Burkett ZA, Day NF, Penagarikano O, Geschwind DH, White SA (2015). VoICE: A semi-automated pipeline for standardizing vocal analysis across models. Science Reports. 5:10237.

Paşca AM, Sloan SA, Clarke LE, Tian Y, Makinson CD, Huber N, Kim CH, Park JY, O’Rourke NA, Nguyen KD, Smith SJ, Huguenard JR, Geschwind DH, Barres BA, Pa?ca SP (2015). Functional cortical neurons and astrocytes from human pluripotent stem cells in 3D culture. Nature Methods. 12(7):671-8.

Werling DM, Geschwind DH (2015). Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins. Molecular Autism. 6: 27.

Bakken TE, Miller JA, Luo R, Bernard A, Bennett JL, Lee CK, Bertagnolli D, Parikshak NN, Smith KA, Sunkin SM, Amaral DG, Geschwind DH, Lein ES (2015). Spatiotemporal dynamics of the postnatal developing primate brain transcriptome. Human Molecular Genetics. 24(15): 4327-39.

Gdalyahu A, Lazaro M, Penagarikano O, Golshani P, Trachtenberg JT, Gescwind DH (2015). The autism-related protein Contactin-Associated Protein-Like 2 (CNTNAP2) stabilizes new spines: An in vivo mouse study. Public Library of Science ONE. 10(5): e0125633. **Correction May 29, 2015 10(5): e0129638.

Legati A, Giovannini D, Nicolas G, López-Sánchez U, Quintáns B, Oliveira J, Sears R, Ramos EM, Spiteri E, Sobrido MJ, Carracedo A, Castro-Fernández C, Cubizolle S, Fogel BL, Goizet C, Jen JC, Kirdlarp S, Lang AE, Miedzybrodzka Z, Mitarnun W, Paucar M, Paulson H, Pariente J, Richard AC, Salins NS, Simpson SA, Striano P, Svenningsson P, Tison F, Unni VK, Vanakker O, Wessels MW, Wetchaphanphesat S, Yang M, Boller F, Campion D, Hannequin D, Sitbon M, Geschwind DH, Battini JL, Coppola G. (2015) Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export. Nature Genetics. 47(6): 579-581.

Yu, H, Su Y, Shin J, Zhong C, Guo JU, Weng YL, Gao F, Geschwind DH, Coppola G, Ming GL, Song H (2015). Tet3 regulates synaptic transmission and homeostatic plasticity via DNA oxidation and repair. Nature Neuroscience. 18(6): 836-43.

Raposo M, Bettencourt C, Maciel P, Gao F, Ramos A, Kazachkova N, Vasconcelos J, Kay T, Rodrigues AJ, Bettencourt B, Bruges-Armas J, Geschwind DH, Coppola G, Lima M (2015). Novel candidate blood-based transcriptional biomarkers of Machado-Joseph disease. Movement Disorders. 30(7):968-75.

Chen JA, Wang Q, Davis-Turak J, Li Y, Karydas A, Hsu S, Sears R, Chatzopoulou D, Huang A, Wojta K, Klein E, Lee J, Beekly D, Boxer A, Faber K, Haase C, Miller J, Poon W, Rosen A, Rosen H, Sapozhnikova A, Shapira J, Varpetian A, Foroud T, Levenson R, Levey A, Kukull W, Mendez M, Ringman J, Chui H, Cotman C, DeCarli C, Miller B, Geschwind D, Coppola G (2015). A multiancestral genome-wide exome array study of Alzheimer’s disease, frontotemporal dementia, and progressive supranuclear palsy. JAMA Neurology. 72(4):414-22.

Winden K, Bragin A, Engel J, Geschwind DH (2015). Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy. Neurobiology of Disease. 78: 35-44.