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Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.Nature Communications|June 26, 2021
Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytesJiwen Li, Lin Pan, William G Pembroke, et al.Human Molecular Genetics|April 25, 2014
Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2Brent L Fogel, Ellen Cho, Amanda Wahnich, et al.Neuron|July 4, 2014
A quantitative framework to evaluate modeling of cortical development by neural stem cellsJason L Stein, Luis de la Torre-Ubieta, Yuan Tian, et al.Environment International|August 18, 2023
Prenatal air pollution, maternal immune activation, and autism spectrum disorderXin Yu, Md Mostafijur Rahman, Sarah A Carter, et al.Proceedings of the National Academy of Sciences of the United States of America|September 2, 2015
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismStanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.Brain : a Journal of Neurology|April 16, 2021
A neurogenetic analysis of female autismAllison Jack, Catherine A W Sullivan, Elizabeth Aylward, et al.Plos Genetics|July 19, 2011
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brainSonja C Vernes, Peter L Oliver, Elizabeth Spiteri, et al.Neuro-Oncology Advances|April 15, 2024
Single-nucleus expression characterization of non-enhancing region of recurrent high-grade gliomaKunal S Patel, Kaleab K Tessema, Riki Kawaguchi, et al.Pageof 65