Associated Papers
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.
Yu Y et al.
Human Molecular Genetics, 2014
Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses.
Won H et al.
Frontiers in Molecular Neuroscience, 2013
No association between the WNT2 gene and autistic disorder.
McCoy PA et al.
American Journal of Medical Genetics, 2002
Evidence supporting WNT2 as an autism susceptibility gene.
Wassink TH et al.
American Journal of Medical Genetics, 2001
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