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SNP information rs167771

RS167771

Normal allele: AA

The dopamine receptor-3 (DRD3) gene is associated with specific repetitive behaviours in autism spectrum disorders.

Polymorphism rs167771 is related to topics like this:

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Research and publications:

  18330705   Physiogenomic analysis of localized FMRI brain activity in schizophrenia.

  18821566   SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.

  19058789   A common variant in DRD3 receptor is associated with autism spectrum disorder.

  19506579   A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms.

  20148275   Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.

  20619616   Searching for functional SNPs or rare variants in exonic regions of DRD3 in risperidone-treated patients.

  21691864   Brief report: the dopamine-3-receptor gene (DRD3) is associated with specific repetitive behavior in autism spectrum disorder (ASD).

  22021758   Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort.

  22309839   Association study of 45 candidate genes in nicotine dependence in Han Chinese.

  22397633   Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.

  23856854   Positive effects of methylphenidate on hyperactivity are moderated by monoaminergic gene variants in children with autism spectrum disorders.

  24927283   Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder.

  24944790   Screening for 392 polymorphisms in 141 pharmacogenes.

  25224105   Autism, DRD3 and repetitive and stereotyped behavior, an overview of the current knowledge.

  25266122   Addiction-related genes in gambling disorders: new insights from parallel human and pre-clinical models.

  25792691   DRD3 gene and striatum in autism spectrum disorder.

  25807276   Analysis of pharmacogenomic variants associated with population differentiation.

  26322220   A comprehensive meta-analysis of common genetic variants in autism spectrum conditions.

  26555434   Prevalence of pain-related single nucleotide polymorphisms in patients of African origin with sickle cell disease.

  27247849   Genetic variation and cognitive dysfunction in opioid-treated patients with cancer.

  30093869   Biological Predictors of Clozapine Response: A Systematic Review.

  30967134   A pharmacogenetic study of patients with schizophrenia from West Siberia gets insight into dopaminergic mechanisms of antipsychotic-induced hyperprolactinemia.

  33644845   Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors.

  34440083   Candidate Genes Encoding Dopamine Receptors as Predictors of the Risk of Antipsychotic-Induced Parkinsonism and Tardive Dyskinesia in Schizophrenic Patients.

  35140610   Genetic Factors Associated With Tardive Dyskinesia: From Pre-clinical Models to Clinical Studies.

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DNA methylation genes

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