R37 CA076404/CA/NCI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	1
2008	2
2009	4
2010	8
2011	9
2012	13
2013	14
2014	11
2015	2
2016	4
2017	3
2024	0

1

Rare-variant association analysis: study designs and statistical tests.

Lee S, Abecasis GR, Boehnke M, Lin X. Lee S, et al. Am J Hum Genet. 2014 Jul 3;95(1):5-23. doi: 10.1016/j.ajhg.2014.06.009. Am J Hum Genet. 2014. PMID: 24995866 Free PMC article. Review.

2

VARIABLE SELECTION FOR HIGH DIMENSIONAL MULTIVARIATE OUTCOMES.

Sofer T, Dicker L, Lin X. Sofer T, et al. Stat Sin. 2014 Oct;24(4):1633-1654. doi: 10.5705/ss.2013.019. Stat Sin. 2014. PMID: 28642637 Free PMC article.

3

B-cell lymphomas with concurrent IGH-BCL2 and MYC rearrangements are aggressive neoplasms with clinical and pathologic features distinct from Burkitt lymphoma and diffuse large B-cell lymphoma.

Snuderl M, Kolman OK, Chen YB, Hsu JJ, Ackerman AM, Dal Cin P, Ferry JA, Harris NL, Hasserjian RP, Zukerberg LR, Abramson JS, Hochberg EP, Lee H, Lee AI, Toomey CE, Sohani AR. Snuderl M, et al. Am J Surg Pathol. 2010 Mar;34(3):327-40. doi: 10.1097/PAS.0b013e3181cd3aeb. Am J Surg Pathol. 2010. PMID: 20118770 Free PMC article.

4

Test for rare variants by environment interactions in sequencing association studies.

Lin X, Lee S, Wu MC, Wang C, Chen H, Li Z, Lin X. Lin X, et al. Biometrics. 2016 Mar;72(1):156-64. doi: 10.1111/biom.12368. Epub 2015 Jul 30. Biometrics. 2016. PMID: 26229047 Free PMC article.

5

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. 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.

6

Fast and robust adjustment of cell mixtures in epigenome-wide association studies with SmartSVA.

Chen J, Behnam E, Huang J, Moffatt MF, Schaid DJ, Liang L, Lin X. Chen J, et al. BMC Genomics. 2017 May 26;18(1):413. doi: 10.1186/s12864-017-3808-1. BMC Genomics. 2017. PMID: 28549425 Free PMC article.

7

Gene set analysis using variance component tests.

Huang YT, Lin X. Huang YT, et al. BMC Bioinformatics. 2013 Jun 28;14:210. doi: 10.1186/1471-2105-14-210. BMC Bioinformatics. 2013. PMID: 23806107 Free PMC article.

8

Genome-wide association analysis for multiple continuous secondary phenotypes.

Schifano ED, Li L, Christiani DC, Lin X. Schifano ED, et al. Am J Hum Genet. 2013 May 2;92(5):744-59. doi: 10.1016/j.ajhg.2013.04.004. Am J Hum Genet. 2013. PMID: 23643383 Free PMC article.

9

Population differences in transcript-regulator expression quantitative trait loci.

Bushel PR, McGovern R, Liu L, Hofmann O, Huda A, Lu J, Hide W, Lin X. Bushel PR, et al. PLoS One. 2012;7(3):e34286. doi: 10.1371/journal.pone.0034286. Epub 2012 Mar 27. PLoS One. 2012. PMID: 22479588 Free PMC article.

10

Sequence kernel association tests for the combined effect of rare and common variants.

Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X. Ionita-Laza I, et al. Am J Hum Genet. 2013 Jun 6;92(6):841-53. doi: 10.1016/j.ajhg.2013.04.015. Epub 2013 May 16. Am J Hum Genet. 2013. PMID: 23684009 Free PMC article.

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