Greenwood CMT - 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: greenwood cmt. 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

Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Greenwood CM, Fujiwara TM, Boothroyd LJ, Miller MA, Frappier D, Fanning EA, Schurr E, Morgan K. Greenwood CM, et al. Am J Hum Genet. 2000 Aug;67(2):405-16. doi: 10.1086/303012. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10882571 Free PMC article.

3

Pedigree selection and tests of linkage in a Hutterite asthma pedigree.

Greenwood CM, Bureau A, Loredo-Osti JC, Roslin NM, Crumley MJ, Brewer CG, Fujiwara TM, Goldstein DR, Morgan K. Greenwood CM, et al. Genet Epidemiol. 2001;21 Suppl 1:S244-51. doi: 10.1002/gepi.2001.21.s1.s244. Genet Epidemiol. 2001. PMID: 11793677

4

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

5

A sequence of methodological changes due to sequencing.

Burkett K, Greenwood C. Burkett K, et al. Curr Opin Allergy Clin Immunol. 2013 Oct;13(5):470-7. doi: 10.1097/ACI.0b013e3283648f68. Curr Opin Allergy Clin Immunol. 2013. PMID: 23974677 Review.

6

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. 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.

7

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. Stat Med. 2016 Mar 15;35(6):905-21. doi: 10.1002/sim.6750. Epub 2015 Sep 29. Stat Med. 2016. PMID: 26420132

8

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. 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.

9

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.

10

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. 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

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