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: rs4246229

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: rs4246229

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

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Functional FLT1 Genetic Variation is a Prognostic Factor for Recurrence in Stage I-III Non-Small-Cell Lung Cancer.

Journal Of Thoracic Oncology : Official Publication Of The International Association For The Study Of Lung Cancer

Glubb, Dylan M DM; Paré-Brunet, Laia L; Jantus-Lewintre, Eloisa E; Jiang, Chen C; Crona, Daniel D; Etheridge, Amy S AS; Mirza, Osman O; Zhang, Wei W; Seiser, Eric L EL; Rzyman, Witold W; Jassem, Jacek J; Auman, Todd T; Hirsch, Fred R FR; Owzar, Kouros K; Camps, Carlos C; Dziadziuszko, Rafal R; Innocenti, Federico F

Publication Date: 2015-07

Variant appearance in text: rs4246229

PubMed Link: 26134224

Variant Present in the following documents:

• Main text

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