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: rs5992500

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Role of novelty seeking personality traits as mediator of the association between COMT and onset age of drug use in Chinese heroin dependent patients.

Plos One

Li, Ting T; Yu, Shunying S; Du, Jiang J; Chen, Hanhui H; Jiang, Haifeng H; Xu, Ke K; Fu, Yingmei Y; Wang, Dongxiang D; Zhao, Min M

Publication Date: 2011

Variant appearance in text: rs5992500

PubMed Link: 21857968

Variant Present in the following documents:

• Main text

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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: rs5992500

PubMed Link: 21808284

Variant Present in the following documents:

• NIHMS305090-supplement-3.pdf

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Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

Croatian Medical Journal

Pal, Prodipto P; Mihanović, Mate M; Molnar, Sven S; Xi, Huifeng H; Sun, Guangyun G; Guha, Saurav S; Jeran, Nina N; Tomljenović, Andrea A; Malnar, Ana A; Missoni, Sasa S; Deka, Ranjan R; Rudan, Pavao P

Publication Date: 2009-08

Variant appearance in text: rs5992500

PubMed Link: 19673036

Variant Present in the following documents:

• Main text

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Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).

Molecular Psychiatry

Strug, L J LJ; Suresh, R R; Fyer, A J AJ; Talati, A A; Adams, P B PB; Li, W W; Hodge, S E SE; Gilliam, T C TC; Weissman, M M MM

Publication Date: 2010-02

Variant appearance in text: rs5992500

PubMed Link: 18663369

Variant Present in the following documents:

• Main text

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