Ruan Y - Search Results

1

Improving polygenic prediction in ancestrally diverse populations.

Ruan Y, Lin YF, Feng YA, Chen CY, Lam M, Guo Z; Stanley Global Asia Initiatives; He L, Sawa A, Martin AR, Qin S, Huang H, Ge T. Ruan Y, et al. Nat Genet. 2022 May;54(5):573-580. doi: 10.1038/s41588-022-01054-7. Epub 2022 May 5. Nat Genet. 2022. PMID: 35513724 Free PMC article.

2

Comparative genome analysis of Prevotella intermedia strain isolated from infected root canal reveals features related to pathogenicity and adaptation.

Ruan Y, Shen L, Zou Y, Qi Z, Yin J, Jiang J, Guo L, He L, Chen Z, Tang Z, Qin S. Ruan Y, et al. BMC Genomics. 2015 Feb 25;16(1):122. doi: 10.1186/s12864-015-1272-3. BMC Genomics. 2015. PMID: 25765460 Free PMC article.

3

Genetic Association of Curative and Adverse Reactions to Tyrosine Kinase Inhibitors in Chinese advanced Non-Small Cell Lung Cancer patients.

Ruan Y, Jiang J, Guo L, Li Y, Huang H, Shen L, Luan M, Li M, Du H, Ma C, He L, Zhang X, Qin S. Ruan Y, et al. Sci Rep. 2016 Mar 18;6:23368. doi: 10.1038/srep23368. Sci Rep. 2016. PMID: 26988277 Free PMC article.

4

Functional Characterization of Human CYP2C9 Allelic Variants in COS-7 Cells.

Du H, Wei Z, Yan Y, Xiong Y, Zhang X, Shen L, Ruan Y, Wu X, Xu Q, He L, Qin S. Du H, et al. Among authors: ruan y. Front Pharmacol. 2016 Apr 25;7:98. doi: 10.3389/fphar.2016.00098. eCollection 2016. Front Pharmacol. 2016. PMID: 27199745 Free PMC article.

5

Genetic Association of Drug Response to Erlotinib in Chinese Advanced Non-small Cell Lung Cancer Patients.

Wang C, Chen F, Liu Y, Xu Q, Guo L, Zhang X, Ruan Y, Shi Y, Shen L, Li M, Du H, Sun X, Ma J, He L, Qin S. Wang C, et al. Among authors: ruan y. Front Pharmacol. 2018 Apr 11;9:360. doi: 10.3389/fphar.2018.00360. eCollection 2018. Front Pharmacol. 2018. PMID: 29695969 Free PMC article.

6

p.E95K mutation in Indian hedgehog causing brachydactyly type A1 impairs IHH/Gli1 downstream transcriptional regulation.

Shen L, Ma G, Shi Y, Ruan Y, Yang X, Wu X, Xiong Y, Wan C, Yang C, Cai L, Xiong L, Gong X, He L, Qin S. Shen L, et al. Among authors: ruan y. BMC Genet. 2019 Jan 16;20(1):10. doi: 10.1186/s12863-018-0697-5. BMC Genet. 2019. PMID: 30651074 Free PMC article.

7

Author Correction: Improving polygenic prediction in ancestrally diverse populations.

Ruan Y, Lin YF, Feng YA, Chen CY, Lam M, Guo Z; Stanley Global Asia Initiatives; He L, Sawa A, Martin AR, Qin S, Huang H, Ge T. Ruan Y, et al. Nat Genet. 2022 Aug;54(8):1259. doi: 10.1038/s41588-022-01144-6. Nat Genet. 2022. PMID: 35789324 No abstract available.

8

Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia.

Hsu YH, Pintacuda G, Liu R, Nacu E, Kim A, Tsafou K, Petrossian N, Crotty W, Suh JM, Riseman J, Martin JM, Biagini JC, Mena D, Ching JKT, Malolepsza E, Li T, Singh T, Ge T, Egri SB, Tanenbaum B, Stanclift CR, Apffel AM; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Stanley Global Asia Initiatives; Carr SA, Schenone M, Jaffe J, Fornelos N, Huang H, Eggan KC, Lage K. Hsu YH, et al. iScience. 2023 Apr 18;26(5):106701. doi: 10.1016/j.isci.2023.106701. eCollection 2023 May 19. iScience. 2023. PMID: 37207277 Free PMC article.

9

An Engineered Rare Codon Device for Optimization of Metabolic Pathways.

Wang Y, Li C, Khan MR, Wang Y, Ruan Y, Zhao B, Zhang B, Ma X, Zhang K, Zhao X, Ye G, Guo X, Feng G, He L, Ma G. Wang Y, et al. Among authors: ruan y. Sci Rep. 2016 Feb 8;6:20608. doi: 10.1038/srep20608. Sci Rep. 2016. PMID: 26852704 Free PMC article.

10

A rare case of pyridoxine-dependent epilepsy with novel ALDH7A1 mutation.

Luo F, Ruan Y, Xiong Y, Zhang H. Luo F, et al. Among authors: ruan y. Asian J Surg. 2024 May 8:S1015-9584(24)00929-1. doi: 10.1016/j.asjsur.2024.05.040. Online ahead of print. Asian J Surg. 2024. PMID: 38724351 No abstract available.

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