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The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders.
Ang CE, Ma Q, Wapinski OL, Fan S, Flynn RA, Lee QY, Coe B, Onoguchi M, Olmos VH, Do BT, Dukes-Rimsky L, Xu J, Tanabe K, Wang L, Elling U, Penninger JM, Zhao Y, Qu K, Eichler EE, Srivastava A, Wernig M, Chang HY. Ang CE, et al. Among authors: coe b. Elife. 2019 Jan 10;8:e41770. doi: 10.7554/eLife.41770. Elife. 2019. PMID: 30628890 Free PMC article.
A genetic model for neurodevelopmental disease.
Coe BP, Girirajan S, Eichler EE. Coe BP, et al. 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.
Genome structural variation discovery and genotyping.
Alkan C, Coe BP, Eichler EE. Alkan C, et al. Nat Rev Genet. 2011 May;12(5):363-76. doi: 10.1038/nrg2958. Epub 2011 Mar 1. Nat Rev Genet. 2011. PMID: 21358748 Free PMC article. Review.
Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Girirajan S, Brkanac Z, Coe BP, Baker C, Vives L, Vu TH, Shafer N, Bernier R, Ferrero GB, Silengo M, Warren ST, Moreno CS, Fichera M, Romano C, Raskind WH, Eichler EE. Girirajan S, et al. Among authors: coe bp. PLoS Genet. 2011 Nov;7(11):e1002334. doi: 10.1371/journal.pgen.1002334. Epub 2011 Nov 10. PLoS Genet. 2011. PMID: 22102821 Free PMC article.
Copy number variation detection and genotyping from exome sequence data.
Krumm N, Sudmant PH, Ko A, O'Roak BJ, Malig M, Coe BP; NHLBI Exome Sequencing Project; Quinlan AR, Nickerson DA, Eichler EE. Krumm N, et al. Genome Res. 2012 Aug;22(8):1525-32. doi: 10.1101/gr.138115.112. Epub 2012 May 14. Genome Res. 2012. PMID: 22585873 Free PMC article.
226 results