Liu Y - Search Results

1

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

Zhang L, Yang Y, Li S, Tai Z, Huang L, Liu Y, Zhu X, Di Y, Qu C, Jiang Z, Li Y, Zhang G, Kim R, Sundaresan P, Yang Z, Zhu X. Zhang L, et al. Among authors: liu y. Genet Test Mol Biomarkers. 2016 Jul;20(7):346-51. doi: 10.1089/gtmb.2015.0322. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27228167

2

Identification of LRP5 mutations in families with familial exudative vitreoretinopathy.

Liu YQ, Zhu X, Li SJ, Yang YM, Yang M, Zhao PQ, Zhu XJ. Liu YQ, et al. Yi Chuan. 2017 Mar 20;39(3):241-249. doi: 10.16288/j.yczz.16-339. Yi Chuan. 2017. PMID: 28420620

3

Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population.

Zhou Y, Saikia BB, Jiang Z, Zhu X, Liu Y, Huang L, Kim R, Yang Y, Qu C, Hao F, Gong B, Tai Z, Niu L, Yang Z, Sundaresan P, Zhu X. Zhou Y, et al. Among authors: liu y. J Hum Genet. 2015 Oct;60(10):625-30. doi: 10.1038/jhg.2015.92. Epub 2015 Aug 6. J Hum Genet. 2015. PMID: 26246154

4

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa.

Li S, Yang M, Liu W, Liu Y, Zhang L, Yang Y, Sundaresan P, Yang Z, Zhu X. Li S, et al. Among authors: liu y, liu w. Genet Test Mol Biomarkers. 2018 Feb;22(2):109-114. doi: 10.1089/gtmb.2017.0223. Genet Test Mol Biomarkers. 2018. PMID: 29425069

5

Loss of Tmem30a leads to photoreceptor degeneration.

Zhang L, Yang Y, Li S, Zhang S, Zhu X, Tai Z, Yang M, Liu Y, Guo X, Chen B, Jiang Z, Lu F, Zhu X. Zhang L, et al. Among authors: liu y. Sci Rep. 2017 Aug 24;7(1):9296. doi: 10.1038/s41598-017-09506-5. Sci Rep. 2017. PMID: 28839191 Free PMC article.

6

Two-person DNA mixture interpretation based on a novel set of SNP-STR markers.

Tan Y, Bai P, Wang L, Wang H, Tian H, Jian H, Zhang R, Liu Y, Liang W, Zhang L. Tan Y, et al. Among authors: liu y. Forensic Sci Int Genet. 2018 Nov;37:37-45. doi: 10.1016/j.fsigen.2018.07.021. Epub 2018 Jul 26. Forensic Sci Int Genet. 2018. PMID: 30075395

7

Evaluation of the microhaplotype markers in kinship analysis.

Zhu J, Chen P, Qu S, Wang Y, Jian H, Cao S, Liu Y, Zhang R, Lv M, Liang W, Zhang L. Zhu J, et al. Among authors: liu y. Electrophoresis. 2019 Apr;40(7):1091-1095. doi: 10.1002/elps.201800351. Epub 2019 Jan 4. Electrophoresis. 2019. PMID: 30557455

8

Establishing a second-tier panel of 18 ancestry informative markers to improve ancestry distinctions among Asian populations.

Qu S, Zhu J, Wang Y, Yin L, Lv M, Wang L, Jian H, Tan Y, Zhang R, Liu Y, Li F, Huang S, Liang W, Zhang L. Qu S, et al. Among authors: liu y. Forensic Sci Int Genet. 2019 Jul;41:159-167. doi: 10.1016/j.fsigen.2019.05.001. Epub 2019 May 10. Forensic Sci Int Genet. 2019. PMID: 31136932

9

A new approach to detect a set of SNP-SNP markers: Combining ARMS-PCR with SNaPshot technology.

Zhang R, Tan Y, Jian H, Qu S, Liu Y, Zhu J, Wang L, Lv M, Liao M, Zhang L, Yang F, Liang W. Zhang R, et al. Among authors: liu y. Electrophoresis. 2020 Jul;41(13-14):1189-1197. doi: 10.1002/elps.202000009. Epub 2020 May 11. Electrophoresis. 2020. PMID: 32333411

10

Multi-Indel: A Microhaplotype Marker Can Be Typed Using Capillary Electrophoresis Platforms.

Qu S, Lv M, Xue J, Zhu J, Wang L, Jian H, Liu Y, Zhang R, Zha L, Liang W, Zhang L. Qu S, et al. Among authors: liu y. Front Genet. 2020 Oct 23;11:567082. doi: 10.3389/fgene.2020.567082. eCollection 2020. Front Genet. 2020. PMID: 33193656 Free PMC article.

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