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  1. No Access

    Article

    Abnormal H3K4 enzyme catalytic activity and neuronal morphology caused by ASH1L mutations in individuals with Tourette syndrome

    ASH1L potentially contributes to Tourette syndrome (TS) and other neuropsychiatric disorders, as our previous studies have shown. It regulates essential developmental genes by counteracting polycomb-mediated tran...

    Cheng Zhang, Wenmiao Liu, Lulu Xu, Shiguo Liu… in European Child & Adolescent Psychiatry (2024)

  2. No Access

    Article

    Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases

    Mutations in DUOX2 are the frequent cause of congenital hypothyroidism (CH), a common neonatal metabolic disorder characterized by great phenotypic variability. CH can be traditionally subclassified into two subt...

    Liangshan Li, Wenmiao Liu, Liqin Zhang, Fang Wang, Fengqi Wang, Maosheng Gu… in Endocrine (2021)

  3. No Access

    Article

    Spontaneous hyperactivity in Ash1l mutant mice, a new model for Tourette syndrome

    Shiguo Liu, Miaomiao Tian, Fan He, Jiani Li, Hong **e, Wenmiao Liu… in Molecular Psychiatry (2020)

  4. No Access

    Article

    Mutations in ASH1L confer susceptibility to Tourette syndrome

    Tourette syndrome (TS) is a childhood-onset neuropsychiatric disorder characterized by repetitive motor movements and vocal tics. The clinical manifestations of TS are complex and often overlap with other neur...

    Shiguo Liu, Miaomiao Tian, Fan He, Jiani Li, Hong **e, Wenmiao Liu… in Molecular Psychiatry (2020)