Comer JD, Pan FCheng, Willet SG, Haldipur P, Millen KJ, Wright CVE, Kaltschmidt JA.  2015.  Sensory and spinal inhibitory dorsal midline crossing is independent of Robo3.. Front Neural Circuits. 9:36.

Jones M, Osawa G, Regal JA, Weinberg DN, Taggart J, Kocak H, Friedman A, Ferguson DO, Keegan CE, Maillard I.  2014.  Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation.. J Clin Invest. 124(1):353-66.

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.

McFadden DG, Vernon A, Santiago PM, Martinez-McFaline R, Bhutkar A, Crowley DM, McMahon M, Sadow PM, Jacks T.  2014.  p53 constrains progression to anaplastic thyroid carcinoma in a Braf-mutant mouse model of papillary thyroid cancer.. Proc Natl Acad Sci U S A. 111(16):E1600-9.

Ebert DH, Gabel HW, Robinson ND, Kastan NR, Hu LS, Cohen S, Navarro AJ, Lyst MJ, Ekiert R, Bird AP et al..  2013.  Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR.. Nature. 499(7458):341-5.

Wise A, Schatoff E, Flores J, Hua S-Y, Ueda A, Wu C-F, Venkatesh T.  2013.  Drosophila-Cdh1 (Rap/Fzr) a regulatory subunit of APC/C is required for synaptic morphology, synaptic transmission and locomotion.. Int J Dev Neurosci. 31(7):624-33.

Lyst MJ, Ekiert R, Ebert DH, Merusi C, Nowak J, Selfridge J, Guy J, Kastan NR, Robinson ND, Alves Fde Lima et al..  2013.  Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.. Nat Neurosci. 16(7):898-902.

Chung YRock, Schatoff E, Abdel-Wahab O.  2012.  Epigenetic alterations in hematopoietic malignancies.. Int J Hematol. 96(4):413-27.

Oikonomou G, Perens EA, Lu Y, Shaham S.  2012.  Some, but not all, retromer components promote morphogenesis of C. elegans sensory compartments.. Dev Biol. 362(1):42-9.

Worthey EA, Mayer AN, Syverson GD, Helbling D, Bonacci BB, Decker B, Serpe JM, Dasu T, Tschannen MR, Veith RL et al..  2011.  Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.. Genet Med. 13(3):255-62.

Furlow PW, Percy MJ, Sutherland S, Bierl C, McMullin MFrances, Master SR, Lappin TRJ, Lee FS.  2009.  Erythrocytosis-associated HIF-2alpha mutations demonstrate a critical role for residues C-terminal to the hydroxylacceptor proline.. J Biol Chem. 284(14):9050-8.

Eakin CM, Knight JD, Morgan CJ, Gelfand MA, Miranker AD.  2002.  Formation of a copper specific binding site in non-native states of beta-2-microglobulin.. Biochemistry. 41(34):10646-56.