Publications

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Van Schil, K., Naessens, S., Van de Sompele, S., Carron, M., Aslanidis, A., Van Cauwenbergh, C., Kathrin Mayer, A., Van Heetvelde, M., Bauwens, M., Verdin, H., Coppieters, F., Greenberg, M.E., Yang, M.G., Karlstetter, M., Langmann, T., De Preter, K., Kohl, S.,Cherry, T.J., Leroy, B.P., De Baere, E. Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations. Genet Med. 2017 Jul 27. PMID:28749477


Andzelm, M.M.*, Cherry, T.J.*, Harmin, D.A., Boeke, A.C., Lee, C., Hemberg, M., Pawlyk, B., Malik, A.N., Flavell, S.W., Sandberg, M.A., Raviola, E., Greenberg, M.E. (2015) MEF2D Drives Photoreceptor Development through a Genome-wide Competition for Tissue-Specific Enhancers. Neuron. 86, 1-17. * equal contribution.


Cherry, T.J., Wang, S., Bormuth, I., Schwab, M., Olson, J., Cepko, C.L. (2011) NeuroD factors regulate cell fate and neurite stratifcation in the developing retina. J. Neurosci. 31(20), 7365-7379.


Cherry, T.J., Trimarchi J.M., Stadler M.B., Cepko C.L. (2009) Development and diversification of retinal amacrine interneurons at single cell resolution. Proc Natl Acad Sci USA 106(23), 9495-9500.


Sun, T., Patoine, C., Abu-Khalil, A., Visvader, J., Sum, E., Cherry, T. J., Orkin, S. H., Geschwind, D. H., and Walsh, C. A. (2005). Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Science 308, 1794-1798.


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