Whitman MC, Andrews C, Chan WM, et al. Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development. Am J Med Genet A. 2016;170A(2):297-305. doi:10.1002/ajmg.a.37362
Publications
T Y Chan C, Lee JW, Cameron E, Bashor CJ, Collins JJ. ’Deadman’ and ’Passcode’ microbial kill switches for bacterial containment. Nat Chem Biol. 2016;12(2):82-6. doi:10.1038/nchembio.1979
Doyle SK, Pop MS, Evans HL, Koehler AN. Advances in discovering small molecules to probe protein function in a systems context. Curr Opin Chem Biol. 2016;30:28-36. doi:10.1016/j.cbpa.2015.10.032
Lu C, Chen Q, Zhou T, et al. Micro-electrode array recordings reveal reductions in both excitation and inhibition in cultured cortical neuron networks lacking Shank3. Mol Psychiatry. 2016;21(2):159-68. doi:10.1038/mp.2015.173
Xia Z, White CC, Owen EK, et al. Genes and Environment in Multiple Sclerosis project: A platform to investigate multiple sclerosis risk. Ann Neurol. 2016;79(2):178-89. doi:10.1002/ana.24560
Spencer NY, Yan Z, Cong L, Zhang Y, Engelhardt JF, Stanton RC. Definitive localization of intracellular proteins: Novel approach using CRISPR-Cas9 genome editing, with glucose 6-phosphate dehydrogenase as a model. Anal Biochem. 2016;494:55-67. doi:10.1016/j.ab.2015.11.002
Hivert MF, Christophi CA, Franks PW, et al. Lifestyle and Metformin Ameliorate Insulin Sensitivity Independently of the Genetic Burden of Established Insulin Resistance Variants in Diabetes Prevention Program Participants. Diabetes. 2016;65(2):520-6. doi:10.2337/db15-0950
Sumner JA, Duncan L, Ratanatharathorn A, Roberts AL, Koenen KC. PTSD has shared polygenic contributions with bipolar disorder and schizophrenia in women. Psychol Med. 2016;46(3):669-71. doi:10.1017/S0033291715002135
Spencer SJ, Tamminen MV, Preheim SP, et al. Massively parallel sequencing of single cells by epicPCR links functional genes with phylogenetic markers. ISME J. 2016;10(2):427-36. doi:10.1038/ismej.2015.124
Mohnke S, Erk S, Schnell K, et al. Theory of mind network activity is altered in subjects with familial liability for schizophrenia. Soc Cogn Affect Neurosci. 2016;11(2):299-307. doi:10.1093/scan/nsv111