Pages that link to "Q24627520"
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The following pages link to Genetics of autistic disorders: review and clinical implications (Q24627520):
Displaying 50 items.
- Autism spectrum disorder in adults: diagnosis, management, and health services development (Q26741443) (← links)
- Neuroimaging endophenotypes in autism spectrum disorder (Q26800176) (← links)
- From genes to environment: using integrative genomics to build a "systems-level" understanding of autism spectrum disorders (Q26825821) (← links)
- Genomics and autism spectrum disorder (Q27015042) (← links)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics (Q27022289) (← links)
- Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE (Q28115364) (← links)
- Major channels involved in neuropsychiatric disorders and therapeutic perspectives (Q28290639) (← links)
- Infant siblings and the investigation of autism risk factors (Q28388355) (← links)
- Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders (Q28655713) (← links)
- Evaluation of Pax6 mutant rat as a model for autism (Q28941192) (← links)
- Stem cells and modeling of autism spectrum disorders (Q30401824) (← links)
- Heterogeneity of subclinical autistic traits among parents of children with autism spectrum disorder: Identifying the broader autism phenotype with a data-driven method. (Q31112787) (← links)
- The autism puzzle: challenging a mechanistic model on conceptual and historical grounds (Q33356952) (← links)
- Associations of hypomelanotic skin disorders with autism: Do they reflect the effects of genetic mutations and epigenetic factors on vitamin-D metabolism in individuals at risk for autism? (Q33358843) (← links)
- Connecting Families to Their Health Record and Care Team: The Use, Utility, and Impact of a Client/Family Health Portal at a Children's Rehabilitation Hospital. (Q33586892) (← links)
- Vitamin D status in autism spectrum disorders and the efficacy of vitamin D supplementation in autistic children. (Q34043762) (← links)
- The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis (Q34432309) (← links)
- Mass spectrometry as a tool for studying autism spectrum disorder (Q34470350) (← links)
- Genetics in autism diagnosis: adding molecular subtypes to neurobehavioral diagnoses (Q35116793) (← links)
- MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders (Q35151007) (← links)
- The ongoing dissection of the genetic architecture of autistic spectrum disorder (Q35166492) (← links)
- Environmental risk factors for autism. (Q35200038) (← links)
- The plausibility of a role for mercury in the etiology of autism: a cellular perspective (Q35214783) (← links)
- Association of hypomelanotic skin disorders with autism: links to possible etiologic role of vitamin-D levels in autism? (Q35225536) (← links)
- Lack of association between autism and four heavy metal regulatory genes (Q35501612) (← links)
- Single nucleotide polymorphisms predict symptom severity of autism spectrum disorder (Q35629165) (← links)
- The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network (Q35683981) (← links)
- GABA system dysfunction in autism and related disorders: from synapse to symptoms (Q35770888) (← links)
- Developmental regulation of expression of schizophrenia susceptibility genes in the primate hippocampal formation. (Q36591363) (← links)
- Genetic testing and genetic counseling among Medicaid-enrolled children with autism spectrum disorder in 2001 and 2007. (Q36614115) (← links)
- Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders (Q36672907) (← links)
- The expanding genomic landscape of autism: discovering the 'forest' beyond the 'trees' (Q36799924) (← links)
- AKAPs integrate genetic findings for autism spectrum disorders (Q36956652) (← links)
- Targeted treatment trials for tuberous sclerosis and autism: no longer a dream (Q37025554) (← links)
- Developing a Predictive Gene Classifier for Autism Spectrum Disorders Based upon Differential Gene Expression Profiles of Phenotypic Subgroups (Q37403123) (← links)
- A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism (Q37589578) (← links)
- Protein signatures of oxidative stress response in a patient specific cell line model for autism (Q37596896) (← links)
- MLPA analysis in a cohort of patients with autism (Q37624868) (← links)
- First evidence of sensory atypicality in mothers of children with Autism Spectrum Disorder (ASD). (Q37684961) (← links)
- Child and adolescent psychiatric genetics (Q37688994) (← links)
- Autism spectrum disorders—A genetics review (Q37847947) (← links)
- Autism spectrum disorders and autistic traits: A decade of new twin studies (Q37857801) (← links)
- Genetic basis of autism: is there a way forward? (Q37860856) (← links)
- Diagnostic Yield of Genetic Testing in Children Diagnosed With Autism Spectrum Disorders at a Regional Referral Center (Q37869643) (← links)
- Are retinoids potential therapeutic agents in disorders of social cognition including autism? (Q37873985) (← links)
- Risk factors for autism: translating genomic discoveries into diagnostics (Q37893976) (← links)
- Autistic traits below the clinical threshold: re-examining the broader autism phenotype in the 21st century (Q37944510) (← links)
- Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research (Q37953135) (← links)
- Genomic and proteomic advances in autism research (Q38060576) (← links)
- Genetic risk in autism: new associations and clinical testing (Q38088742) (← links)