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1. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

2. Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

3. CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

4. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

5. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

7. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

9. Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management.

10. Mutations in the PH Domain of <italic>DNM1</italic> are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities.

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