Wei Q - Search Results

1

Genome sequencing unveils a regulatory landscape of platelet reactivity.

Keramati AR, Chen MH, Rodriguez BAT, Yanek LR, Bhan A, Gaynor BJ, Ryan K, Brody JA, Zhong X, Wei Q; NHLBI Trans-Omics for Precision (TOPMed) Consortium; Kammers K, Kanchan K, Iyer K, Kowalski MH, Pitsillides AN, Cupples LA, Li B, Schlaeger TM, Shuldiner AR, O'Connell JR, Ruczinski I, Mitchell BD, Faraday N, Taub MA, Becker LC, Lewis JP, Mathias RA, Johnson AD. Keramati AR, et al. Among authors: wei q. Nat Commun. 2021 Jun 15;12(1):3626. doi: 10.1038/s41467-021-23470-9. Nat Commun. 2021. PMID: 34131117 Free PMC article.

2

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.

3

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.

4

Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.

Li B, Wei Q, Zhan X, Zhong X, Chen W, Li C, Haines J. Li B, et al. Among authors: wei q. PLoS Genet. 2015 Jun 4;11(6):e1005271. doi: 10.1371/journal.pgen.1005271. eCollection 2015 Jun. PLoS Genet. 2015. PMID: 26043085 Free PMC article.

5

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.

6

A common TCN1 loss-of-function variant is associated with lower vitamin B₁₂ concentration in African Americans.

Hu Y, Raffield LM, Polfus LM, Moscati A, Nadkarni G, Preuss MH, Zhong X, Wei Q, Rich SS, Li Y, Wilson JG, Correa A, Loos RJF, Li B, Auer PL, Reiner AP; NHLBI Trans-Omics for Precision Medicine Consortium. Hu Y, et al. Among authors: wei q. Blood. 2018 Jun 21;131(25):2859-2863. doi: 10.1182/blood-2018-03-841023. Epub 2018 May 15. Blood. 2018. PMID: 29764838 Free PMC article. No abstract available.

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

A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.

Wang Q, Chen R, Cheng F, Wei Q, Ji Y, Yang H, Zhong X, Tao R, Wen Z, Sutcliffe JS, Liu C, Cook EH, Cox NJ, Li B. Wang Q, et al. Among authors: wei q. Nat Neurosci. 2019 May;22(5):691-699. doi: 10.1038/s41593-019-0382-7. Epub 2019 Apr 15. Nat Neurosci. 2019. PMID: 30988527 Free PMC article.

9

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.

10

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.

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