Wang M - Search Results

1

FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triads.

Wang M, Lin S. Wang M, et al. Bioinformatics. 2014 Sep 15;30(18):2611-8. doi: 10.1093/bioinformatics/btu347. Epub 2014 May 21. Bioinformatics. 2014. PMID: 24849576 Free PMC article.

2

Detecting associations of rare variants with common diseases: collapsing or haplotyping?

Wang M, Lin S. Wang M, et al. Brief Bioinform. 2015 Sep;16(5):759-68. doi: 10.1093/bib/bbu050. Epub 2015 Jan 17. Brief Bioinform. 2015. PMID: 25596401 Free PMC article.

3

Logistic Bayesian LASSO for detecting association combining family and case-control data.

Zhou X, Wang M, Zhang H, Stewart WCL, Lin S. Zhou X, et al. Among authors: wang m. BMC Proc. 2018 Sep 17;12(Suppl 9):54. doi: 10.1186/s12919-018-0139-4. eCollection 2018. BMC Proc. 2018. PMID: 30263052 Free PMC article.

4

Detecting rare haplotypes associated with complex diseases using both population and family data: Combined logistic Bayesian Lasso.

Zhou X, Wang M, Lin S. Zhou X, et al. Among authors: wang m. Stat Methods Med Res. 2020 Nov;29(11):3340-3350. doi: 10.1177/0962280220927728. Epub 2020 Jun 4. Stat Methods Med Res. 2020. PMID: 32493129

5

Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy.

Wang M, Greenberg DA, Stewart WCL. Wang M, et al. Epilepsia. 2019 Mar;60(3):539-546. doi: 10.1111/epi.14654. Epub 2019 Feb 4. Epilepsia. 2019. PMID: 30719716

6

A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent Cases.

Wang M, Stewart WCL. Wang M, et al. Front Genet. 2017 May 9;8:49. doi: 10.3389/fgene.2017.00049. eCollection 2017. Front Genet. 2017. PMID: 28536599 Free PMC article.

7

Chromatin structure in cancer.

Wang M, Sunkel BD, Ray WC, Stanton BZ. Wang M, et al. BMC Mol Cell Biol. 2022 Jul 28;23(1):35. doi: 10.1186/s12860-022-00433-6. BMC Mol Cell Biol. 2022. PMID: 35902807 Free PMC article. Review.

8

In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy.

Wang M, Greenberg DA, Stewart WCL. Wang M, et al. Epilepsia. 2019 Sep;60(9):2001-2002. doi: 10.1111/epi.16303. Epub 2019 Jul 29. Epilepsia. 2019. PMID: 31353459 No abstract available.

9

A SNAI2/CTCF Interaction is Required for NOTCH1 Expression in Rhabdomyosarcoma.

Sreenivas P, Wang L, Wang M, Challa A, Modi P, Hensch NR, Gryder B, Chou HC, Zhao XR, Sunkel B, Moreno-Campos R, Khan J, Stanton BZ, Ignatius MS. Sreenivas P, et al. Among authors: wang l, wang m. Mol Cell Biol. 2023;43(11):547-565. doi: 10.1080/10985549.2023.2256640. Epub 2023 Nov 17. Mol Cell Biol. 2023. PMID: 37882064 Free PMC article.

10

Evidence of pioneer factor activity of an oncogenic fusion transcription factor.

Sunkel BD, Wang M, LaHaye S, Kelly BJ, Fitch JR, Barr FG, White P, Stanton BZ. Sunkel BD, et al. Among authors: wang m. iScience. 2021 Jul 16;24(8):102867. doi: 10.1016/j.isci.2021.102867. eCollection 2021 Aug 20. iScience. 2021. PMID: 34386729 Free PMC article.

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