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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.
French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, Waskiewicz AJ, Lehmann OJ. French CR, et al. Among authors: waskiewicz aj. J Clin Invest. 2014 Nov;124(11):4877-81. doi: 10.1172/JCI75109. Epub 2014 Sep 24. J Clin Invest. 2014. PMID: 25250569 Free PMC article.
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ. Chrystal PW, et al. Among authors: waskiewicz aj. Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170. Genes (Basel). 2021. PMID: 33530637 Free PMC article.
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
Ye M, Berry-Wynne KM, Asai-Coakwell M, Sundaresan P, Footz T, French CR, Abitbol M, Fleisch VC, Corbett N, Allison WT, Drummond G, Walter MA, Underhill TM, Waskiewicz AJ, Lehmann OJ. Ye M, et al. Among authors: waskiewicz aj. Hum Mol Genet. 2010 Jan 15;19(2):287-98. doi: 10.1093/hmg/ddp496. Epub 2009 Oct 28. Hum Mol Genet. 2010. PMID: 19864492
GDF6, a novel locus for a spectrum of ocular developmental anomalies.
Asai-Coakwell M, French CR, Berry KM, Ye M, Koss R, Somerville M, Mueller R, van Heyningen V, Waskiewicz AJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: waskiewicz aj. Am J Hum Genet. 2007 Feb;80(2):306-15. doi: 10.1086/511280. Epub 2006 Dec 29. Am J Hum Genet. 2007. PMID: 17236135 Free PMC article.
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies.
Asai-Coakwell M, March L, Dai XH, Duval M, Lopez I, French CR, Famulski J, De Baere E, Francis PJ, Sundaresan P, Sauvé Y, Koenekoop RK, Berry FB, Allison WT, Waskiewicz AJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: waskiewicz aj. Hum Mol Genet. 2013 Apr 1;22(7):1432-42. doi: 10.1093/hmg/dds560. Epub 2013 Jan 9. Hum Mol Genet. 2013. PMID: 23307924
51 results