Wu J - Search Results

1

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.

Li J, Cai T, Jiang Y, Chen H, He X, Chen C, Li X, Shao Q, Ran X, Li Z, Xia K, Liu C, Sun ZS, Wu J. Li J, et al. Among authors: wu j. Mol Psychiatry. 2016 Feb;21(2):290-7. doi: 10.1038/mp.2015.40. Epub 2015 Apr 7. Mol Psychiatry. 2016. PMID: 25849321 Free PMC article.

2

Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing.

Wu J, Shen E, Shi D, Sun Z, Cai T. Wu J, et al. Genet Med. 2012 Sep;14(9):823-6. doi: 10.1038/gim.2012.50. Epub 2012 May 17. Genet Med. 2012. PMID: 22595939 Free article.

3

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

Bi C, Wu J, Jiang T, Liu Q, Cai W, Yu P, Cai T, Zhao M, Jiang YH, Sun ZS. Bi C, et al. Among authors: wu j. Hum Mutat. 2012 Dec;33(12):1635-8. doi: 10.1002/humu.22174. Epub 2012 Aug 24. Hum Mutat. 2012. PMID: 22865819

4

Exome-assistant: a rapid and easy detection of disease-related genes and genetic variations from exome sequencing.

Liu Q, Shen E, Min Q, Li X, Wang X, Li X, Sun ZS, Wu J. Liu Q, et al. Among authors: wu j. BMC Genomics. 2012 Dec 11;13:692. doi: 10.1186/1471-2164-13-692. BMC Genomics. 2012. PMID: 23231371 Free PMC article.

5

RRBS-analyser: a comprehensive web server for reduced representation bisulfite sequencing data analysis.

Wang T, Liu Q, Li X, Wang X, Li J, Zhu X, Sun ZS, Wu J. Wang T, et al. Among authors: wu j. Hum Mutat. 2013 Dec;34(12):1606-10. doi: 10.1002/humu.22444. Epub 2013 Oct 10. Hum Mutat. 2013. PMID: 24106010

6

Ras-induced epigenetic inactivation of the RRAD (Ras-related associated with diabetes) gene promotes glucose uptake in a human ovarian cancer model.

Wang Y, Li G, Mao F, Li X, Liu Q, Chen L, Lv L, Wang X, Wu J, Dai W, Wang G, Zhao E, Tang KF, Sun ZS. Wang Y, et al. Among authors: wu j. J Biol Chem. 2014 May 16;289(20):14225-38. doi: 10.1074/jbc.M113.527671. Epub 2014 Mar 19. J Biol Chem. 2014. PMID: 24648519 Free PMC article.

7

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.

Ran X, Cai WJ, Huang XF, Liu Q, Lu F, Qu J, Wu J, Jin ZB. Ran X, et al. Among authors: wu j. Database (Oxford). 2014 Jun 17;2014:bau047. doi: 10.1093/database/bau047. Print 2014. Database (Oxford). 2014. PMID: 24939193 Free PMC article.

8

A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing data.

Xie Q, Liu Q, Mao F, Cai W, Wu H, You M, Wang Z, Chen B, Sun ZS, Wu J. Xie Q, et al. Among authors: wu h, wu j. PLoS Comput Biol. 2014 Sep 25;10(9):e1003853. doi: 10.1371/journal.pcbi.1003853. eCollection 2014 Sep. PLoS Comput Biol. 2014. PMID: 25255082 Free PMC article.

9

EpilepsyGene: a genetic resource for genes and mutations related to epilepsy.

Ran X, Li J, Shao Q, Chen H, Lin Z, Sun ZS, Wu J. Ran X, et al. Among authors: wu j. Nucleic Acids Res. 2015 Jan;43(Database issue):D893-9. doi: 10.1093/nar/gku943. Epub 2014 Oct 16. Nucleic Acids Res. 2015. PMID: 25324312 Free PMC article.

10

[Whole-genome sequencing and its application in the research and diagnoses of genetic diseases].

Shao Q, Jiang Y, Wu J. Shao Q, et al. Among authors: wu j. Yi Chuan. 2014 Nov;36(11):1087-98. Yi Chuan. 2014. PMID: 25567867 Review. Chinese.

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