DRD2 c.-31-1215G>A

Variant ID: 11-113296619-C-T

NM_000795.3(DRD2):c.-31-1215G>A

This variant was identified in 19 publications

View GRCh38 version.




Publications:


Haplotype of ESR1 and PPARD Genes Is Associated with Higher Anthropometric Changes in Han Chinese Obesity by Adjusting Dietary Factors-An 18-Month Follow-Up.

Nutrients
Huang, Yu-Min YM; Wang, Weu W; Hsieh, Po-Pin PP; Chen, Hsin-Hung HH
Publication Date: 2022-10-21

Variant appearance in text: rs1079596
PubMed Link: 36297109
Variant Present in the following documents:
  • Main text
  • nutrients-14-04425.pdf
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A novel quantitative electroencephalography subtype with high alpha power in ADHD: ADHD or misdiagnosed ADHD?

Plos One
Byeon, Jun J; Choi, Tae Young TY; Won, Geun Hui GH; Lee, Jaewon J; Kim, Jun Won JW
Publication Date: 2020

Variant appearance in text: rs1079596
PubMed Link: 33201920
Variant Present in the following documents:
  • Main text
  • pone.0242566.pdf
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Expression of Dopamine-Related Genes in Four Human Brain Regions.

Brain Sciences
Stanfill, Ansley Grimes AG; Cao, Xueyuan X
Publication Date: 2020-08-18

Variant appearance in text: rs1079596
PubMed Link: 32824878
Variant Present in the following documents:
  • Main text
  • brainsci-10-00567.pdf
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Does L-Methylfolate Supplement Methylphenidate Pharmacotherapy in Attention-Deficit/Hyperactivity Disorder?: Evidence of Lack of Benefit From a Double-Blind, Placebo-Controlled, Randomized Clinical Trial.

Journal Of Clinical Psychopharmacology
Surman, Craig C; Ceranoglu, Atilla A; Vaudreuil, Carrie C; Albright, Brittany B; Uchida, Mai M; Yule, Amy A; Spencer, Andrea A; Boland, Heidi H; Grossman, Rebecca R; Rhodewalt, Lauren L; Fitzgerald, Maura M; Biederman, Joseph J
Publication Date: 2019

Variant appearance in text: rs1079596
PubMed Link: 30566416
Variant Present in the following documents:
  • Main text
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs1079596
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-6.xlsx, sheet 1
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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Transcranial direct current brain stimulation decreases impulsivity in ADHD.

Brain Stimulation
Allenby, Cheyenne C; Falcone, Mary M; Bernardo, Leah L; Wileyto, E Paul EP; Rostain, Anthony A; Ramsay, J Russell JR; Lerman, Caryn C; Loughead, James J
Publication Date: 2018

Variant appearance in text: rs1079596
PubMed Link: 29885858
Variant Present in the following documents:
  • Main text
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Using an Event-History with Risk-Free Model to Study the Genetics of Alcoholism.

Scientific Reports
Yang, Hsin-Chou HC; Chen, I-Chen IC; Tsay, Yuh-Chyuan YC; Li, Zheng-Rong ZR; Chen, Chun-Houh CH; Hwu, Hai-Gwo HG; Chen, Chen-Hsin CH
Publication Date: 2017-05-16

Variant appearance in text: rs1079596
PubMed Link: 28512340
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_1791.pdf
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Peer Influence, Genetic Propensity, and Binge Drinking: A Natural Experiment and a Replication.

Ajs; American Journal Of Sociology
Guo, Guang G; Li, Yi Y; Wang, Hongyu H; Cai, Tianji T; Duncan, Greg J GJ
Publication Date: 2015-11

Variant appearance in text: rs1079596
PubMed Link: 26900620
Variant Present in the following documents:
  • Main text
View BVdb publication page



Overlapping dopaminergic pathway genetic susceptibility to heroin and cocaine addictions in African Americans.

Annals Of Human Genetics
Levran, Orna O; Randesi, Matthew M; da Rosa, Joel Correa JC; Ott, Jurg J; Rotrosen, John J; Adelson, Miriam M; Kreek, Mary Jeanne MJ
Publication Date: 2015-05

Variant appearance in text: rs1079596
PubMed Link: 25875614
Variant Present in the following documents:
  • Main text
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Association of genetic variation in pharmacodynamic factors with methadone dose required for effective treatment of opioid addiction.

Pharmacogenomics
Levran, Orna O; Peles, Einat E; Randesi, Matthew M; Shu, Xu X; Ott, Jurg J; Shen, Pei-Hong PH; Adelson, Miriam M; Kreek, Mary Jeanne MJ
Publication Date: 2013-05

Variant appearance in text: rs1079596
PubMed Link: 23651024
Variant Present in the following documents:
  • Main text
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Candidate gene studies of a promising intermediate phenotype: failure to replicate.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Hart, Amy B AB; de Wit, Harriet H; Palmer, Abraham A AA
Publication Date: 2013-04

Variant appearance in text: rs1079596
PubMed Link: 23303064
Variant Present in the following documents:
  • Main text
View BVdb publication page



The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHD.

Behavioral And Brain Functions : Bbf
Matthews, Natasha N; Vance, Alasdair A; Cummins, Tarrant D R TD; Wagner, Joseph J; Connolly, Amanda A; Yamada, Jacqueline J; Lockhart, Paul J PJ; Panwar, Ajay A; Wallace, Robyn H RH; Bellgrove, Mark A MA
Publication Date: 2012-05-28

Variant appearance in text: rs1079596
PubMed Link: 22640745
Variant Present in the following documents:
  • Main text
  • 1744-9081-8-25.pdf
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DRD2 polymorphisms modulate reward and emotion processing, dopamine neurotransmission and openness to experience.

Cortex; A Journal Devoted To The Study Of The Nervous System And Behavior
Peciña, Marta M; Mickey, Brian J BJ; Love, Tiffany T; Wang, Heng H; Langenecker, Scott A SA; Hodgkinson, Colin C; Shen, Pei-Hong PH; Villafuerte, Sandra S; Hsu, David D; Weisenbach, Sara L SL; Stohler, Christian S CS; Goldman, David D; Zubieta, Jon-Kar JK
Publication Date: 2013-03

Variant appearance in text: rs1079596
PubMed Link: 22424959
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epigenetics in Developmental Disorder: ADHD and Endophenotypes.

Journal Of Genetic Syndromes & Gene Therapy
Archer, Trevor T; Oscar-Berman, Marlene M; Blum, Kenneth K
Publication Date: 2011-06-30

Variant appearance in text: rs1079596
PubMed Link: 22224195
Variant Present in the following documents:
  • Main text
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Different phenotypic and genotypic presentations in alcohol dependence: age at onset matters.

Journal Of Studies On Alcohol And Drugs
Chen, Yu-Chu YC; Prescott, Carol A CA; Walsh, Dermot D; Patterson, Diana G DG; Riley, Brien P BP; Kendler, Kenneth S KS; Kuo, Po-Hsiu PH
Publication Date: 2011-09

Variant appearance in text: rs1079596
PubMed Link: 21906503
Variant Present in the following documents:
  • Main text
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Intronic polymorphisms affecting alternative splicing of human dopamine D2 receptor are associated with cocaine abuse.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Moyer, Robert A RA; Wang, Danxin D; Papp, Audrey C AC; Smith, Ryan M RM; Duque, Linda L; Mash, Deborah C DC; Sadee, Wolfgang W
Publication Date: 2011-03

Variant appearance in text: rs1079596
PubMed Link: 21150907
Variant Present in the following documents:
  • Main text
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Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participants.

Experimental And Clinical Psychopharmacology
Hamidovic, Ajna A; Dlugos, Andrea A; Skol, Andrew A; Palmer, Abraham A AA; de Wit, Harriet H
Publication Date: 2009-12

Variant appearance in text: rs1079596
PubMed Link: 19968402
Variant Present in the following documents:
  • Main text
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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.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE
Publication Date: 2008-12-05

Variant appearance in text: rs1079596
PubMed Link: 18821566
Variant Present in the following documents:
  • Main text
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Genome-wide association with select biomarker traits in the Framingham Heart Study.

Bmc Medical Genetics
Benjamin, Emelia J EJ; Dupuis, Josée J; Larson, Martin G MG; Lunetta, Kathryn L KL; Booth, Sarah L SL; Govindaraju, Diddahally R DR; Kathiresan, Sekar S; Keaney, John F JF; Keyes, Michelle J MJ; Lin, Jing-Ping JP; Meigs, James B JB; Robins, Sander J SJ; Rong, Jian J; Schnabel, Renate R; Vita, Joseph A JA; Wang, Thomas J TJ; Wilson, Peter W F PW; Wolf, Philip A PA; Vasan, Ramachandran S RS
Publication Date: 2007-09-19

Variant appearance in text: rs1079596
PubMed Link: 17903293
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S11.pdf
View BVdb publication page