Zhang J - Search Results

1

Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

Jespersgaard C, Fang M, Bertelsen M, Dang X, Jensen H, Chen Y, Bech N, Dai L, Rosenberg T, Zhang J, Møller LB, Tümer Z, Brøndum-Nielsen K, Grønskov K. Jespersgaard C, et al. Among authors: zhang j. Sci Rep. 2019 Feb 4;9(1):1219. doi: 10.1038/s41598-018-38007-2. Sci Rep. 2019. PMID: 30718709 Free PMC article.

2

Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions.

Fang M, Abolhassani H, Lim CK, Zhang J, Hammarström L. Fang M, et al. Among authors: zhang j. J Clin Immunol. 2016 May;36 Suppl 1:68-75. doi: 10.1007/s10875-016-0260-y. Epub 2016 Mar 18. J Clin Immunol. 2016. PMID: 26993986 Review.

3

Gene pathogenicity prediction of Mendelian diseases via the random forest algorithm.

He S, Chen W, Liu H, Li S, Lei D, Dang X, Chen Y, Zhang X, Zhang J. He S, et al. Among authors: zhang j, zhang x. Hum Genet. 2019 Jun;138(6):673-679. doi: 10.1007/s00439-019-02021-9. Epub 2019 May 8. Hum Genet. 2019. PMID: 31069506

4

The complete mitochondrial genome of the Poecilia formosa (Amazon molly).

Dang X, Xia Y, Xu Q, Zhang J. Dang X, et al. Among authors: zhang j. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3523-4. doi: 10.3109/19401736.2015.1074200. Epub 2015 Aug 11. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26260185

5

The complete mitochondrial genome of the Sorex araneus.

Huang T, Dang X, An M, Chen L, Zhang J. Huang T, et al. Among authors: zhang j. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3655-6. doi: 10.3109/19401736.2015.1079841. Epub 2015 Sep 2. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26328473

6

Search for the potential "second-hit" mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysis.

Gao L, Dang X, Huang L, Zhu L, Fang M, Zhang J, Xu X, Zhu L, Li T, Zhao L, Wei J, Zhou J. Gao L, et al. Among authors: zhang j. Transl Res. 2016 Apr;170:26-39. doi: 10.1016/j.trsl.2015.12.004. Epub 2015 Dec 15. Transl Res. 2016. PMID: 26739415

7

Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder.

Nafisinia M, Guo Y, Dang X, Li J, Chen Y, Zhang J, Lake NJ, Gold WA, Riley LG, Thorburn DR, Keating B, Xu X, Hakonarson H, Christodoulou J. Nafisinia M, et al. Among authors: zhang j. JIMD Rep. 2017;32:117-124. doi: 10.1007/8904_2016_541. Epub 2016 Jun 26. JIMD Rep. 2017. PMID: 27344648 Free PMC article.

8

FBN3 gene involved in pathogenesis of a Chinese family with Bardet-Biedl syndrome.

Wang Y, Garraoui A, Zeng L, Lai M, He F, Wang H, Jiang C, Chen Y, Dai L, Fan N, Yang H, Zhang J, Liu X. Wang Y, et al. Among authors: zhang j. Oncotarget. 2017 Sep 30;8(49):86718-86725. doi: 10.18632/oncotarget.21415. eCollection 2017 Oct 17. Oncotarget. 2017. PMID: 29156830 Free PMC article.

9

Letter regarding the article "two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disability" (Isidor et al., 2015).

Latypova X, Dang X, Zhang J, Isidor B. Latypova X, et al. Among authors: zhang j. Eur J Med Genet. 2021 Apr;64(4):104179. doi: 10.1016/j.ejmg.2021.104179. Epub 2021 Feb 23. Eur J Med Genet. 2021. PMID: 33636376 No abstract available.

10

Mutation analysis of Leber congenital amaurosis‑associated genes in patients with retinitis pigmentosa.

Shen T, Guan L, Li S, Zhang J, Xiao X, Jiang H, Yang J, Guo X, Wang J, Zhang Q. Shen T, et al. Among authors: zhang q, zhang j. Mol Med Rep. 2015 Mar;11(3):1827-32. doi: 10.3892/mmr.2014.2894. Epub 2014 Nov 7. Mol Med Rep. 2015. PMID: 25377065

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