DRD2 c.723+227G>A

Variant ID: 11-113285916-C-T

NM_000795.3(DRD2):c.723+227G>A

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research.

Cns Drugs
Elsayed, Nada A NA; Yamamoto, Kaila M KM; Froehlich, Tanya E TE
Publication Date: 2020-04

Variant appearance in text: rs12363125
PubMed Link: 32133580
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs12363125
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.

International Journal Of Molecular Medicine
Yamada, Yoshiji Y; Sakuma, Jun J; Takeuchi, Ichiro I; Yasukochi, Yoshiki Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Muramatsu, Masaaki M; Sawabe, Motoji M; Fujiwara, Yoshinori Y; Taniguchi, Yu Y; Obuchi, Shuichi S; Kawai, Hisashi H; Shinkai, Shoji S; Mori, Seijiro S; Arai, Tomio T; Tanaka, Masashi M
Publication Date: 2017-05

Variant appearance in text: rs12363125
PubMed Link: 28339009
Variant Present in the following documents:
  • Main text
  • ijmm-39-05-1091.pdf
View BVdb publication page



Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry
Bonvicini, C C; Faraone, S V SV; Scassellati, C C
Publication Date: 2016-07

Variant appearance in text: rs12363125
PubMed Link: 27217152
Variant Present in the following documents:
View BVdb publication page



Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent.

Bmc Research Notes
Al-Eitan, Laith N LN; Jaradat, Saied A SA; Hulse, Gary K GK; Tay, Guan K GK
Publication Date: 2012-09-10

Variant appearance in text: rs12363125
PubMed Link: 22963930
Variant Present in the following documents:
  • Main text
  • 1756-0500-5-497.pdf
View BVdb publication page



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: rs12363125
PubMed Link: 21150907
Variant Present in the following documents:
  • Main text
View BVdb publication page



Two-stage case-control association study of dopamine-related genes and migraine.

Bmc Medical Genetics
Corominas, Roser R; Ribases, Marta M; Camiña, Montserrat M; Cuenca-León, Ester E; Pardo, Julio J; Boronat, Susana S; Sobrido, María-Jesús MJ; Cormand, Bru B; Macaya, Alfons A
Publication Date: 2009-09-21

Variant appearance in text: rs12363125
PubMed Link: 19772578
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-95.pdf
View BVdb publication page



Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Zhang, Ying Y; Bertolino, Alessandro A; Fazio, Leonardo L; Blasi, Giuseppe G; Rampino, Antonio A; Romano, Raffaella R; Lee, Mei-Ling T ML; Xiao, Tao T; Papp, Audrey A; Wang, Danxin D; Sadée, Wolfgang W
Publication Date: 2007-12-18

Variant appearance in text: rs12363125
PubMed Link: 18077373
Variant Present in the following documents:
  • Main text
View BVdb publication page