SnapShot: Reporting practices for publishing results with human PSCs and tissue stem cells.
Research Articles
Peripheral temperature dysregulation associated with functionally altered NaV1.8 channels.
Caregiver-reported dental manifestations in individuals with genetic neurodevelopmental disorders.
Large-scale whole genome sequence analysis of >22,000 subjects provides no evidence of FMR1 premutation allele involvement in autism spectrum disorder.
The emotion dysregulation inventory-young child: Psychometric properties and item response theory calibration in 2- to 5-year-olds.
Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice.
Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-function.
The phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.
Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.
Repetitive and restricted behaviors and interests in autism spectrum disorder: relation to individual characteristics and mental health problems.
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