Varaico: Literature-Extracted Genetic Variants

Gene:DRD3
Variant:p.G9S
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DRD3

NM_000796.6:p.G9S

Associated Papers

Genomic alterations in ovarian endometriosis and subsequently diagnosed ovarian carcinoma.

Linder A et al.

Human Reproduction (oxford, England), 2024

38459814 (PubMed )
Supplement: deae043_supplementary_table_s3.xlsx › Endometriosis

Functional single nucleotide polymorphisms in dopaminergic receptors D2 predict clinical response to Cariprazine.

De Pieri M et al.

Frontiers in Pharmacology, 2023

Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.

Boukhalfa W et al.

Frontiers in Aging Neuroscience, 2023

37342358 (PubMed )
Supplement: Table_2.XLSX › Table_2_SNPnexus_annotation

New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes.

Mestiri S et al.

Molecular Genetics & Genomic Medicine, 2022

Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.

Bateman NW et al.

Iscience, 2022

35036865 (PubMed )
Supplement: mmc2.xlsx › SupplementalTable1A

Genomic Markers for Essential Tremor.

Jiménez-Jiménez FJ et al.

Pharmaceuticals (basel, Switzerland), 2021

Introducing the first whole genomes of nationals from the United Arab Emirates.

AlSafar HS et al.

Scientific Reports, 2019

31604968 (PubMed )
Supplement: 41598_2019_50876_MOESM1_ESM.xlsx › UAE_S001

Dopaminergic Pathway Genes Influence Adverse Events Related to Dopaminergic Treatment in Parkinson's Disease.

Redenšek S et al.

Frontiers in Pharmacology, 2019

Non-invasive genotyping with a massively parallel sequencing panel for the detection of SNPs in HPA-axis genes.

Gutleb DR et al.

Scientific Reports, 2018

30374157 (PubMed )
Supplement: 41598_2018_34223_MOESM2_ESM.xlsx › Table_S1

Pharmacogenomics of GPCR Drug Targets.

Hauser AS et al.

Cell, 2018

Polymorphisms of Dopamine Receptor Genes and Risk of L-Dopa-Induced Dyskinesia in Parkinson's Disease.

Comi C et al.

International Journal of Molecular Sciences, 2017

Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients.

Ferrari M et al.

European Journal of Clinical Pharmacology, 2016

Influence of dopamine receptor gene polymorphisms on circulating T lymphocytes: A pilot study in healthy subjects.

Cosentino M et al.

Human Immunology, 2015

Meta-analysis of the influence of DRD3 Ser9Gly variant on susceptibility for essential tremor.

Mao X et al.

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2013

Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia.

Proitsi P et al.

Neurobiology of Aging, 2012

Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.

Muglia P et al.

Molecular Psychiatry, 2010

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients.

Lorenz D et al.

European Journal of Human Genetics : Ejhg, 2009

Pathway-based association analysis of genome-wide screening data suggest that genes associated with the gamma-aminobutyric acid receptor signaling pathway are involved in neuroleptic-induced, treatment-resistant tardive dyskinesia.

Inada T et al.

Pharmacogenetics and Genomics, 2008

Cebus apella, a nonhuman primate highly susceptible to neuroleptic side effects, carries the GLY9 dopamine receptor D3 associated with tardive dyskinesia in humans.

Werge T et al.

The Pharmacogenomics Journal, 2003

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases.

Rietschel M et al.

Schizophrenia Research, 1996

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."