Greenwood CMT - Search Results

1

Constrained instruments and their application to Mendelian randomization with pleiotropy.

Jiang L, Oualkacha K, Didelez V, Ciampi A, Rosa-Neto P, Benedet AL, Mathotaarachchi S, Richards JB, Greenwood CMT; Alzheimer’s Disease Neuroimaging Initiative. Jiang L, et al. Among authors: greenwood cmt. Genet Epidemiol. 2019 Jun;43(4):373-401. doi: 10.1002/gepi.22184. Epub 2019 Jan 12. Genet Epidemiol. 2019. PMID: 30635941 Free PMC article.

2

Validation of linkage by sampling based on environmental exposures.

Greenwood CM, Brewer CG, Morgan K. Greenwood CM, et al. Genet Epidemiol. 1999;17 Suppl 1:S593-8. doi: 10.1002/gepi.1370170796. Genet Epidemiol. 1999. PMID: 10597498

3

Multiple regression methods show great potential for rare variant association tests.

Xu C, Ladouceur M, Dastani Z, Richards JB, Ciampi A, Greenwood CM. Xu C, et al. PLoS One. 2012;7(8):e41694. doi: 10.1371/journal.pone.0041694. Epub 2012 Aug 8. PLoS One. 2012. PMID: 22916111 Free PMC article.

4

Effect of genome-wide genotyping and reference panels on rare variants imputation.

Zheng HF, Ladouceur M, Greenwood CM, Richards JB. Zheng HF, et al. J Genet Genomics. 2012 Oct 20;39(10):545-50. doi: 10.1016/j.jgg.2012.07.002. Epub 2012 Jul 24. J Genet Genomics. 2012. PMID: 23089364

5

Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals.

Ladouceur M, Zheng HF, Greenwood CM, Richards JB. Ladouceur M, et al. Eur J Hum Genet. 2013 Sep;21(9):1027-30. doi: 10.1038/ejhg.2012.284. Epub 2013 Jan 16. Eur J Hum Genet. 2013. PMID: 23321613 Free PMC article.

6

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

7

The shared allelic architecture of adiponectin levels and coronary artery disease.

Dastani Z, Johnson T, Kronenberg F, Nelson CP, Assimes TL, März W; CARDIoGRAM Consortium; ADIPOGen Consortium; Richards JB. Dastani Z, et al. Atherosclerosis. 2013 Jul;229(1):145-8. doi: 10.1016/j.atherosclerosis.2013.03.034. Epub 2013 Apr 22. Atherosclerosis. 2013. PMID: 23664276 Free PMC article.

8

Somatic point mutations occurring early in development: a monozygotic twin study.

Li R, Montpetit A, Rousseau M, Wu SY, Greenwood CM, Spector TD, Pollak M, Polychronakos C, Richards JB. Li R, et al. J Med Genet. 2014 Jan;51(1):28-34. doi: 10.1136/jmedgenet-2013-101712. Epub 2013 Oct 11. J Med Genet. 2014. PMID: 24123875

9

Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation.

Xu C, Ciampi A, Greenwood CM; UK10K Consortium. Xu C, et al. Front Genet. 2014 Jan 29;5:11. doi: 10.3389/fgene.2014.00011. eCollection 2014. Front Genet. 2014. PMID: 24523729 Free PMC article.

10

Estimating genome-wide significance for whole-genome sequencing studies.

Xu C, Tachmazidou I, Walter K, Ciampi A, Zeggini E, Greenwood CM; UK10K Consortium. Xu C, et al. Genet Epidemiol. 2014 May;38(4):281-90. doi: 10.1002/gepi.21797. Epub 2014 Feb 14. Genet Epidemiol. 2014. PMID: 24676807 Free PMC article.

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