| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.090 | GeneticVariation | group | BEFREE | The 5-HTTLPR polymorphism of the serotonin transporter gene and child's sex moderate the relationship between disaster-related prenatal maternal stress and autism spectrum disorder traits: The QF2011 Queensland flood study. | 30394245 | 2019 | ||||
|
0.090 | GeneticVariation | group | BEFREE | The influence of 5-HTTLPR transporter genotype on amygdala-subgenual anterior cingulate cortex connectivity in autism spectrum disorder. | 28088648 | 2017 | ||||
|
0.090 | GeneticVariation | group | BEFREE | Association of the FGA and SLC6A4 genes with autistic spectrum disorder in a Korean population. | 24192574 | 2013 | ||||
|
0.090 | GeneticVariation | group | BEFREE | Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder. | 23123360 | 2013 | ||||
|
0.090 | GeneticVariation | group | BEFREE | 5-HTTLPR polymorphism influences prefrontal neurochemical metabolites in autism spectrum disorder. | 20619617 | 2010 | ||||
|
0.090 | GeneticVariation | group | BEFREE | Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. | 17280648 | 2007 | ||||
|
0.090 | GeneticVariation | group | BEFREE | A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder. | 16698432 | 2006 | ||||
|
0.090 | GeneticVariation | group | BEFREE | Genotyping data obtained from the 2 mM magnesium protocol increased the significance of linkage and gave suggestive (P=0.06) association with autism spectrum disorder, whereas the corrected genotypes of 5-HTTLPR provide no linkage information beyond the results we have previously published and no evidence of association with autism spectrum disorder. | 16395127 | 2006 | ||||
|
0.090 | GeneticVariation | group | BEFREE | Dutch patients diagnosed with PDD (N = 125, age range 5-20 years, DSM-IV-TR based criteria, ADI-R and ADOS behavioral assessments) and their parents (N = 230) were genotyped for promoter ins/del (5-HTTLPR) and intron 2 variable number of tandem repeats (VNTR) alleles. | 15635668 | 2005 |