Dang X - 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: dang x. Sci Rep. 2019 Feb 4;9(1):1219. doi: 10.1038/s41598-018-38007-2. Sci Rep. 2019. PMID: 30718709 Free PMC article.

2

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: dang 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

3

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

Dang X, Xia Y, Xu Q, Zhang J. Dang X, et al. 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

4

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: dang x. Transl Res. 2016 Apr;170:26-39. doi: 10.1016/j.trsl.2015.12.004. Epub 2015 Dec 15. Transl Res. 2016. PMID: 26739415

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: dang x. 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

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: dang x. JIMD Rep. 2017;32:117-124. doi: 10.1007/8904_2016_541. Epub 2016 Jun 26. JIMD Rep. 2017. PMID: 27344648 Free PMC article.

7

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: dang x. 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.

8

Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome.

Gualandi F, Zaraket F, Malagù M, Parmeggiani G, Trabanelli C, Fini S, Dang X, Wei X, Fang M, Bertini M, Ferrari R, Ferlini A. Gualandi F, et al. Among authors: dang x. Cardiology. 2017;137(4):256-260. doi: 10.1159/000471792. Epub 2017 May 12. Cardiology. 2017. PMID: 28494446

9

Implementing targeted region capture sequencing for the clinical detection of Alagille syndrome: An efficient and cost‑effective method.

Huang T, Yang G, Dang X, Ao F, Li J, He Y, Tang Q, He Q. Huang T, et al. Among authors: dang x. Mol Med Rep. 2017 Nov;16(5):6876-6881. doi: 10.3892/mmr.2017.7429. Epub 2017 Sep 7. Mol Med Rep. 2017. PMID: 28901437

10

The first complete mitochondrial genome of the Microtus ochrogaster.

Cao W, Xia Y, Dang X, Xu Q. Cao W, et al. Among authors: dang x. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3682-3. doi: 10.3109/19401736.2015.1079854. Epub 2015 Aug 24. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26305486

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,041 results

Search Page