Journal of Neurodevelopmental Disorders
A multimeasure approach to investigating affective appraisal of social information in Williams syndrome
Approach to epigenetic analysis in language disorders
Contributions of phonological and verbal working memory to language development in adolescents with fragile X syndrome
Dissection of genetic associations with language-related traits in population-based cohorts
Epigenetic modifications may play a role in the developmental consequences of early life events
Genetic approaches to understanding the causes of stuttering
Genetics and language: a neurobiological perspective on the missing link (-ing hypotheses)
Language development after cochlear implantation: an epigenetic model
Prenatal exposure to ß2-adrenergic receptor agonists and risk of autism spectrum disorders
Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader–Willi syndrome
Turner syndrome and sexual differentiation of the brain: implications for understanding male-biased neurodevelopmental disorders
A new synaptic player leading to autism risk: Met receptor tyrosine kinase
DNA methylation, the early-life social environment and behavioral disorders
FMR1 premutation and full mutation molecular mechanisms related to autism
Language and sociability: insights from Williams syndrome
Prader–Willi syndrome and autism spectrum disorders: an evolving story
Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders
Role of MeCP2, DNA methylation, and HDACs in regulating synapse function
Targeted treatments for fragile X syndrome
The neurobiology of mouse models syntenic to human chromosome 15q
Treatment effects of stimulant medication in young boys with fragile X syndrome