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: rs2009181

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs2009181

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

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Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.

Molecular Psychiatry

Gelernter, J J; Kranzler, H R HR; Sherva, R R; Almasy, L L; Koesterer, R R; Smith, A H AH; Anton, R R; Preuss, U W UW; Ridinger, M M; Rujescu, D D; Wodarz, N N; Zill, P P; Zhao, H H; Farrer, L A LA

Publication Date: 2014-01

Variant appearance in text: rs2009181

PubMed Link: 24166409

Variant Present in the following documents:

• Main text

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