Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55879
Gene Symbol: GABRQ
GABRQ
0.300 Biomarker disease GENOMICS_ENGLAND Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204 2015
Entrez Id: 9320
Gene Symbol: TRIP12
TRIP12
0.300 Biomarker disease GENOMICS_ENGLAND CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. 25294932 2014
Entrez Id: 23040
Gene Symbol: MYT1L
MYT1L
0.300 Biomarker disease GENOMICS_ENGLAND CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. 25294932 2014
Entrez Id: 4908
Gene Symbol: NTF3
NTF3
0.200 Biomarker disease MGD LIG family receptor tyrosine kinase-associated proteins modulate growth factor signals during neural development. 19755105 2009
Entrez Id: 3491
Gene Symbol: CCN1
CCN1
0.200 Biomarker disease MGD The matricellular protein CCN1 is essential for cardiac development. 17023674 2006
Entrez Id: 4908
Gene Symbol: NTF3
NTF3
0.200 Biomarker disease MGD Loss of brain-derived neurotrophic factor-dependent neural crest-derived sensory neurons in neurotrophin-4 mutant mice. 10681461 2000
Entrez Id: 4908
Gene Symbol: NTF3
NTF3
0.200 Biomarker disease MGD Absence of sensory neurons before target innervation in brain-derived neurotrophic factor-, neurotrophin 3-, and TrkC-deficient embryonic mice. 9364058 1997
Entrez Id: 4908
Gene Symbol: NTF3
NTF3
0.200 Biomarker disease MGD Identification of an essential nonneuronal function of neurotrophin 3 in mammalian cardiac development. 8841198 1996
Entrez Id: 4908
Gene Symbol: NTF3
NTF3
0.200 Biomarker disease MGD Targeted mutation in the neurotrophin-3 gene results in loss of muscle sensory neurons. 7991545 1994
Entrez Id: 85358
Gene Symbol: SHANK3
SHANK3
0.110 Biomarker disease BEFREE Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish. 27562614 2016
Entrez Id: 85358
Gene Symbol: SHANK3
SHANK3
0.110 CausalMutation disease CLINVAR Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions. 25356970 2015
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 GeneticVariation disease BEFREE We aimed to develop and internally validate a scoring system, the adult spinal deformity surgical decision-making (ASD-SDM) score, to guide the decision-making process for ASD patients aged above 40 years. 31317308 2020
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE This study was designed to (1) describe ASD symptoms in adolescent and young adult males with FXS (n = 44) and (2) evaluate the contributions to ASD severity of cognitive, language, and psychiatric factors, as well as FMRP (the protein deficient in FXS). 30382442 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE At the group-level, we observed weaknesses in the language skills of boys with <sub>n</sub>ASD relative to those with FXS (e.g., when considering raw score performance, standard score performance relative to nonverbal cognitive skills, frequency of talk in play), after controlling for nonverbal IQ and ASD symptom severity. 30783899 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE The research put forward that in individuals with ASD, while gluten-free/casein-free and ketogenic diets, camel milk, curcumin, probiotics, and fermentable foods can play a role in alleviating ASD symptoms, consumption of sugar, additives, pesticides, genetically modified organisms, inorganic processed foods, and hard-to-digest starches may aggravate symptoms. 28762296 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE Results revealed a pragmatic continuum with significantly better scores for HR-TD than HR-BAP or HR-ASD, and HR-BAP than HR-ASD. 30488153 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 GeneticVariation disease BEFREE To investigate possible correlates of generalised anxiety disorder (GAD) in young males with ASD, a test of the mediation effects of sensory features (SF) upon the association between ASD symptoms and GAD was conducted with 150 males aged 6 to 18 years. 30771129 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE Heart rate variability (HRV) has been separately shown to be associated with ASD symptomatology, psychological wellbeing and emotion regulation (ER) in specific samples consisting of either individuals with ASD, those without ASD, or combined. 30578793 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 AlteredExpression disease BEFREE One hundred children, aged 3-12 y, diagnosed as Autistic spectrum disorder; ASD (DSM-V) and 100 age and sex matched controls were studied. 31612302 2019
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 GeneticVariation disease BEFREE Doing so represents a first step in evaluating whether ABRs yield potential for informing the etiology of ASD risk and/or ASD symptom profiles. 29603654 2018
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE Evidence supporting that gut problems are linked to ASD symptoms has been accumulating both in humans and animal models of ASD. 29274915 2018
Entrez Id: 7168
Gene Symbol: TPM1
TPM1
0.100 GeneticVariation disease CLINVAR Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects. 28359939 2017
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 Biomarker disease BEFREE Findings indicate that ASD may be favored by consanguineous marriage and that NKX2-5 variant rate in ASD patients may be affected by ethnicity. 27752029 2017
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.100 GeneticVariation disease BEFREE In view of the high prevalence of familial occurrence of secundum ASD (10% of all ASD patients), we recommend screening all first degree relatives of ASD patients for cardiac, conduction and skeletal anomalies. 17462063 2007
Entrez Id: 6910
Gene Symbol: TBX5
TBX5
0.100 CausalMutation disease CLINVAR