Yip WK - Search Results

1

Clinical and analytical validation of FoundationOne®CDx, a comprehensive genomic profiling assay for solid tumors.

Milbury CA, Creeden J, Yip WK, Smith DL, Pattani V, Maxwell K, Sawchyn B, Gjoerup O, Meng W, Skoletsky J, Concepcion AD, Tang Y, Bai X, Dewal N, Ma P, Bailey ST, Thornton J, Pavlick DC, Frampton GM, Lieber D, White J, Burns C, Vietz C. Milbury CA, et al. Among authors: yip wk. PLoS One. 2022 Mar 16;17(3):e0264138. doi: 10.1371/journal.pone.0264138. eCollection 2022. PLoS One. 2022. PMID: 35294956 Free PMC article.

2

A novel method for detecting association between DNA methylation and diseases using spatial information.

Yip WK, Fier H, DeMeo DL, Aryee M, Laird N, Lange C. Yip WK, et al. Genet Epidemiol. 2014 Dec;38(8):714-21. doi: 10.1002/gepi.21851. Epub 2014 Sep 22. Genet Epidemiol. 2014. PMID: 25250875 Free PMC article.

3

Quantitative trait prediction based on genetic marker-array data, a simulation study.

Yip WK, Lange C. Yip WK, et al. Bioinformatics. 2011 Mar 15;27(6):745-8. doi: 10.1093/bioinformatics/btr024. Epub 2011 Jan 31. Bioinformatics. 2011. PMID: 21285022 Free PMC article.

4

On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.

Lipman PJ, Yip WK, AlChawa T, Ludwig KU, Mangold E, Lange C. Lipman PJ, et al. Among authors: yip wk. Genet Epidemiol. 2011 Dec;35(8):880-6. doi: 10.1002/gepi.20638. Genet Epidemiol. 2011. PMID: 22125225 Free PMC article.

5

A general semi-parametric approach to the analysis of genetic association studies in population-based designs.

Lutz S, Yip WK, Hokanson J, Laird N, Lange C. Lutz S, et al. Among authors: yip wk. BMC Genet. 2013 Feb 28;14:13. doi: 10.1186/1471-2156-14-13. BMC Genet. 2013. PMID: 23448186 Free PMC article.

6

A comparative analysis of family-based and population-based association tests using whole genome sequence data.

Zhou JJ, Yip WK, Cho MH, Qiao D, McDonald ML, Laird NM. Zhou JJ, et al. Among authors: yip wk. BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S33. doi: 10.1186/1753-6561-8-S1-S33. eCollection 2014. BMC Proc. 2014. PMID: 25519381 Free PMC article.

7

Rare variant analysis for family-based design.

De G, Yip WK, Ionita-Laza I, Laird N. De G, et al. Among authors: yip wk. PLoS One. 2013;8(1):e48495. doi: 10.1371/journal.pone.0048495. Epub 2013 Jan 15. PLoS One. 2013. PMID: 23341868 Free PMC article.

8

Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data.

Qiao D, Yip WK, Lange C. Qiao D, et al. Among authors: yip wk. BMC Bioinformatics. 2012 May 16;13:100. doi: 10.1186/1471-2105-13-100. BMC Bioinformatics. 2012. PMID: 22591016 Free PMC article.

9

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set.

Yip WK, De G, Raby BA, Laird N. Yip WK, et al. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S21. doi: 10.1186/1753-6561-5-S9-S21. BMC Proc. 2011. PMID: 22373204 Free PMC article.

10

The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.

Hooli BV, Parrado AR, Mullin K, Yip WK, Liu T, Roehr JT, Qiao D, Jessen F, Peters O, Becker T, Ramirez A, Lange C, Bertram L, Tanzi RE. Hooli BV, et al. Among authors: yip wk. Neurology. 2014 Oct 7;83(15):1353-8. doi: 10.1212/WNL.0000000000000855. Epub 2014 Sep 3. Neurology. 2014. PMID: 25186855 Free PMC article.

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