Associated Papers
Abnormal H3K4 enzyme catalytic activity and neuronal morphology caused by ASH1L mutations in individuals with Tourette syndrome.
Zhang C et al.
European Child & Adolescent Psychiatry, 2024
ASH1L may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.
Liu W et al.
Brain and Behavior, 2022
Role of Ash1l in Tourette syndrome and other neurodevelopmental disorders.
Zhang C et al.
Developmental Neurobiology, 2021
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM6_ESM.xlsx › Supplementary_Data_4
Mutations in ASH1L confer susceptibility to Tourette syndrome.
Liu S et al.
Molecular Psychiatry, 2020
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