Fu Q - Search Results

1

MET mutation causes muscular dysplasia and arthrogryposis.

Zhou H, Lian C, Wang T, Yang X, Xu C, Su D, Zheng S, Huang X, Liao Z, Zhou T, Qiu X, Chen Y, Gao B, Li Y, Wang X, You G, Fu Q, Gurnett C, Huang D, Su P. Zhou H, et al. Among authors: fu q. EMBO Mol Med. 2019 Mar;11(3):e9709. doi: 10.15252/emmm.201809709. EMBO Mol Med. 2019. PMID: 30777867 Free PMC article.

2

A novel missense mutation of TNNI2 in a Chinese family cause distal arthrogryposis type 1.

Wang B, Zheng Z, Wang Z, Zhang X, Yang H, Cai H, Fu Q. Wang B, et al. Among authors: fu q. Am J Med Genet A. 2016 Jan;170A(1):135-41. doi: 10.1002/ajmg.a.37391. Epub 2015 Sep 16. Am J Med Genet A. 2016. PMID: 26374086

3

Association between ABO Blood Group and Risk of Congenital Heart Disease: A 6-year large cohort study.

Zu B, You G, Fu Q, Wang J. Zu B, et al. Among authors: fu q. Sci Rep. 2017 Feb 17;7:42804. doi: 10.1038/srep42804. Sci Rep. 2017. PMID: 28211529 Free PMC article.

4

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly.

You G, Zu B, Wang B, Wang Z, Xu Y, Fu Q. You G, et al. Among authors: fu q. Int J Mol Sci. 2017 Apr 5;18(4):626. doi: 10.3390/ijms18040626. Int J Mol Sci. 2017. PMID: 28379158 Free PMC article.

5

Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.

Wang B, You G, Fu Q. Wang B, et al. Among authors: fu q. Sci Rep. 2017 Apr 24;7:46760. doi: 10.1038/srep46760. Sci Rep. 2017. PMID: 28436429 Free PMC article.

6

A Novel Multiplex HRM Assay to Detect Clopidogrel Resistance.

Zhang L, Ma X, You G, Zhang X, Fu Q. Zhang L, et al. Among authors: fu q. Sci Rep. 2017 Nov 22;7(1):16021. doi: 10.1038/s41598-017-16310-8. Sci Rep. 2017. PMID: 29167499 Free PMC article.

7

A novel dNTP-limited PCR and HRM assay to detect Williams-Beuren syndrome.

Zhang L, Zhang X, You G, Yu Y, Fu Q. Zhang L, et al. Among authors: fu q. Clin Chim Acta. 2018 Jun;481:171-176. doi: 10.1016/j.cca.2018.03.011. Epub 2018 Mar 14. Clin Chim Acta. 2018. PMID: 29550276

8

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting.

Zhang X, Wang B, Zhang L, You G, Palais RA, Zhou L, Fu Q. Zhang X, et al. Among authors: fu q. BMC Genomics. 2018 Jun 20;19(1):485. doi: 10.1186/s12864-018-4833-4. BMC Genomics. 2018. PMID: 29925309 Free PMC article.

9

Identification of a novel ANO5 missense mutation in a Chinese family with familial florid osseous dysplasia.

Lv M, You G, Wang J, Fu Q, Gupta A, Li J, Sun J. Lv M, et al. Among authors: fu q. J Hum Genet. 2019 Jul;64(7):599-607. doi: 10.1038/s10038-019-0601-9. Epub 2019 Apr 17. J Hum Genet. 2019. PMID: 30996299

10

Identification of miRNA-mRNA-TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot.

You G, Zu B, Wang B, Fu Q, Li F. You G, et al. Among authors: fu q. Front Genet. 2020 Jun 12;11:552. doi: 10.3389/fgene.2020.00552. eCollection 2020. Front Genet. 2020. PMID: 32595699 Free PMC article.

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