Paquet D, Kwart D, Chen A, Sproul A, Jacob S, Teo S, Olsen KMoore, Gregg A, Noggle S, Tessier-Lavigne M.  2016.  Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9.. Nature. 533(7601):125-9.

Heath JL, Weiss JM, Lavau CP, Wechsler DS.  2014.  Effects of iron depletion on CALM-AF10 leukemias.. Exp Hematol. 42(12):1022-1030.e1.

González F, Zhu Z, Shi Z-D, Lelli K, Verma N, Li QV, Huangfu D.  2014.  An iCRISPR platform for rapid, multiplexable, and inducible genome editing in human pluripotent stem cells.. Cell Stem Cell. 15(2):215-226.

Cederquist GY, Luchniak A, Tischfield MA, Peeva M, Song Y, Menezes MP, Chan W-M, Andrews C, Chew S, Jamieson RV et al..  2012.  An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.. Hum Mol Genet. 21(26):5484-99.

Ozaki Y, Nomura M, Saito J, Luedke CE, Muglia LJ, Matsumoto T, Ogawa S, Ueta Y, Pfaff DW.  2004.  Expression of the arginine vasopressin gene in response to salt loading in oxytocin gene knockout mice.. J Neuroendocrinol. 16(1):39-44.

Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R et al..  2001.  Linkage disequilibrium in the human genome.. Nature. 411(6834):199-204.