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Proceedings of the National Academy of Sciences of the United States of America|October 21, 2006
A genetic variant that disrupts MET transcription is associated with autismDaniel B Campbell, James S Sutcliffe, Philip J Ebert, et al.Nature Neuroscience|November 9, 2010
An age-related sprouting transcriptome provides molecular control of axonal sprouting after strokeSonglin Li, Justine J Overman, Diana Katsman, et al.Molecular Autism|August 4, 2021
Abnormal sleep physiology in children with 15q11.2-13.1 duplication (Dup15q) syndromeVidya Saravanapandian, Divya Nadkarni, Sheng-Hsiou Hsu, et al.Proceedings of the National Academy of Sciences of the United States of America|December 24, 2005
PTEN negatively regulates neural stem cell self-renewal by modulating G0-G1 cell cycle entryMatthias Groszer, Rebecca Erickson, Deirdre D Scripture-Adams, et al.Neuron|August 28, 2012
Human-specific transcriptional networks in the brainGenevieve Konopka, Tara Friedrich, Jeremy Davis-Turak, et al.Journal of Autism and Developmental Disorders|March 15, 2017
Association of Rigid-Compulsive Behavior with Functional Constipation in Autism Spectrum DisorderSarah Marler, Bradley J Ferguson, Evon Batey Lee, et al.Nature|May 20, 2026
Feature-specific threat coding in lateral septum guides defensive actionDionnet Leandro Bhatti Mazo, Marc Z C Berger, Amanda Loren Pasqualini, et al.Research Square|June 30, 2025
Feature-specific threat coding in lateral septum guides defensive actionDionnet Leandro Bhatti Mazo, Amanda Loren Pasqualini, Sherry Jingjing Wu, et al.Neurocase|August 26, 2015
Early-onset Alzheimer's disease versus frontotemporal dementia: resolution with genetic diagnoses?Sharon J Sha, Anna M Khazenzon, Pia M Ghosh, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2012
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxiaBrent L Fogel, Ji Yong Lee, Jessica Lane, et al.Pageof 65