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On the frequency of copy number variants.
Ionita-Laza I, Laird NM, Raby BA, Weiss ST, Lange C. Ionita-Laza I, et al. Bioinformatics. 2008 Oct 15;24(20):2350-5. doi: 10.1093/bioinformatics/btn421. Epub 2008 Aug 8. Bioinformatics. 2008. PMID: 18689430 Free PMC article.
Copy number variation genotyping using family information.
Chu JH, Rogers A, Ionita-Laza I, Darvishi K, Mills RE, Lee C, Raby BA. Chu JH, et al. BMC Bioinformatics. 2013 May 9;14:157. doi: 10.1186/1471-2105-14-157. BMC Bioinformatics. 2013. PMID: 23656838 Free PMC article.
Estimating the number of unseen variants in the human genome.
Ionita-Laza I, Lange C, M Laird N. Ionita-Laza I, et al. Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5008-13. doi: 10.1073/pnas.0807815106. Epub 2009 Mar 10. Proc Natl Acad Sci U S A. 2009. PMID: 19276111 Free PMC article.
Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.
Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, Allen MH, Bowden CL, Calabrese JR, Fossey MD, Friedman ES, Gyulai L, Hauser P, Ketter TB, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel JK, Sachs GS, Thase ME, Molay FB, Escamilla MA, Nimgaonkar VL, Sklar P, Laird NM, Smoller JW. Fan J, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):29-37. doi: 10.1002/ajmg.b.30942. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19308960 Free PMC article.
88 results