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.

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.)

Wang S, Chandler-Militello D, Lu G, Roy N, Auvergne R, Zielke A, Stanwood N, Geschwind DH, Coppola G, Nicolis S, Sim F, Goldman S (2010). Prospective identification, isolation, and profiling of a telomerase expressing subpopulation of human neural stem cells, using sox2 enhancer-directed FACS. Journal of Neuroscience. 30(44): 14635-48.

Lajonchere CM, Brown WT, Bucan M, Cantor R, Constantino J, Geschwind DH, Gilliam TC, Herbert M, Ledbetter DH, Miller J, Nelson SF, Samango-Sprouse C, Schellenberg GD, Shestack J, Spence S, State M, Tanzi RE, Deutsch C, Hallmeyer J (2010). Changing the landscape of autism research: The Autism Genetic Resource Exchange. Neuron. 68(2): 187-91.

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J (2010). A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19(20): 4072-82.

Mumford JA, Horvath S, Oldham MC, Langfelder P, Geschwind DH, Poldrack RA (2010). Detecting network modules in fMRI time series: A weighted network analysis approach. Neuroimage. 52(4): 1465-76.

Strom SP, Stone JL, Ten Bosch JR, Merriman B, Cantor RM, Geschwind DH, Nelson SF (2010). High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. Molecular Psychiatry. 15(10): 996-1005.

Lu PH, Thompson PM, Leow A, Lee GJ, Yanovsky I, Parikshak N, Khoo T, Wu S, Geschwind DH, Bartzokis G (2010). Apolipoprotein E genotype is associated with temporal and hippocampal atrophy rates in healthy elderly adults: A tensor-based morphometry study. Journal of Alzheimer’s Disease. 23(3): 433-42.