Ou S - Search Results

1

[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].

Luo S, Fu C, Zhang S, Wang J, Fan X, Luo J, Chen R, Hu X, Qin H, Li C, Ou S, Li Q, Chen S. Luo S, et al. Among authors: ou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):321-326. doi: 10.3760/cma.j.issn.1003-9406.2017.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604947 Chinese.

2

[Cytogenetic analysis of 105 new human abnormal karyotypes].

Ou S, Du J, Chen SK, Zheng CG, Meng DH, Zhang HY, Qiu QM, Liu TS, Tang B. Ou S, et al. Yi Chuan. 2013 Jul;35(7):885-9. doi: 10.3724/sp.j.1005.2013.00885. Yi Chuan. 2013. PMID: 23853359 Chinese.

3

[Analysis of chromosomal abnormalities and a report of eight new karyotypes among children in genetic counseling].

Ou S, Ou H, Tang B, Chen SK, Xu YQ, Zheng CG. Ou S, et al. Among authors: ou h. Zhongguo Dang Dai Er Ke Za Zhi. 2014 Jul;16(7):725-8. Zhongguo Dang Dai Er Ke Za Zhi. 2014. PMID: 25008881 Free article. Chinese.

4

A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.

Wang J, Fu C, Zhang S, Luo J, Ouyang L, Xie B, Sun W, He S, Su J, Hu X, Fei D, Chen R, Fan X, Ou S, Chen S, Shen Y. Wang J, et al. Among authors: ou s. Gene. 2016 Dec 5;594(1):59-65. doi: 10.1016/j.gene.2016.08.042. Epub 2016 Aug 31. Gene. 2016. PMID: 27591971

5

Genetic polymorphisms in complement receptor 1 gene and its association with HBV-related liver disease: A case-control study.

Luo J, Chen S, Wang J, Ou S, Zhang W, Liu Y, Qin Z, Xu J, Lu Q, Mo C, Li S, Qin X. Luo J, et al. Among authors: ou s. Gene. 2019 Mar 10;688:107-118. doi: 10.1016/j.gene.2018.11.082. Epub 2018 Dec 5. Gene. 2019. PMID: 30529247

6

[Application of flat-sided culture tubes during prenatal diagnosis].

Liu T, Huang H, Su J, Qin W, Fei D, Ouyang L, Huang M, Yu J, Lei Y, Ou S, Sun W, Qiu Q, Zheng Q. Liu T, et al. Among authors: ou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Oct 10;40(10):1306-1311. doi: 10.3760/cma.j.cn511374-20221223-00888. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37730237 Chinese.

7

Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, café-au-lait spots, and metabolic abnormality.

Yang Q, Ou S, Zhou X, Yi S, Lin L, Yi S, Zhang S, Qin Z, Luo J. Yang Q, et al. Among authors: ou s. Mol Genet Genomic Med. 2024 Feb;12(2):e2408. doi: 10.1002/mgg3.2408. Mol Genet Genomic Med. 2024. PMID: 38404251 Free PMC article.

8

Excessive Initial Renal Function Decline Following Sodium-Glucose Cotransporter-2 Inhibitor Treatment Predicts Major Adverse Cardiorenal Outcomes.

Chen CY, Huang SS, Ou SM, Ho Y, Chen TH, Lee KH, Chu YC, Lin YP, Tseng WC, Tarng DC. Chen CY, et al. Among authors: ou sm. Mayo Clin Proc. 2025 Jan 11:S0025-6196(24)00475-0. doi: 10.1016/j.mayocp.2024.08.028. Online ahead of print. Mayo Clin Proc. 2025. PMID: 39797864

9

Consolidation ALK Tyrosine Kinase Inhibitor in Definitively Treated Unresectable Stage III ALK+ NSCLC: Can Real-World Data Inform Clinical Decision in the Absence of a LAURA-Type Designed Trial?

Arter ZL, Ou SI, Nagasaka M. Arter ZL, et al. Among authors: ou si. J Thorac Oncol. 2025 Jan;20(1):12-16. doi: 10.1016/j.jtho.2024.10.001. J Thorac Oncol. 2025. PMID: 39794098 No abstract available.

10

ALK Tyrosine Kinase Inhibitors Induced Weight Gain: More Refined Definition of Weight Gain, Glucagon-Like Peptide-1 Agonist Treatment, and Therapeutic Drug Monitoring of ALK+ Non-Small Cell Lung Cancer?

Park CJ, Lee ATM, Ou SI. Park CJ, et al. Among authors: ou si. J Clin Oncol. 2025 Jan 7:JCO2402514. doi: 10.1200/JCO-24-02514. Online ahead of print. J Clin Oncol. 2025. PMID: 39772872 No abstract available.

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