Parikshak NN, Swarup V, Belgard TG, Irimia M, Ramaswami G, Gandal MJ, Hartl C, Leppa V, Ubieta LT, Huang J, Lowe JK, Blencowe BJ, Horvath S, Geschwind DH (2016). Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism. Nature. 540(7633): 423-427.

Lee SE, Sias AC, Mandelli ML, Brown JA, Brown AB, Khazenzon AM, Vidovszky AA, Zanto TP, Karydas AM, Pribadi M, Dokuru D, Coppola G, Geschwind DH, Rademakers R, Gorno-Tempini ML, Rosen HJ, Miller BL, Seeley WW (2017). Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers. Neuroimage: Clinical. 14:286-297.

Sun W, Poschmann J, Cruz-Herrera Del Rosario R, Parikshak NN, Hajan HS, Kumar V, Ramasamy R, Belgard TG, Elanggovan B, Wong CC, Mill J, Geschwind DH, Prabhakar S (2016). Histone Acetylome-wide Association Study of Autism Spectrum Disorder. Cell. 167(5): 1385-1397.e11.

Sharon G, Sampson TR, Geschwind DH, Mazmanian SK (2016). The Central Nervous System and the Gut Microbiome. Cell. 167(4): 915-932.

Miller ZA, Sturm VE, Camsari GB, Karydas A, Yokoyama JS, Grinberg LT, Boxer AL, Rosen HJ, Rankin KP, Gorno-Tempini ML, Coppola G, Geschwind DH, Rademakers R, Seeley WW, Graff-Radford NR, Miller BL (2016). Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture. Neurology: Neuroimmunology & Neuroinflammation. 3(6): e301.

Won H, de la Torre-Ubieta L, Stein JL, Parikshak NN, Huang J, Opland CK, Gandal MJ, Sutton GJ, Hormozdiari F, Lu D, Lee C, Eskin E, Voineagu I, Ernst J, Geschwind DH (2016). Chromosome conformation elucidates regulatory relationships in developing human brain. Nature. 538(7626): 523-527.

Gandal MJ, Leppa V, Won H, Parikshak NN, Geschwind DH (2016). The road to precision psychiatry: translating genetics into disease mechanisms. Nature Neuroscience. 19(11): 1397-1407.

Vatsavayai SC, Yoon SJ, Gardner RC, Gendron TF, Vargas JN, Trujillo A, Pribadi M, Phillips JJ, Gaus SE, Hixson JD, Garcia PA, Rabinovici GD, Coppola G, Geschwind DH, Petrucelli L, Miller BL, Seeley WW (2016). Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementia. Brain. 139(Pt 12): 3202-3216

Silva SM, Cheng C, Mair W, Almeida S, Fong H, Biswas HU, Zhang Z, Huang Y, Temple S, Coppola, G, Geschwind DH, Karydas A, Miller BL, Kosik KS, Gao FB, Steen JA, & Haggerty SJ (2016). Human iPSC-derived neuronal model of tau-A152T frontotemporal dementia reveals tau-mediated mechanisms of neuronal vulnerability. Stem Cell Reports. Online access Sep 1, 2016.

Ranasinghe KG, Rankin KP, Pressman PS, Perry DC, Lobach IV, Seeley WW, Coppola G, Karydas AM, Grinberg LT, Shany-Ur T, Lee SE, Rabinovici GD, Rosen HJ, Gorno-Tempini ML, Boxer AL, Miller ZA, Chiong W, DeMay M, Kramer JH, Possin KL, Sturm VE, Bettcher BM, Neylan M, Zackey DD, Nguyen LA, Ketelle R, Block N, Wu TQ, Dallich A, Russek N, Caplan A, Geschwind DH, Vossel KA, Miller BL (2016). Distinct Subtypes of Behavioral Variant Frontotemporal Dementia Based on Patterns of Network Degeneration. JAMA Neurology. 73(9): 1078-88.