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: rs4947488

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Germline genetic variants in somatically significantly mutated genes in tumors are associated with renal cell carcinoma risk and outcome.

Carcinogenesis

Shu, Xiang X; Gu, Jianchun J; Huang, Maosheng M; Tannir, Nizar M NM; Matin, Surena F SF; Karam, Jose A JA; Wood, Christopher G CG; Wu, Xifeng X; Ye, Yuanqing Y

Publication Date: 2018-05-28

Variant appearance in text: rs4947488

PubMed Link: 29635281

Variant Present in the following documents:

• Main text

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Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women.

Plos One

Zhou, Qiu-Hong QH; Zhao, Lan-Juan LJ; Wang, Ping P; Badr, Rhamee R; Xu, Xiao-Jing XJ; Bu, Feng-Xiao FX; Lappe, Joan J; Recker, Robert R; Zhou, Yu Y; Ye, An A; Zhou, Bo-Ting BT

Publication Date: 2014

Variant appearance in text: rs4947488

PubMed Link: 25396734

Variant Present in the following documents:

• Main text
• pone.0112358.pdf

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