Chang YS - Search Results

1

Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males.

Tseng YP, Chang YS, Mekala VR, Liu TY, Chang JG, Shieh GS. Tseng YP, et al. Among authors: chang jg, chang ys. Front Genet. 2024 Sep 25;15:1423714. doi: 10.3389/fgene.2024.1423714. eCollection 2024. Front Genet. 2024. PMID: 39385933 Free PMC article.

2

Evaluation of whole exome sequencing by targeted gene sequencing and Sanger sequencing.

Chang YS, Huang HD, Yeh KT, Chang JG. Chang YS, et al. Among authors: chang jg. Clin Chim Acta. 2017 Aug;471:222-232. doi: 10.1016/j.cca.2017.06.015. Epub 2017 Jun 15. Clin Chim Acta. 2017. PMID: 28624499

3

Cancer carrier screening in the general population using whole-genome sequencing.

Chang YS, Chao DS, Chung CC, Chou YP, Chang CM, Lin CL, Chu HW, Chen HD, Liu TY, Juan YH, Chang SJ, Chang JG. Chang YS, et al. Among authors: chang jg, chang cm, chang sj. Cancer Med. 2023 Jan;12(2):1972-1983. doi: 10.1002/cam4.5034. Epub 2022 Jul 21. Cancer Med. 2023. PMID: 35861108 Free PMC article.

4

Polygenic risk score trend and new variants on chromosome 1 are associated with male gout in genome-wide association study.

Chang YS, Lin CY, Liu TY, Huang CM, Chung CC, Chen YC, Tsai FJ, Chang JG, Chang SJ. Chang YS, et al. Among authors: chang jg, chang sj. Arthritis Res Ther. 2022 Oct 11;24(1):229. doi: 10.1186/s13075-022-02917-4. Arthritis Res Ther. 2022. PMID: 36221101 Free PMC article.

5

Down-regulated and Commonly mutated ALPK1 in Lung and Colorectal Cancers.

Liao HF, Lee HH, Chang YS, Lin CL, Liu TY, Chen YC, Yen JC, Lee YT, Lin CY, Wu SH, Ko YC, Chang JG. Liao HF, et al. Among authors: chang jg, chang ys. Sci Rep. 2016 Jun 10;6:27350. doi: 10.1038/srep27350. Sci Rep. 2016. PMID: 27283888 Free PMC article.

6

Determination of the mutational landscape in Taiwanese patients with papillary thyroid cancer by whole-exome sequencing.

Chang CC, Chang YS, Huang HY, Yeh KT, Liu TC, Chang JG. Chang CC, et al. Among authors: chang jg, chang ys. Hum Pathol. 2018 Aug;78:151-158. doi: 10.1016/j.humpath.2018.04.023. Epub 2018 May 9. Hum Pathol. 2018. PMID: 29753010

7

Detection of Molecular Alterations in Taiwanese Patients with Medullary Thyroid Cancer Using Whole-Exome Sequencing.

Chang YS, Chang CC, Huang HY, Lin CY, Yeh KT, Chang JG. Chang YS, et al. Among authors: chang cc, chang jg. Endocr Pathol. 2018 Dec;29(4):324-331. doi: 10.1007/s12022-018-9543-6. Endocr Pathol. 2018. PMID: 30120715

8

Molecular characterization of colorectal cancer using whole-exome sequencing in a Taiwanese population.

Chang YS, Lee CC, Ke TW, Chang CM, Chao DS, Huang HY, Chang JG. Chang YS, et al. Among authors: chang jg, chang cm. Cancer Med. 2019 Jul;8(8):3738-3747. doi: 10.1002/cam4.2282. Epub 2019 May 24. Cancer Med. 2019. PMID: 31127692 Free PMC article.

9

Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.

Chang YS, Lin CY, Huang HY, Chang JG, Kuo HT. Chang YS, et al. Among authors: chang jg. Mol Genet Genomic Med. 2019 Dec;7(12):e996. doi: 10.1002/mgg3.996. Epub 2019 Oct 8. Mol Genet Genomic Med. 2019. PMID: 31595719 Free PMC article.

10

Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing.

Lin PC, Cheng CN, Huang HY, Tseng YH, Chang YS, Lin CY, Chang JG. Lin PC, et al. Among authors: chang jg, chang ys. Mol Genet Genomic Med. 2020 May;8(5):e1220. doi: 10.1002/mgg3.1220. Epub 2020 Mar 11. Mol Genet Genomic Med. 2020. PMID: 32160409 Free PMC article.

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