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Article

Association of Alcohol Use Disorder Risk With ADH1B, DRD2, FAAH, SLC39A8, GCKR, and PDYN Genetic Polymorphisms.

In vivo (Athens, Greece) - 1 Jan 2000

Legaki Evangelia, Tsaklakidou Domna, Hatzimanolis Alex, Segredou Eirini, Petalotis Markos, Moularogiorgou Giannoula, Mouchtouri Varvara, Lykouras Lefteris, Stefanis Nikos C, Gazouli Maria

Abstract excerpt

BACKGROUND/AIM: Alcohol use disorder (AUD) is a chronic, multifactorial psychiatric condition with an enormous impact on public health and social cost. Genetic studies suggest a heritability, and genome-wide association studies (GWAS) have revealed genetic polymorphisms influencing AUD development. Our study aimed to investigate known variants located in ADH1B, DRD2, FAAH, SLC39A8, GCKR, and PDYN genes...

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Adaptor Proteins, Signal Transducing
Alcohol Dehydrogenase
Alcoholism
Genome-Wide Association Study
Neurotransmitter Receptor Influence on Behavior

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Polymorphism, Single Nucleotide

Receptors, Dopamine D2

Substance Abuse Treatment and Outcomes

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Identifiers

PMID: 36099111
DOI: 10.21873/invivo.12935
PMCID: PMC9463892

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