Hernandez LM, Krasileva K, Green SA, Sherman LE, Ponting C, McCarron R, Lowe JK, Geschwind DH, Bookheimer SY, Dapretto M (2017). Additive effects of oxytocin receptor gene polymorphisms on reward circuitry in youth with autism. Molecular Psychiatry. 22(8): 1134-1139.

Carter CS, Bearden CE, Bullmore ET, Geschwind DH, Glahn DC, Gur RE, Meyer-Lindenberg A, Weinberger DR (2017). Enhancing the Informativeness and Replicability of Imaging Genomics Studies. Biological Psychiatry. 82(3): 157-164.

Nicolas G, Sanchez-Contreras M, Ramos EM, Lemos RR, Ferreira J, Moura D, Sobrido MJ, Richard AC, Lopez AR, Legati A, Deleuze JF, Boland A, Quenez O, Krystkowiak P, Favrole P, Geschwind DH, Aran A, Segel R, Levy-Lahad E, Dickson DW, Coppola G, Rademakers R, de Oliveira JRM (2017). Brain calcifications and PCDH12 variants. Neurology Genetics. 3(4): e166.

Valera JM, Diaz T, Petty LE, Quintáns B, Yáñez Z, Boerwinkle E, Muzny D, Akhmedov D, Berdeaux R, Sobrido MJ, Gibbs R, Lupski JR, Geschwind DH, Perlman S, Below JE, Fogel BL (2017). Prevalence of spinocerebellar ataxia 36 in a US population. Neurology Genetics. 3(4): e174.

Sims R, van der Lee SJ, Naj AC, …, Geschwind DH, …, Schellenberg GD (2017). Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer’s disease. Nature Genetics. 49(9): 1373-1384.

Singh T, Walters JTR, Johnstone M, Curtis D, Suvisaari J, Torniainen M, Rees E, Iyegbe C, Blackwood D, McIntosh AM, Kirov G, Geschwind D, Murray RM, Di Forti M, Bramon E, Gandal M, Hultman CM, Sklar P; INTERVAL Study; UK10K Consortium, Palotie A, Sullivan PF, O’Donovan MC, Owen MJ, Barrett JC (2017). The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics. 49(8): 1167-1173.

Marchetto MC, Belinson H, Tian Y, Freitas BC, Fu C, Vadodaria K, Beltrao-Braga P, Trujillo CA, Mendes APD, Padmanabhan K, Nunez Y, Ou J, Ghosh H, Wright R, Brennand K, Pierce K, Eichenfield L, Pramparo T, Eyler L, Barnes CC, Courchesne E, Geschwind DH, Gage FH, Wynshaw-Boris A, Muotri AR (2017). Altered proliferation and networks in neural cells derived from idiopathic autistic individuals. Molecular Psychiatry. 22(6): 820-835.

Cantor RM, Navarro L, Won H, Walker RL, Lowe JK, Geschwind DH (2017). ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains. Molecular Psychiatry. Epub May 23, 2017.

Lu AT, Hannon E, Levine ME, Crimmins EM, Lunnon K, Mill J, Geschwind DH, Horvath S (2017). Genetic architecture of epigenetic and neuronal ageing rates in human brain regions. Nature Communications. 8: 15353.

Hinz FI, Geschwind DH (2017). Molecular Genetics of Neurodegenerative Dementias. Cold Spring Harbor Perspectives in Biology. 9(4).