Associated Papers
Identification of Neurotransmission and Synaptic Biological Processes Disrupted in Autism Spectrum Disorder Using Interaction Networks and Community Detection Analysis.
Vilela J et al.
Biomedicines, 2023
38001974 (PubMed )
Supplement: biomedicines-11-02971-s001.zip › Supplementary_Table_S5.xlsx › S5
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
Marcogliese PC et al.
Cell Reports, 2022
35294868 (PubMed )
Supplement: NIHMS1789669-supplement-4.xlsx › S3
Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics.
Nguyen TA et al.
Frontiers in Synaptic Neuroscience, 2020
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.
Quartier A et al.
Human Mutation, 2019
De novo genic mutations among a Chinese autism spectrum disorder cohort.
Wang T et al.
Nature Communications, 2016
27824329 (PubMed )
Supplement: ncomms13316-s7.xlsx › Supplementary_Data_6
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