Prader-Willi syndrome phenotype

Aliases

PWS

Related entities (1)

Mentioned in (20)

Papers in which this entity is mentioned.

• Genome-wide association testing beyond SNPs. (2025)
• Neurodevelopmental Trajectories Following Prenatal Alcohol Exposure. (2021)
• Neurodevelopment in adolescents and adults with fetal alcohol spectrum disorders (FASD): A magnetic resonance region of interest analysis. (2020)
• Hippocampal deficits in neurodevelopmental disorders. (2019)
• Abnormal Eating Behaviors Are Common in Children with Fetal Alcohol Spectrum Disorder. (2016)
• What Happens When Children with Fetal Alcohol Spectrum Disorders Become Adults? (2015)
• Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure. (2014)
• Fetal alcohol spectrum disorders and their transmission through genetic and epigenetic mechanisms. (2014)
• Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. (2013)
• Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
• Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice. (2013)
• DNA methylation program in developing hippocampus and its alteration by alcohol. (2013)
• Recurrent variations in DNA methylation in human pluripotent stem cells and their differentiated derivatives. (2012)
• Pilot study of iPS-derived neural cells to examine biologic effects of alcohol on human neurons in vitro. (2012)
• Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs. (2012)
• The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
• DNA methylation and methyl-CpG binding proteins: developmental requirements and function. (2009)
• Large histone H3 lysine 9 dimethylated chromatin blocks distinguish differentiated from embryonic stem cells. (2009)
• Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. (2005)
• Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. (1998)

Merged raw entities (2)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.