Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH (2008). Association of common variants in the Joubert syndrome gene (AHI1) with autism. Human Molecular Genetics. 17(24): 3887-96.

Ratan RR, Siddiq A, Aminova L, Langley B, McConoughey S, Karpisheva K, Lee HH, Carmichael T, Kornblum H, Coppola G, Geschwind DH, Hoke A, Smirnova N, Rink C, Roy S, Sen C, Beattie MS, Hart RP, Grumet M, Sun D, Freeman RS, Semenza GL, Gazaryan I (2008). Small molecule activation of adaptive gene expression: Tilorone or its analogs are novel potent activators of hypoxia inducible factor-1 that provide prophylaxis against stroke and spinal cord injury. Annals of the New York Academy of Sciences. 1147: 383-94.

Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE (2008). A functional genetic link between distinct developmental language disorders. New England Journal of Medicine. 359(22): 2337-45.

Carmichael ST, Vespa PM, Saver JL, Coppola G, Geschwind DH, Starkman S, Miller CM, Kidwell CS, Liebeskind DS, Martin NA (2008). Genomic profiles of damage and protection in human intracerebral hemorrhage. Journal of Cerebral Blood Flow and Metabolism. 28(11):1860-75.

Oldham MC, Konopka G, Iwamoto K, Langfelder P, Kato T, Horvath S, Geschwind DH (2008). Functional organization of the transcriptome in human brain. Nature Neuroscience. 11(11): 1271-82.

Schaffer B, Bertram L, Miller BL, Mullin K, Weintraub S, Johnson N, Bigio EH, Mesulam M-M, Wiedau-Pazos M, Jackson GR, Cummings JL, Cantor RM, Tanzi RE, Geschwind DH (2008). Association of GSK3B with Alzheimer’s disease and frontotemporal dementia. Archives of Neurology. 65(10): 1368-74.

Miller JE, Spiteri E, Condro MC, Dosumu-Johnson RT, Geschwind DH, White SA (2008). Birdsong decreases protein levels of FoxP2, a molecule required for human speech. Journal of Neurophysiology. 100(4): 2015-25.

Liu XQ, Paterson AD, Szatmari P, Bailey AJ,Baird G, Bartlett C, Battaglia A, Berney T, Betancur C, Bölte S, Bolton PF, Brian J, Bryson SE, Buxbaum JD, Cantor RM, Cook EH, Coon H, Corsello C, Cuccaro ML, Davis KL, Dawson G, de Jonge M, Devlin B, Ennis S, Estes A, Fombonne E, Freitag CM, Gallagher L, Geschwind DH, Gilbert J, Gill M, Gillberg C, Goldberg J, Green A, Green J, Guter SJ, Haines JL, Hallmayer J, Hus V, Klauck SM, Korvatska O, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lotspeich L, Maestrini E, Mahoney W, Mantoulan C, McConachie H, McDougle CJ, McMahon WM, Miller J, Monaco AP, Munson J, Nurnberger JI Jr, Oliveira G, Papanikolaou K, Parr JR, Pericak-Vance MA, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Renshaw K, Roberts W, Roge B, Rutter ML, Salt J, Schellenberg GD, Scherer SW, Sheffield VC, Sutcliffe JS, Thompson AP, Tsiantis J, Van Engeland H, Vicente AM, Vieland VJ, Volkmar F, Wallace S, Wassink TH, Wijsman EM, Wittemeyer K, Zwaigenbaum L (2008). Genome-wide linkage analysis of quantitative and categorical autism subphenotypes. Biological Psychiatry. 64(7): 561-70.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind DH, Bolton P, Craig IW (2008). Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism. Genes Brain and Behavior. 7(7): 754-60.

Thomas EA, Coppola G, Desplats PA, Tang B, Soragni E, Burnett R, Gao F, Fitzgerald KM, Borok JF, Herman D, Geschwind DH, Gottesfeld JM (2008). The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington’s disease transgenic mice. Proceedings of the National Academy of Sciences USA. 105(40): 15564-9.