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: rs1564370

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Allele Frequencies of the Single Nucleotide Polymorphisms Related to the Body Burden of Heavy Metals in the Korean Population and Their Ethnic Differences.

Toxicological Research

Eom, Sang-Yong SY; Lim, Ji-Ae JA; Kim, Yong-Dae YD; Choi, Byung-Sun BS; Hwang, Myung Sil MS; Park, Jung-Duck JD; Kim, Heon H; Kwon, Ho-Jang HJ

Publication Date: 2016-07

Variant appearance in text: rs1564370

PubMed Link: 27437086

Variant Present in the following documents:

• Main text
• tr-32-195.pdf

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SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study.

Toxicological Sciences : An Official Journal Of The Society Of Toxicology

Gribble, Matthew O MO; Voruganti, Venkata Saroja VS; Cropp, Cheryl D CD; Francesconi, Kevin A KA; Goessler, Walter W; Umans, Jason G JG; Silbergeld, Ellen K EK; Laston, Sandra L SL; Haack, Karin K; Kao, Wen Hong Linda WH; Fallin, Margaret Daniele MD; Maccluer, Jean W JW; Cole, Shelley A SA; Navas-Acien, Ana A

Publication Date: 2013-11

Variant appearance in text: rs1564370

PubMed Link: 23970802

Variant Present in the following documents:

• Main text

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