Similar articles for PMID: 27221085

Year	Number of Results
2009	3
2010	1
2011	18
2012	7
2013	11
2014	23
2015	13
2016	17
2017	8
2018	8
2019	6
2020	8
2021	7
2022	6
2023	1
2024	0

1

Discovery of rare variants for complex phenotypes.

Kosmicki JA, Churchhouse CL, Rivas MA, Neale BM. Kosmicki JA, et al. Hum Genet. 2016 Jun;135(6):625-34. doi: 10.1007/s00439-016-1679-1. Epub 2016 May 24. Hum Genet. 2016. PMID: 27221085 Free PMC article. Review.

2

Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.

Wagner MJ. Wagner MJ. Pharmacogenomics. 2013 Mar;14(4):413-24. doi: 10.2217/pgs.13.36. Pharmacogenomics. 2013. PMID: 23438888 Review.

3

Rare variant association test with multiple phenotypes.

Lee S, Won S, Kim YJ, Kim Y; T2D-Genes Consortium; Kim BJ, Park T. Lee S, et al. Genet Epidemiol. 2017 Apr;41(3):198-209. doi: 10.1002/gepi.22021. Epub 2016 Dec 31. Genet Epidemiol. 2017. PMID: 28039885 Free PMC article.

4

SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data.

Zhang D, Zhao L, Li B, He Z, Wang GT, Liu DJ, Leal SM. Zhang D, et al. Am J Hum Genet. 2017 Jul 6;101(1):115-122. doi: 10.1016/j.ajhg.2017.05.017. Epub 2017 Jun 29. Am J Hum Genet. 2017. PMID: 28669402 Free PMC article.

5

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.

Moutsianas L, Agarwala V, Fuchsberger C, Flannick J, Rivas MA, Gaulton KJ, Albers PK; GoT2D Consortium; McVean G, Boehnke M, Altshuler D, McCarthy MI. Moutsianas L, et al. PLoS Genet. 2015 Apr 23;11(4):e1005165. doi: 10.1371/journal.pgen.1005165. eCollection 2015 Apr. PLoS Genet. 2015. PMID: 25906071 Free PMC article.

6

Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.

Hammer MF, Ishii A, Johnstone L, Tchourbanov A, Lau B, Sprissler R, Hallmark B, Zhang M, Zhou J, Watkins J, Hirose S. Hammer MF, et al. PLoS One. 2017 Jul 7;12(7):e0180485. doi: 10.1371/journal.pone.0180485. eCollection 2017. PLoS One. 2017. PMID: 28686619 Free PMC article.

7

Rare variants in complex traits: novel identification strategies and the role of de novo mutations.

Jouan L, Gauthier J, Dion PA, Rouleau GA. Jouan L, et al. Hum Hered. 2012;74(3-4):215-25. doi: 10.1159/000346478. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594499 Free article.

8

Assessing the Power of Exome Chips.

Page CM, Baranzini SE, Mevik BH, Bos SD, Harbo HF, Andreassen BK. Page CM, et al. PLoS One. 2015 Oct 5;10(10):e0139642. doi: 10.1371/journal.pone.0139642. eCollection 2015. PLoS One. 2015. PMID: 26437075 Free PMC article.

9

The Rise and Rise of Exome Sequencing.

Ku CS, Cooper DN, Patrinos GP. Ku CS, et al. Public Health Genomics. 2016;19(6):315-324. doi: 10.1159/000450991. Epub 2016 Nov 30. Public Health Genomics. 2016. PMID: 27898412 Free article. Review.

10

Exome versus transcriptome sequencing in identifying coding region variants.

Ku CS, Wu M, Cooper DN, Naidoo N, Pawitan Y, Pang B, Iacopetta B, Soong R. Ku CS, et al. Expert Rev Mol Diagn. 2012 Apr;12(3):241-51. doi: 10.1586/erm.12.10. Expert Rev Mol Diagn. 2012. PMID: 22468815 Review.

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