Wei Q - Search Results

1

Molecular signature incorporating the immune microenvironment enhances thyroid cancer outcome prediction.

Xu GJ, Loberg MA, Gallant JN, Sheng Q, Chen SC, Lehmann BD, Shaddy SM, Tigue ML, Phifer CJ, Wang L, Saab-Chalhoub MW, Dehan LM, Wei Q, Chen R, Li B, Kim CY, Ferguson DC, Netterville JL, Rohde SL, Solórzano CC, Bischoff LA, Baregamian N, Shaver AC, Mehrad M, Ely KA, Byrne DW, Stricker TP, Murphy BA, Choe JH, Kagohara LT, Jaffee EM, Huang EC, Ye F, Lee E, Weiss VL. Xu GJ, et al. Among authors: wei q. Cell Genom. 2023 Sep 14;3(10):100409. doi: 10.1016/j.xgen.2023.100409. eCollection 2023 Oct 11. Cell Genom. 2023. PMID: 37868034 Free PMC article.

2

Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association Studies.

Ji Y, Chen R, Wang Q, Wei Q, Tao R, Li B. Ji Y, et al. Among authors: wei q. Genes (Basel). 2022 Feb 19;13(2):381. doi: 10.3390/genes13020381. Genes (Basel). 2022. PMID: 35205424 Free PMC article.

3

A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization.

Ji Y, Chen R, Wang Q, Wei Q, Tao R, Li B. Ji Y, et al. Among authors: wei q. BMC Bioinformatics. 2022 Apr 22;23(1):146. doi: 10.1186/s12859-022-04616-y. BMC Bioinformatics. 2022. PMID: 35459094 Free PMC article.

4

Integration of multidimensional splicing data and GWAS summary statistics for risk gene discovery.

Ji Y, Wei Q, Chen R, Wang Q, Tao R, Li B. Ji Y, et al. Among authors: wei q. PLoS Genet. 2022 Jun 30;18(6):e1009814. doi: 10.1371/journal.pgen.1009814. eCollection 2022 Jun. PLoS Genet. 2022. PMID: 35771864 Free PMC article.

5

TVAR: assessing tissue-specific functional effects of non-coding variants with deep learning.

Yang H, Chen R, Wang Q, Wei Q, Ji Y, Zhong X, Li B. Yang H, et al. Among authors: wei q. Bioinformatics. 2022 Oct 14;38(20):4697-4704. doi: 10.1093/bioinformatics/btac608. Bioinformatics. 2022. PMID: 36063453 Free PMC article.

6

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.

Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B. Chen R, et al. Among authors: wei q. Mol Autism. 2017 Mar 21;8:14. doi: 10.1186/s13229-017-0130-3. eCollection 2017. Mol Autism. 2017. PMID: 28344757 Free PMC article.

7

De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.

Yang H, Chen R, Wang Q, Wei Q, Ji Y, Zheng G, Zhong X, Cox NJ, Li B. Yang H, et al. Among authors: wei q. Bioinformatics. 2019 May 1;35(9):1453-1460. doi: 10.1093/bioinformatics/bty826. Bioinformatics. 2019. PMID: 30256891 Free PMC article.

8

Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework.

Yang H, Wei Q, Zhong X, Yang H, Li B. Yang H, et al. Among authors: wei q. Bioinformatics. 2017 Feb 15;33(4):483-490. doi: 10.1093/bioinformatics/btw662. Bioinformatics. 2017. PMID: 27797769 Free PMC article.

9

A Bayesian framework for de novo mutation calling in parents-offspring trios.

Wei Q, Zhan X, Zhong X, Liu Y, Han Y, Chen W, Li B. Wei Q, et al. Bioinformatics. 2015 May 1;31(9):1375-81. doi: 10.1093/bioinformatics/btu839. Epub 2014 Dec 21. Bioinformatics. 2015. PMID: 25535243 Free PMC article.

10

A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.

Chen R, Wei Q, Zhan X, Zhong X, Sutcliffe JS, Cox NJ, Cook EH, Li C, Chen W, Li B. Chen R, et al. Among authors: wei q. Bioinformatics. 2015 May 1;31(9):1452-9. doi: 10.1093/bioinformatics/btu860. Epub 2015 Jan 6. Bioinformatics. 2015. PMID: 25568282 Free PMC article.

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