Publications:

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: rs12800853

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Selection in the dopamine receptor 2 gene: a candidate SNP study.

Peerj

Göllner, Tobias T; Fieder, Martin M

Publication Date: 2015

Variant appearance in text: rs12800853

PubMed Link: 26290802

Variant Present in the following documents:

• Main text
• peerj-03-1149.pdf

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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: rs12800853

PubMed Link: 25178928

Variant Present in the following documents:

• Main text
• 1744-9081-10-29.pdf

View BVdb publication page