DRD2 c.286-324A>G

Variant ID: 11-113289182-T-C

NM_000795.3(DRD2):c.286-324A>G

This variant was identified in 16 publications

View GRCh38 version.




Publications:


Association of DRD2 gene polymorphisms with schizophrenia in the young Bangladeshi population: A pilot study.

Heliyon
Hussain, Md Saddam MS; Siddiqui, Shafayet Ahmed SA; Mondal, Susmita S; Millat, Md Shalahuddin MS; Marzan, Sadiatul S; Uddin, Md Giash MG; Aziz, Md Abdul MA; Alam, Md Faruq MF; Islam, Mohammad Safiqul MS
Publication Date: 2020-10

Variant appearance in text: rs1079727
PubMed Link: 33043160
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



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: rs1079727
PubMed Link: 32824878
Variant Present in the following documents:
  • Main text
  • brainsci-10-00567.pdf
View BVdb publication page



Identifying interactive biological pathways associated with reading disability.

Brain And Behavior
Lancaster, Hope Sparks HS; Liu, Xiaonan X; Dinu, Valentin V; Li, Jing J
Publication Date: 2020-08

Variant appearance in text: rs1079727
PubMed Link: 32596987
Variant Present in the following documents:
  • Main text
View BVdb publication page



Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally?

Genes
Nishiyama, Kumiko V KV; Satta, Yoko Y; Gojobori, Jun J
Publication Date: 2020-06-17

Variant appearance in text: rs1079727
PubMed Link: 32560373
Variant Present in the following documents:
  • Main text
  • genes-11-00658-s001.pdf
  • genes-11-00658.pdf
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Psychiatric research in the Northern Finland Birth Cohort 1986 - a systematic review.

International Journal Of Circumpolar Health
Miettunen, Jouko J; Haapea, Marianne M; Björnholm, Lassi L; Huhtaniska, Sanna S; Juola, Teija T; Kinnunen, Lotta L; Lehtiniemi, Heli H; Lieslehto, Johannes J; Rautio, Nina N; Nordström, Tanja T
Publication Date: 2019-12

Variant appearance in text: rs1079727
PubMed Link: 30744507
Variant Present in the following documents:
  • Main text
  • ZICH_78_1571382.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: DRD2: 286-324A>G; rs1079727
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
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: rs1079727
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Biological Predictors of Clozapine Response: A Systematic Review.

Frontiers In Psychiatry
Samanaite, Ruta R; Gillespie, Amy A; Sendt, Kyra-Verena KV; McQueen, Grant G; MacCabe, James H JH; Egerton, Alice A
Publication Date: 2018

Variant appearance in text: rs1079727
PubMed Link: 30093869
Variant Present in the following documents:
  • fpsyt-09-00327.pdf
View BVdb publication page



[Effects of rs4274224 polymorphisms in the DRD2 gene and family factors on the regularity based on the temperament in school-age children].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics
Li, Yu-Ling YL; Enherbayaer, Enherbayaer E; Guan, Hong-Yan HY
Publication Date: 2016-06

Variant appearance in text: rs1079727
PubMed Link: 27324537
Variant Present in the following documents:
  • Main text
View BVdb publication page



Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population.

Behavioral And Brain Functions : Bbf
Chen, Huan H; Wang, Guoqing G; Xia, Jiguang J; Zhou, Yuxi Y; Gao, Yong Y; Xu, Junquan J; Huen, Michael Sy MS; Siok, Wai Ting WT; Jiang, Yuyang Y; Tan, Li Hai LH; Sun, Yimin Y
Publication Date: 2014-09-01

Variant appearance in text: rs1079727
PubMed Link: 25178928
Variant Present in the following documents:
  • Main text
  • 1744-9081-10-29.pdf
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The association between DRD2/ANKK1 and genetically informed measures of alcohol use and problems.

Addiction Biology
Meyers, Jacquelyn L JL; Nyman, Emma E; Loukola, Anu A; Rose, Richard J RJ; Kaprio, Jaakko J; Dick, Danielle M DM
Publication Date: 2013-05

Variant appearance in text: rs1079727
PubMed Link: 22970887
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic influences on craving for alcohol.

Addictive Behaviors
Agrawal, Arpana A; Wetherill, Leah L; Bucholz, Kathleen K KK; Kramer, John J; Kuperman, Samuel S; Lynskey, Michael T MT; Nurnberger, John I JI; Schuckit, Marc M; Tischfield, Jay A JA; Edenberg, Howard J HJ; Foroud, Tatiana T; Bierut, Laura J LJ
Publication Date: 2013-02

Variant appearance in text: rs1079727
PubMed Link: 22481050
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs1079727
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.

Human Genetics
Chiang, Charleston W K CW; Gajdos, Zofia K Z ZK; Korn, Joshua M JM; Butler, Johannah L JL; Hackett, Rachel R; Guiducci, Candace C; Nguyen, Thutrang T TT; Wilks, Rainford R; Forrester, Terrence T; Henderson, Katherine D KD; Le Marchand, Loic L; Henderson, Brian E BE; Haiman, Christopher A CA; Cooper, Richard S RS; Lyon, Helen N HN; Zhu, Xiaofeng X; McKenzie, Colin A CA; Palmert, Mark R MR; Hirschhorn, Joel N JN
Publication Date: 2011-11

Variant appearance in text: rs1079727
PubMed Link: 21424828
Variant Present in the following documents:
  • Main text
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: rs1079727
PubMed Link: 21150907
Variant Present in the following documents:
  • Main text
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Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.

Molecular Psychiatry
Glatt, S J SJ; Faraone, S V SV; Lasky-Su, J A JA; Kanazawa, T T; Hwu, H-G HG; Tsuang, M T MT
Publication Date: 2009-09

Variant appearance in text: rs1079727
PubMed Link: 18332877
Variant Present in the following documents:
  • Main text
View BVdb publication page