Asimit J - Search Results

1

Rare variant association analysis methods for complex traits.

Asimit J, Zeggini E. Asimit J, et al. Annu Rev Genet. 2010;44:293-308. doi: 10.1146/annurev-genet-102209-163421. Annu Rev Genet. 2010. PMID: 21047260 Review.

2

An evaluation of power to detect low-frequency variant associations using allele-matching tests that account for uncertainty.

Zeggini E, Asimit JL. Zeggini E, et al. Among authors: asimit jl. Pac Symp Biocomput. 2011:100-5. doi: 10.1142/9789814335058_0011. Pac Symp Biocomput. 2011. PMID: 21121037 Free PMC article.

3

Testing for rare variant associations in complex diseases.

Asimit J, Zeggini E. Asimit J, et al. Genome Med. 2009;1(11):24. doi: 10.1186/gm238. Epub 2011 Apr 27. Genome Med. 2009. PMID: 21542888 Free PMC article.

4

Defining the power limits of genome-wide association scan meta-analyses.

Chapman K, Ferreira T, Morris A, Asimit J, Zeggini E. Chapman K, et al. Among authors: asimit j. Genet Epidemiol. 2011 Dec;35(8):781-9. doi: 10.1002/gepi.20627. Epub 2011 Sep 15. Genet Epidemiol. 2011. PMID: 21922540 Free PMC article.

5

A combined functional annotation score for non-synonymous variants.

Lopes MC, Joyce C, Ritchie GR, John SL, Cunningham F, Asimit J, Zeggini E. Lopes MC, et al. Among authors: asimit j. Hum Hered. 2012;73(1):47-51. doi: 10.1159/000334984. Epub 2012 Jan 18. Hum Hered. 2012. PMID: 22261837 Free PMC article.

6

An evaluation of different meta-analysis approaches in the presence of allelic heterogeneity.

Asimit J, Day-Williams A, Zgaga L, Rudan I, Boraska V, Zeggini E. Asimit J, et al. Eur J Hum Genet. 2012 Jun;20(6):709-12. doi: 10.1038/ejhg.2011.274. Epub 2012 Feb 1. Eur J Hum Genet. 2012. PMID: 22293689 Free PMC article.

7

ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data.

Asimit JL, Day-Williams AG, Morris AP, Zeggini E. Asimit JL, et al. Hum Hered. 2012;73(2):84-94. doi: 10.1159/000336982. Epub 2012 Mar 22. Hum Hered. 2012. PMID: 22441326 Free PMC article.

8

Genome-wide association analysis of imputed rare variants: application to seven common complex diseases.

Mägi R, Asimit JL, Day-Williams AG, Zeggini E, Morris AP. Mägi R, et al. Genet Epidemiol. 2012 Dec;36(8):785-96. doi: 10.1002/gepi.21675. Epub 2012 Sep 5. Genet Epidemiol. 2012. PMID: 22951892 Free PMC article.

9

Imputation of rare variants in next-generation association studies.

Asimit JL, Zeggini E. Asimit JL, et al. Hum Hered. 2012;74(3-4):196-204. doi: 10.1159/000345602. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594497 Free PMC article.

10

Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan.

Carss KJ, Stevens E, Foley AR, Cirak S, Riemersma M, Torelli S, Hoischen A, Willer T, van Scherpenzeel M, Moore SA, Messina S, Bertini E, Bönnemann CG, Abdenur JE, Grosmann CM, Kesari A, Punetha J, Quinlivan R, Waddell LB, Young HK, Wraige E, Yau S, Brodd L, Feng L, Sewry C, MacArthur DG, North KN, Hoffman E, Stemple DL, Hurles ME, van Bokhoven H, Campbell KP, Lefeber DJ; UK10K Consortium; Lin YY, Muntoni F. Carss KJ, et al. Am J Hum Genet. 2013 Jul 11;93(1):29-41. doi: 10.1016/j.ajhg.2013.05.009. Epub 2013 Jun 13. Am J Hum Genet. 2013. PMID: 23768512 Free PMC article.

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