Lin X - Search Results

1

A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes.

Epstein MP, Hunter JE, Allen EG, Sherman SL, Lin X, Boehnke M. Epstein MP, et al. Among authors: lin x. Stat Biosci. 2009 Nov;1(2):181-198. doi: 10.1007/s12561-009-9010-5. Stat Biosci. 2009. PMID: 20436936 Free PMC article.

2

Ascertainment-adjusted parameter estimates revisited.

Epstein MP, Lin X, Boehnke M. Epstein MP, et al. Among authors: lin x. Am J Hum Genet. 2002 Apr;70(4):886-95. doi: 10.1086/339517. Epub 2002 Mar 5. Am J Hum Genet. 2002. PMID: 11880949 Free PMC article.

3

A tobit variance-component method for linkage analysis of censored trait data.

Epstein MP, Lin X, Boehnke M. Epstein MP, et al. Among authors: lin x. Am J Hum Genet. 2003 Mar;72(3):611-20. doi: 10.1086/367924. Epub 2003 Feb 13. Am J Hum Genet. 2003. PMID: 12587095 Free PMC article.

4

A powerful and flexible multilocus association test for quantitative traits.

Kwee LC, Liu D, Lin X, Ghosh D, Epstein MP. Kwee LC, et al. Among authors: lin x. Am J Hum Genet. 2008 Feb;82(2):386-97. doi: 10.1016/j.ajhg.2007.10.010. Am J Hum Genet. 2008. PMID: 18252219 Free PMC article.

5

Powerful SNP-set analysis for case-control genome-wide association studies.

Wu MC, Kraft P, Epstein MP, Taylor DM, Chanock SJ, Hunter DJ, Lin X. Wu MC, et al. Among authors: lin x. Am J Hum Genet. 2010 Jun 11;86(6):929-42. doi: 10.1016/j.ajhg.2010.05.002. Am J Hum Genet. 2010. PMID: 20560208 Free PMC article.

6

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, Freeman SB, Torfs CP, Cua CL, Epstein MP, Wu MC, Lin X, Capone G, Sherman SL, Bean LJ. Locke AE, et al. Among authors: lin x. Genet Epidemiol. 2010 Sep;34(6):613-23. doi: 10.1002/gepi.20518. Genet Epidemiol. 2010. PMID: 20718043 Free PMC article.

7

Estimating Causal Effects in Trials Involving Multi-Treatment Arms Subject to Non-compliance: A Bayesian framework.

Long Q, Little RJ, Lin X. Long Q, et al. Among authors: lin x. J R Stat Soc Ser C Appl Stat. 2010 May;59(3):513-531. doi: 10.1111/j.1467-9876.2009.00709.x. J R Stat Soc Ser C Appl Stat. 2010. PMID: 21637737 Free PMC article.

8

Rare-variant association testing for sequencing data with the sequence kernel association test.

Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X. Wu MC, et al. Among authors: lin x. Am J Hum Genet. 2011 Jul 15;89(1):82-93. doi: 10.1016/j.ajhg.2011.05.029. Epub 2011 Jul 7. Am J Hum Genet. 2011. PMID: 21737059 Free PMC article.

9

Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies.

Lee S, Epstein MP, Duncan R, Lin X. Lee S, et al. Among authors: lin x. Genet Epidemiol. 2012 May;36(4):293-302. doi: 10.1002/gepi.21621. Epub 2012 Apr 16. Genet Epidemiol. 2012. PMID: 22508067 Free PMC article.

10

SNP set association analysis for familial data.

Schifano ED, Epstein MP, Bielak LF, Jhun MA, Kardia SL, Peyser PA, Lin X. Schifano ED, et al. Among authors: lin x. Genet Epidemiol. 2012 Dec;36(8):797-810. doi: 10.1002/gepi.21676. Epub 2012 Sep 11. Genet Epidemiol. 2012. PMID: 22968922 Free PMC article.

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