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In vivo modeling of the morbid human genome using Danio rerio.
J Vis Exp. 2013 Aug 24;(78):e50338. doi: 10.3791/50338.
J Vis Exp. 2013.
PMID: 23995499
Free PMC article.
Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network.
Chassaing N, Davis EE, McKnight KL, Niederriter AR, Causse A, David V, Desmaison A, Lamarre S, Vincent-Delorme C, Pasquier L, Coubes C, Lacombe D, Rossi M, Dufier JL, Dollfus H, Kaplan J, Katsanis N, Etchevers HC, Faguer S, Calvas P.
Chassaing N, et al. Among authors: niederriter ar.
Genome Res. 2016 Apr;26(4):474-85. doi: 10.1101/gr.196048.115. Epub 2016 Feb 18.
Genome Res. 2016.
PMID: 26893459
Free PMC article.
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Super Enhancers in Cancers, Complex Disease, and Developmental Disorders.
Niederriter AR, Varshney A, Parker SC, Martin DM.
Niederriter AR, et al.
Genes (Basel). 2015 Nov 9;6(4):1183-200. doi: 10.3390/genes6041183.
Genes (Basel). 2015.
PMID: 26569311
Free PMC article.
Review.
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Identification of cis-suppression of human disease mutations by comparative genomics.
Jordan DM, Frangakis SG, Golzio C, Cassa CA, Kurtzberg J; Task Force for Neonatal Genomics; Davis EE, Sunyaev SR, Katsanis N.
Jordan DM, et al.
Nature. 2015 Aug 13;524(7564):225-9. doi: 10.1038/nature14497. Epub 2015 Jun 29.
Nature. 2015.
PMID: 26123021
Free PMC article.
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