Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 Biomarker group BEFREE Prematurity was independently associated with diagnosis of a ND (adjusted odds ratio [AOR] 3.46, 95% CI 1.15 - 7.92), as well as with ADHD and ASD diagnosis after a multiple logistic regression analysis. 31552529 2020
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 Biomarker group BEFREE These findings show that melatonin was useful in improving some sleep outcomes in the short term, particularly those with comorbid ASD and neurodevelopmental disorders. 30674203 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 Biomarker group BEFREE We further demonstrate that deamidated 4E-BP2 regulates the translation of a distinct pool of mRNAs linked to cerebral development, mitochondria, and NF-κB activity, and thus may be crucial for postnatal brain development in neurodevelopmental disorders, such as ASD. 31825840 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 Biomarker group BEFREE These results have significant implications for understanding the neural basis of autism and related neurodevelopmental disorders.<b>SIGNIFICANCE STATEMENT</b> The recurrent ∼600 kb deletion at 16p11.2 (BP4-BP5) is one of the most common genetic etiologies of ASD and, more generally, of neurodevelopmental disorders. 31270155 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 GeneticVariation group BEFREE One or more ND was diagnosed in 226 children (55.5%; 69.9% boys): ADHD (44.5%; 68.5% boys); TD (17.7%; 77.8% boys) and ASD (6.1%; 76% boys). 29488416 2018
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 Biomarker group BEFREE The ASI, School-Age was administered by interviewers with minimal training to parents of children ages 5 to 12 who had all been previously identified with (or referred for assessment of) ASD or another neurodevelopmental disorder. 27282463 2017
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.070 GeneticVariation group BEFREE This review addresses the particular issues that attend gene discovery in neuropsychiatric and neurodevelopmental disorders and ASDs in particular, summarizes recent findings in human genetics broadly that are driving the reevaluation of the conventional wisdom regarding the allelic architecture of common psychiatric conditions, reviews selected discoveries in ASDs and their relevance to models of pathology, highlights the conceptual and practical issues raised by the observation of a convergence of ASD genetic risks with distinct psychiatric disorders, and considers the important interplay of studies of neurobiology and genetics in clarifying and extending our understanding of social disability syndromes. 22037497 2011