Prader–Willi syndrome (PWS) and Angelman syndrome (AS) are oppositely imprinted
autism-spectrum disorders with known genetic bases, but complex epigenetic mechanisms …

Prader–Willi syndrome (PWS), a genetic disorder of obesity, intellectual disability and sleep
abnormalities, is caused by loss of non-coding RNAs on paternal chromosome 15q11-q13. …

Rare variants enriched for functions in chromatin regulation and neuronal synapses have
been linked to autism. How chromatin and DNA methylation interact with environmental …

DNA methylation acts at the interface of genetic and environmental factors relevant for autism
spectrum disorder (ASD). Placenta, normally discarded at birth, is a potentially rich source …

Prader-Willi syndrome (PWS) is an imprinted neurodevelopmental disease caused by a loss
of paternal genes on chromosome 15q11-q13. It is characterized by cognitive impairments, …

Rhythmic oscillations of physiological processes depend on integrating the circadian clock
and diurnal environment. DNA methylation is epigenetically responsive to daily rhythms, as a …

Neurological disorders encompass an extremely broad range of conditions, including those
that present early in development and those that progress slowly or manifest with advanced …

Neural tube defects (NTDs) is a general term for central nervous system malformations
secondary to a failure of closure or development of the neural tube. The resulting pathologies …

Augmented maternal care during the first postnatal week promotes life-long stress resilience
and improved memory compared with the outcome of routine rearing conditions. Recent …

Prader–Willi syndrome (PWS), an imprinted neurodevelopmental disorder characterized by
metabolic, sleep and neuropsychiatric features, is caused by the loss of paternal SNORD116…