Oualkacha K - Search Results

1

Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models.

Bhatnagar SR, Yang Y, Lu T, Schurr E, Loredo-Osti JC, Forest M, Oualkacha K, Greenwood CMT. Bhatnagar SR, et al. Among authors: oualkacha k. PLoS Genet. 2020 May 4;16(5):e1008766. doi: 10.1371/journal.pgen.1008766. eCollection 2020 May. PLoS Genet. 2020. PMID: 32365090 Free PMC article.

2

Adjusted sequence kernel association test for rare variants controlling for cryptic and family relatedness.

Oualkacha K, Dastani Z, Li R, Cingolani PE, Spector TD, Hammond CJ, Richards JB, Ciampi A, Greenwood CM. Oualkacha K, et al. Genet Epidemiol. 2013 May;37(4):366-76. doi: 10.1002/gepi.21725. Epub 2013 Mar 25. Genet Epidemiol. 2013. PMID: 23529756

3

Pathway analysis for genetic association studies: to do, or not to do? That is the question.

Dufresne L, Oualkacha K, Forgetta V, Greenwood CM. Dufresne L, et al. Among authors: oualkacha k. BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S103. doi: 10.1186/1753-6561-8-S1-S103. eCollection 2014. BMC Proc. 2014. PMID: 25519357 Free PMC article.

4

Whole-genome sequence-based analysis of thyroid function.

Taylor PN, Porcu E, Chew S, Campbell PJ, Traglia M, Brown SJ, Mullin BH, Shihab HA, Min J, Walter K, Memari Y, Huang J, Barnes MR, Beilby JP, Charoen P, Danecek P, Dudbridge F, Forgetta V, Greenwood C, Grundberg E, Johnson AD, Hui J, Lim EM, McCarthy S, Muddyman D, Panicker V, Perry JR, Bell JT, Yuan W, Relton C, Gaunt T, Schlessinger D, Abecasis G, Cucca F, Surdulescu GL, Woltersdorf W, Zeggini E, Zheng HF, Toniolo D, Dayan CM, Naitza S, Walsh JP, Spector T, Davey Smith G, Durbin R, Richards JB, Sanna S, Soranzo N, Timpson NJ, Wilson SG; UK0K Consortium. Taylor PN, et al. Nat Commun. 2015 Mar 6;6:5681. doi: 10.1038/ncomms6681. Nat Commun. 2015. PMID: 25743335 Free PMC article.

5

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel.

Huang J, Howie B, McCarthy S, Memari Y, Walter K, Min JL, Danecek P, Malerba G, Trabetti E, Zheng HF; UK10K Consortium; Gambaro G, Richards JB, Durbin R, Timpson NJ, Marchini J, Soranzo N. Huang J, et al. Nat Commun. 2015 Sep 14;6:8111. doi: 10.1038/ncomms9111. Nat Commun. 2015. PMID: 26368830 Free PMC article.

6

A rare variant association test in family-based designs and non-normal quantitative traits.

Lakhal-Chaieb L, Oualkacha K, Richards BJ, Greenwood CM. Lakhal-Chaieb L, et al. Among authors: oualkacha k. Stat Med. 2016 Mar 15;35(6):905-21. doi: 10.1002/sim.6750. Epub 2015 Sep 29. Stat Med. 2016. PMID: 26420132

7

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects.

Sun J, Oualkacha K, Forgetta V, Zheng HF, Brent Richards J, Ciampi A, Greenwood CM; UK10K Consortium. Sun J, et al. Among authors: oualkacha k. Eur J Hum Genet. 2016 Aug;24(9):1344-51. doi: 10.1038/ejhg.2016.8. Epub 2016 Feb 10. Eur J Hum Genet. 2016. PMID: 26860061 Free PMC article.

8

Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits.

Oualkacha K, Lakhal-Chaieb L, Greenwood CM. Oualkacha K, et al. Int J Epidemiol. 2016 Apr;45(2):402-7. doi: 10.1093/ije/dyw047. Epub 2016 Apr 16. Int J Epidemiol. 2016. PMID: 27085080 Free PMC article.

9

Principal component of explained variance: An efficient and optimal data dimension reduction framework for association studies.

Turgeon M, Oualkacha K, Ciampi A, Miftah H, Dehghan G, Zanke BW, Benedet AL, Rosa-Neto P, Greenwood CM, Labbe A; Alzheimer’s Disease Neuroimaging Initiative. Turgeon M, et al. Among authors: oualkacha k. Stat Methods Med Res. 2018 May;27(5):1331-1350. doi: 10.1177/0962280216660128. Epub 2016 Jul 26. Stat Methods Med Res. 2018. PMID: 27460538

10

Gene Coexpression Analyses Differentiate Networks Associated with Diverse Cancers Harboring TP53 Missense or Null Mutations.

Oros Klein K, Oualkacha K, Lafond MH, Bhatnagar S, Tonin PN, Greenwood CM. Oros Klein K, et al. Among authors: oualkacha k. Front Genet. 2016 Aug 3;7:137. doi: 10.3389/fgene.2016.00137. eCollection 2016. Front Genet. 2016. PMID: 27536319 Free PMC article.

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