Associated Papers
Genetic Diversity in Schizophrenia: Developmental Implications of Ultra-Rare, Protein-Truncating Mutations.
Clarin JD et al.
Genes, 2024
SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases.
Colijn MA et al.
Progress in Neuro-psychopharmacology & Biological Psychiatry, 2024
Case report: De novo variant of SETD1A causes infantile epileptic spasms syndrome.
Lan M et al.
Frontiers in Neurology, 2023
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Weerts MJA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders.
Wang S et al.
Frontiers in Molecular Neuroscience, 2021
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy.
Yu X et al.
Neuroscience Bulletin, 2019
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