Liu Y - Search Results

1

Non-syndromic hereditary gingival fibromatosis in three Chinese families is not due to SOS1 gene mutations.

Ma Y, Sun Z, Hu Y, Liu Y, Jin L, Zhang F. Ma Y, et al. Among authors: liu y. Cell Biochem Biophys. 2014 Dec;70(3):1869-73. doi: 10.1007/s12013-014-0144-9. Cell Biochem Biophys. 2014. PMID: 25062969

2

Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia.

Jin L, Liu Y, Sun F, Collins MT, Blackwell K, Woo AS, Reichenberger EJ, Hu Y. Jin L, et al. Among authors: liu y. Sci Rep. 2017 Feb 8;7:40935. doi: 10.1038/srep40935. Sci Rep. 2017. PMID: 28176803 Free PMC article.

3

A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia.

Ma T, Liu Y, Zhao X, Wu J, Wang H, Chen J, Liu P, Zhang X, Zhang X. Ma T, et al. Among authors: liu y, liu p. Ann Hum Genet. 2020 Jan;84(1):97-101. doi: 10.1111/ahg.12348. Epub 2019 Aug 30. Ann Hum Genet. 2020. PMID: 31469409

4

A novel missense mutation of LRP6 identified by whole-exome sequencing in a Chinese family with non-syndromic tooth agenesis.

Wang H, Liu Y, Zheng Y, Zhao X, Lin S, Zhang Q, Zhang X. Wang H, et al. Among authors: liu y. Orthod Craniofac Res. 2021 May;24(2):233-240. doi: 10.1111/ocr.12424. Epub 2020 Sep 10. Orthod Craniofac Res. 2021. PMID: 32844563

5

[Clinical and ASS1 gene variant analysis of three Chinese pedigrees affected with Citrullinemia type I].

Dong R, Zhang K, Guo H, Zhang G, Lyu Y, Gao M, Gai Z, Liu Y. Dong R, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Nov 10;40(11):1345-1349. doi: 10.3760/cma.j.cn511374-20210702-00566. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37906139 Chinese.

6

Improving methylmalonic acidemia (MMA) screening and MMA genotype prediction using random forest classifier in two Chinese populations.

Yin Z, Zhang C, Dong R, Zhang X, Song Y, Hao S, Gai Z, Zhou B, Hui L, Wang S, Xue H, Cao Z, Liu Y, Ma X. Yin Z, et al. Among authors: liu y. Eur J Med Res. 2024 Nov 10;29(1):540. doi: 10.1186/s40001-024-02115-9. Eur J Med Res. 2024. PMID: 39523381 Free PMC article.

7

[Analysis of clinical characteristics and genetic variants in two pedigrees affected with Autosomal dominant intellectual developmental disorder 49].

Lyu Y, Zhang Y, Li N, Zhang K, Gao M, Ma J, Guo W, Liu Y, Gai Z. Lyu Y, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Nov 10;41(11):1296-1301. doi: 10.3760/cma.j.cn-511374-20240102-00002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 39528278 Chinese.

8

Enhancing Osteogenesis and Mechanical Properties through Scaffold Design in 3D Printed Bone Substitutes.

Cao X, Sun K, Luo J, Chen A, Wan Q, Zhou H, Zhou H, Liu Y, Chen X. Cao X, et al. Among authors: liu y. ACS Biomater Sci Eng. 2025 Jan 17. doi: 10.1021/acsbiomaterials.4c01661. Online ahead of print. ACS Biomater Sci Eng. 2025. PMID: 39818724 Review.

9

Electromechanics of the Molecule-Electrode Interface and Interface-Mediated Effects in Single-Molecule Junctions.

Zhu Y, Xu Y, Liu Y, Liu H, Hong W. Zhu Y, et al. Among authors: liu y. ACS Appl Mater Interfaces. 2025 Jan 16. doi: 10.1021/acsami.4c18286. Online ahead of print. ACS Appl Mater Interfaces. 2025. PMID: 39818711 Review.

10

Concentration-Dependent Control of the Band Gap Energy of a Low-Dimensional Lepidocrocite Titanate.

Walter AD, Schwenk GR, Liu Y, Bugallo Ferron D, Wilk JT, Ferrer LM, Li CY, Hu YJ, Barsoum MW. Walter AD, et al. Among authors: liu y. ACS Nano. 2025 Jan 16. doi: 10.1021/acsnano.4c16410. Online ahead of print. ACS Nano. 2025. PMID: 39818710

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