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A splicing mutation in VPS4B causes dentin dysplasia I.
Yang Q, Chen D, Xiong F, Chen D, Liu C, Liu Y, Yu Q, Xiong J, Liu J, Li K, Zhao L, Ye Y, Zhou H, Hu L, Tian Z, Shang X, Zhang L, Wei X, Zhou W, Li D, Zhang W, Xu X. Yang Q, et al. Among authors: ye y. J Med Genet. 2016 Sep;53(9):624-33. doi: 10.1136/jmedgenet-2015-103619. Epub 2016 May 31. J Med Genet. 2016. PMID: 27247351
Human STEAP3 mutations with no phenotypic red cell changes.
Liu D, Yi S, Zhang X, Fang P, Zheng C, Lin L, Cai R, Ye Y, Zhou Y, Liang Y, Cheng F, Zhang X, Zhou W, Mohandas N, An X, Xu X. Liu D, et al. Among authors: ye y. Blood. 2016 Feb 25;127(8):1067-71. doi: 10.1182/blood-2015-09-670174. Epub 2015 Dec 16. Blood. 2016. PMID: 26675350 Free PMC article. No abstract available.
A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression.
Chen D, Zuo Y, Zhang X, Ye Y, Bao X, Huang H, Tepakhan W, Wang L, Ju J, Chen G, Zheng M, Liu D, Huang S, Zong L, Li C, Chen Y, Zheng C, Shi L, Zhao Q, Wu Q, Fucharoen S, Zhao C, Xu X. Chen D, et al. Among authors: ye y. Am J Hum Genet. 2017 Jul 6;101(1):130-138. doi: 10.1016/j.ajhg.2017.05.012. Epub 2017 Jun 29. Am J Hum Genet. 2017. PMID: 28669403 Free PMC article.
Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies.
Shang X, Peng Z, Ye Y, Asan, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Huang S, Liu Y, Chen B, Yan S, Chen Y, Ding H, Yin X, Wu L, He J, Huang D, He S, Yan T, Fan X, Zhou Y, Wei X, Zhao S, Cai D, Guo F, Zhang Q, Li Y, Zhang X, Lu H, Huang H, Guo J, Zhu F, Yuan Y, Zhang L, Liu N, Li Z, Jiang H, Zhang Q, Zhang Y, Juhari WKW, Hanafi S, Zhou W, Xiong F, Yang H, Wang J, Zilfalil BA, Qi M, Yang Y, Yin Y, Mao M, Xu X. Shang X, et al. Among authors: ye y. EBioMedicine. 2017 Sep;23:150-159. doi: 10.1016/j.ebiom.2017.08.015. Epub 2017 Aug 17. EBioMedicine. 2017. PMID: 28865746 Free PMC article.
miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells.
Li Y, Liu D, Zhang X, Li Z, Ye Y, Liu Q, Shen J, Chen Z, Huang H, Liang Y, Han X, Liu J, An X, Mohandas N, Xu X. Li Y, et al. Among authors: ye y. Exp Hematol. 2018 Jul;63:33-40.e2. doi: 10.1016/j.exphem.2018.03.004. Epub 2018 Mar 27. Exp Hematol. 2018. PMID: 29601850 Free article.
A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia.
Yang X, Zhou Q, Zhou W, Zhong M, Guo X, Wang X, Fan X, Yan S, Li L, Lai Y, Wang Y, Huang J, Ye Y, Zeng H, Chuan J, Du Y, Ma C, Li P, Song Z, Xu X. Yang X, et al. Among authors: ye y. Adv Sci (Weinh). 2019 Apr 1;6(11):1802332. doi: 10.1002/advs.201802332. eCollection 2019 Jun 5. Adv Sci (Weinh). 2019. PMID: 31179213 Free PMC article.
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies.
Zhang L, Zhang Q, Tang Y, Cong P, Ye Y, Chen S, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Zou J, Liu Y, Chen B, Yan S, Chen Y, Zhou Y, Ding H, Li X, Chen D, Zhong J, Shang X, Liu X, Qi M, Xu X. Zhang L, et al. Among authors: ye y. Hum Mutat. 2019 Dec;40(12):2221-2229. doi: 10.1002/humu.23863. Epub 2019 Sep 11. Hum Mutat. 2019. PMID: 31286593 Free PMC article.
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