Wei Q - Search Results

1

Molecular and epidemiologic characterization of Wilms tumor from Baghdad, Iraq.

Phelps HM, Al-Jadiry MF, Corbitt NM, Pierce JM, Li B, Wei Q, Flores RR, Correa H, Uccini S, Frangoul H, Alsaadawi AR, Al-Badri SAF, Al-Darraji AF, Al-Saeed RM, Al-Hadad SA, Lovvorn Iii HN. Phelps HM, et al. Among authors: wei q. World J Pediatr. 2018 Dec;14(6):585-593. doi: 10.1007/s12519-018-0181-3. Epub 2018 Aug 28. World J Pediatr. 2018. PMID: 30155617 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

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.

4

Genetic and chromosomal alterations in Kenyan Wilms Tumor.

Lovvorn HN 3rd, Pierce J, Libes J, Li B, Wei Q, Correa H, Gouffon J, Clark PE, Axt JR, Hansen E, Newton M, O'Neill JA Jr; Kenyan Wilms Tumor Consortium. Lovvorn HN 3rd, et al. Among authors: wei q. Genes Chromosomes Cancer. 2015 Nov;54(11):702-15. doi: 10.1002/gcc.22281. Epub 2015 Aug 14. Genes Chromosomes Cancer. 2015. PMID: 26274016 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

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

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.

9

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.

10

A computational framework to unify orthogonal information in DNA methylation and copy number aberrations in cell-free DNA for early cancer detection.

Wei Q, Jin C, Wang Y, Guo S, Guo X, Liu X, An J, Xing J, Li B. Wei Q, et al. Brief Bioinform. 2022 Jul 18;23(4):bbac200. doi: 10.1093/bib/bbac200. Brief Bioinform. 2022. PMID: 35649341

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