Publications

2012-2014

Transcriptional architecture of the primate neocortex

Bernard A, Lubbers LS, Tanis KQ, Luo R, Podtelezhnikov AA, Finney EM, McWhorter M M.E., Serikawa K, Lemon T, Morgan R, Copeland C, Smith K, Cullen V, Davis-Turak J, Lee C-H, Sunkin S, Loboda AP, Levine DM, Stone DJ, Hawrylycz M, Roberts CJ, Jones AR, Geschwind DH, Lein E (2012). Transcriptional architecture of the primate neocortex. Neuron. 73(6): 1083-1099.

Autism recurrence in half siblings: Strong support for genetic mechanisms of transmission in ASD

Constantino JN, Todorov A, Hilton C, Law P, Zhang Y, Molloy E, Fitzgerald R, Geschwind DH (2012). Autism recurrence in half siblings: Strong support for genetic mechanisms of transmission in ASD. Molecular Psychiatry. (18)2: 137-8.

Increased fMRI signal with age in familial Alzheimer’s disease mutation carriers

Braskie MN, Medina LD, Rodriguez-Agudelo Y, Geschwind DH, Macias-Islas MA, Cummings JL, Bookheimer SY, Ringman JM (2012). Increased fMRI signal with age in familial Alzheimer’s disease mutation carriers. Neurobiology of Aging. 33(2): 424e11-21.

Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia

Fogel BL, Lee JY, Lane J, Wahnich A, Chan S, Huang A, Osborn GE, Klein E, Mamah C, Perlman S, Geschwind DH, Coppola G (2012). Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia. Movement Disorders. 27(3): 442-6.

Proteomic changes in cerebrospinal fluid of presymptomatic and affected persons carrying familial Alzheimer disease mutations

Ringman JM, Schulman H, Becker C, Jones T, Bai Y, Immermann F, Cole G, Sokolow S, Gylys K, Geschwind DH, Cummings JL, Wan HI (2012). Proteomic changes in cerebrospinal fluid of presymptomatic and affected persons carrying familial Alzheimer disease mutations. Archives of Neurology. 69(1): 96-104.

Modeling the functional genomics of autism using human neurons

Konopka G, Wexler E, Rosen E, Mukamel Z, Osborn GE, Chen L, Lu D, Gao F, Gao K, Lowe JK, Geschwind DH (2012). Modeling the functional genomics of autism using human neurons. Molecular Psychiatry. 17(2): 202-14.

Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice

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.