rs1144333 - MSH4
Magnitude 2.8 · 1 study on file
Reported associations
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New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. - American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2020) · Alemany S, Ribasés M, Vilor-Tejedor N, Bustamante M, Sánchez-Mora C, Bosch R, Richarte V, Cormand B, Casas M, Ramos-Quiroga JA, Sunyer J · PubMed 26174813
Attention deficit is one of the core symptoms of the attention-deficit/hyperactivity disorder (ADHD). However, the specific genetic variants that may be associated with attention function in adult ADHD remain largely unknown. The present study aimed to identifying SNPs associated with attention function in adult ADHD and tested whether these associations were enriched for specific biological pathways. Commissions, hit-reaction time (HRT), the standard error of HRT (HRTSE), and intraindividual coefficient variability (ICV) of the Conners Continuous Performance Test (CPT-II) were assessed in 479 unmedicated adult ADHD individuals. A Genome-Wide Association Study (GWAS) was conducted for each outcome and, subsequently, gene set enrichment analyses were performed. Although no SNPs reached geno
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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ADHD assessment or attention screening Moderate
Variant associates with attention function and ADHD in genetic studies; affects brain MSH4 expression
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