qi m. Yi Chuan. 2019 Aug 20;41(8):746-753. doi: 10.16288/j.yczz.19-136. Yi Chuan. 2019. PMID: 31447425 Chinese.

8

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.

Hong N, Chen YH, Xie C, Xu BS, Huang H, Li X, Yang YQ, Huang YP, Deng JL, Qi M, Gu YS. Hong N, et al. Among authors: qi m. J Zhejiang Univ Sci B. 2014 Aug;15(8):727-34. doi: 10.1631/jzus.B1300321. J Zhejiang Univ Sci B. 2014. PMID: 25091991 Free PMC article.

9

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis.

Chiang PW, Wang J, Chen Y, Fu Q, Zhong J, Chen Y, Yi X, Wu R, Gan H, Shi Y, Chen Y, Barnett C, Wheaton D, Day M, Sutherland J, Heon E, Weleber RG, Gabriel LA, Cong P, Chuang K, Ye S, Sallum JM, Qi M. Chiang PW, et al. Among authors: qi m. Nat Genet. 2012 Sep;44(9):972-4. doi: 10.1038/ng.2370. Epub 2012 Jul 29. Nat Genet. 2012. PMID: 22842231

10

Identification of a novel missense mutation of MIP in a Chinese family with congenital cataracts by target region capture sequencing.

Jiang B, Chen Y, Xu B, Hong N, Liu R, Qi M, Shen L. Jiang B, et al. Among authors: qi m. Sci Rep. 2017 Jan 6;7:40129. doi: 10.1038/srep40129. Sci Rep. 2017. PMID: 28059152 Free PMC article.

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