Gene: NOS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4842
Gene Symbol: NOS1
NOS1 		0.040 GeneticVariation disease BEFREE The aim of this study was to examine the association between rs2199161 and rs478597 polymorphisms at MAP1B and NOS1 genes with verbal working memory in children and adolescents with ADHD. 26233433 2016
Entrez Id: 4842
Gene Symbol: NOS1
NOS1 		0.040 GeneticVariation disease BEFREE The aim of the present study was to examine possible associations between polymorphisms in SNAP25, MAP1B and NOS1 genes and ADHD symptoms in Brazilian samples of children/adolescents and adults with ADHD. 26821215 2016
Entrez Id: 4842
Gene Symbol: NOS1
NOS1 		0.040 Biomarker disease BEFREE The substantial heritability of ADHD is well documented and recent genome-wide analyses for risk genes revealed synaptic adhesion molecules (e.g. latrophilin-3, LPHN3; fibronectin leucine-rich repeat transmembrane protein-3, FLRT3), glutamate receptors (e.g. metabotropic glutamate receptor-5, GRM5) and mediators of intracellular signalling pathways (e.g. nitric oxide synthase-1, NOS1). 22939004 2013
Entrez Id: 4842
Gene Symbol: NOS1
NOS1 		0.040 GeneticVariation disease BEFREE However, independent of disease status, homozygous carriers of the short allele of NOS1, the ADHD risk genotype, demonstrated higher ventral striatal activity than carriers of the other NOS1 VNTR genotypes. 21724667 2011