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Year | Number of Results |
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2009 | 1 |
2010 | 2 |
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Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.
Arch Neurol. 2009 Aug;66(8):1028-32. doi: 10.1001/archneurol.2009.139.
Arch Neurol. 2009.
PMID: 19667227
Free PMC article.
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions.
Liu DJ, Leal SM.
Liu DJ, et al.
PLoS Genet. 2010 Oct 14;6(10):e1001156. doi: 10.1371/journal.pgen.1001156.
PLoS Genet. 2010.
PMID: 20976247
Free PMC article.
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Replication strategies for rare variant complex trait association studies via next-generation sequencing.
Liu DJ, Leal SM.
Liu DJ, et al.
Am J Hum Genet. 2010 Dec 10;87(6):790-801. doi: 10.1016/j.ajhg.2010.10.025.
Am J Hum Genet. 2010.
PMID: 21129725
Free PMC article.
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A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data.
Liu DJ, Leal SM.
Liu DJ, et al.
Eur J Hum Genet. 2012 Apr;20(4):449-56. doi: 10.1038/ejhg.2011.211. Epub 2011 Dec 14.
Eur J Hum Genet. 2012.
PMID: 22166943
Free PMC article.
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