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Page 1
Clinical and genetic architecture of a large cohort with auditory neuropathy.
Wang H, Guan L, Wu X, Guan J, Li J, Li N, Wu K, Gao Y, Bing D, Zhang J, Lan L, Shi T, Li D, Wang W, Xie L, Xiong F, Shi W, Zhao L, Wang D, Yin Y, Wang Q. Wang H, et al. Among authors: zhao l. Hum Genet. 2024 Mar;143(3):293-309. doi: 10.1007/s00439-024-02652-7. Epub 2024 Mar 8. Hum Genet. 2024. PMID: 38456936 Free PMC article.
Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.
Wang Q, Xiang J, Sun J, Yang Y, Guan J, Wang D, Song C, Guo L, Wang H, Chen Y, Leng J, Wang X, Zhang J, Han B, Zou J, Yan C, Zhao L, Luo H, Han Y, Yuan W, Zhang H, Wang W, Wang J, Yang H, Xu X, Yin Y, Morton CC, Zhao L, Zhu S, Shen J, Peng Z. Wang Q, et al. Among authors: zhao l. Genet Med. 2019 Oct;21(10):2231-2238. doi: 10.1038/s41436-019-0481-6. Epub 2019 Mar 20. Genet Med. 2019. PMID: 30890784 Free article.
Concurrent hearing and genetic screening in a general newborn population.
Guo L, Xiang J, Sun L, Yan X, Yang J, Wu H, Guo K, Peng J, Xie X, Yin Y, Wang J, Yang H, Shen J, Zhao L, Peng Z. Guo L, et al. Among authors: zhao l. Hum Genet. 2020 Apr;139(4):521-530. doi: 10.1007/s00439-020-02118-6. Epub 2020 Jan 30. Hum Genet. 2020. PMID: 32002660 Clinical Trial.
[Positive maternal blood cfDNA test caused by confined placental mosaicism in a case].
Gao Y, Yao H, Su F, Zhang R, Hu H, Xu J, Xu L, Zhao L, Chen F, Liang Z. Gao Y, et al. Among authors: zhao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):627-628. doi: 10.3760/cma.j.issn.1003-9406.2020.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472538 Chinese. No abstract available.
Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype.
Li J, Lu J, Su F, Yang J, Ju J, Lin Y, Xu J, Qi Y, Hou Y, Wu J, He W, Yang Z, Wu Y, Tang Z, Huang Y, Zhang G, Yang Y, Long Z, Cheng X, Liu P, Xia J, Zhang Y, Wang Y, Chen F, Zhang J, Zhao L, Jin X, Gao Y, Yin A. Li J, et al. Among authors: zhao l. Front Genet. 2022 Jul 1;13:911369. doi: 10.3389/fgene.2022.911369. eCollection 2022. Front Genet. 2022. PMID: 35846127 Free PMC article.
Genome-wide association study of maternal plasma metabolites during pregnancy.
Liu S, Yao J, Lin L, Lan X, Wu L, He X, Kong N, Li Y, Deng Y, Xie J, Zhu H, Wu X, Li Z, Xiong L, Wang Y, Ren J, Qiu X, Zhao W, Gao Y, Chen Y, Su F, Zhou Y, Rao W, Zhang J, Hou G, Huang L, Li L, Liu X, Nie C, Luo L, Zhao M, Liu Z, Chen F, Lin S, Zhao L, Fu Q, Jiang D, Yin Y, Xu X, Wang J, Yang H, Wang R, Niu J, Wei F, Jin X, Liu S. Liu S, et al. Among authors: zhao w, zhao l, zhao m. Cell Genom. 2024 Oct 9;4(10):100657. doi: 10.1016/j.xgen.2024.100657. Cell Genom. 2024. PMID: 39389015 Free PMC article.
Noninvasive preeclampsia prediction using plasma cell-free RNA signatures.
Zhou S, Li J, Yang W, Xue P, Yin Y, Wang Y, Tian P, Peng H, Jiang H, Xu W, Huang S, Zhang R, Wei F, Sun HX, Zhang J, Zhao L. Zhou S, et al. Among authors: zhao l. Am J Obstet Gynecol. 2023 Nov;229(5):553.e1-553.e16. doi: 10.1016/j.ajog.2023.05.015. Epub 2023 May 19. Am J Obstet Gynecol. 2023. PMID: 37211139 Free article.
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