Iwamoto K, Bundo M, Ueda J, Oldham MC, Ukai W, Hashimoto E, Saito T, Geschwind DH, Kato T (2011). Neurons show distinctive DNA methylation profile and higher interindividual variations compared to non-neurons. Genome Research. 21(5): 688-96.
Publications
Ringman JM, Medina LD, Braskie M, Rodriguez-Agudelo Y, Geschwind DH, Macias-Islas MA, Cummings JL, Bookheimer S (2011). Effects of risk genes on BOLD activation in presymptomatic carriers of familial Alzheimer’s disease mutations during a novelty-encoding task. Cerebral Cortex. 21(4): 877-83.
Thomas EA, Coppola G, Tang B, Kuhn A, Ho Kim S, Geschwind DH, Brown TB, Luthi-Carter R, Ehrlich ME (2011). In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons. Human Molecular Genetics. 20(6): 1049-60.
Finch N, Carrasquillo MM, Baker M, Rutherford NJ, Coppola G, DeJesus-Hernandez M, Crook R, Hunter T, Ghidoni R, Benussi L, Crook J, Finger E, Hantanpaa KJ, Karydas AM, Sengdy P, Gonzalez J, Seeley WW, Johnson N, Beach TG, Mesulam M, Forloni G, Kertesz A, Knopman DS, Uitti R, White CL, Caselli R, Lippa C, Bigio EH, Wszolek ZK, Binetti G, Mackenzie IR, Miller BL, Boeve BF, Younkin SG, Dickson DW, Graff-Radford N, Geschwind DH, Rademakers R (2011). TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers. Neurology. 76(5): 467-74.
Marques F, Sousa JC, Coppola G, Gao FY, Puga R, Brentani H, Geschwind DH, Sousa N, Correia-Neves M, Palha JA (2011). Transcriptome signature of the adult mouse choroid plexus. Fluids and Barriers of the CNS. 8(1): 10.
Newbern JM, Li X, Shoemaker SE, Zhou J, Zhong J, Wu Y, Bonder D, Hollenback S, Coppola G, Geschwind DH, Landreth GE, Snider WD (2011). Specific functions for ERK/MAPK signaling during PNS development. Neuron. 69(1): 91-105.
Li S, Overman JJ, Katsman D, Donnelly CJ, Twiss JL, Giger RJ, Coppola G, Geschwind DH, Carmichael ST (2010). An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke. Nature Neuroscience. 13(12): 1496-504.
Ehninger D, Sano Y, de Vries PJ, Dies K, Franz D, Geschwind DH, Kaur M, Lee YS, Li W, Lowe JK, Nakagawa JA, Sahin M, Smith K, Whittemore V, Silva AJ (2010). Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice. Molecular Psychiatry. 17(1):62-70.
Ehninger D, Sano Y, de Vries PJ, Dies K, Franz D, Geschwind DH, Kaur M, Lee YS, Li W, Lowe K, Nakagawa JA, Sahin M, Smith K, Whittemore V, Silva AJ (2012). Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice. Molecular Psychiatry. 17(1): 62-70.
Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford J, Poldrack RA, Dapretto M, Geschwind DH*, Bookheimer SY* (2010). Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Science Translational Medicine. 2(56): 56ra80. (*Senior authors, co-supervised this study.)