Strug LJ - Search Results

1

Genetic association analysis with pedigrees: Direct inference using the composite likelihood ratio.

Baskurt Z, Strug LJ. Baskurt Z, et al. Among authors: strug lj. Genet Epidemiol. 2018 Dec;42(8):826-837. doi: 10.1002/gepi.22153. Epub 2018 Sep 17. Genet Epidemiol. 2018. PMID: 30221395

2

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).

Strug LJ, Clarke T, Chiang T, Chien M, Baskurt Z, Li W, Dorfman R, Bali B, Wirrell E, Kugler SL, Mandelbaum DE, Wolf SM, McGoldrick P, Hardison H, Novotny EJ, Ju J, Greenberg DA, Russo JJ, Pal DK. Strug LJ, et al. Eur J Hum Genet. 2009 Sep;17(9):1171-81. doi: 10.1038/ejhg.2008.267. Epub 2009 Jan 28. Eur J Hum Genet. 2009. PMID: 19172991 Free PMC article.

3

Evidence of shared genetic risk factors for migraine and rolandic epilepsy.

Clarke T, Baskurt Z, Strug LJ, Pal DK. Clarke T, et al. Among authors: strug lj. Epilepsia. 2009 Nov;50(11):2428-33. doi: 10.1111/j.1528-1167.2009.02240.x. Epub 2009 Aug 8. Epilepsia. 2009. PMID: 19674062 Free article.

4

A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysis.

Strug LJ, Hodge SE, Chiang T, Pal DK, Corey PN, Rohde C. Strug LJ, et al. Eur J Hum Genet. 2010 Aug;18(8):933-41. doi: 10.1038/ejhg.2010.47. Epub 2010 Apr 28. Eur J Hum Genet. 2010. PMID: 20424645 Free PMC article.

5

Using parametric multipoint lods and mods for linkage analysis requires a shift in statistical thinking.

Hodge SE, Baskurt Z, Strug LJ. Hodge SE, et al. Among authors: strug lj. Hum Hered. 2011;72(4):264-75. doi: 10.1159/000331463. Epub 2011 Dec 23. Hum Hered. 2011. PMID: 22189469 Free PMC article.

6

The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.

Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK. Strug LJ, et al. PLoS One. 2012;7(7):e40696. doi: 10.1371/journal.pone.0040696. Epub 2012 Jul 18. PLoS One. 2012. PMID: 22815793 Free PMC article.

7

Prioritizing rare variants with conditional likelihood ratios.

Li W, Dobbins S, Tomlinson I, Houlston R, Pal DK, Strug LJ. Li W, et al. Among authors: strug lj. Hum Hered. 2015;79(1):5-13. doi: 10.1159/000371579. Epub 2015 Feb 3. Hum Hered. 2015. PMID: 25659987 Free PMC article.

8

Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels.

Dennis J, Medina-Rivera A, Truong V, Antounians L, Zwingerman N, Carrasco G, Strug L, Wells P, Trégouët DA, Morange PE, Wilson MD, Gagnon F. Dennis J, et al. Genet Epidemiol. 2017 Jul;41(5):455-466. doi: 10.1002/gepi.22049. Epub 2017 Apr 18. Genet Epidemiol. 2017. PMID: 28421636

9

Improving imputation in disease-relevant regions: lessons from cystic fibrosis.

Panjwani N, Xiao B, Xu L, Gong J, Keenan K, Lin F, He G, Baskurt Z, Kim S, Zhang L, Esmaeili M, Blackman S, Scherer SW, Corvol H, Drumm M, Knowles M, Cutting G, Rommens JM, Sun L, Strug LJ. Panjwani N, et al. Among authors: strug lj. NPJ Genom Med. 2018 Mar 20;3:8. doi: 10.1038/s41525-018-0047-6. eCollection 2018. NPJ Genom Med. 2018. PMID: 29581887 Free PMC article.

10

The evidential statistical paradigm in genetics.

Strug LJ. Strug LJ. Genet Epidemiol. 2018 Oct;42(7):590-607. doi: 10.1002/gepi.22151. Epub 2018 Aug 18. Genet Epidemiol. 2018. PMID: 30120797 Free PMC article. Review.

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