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Haplotype sorting using human fosmid clone end-sequence pairs.
Kidd JM, Cheng Z, Graves T, Fulton B, Wilson RK, Eichler EE. Kidd JM, et al. Among authors: eichler ee. Genome Res. 2008 Dec;18(12):2016-23. doi: 10.1101/gr.081786.108. Epub 2008 Oct 3. Genome Res. 2008. PMID: 18836033 Free PMC article.
De novo rates and selection of large copy number variation.
Itsara A, Wu H, Smith JD, Nickerson DA, Romieu I, London SJ, Eichler EE. Itsara A, et al. Among authors: eichler ee. Genome Res. 2010 Nov;20(11):1469-81. doi: 10.1101/gr.107680.110. Epub 2010 Sep 14. Genome Res. 2010. PMID: 20841430 Free PMC article.
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, Eichler EE. O'Roak BJ, et al. Among authors: eichler ee. Nat Genet. 2011 Jun;43(6):585-9. doi: 10.1038/ng.835. Epub 2011 May 15. Nat Genet. 2011. PMID: 21572417 Free PMC article.
The genetic variability and commonality of neurodevelopmental disease.
Coe BP, Girirajan S, Eichler EE. Coe BP, et al. Among authors: eichler ee. Am J Med Genet C Semin Med Genet. 2012 May 15;160C(2):118-29. doi: 10.1002/ajmg.c.31327. Epub 2012 Apr 12. Am J Med Genet C Semin Med Genet. 2012. PMID: 22499536 Free PMC article. Review.
A genetic model for neurodevelopmental disease.
Coe BP, Girirajan S, Eichler EE. Coe BP, et al. Among authors: eichler ee. Curr Opin Neurobiol. 2012 Oct;22(5):829-36. doi: 10.1016/j.conb.2012.04.007. Epub 2012 May 2. Curr Opin Neurobiol. 2012. PMID: 22560351 Free PMC article. Review.
613 results