|?|| (A;A) (A;G) (G;G) ||28|
] White matter abnormalities in 22q11.2 deletion syndrome: Preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis
[PMID 19052207] Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
|| [PMID 23251661]
|| Obesity-related traits
|| Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
| Risk Allele
| Odds Ratio
|| .04 [NR] pg/mL increase
[PMID 28139055] Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.