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American Journal of Human Genetics|August 30, 2016
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex FamiliesVirpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, et al.Nature Communications|June 26, 2021
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disordersBenxia Hu, Hyejung Won, Won Mah, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autismChrista Lese Martin, Jacqueline A Duvall, Yesim Ilkin, et al.Neuron|December 12, 2023
Genome-wide study reveals novel roles for formin-2 in axon regeneration as a microtubule dynamics regulator and therapeutic target for nerve repairNgan Pan Bennett Au, Tan Wu, Xinyu Chen, et al.JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.Science Translational Medicine|January 23, 2015
Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autismOlga Peñagarikano, María T Lázaro, Xiao-Hong Lu, et al.Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.Nucleic Acids Research|March 14, 2015
Genome engineering of isogenic human ES cells to model autism disordersRefugio A Martinez, Jason L Stein, Anne-Rachel F Krostag, et al.Pageof 65