Associated Papers
A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.
Hara T et al.
Psychiatry and Clinical Neurosciences, 2024
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
Kummeling J et al.
Molecular Psychiatry, 2021
SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders.
Wang S et al.
Frontiers in Molecular Neuroscience, 2021
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