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: rs12720898

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Multiple linear combination (MLC) regression tests for common variants adapted to linkage disequilibrium structure.

Genetic Epidemiology

Yoo, Yun Joo YJ; Sun, Lei L; Poirier, Julia G JG; Paterson, Andrew D AD; Bull, Shelley B SB

Publication Date: 2017-02

Variant appearance in text: rs12720898

PubMed Link: 27885705

Variant Present in the following documents:

• Main text
• GEPI-41-108.pdf

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c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One

Ganesan, Mala M; Nizamuddin, Sheikh S; Katkam, Shiva Krishna SK; Kumaraswami, Konda K; Hosad, Uday Kumar UK; Lobo, Limmy Loret LL; Kutala, Vijay Kumar VK; Thangaraj, Kumarasamy K

Publication Date: 2016

Variant appearance in text: rs12720898

PubMed Link: 27768712

Variant Present in the following documents:

• Main text
• pone.0164151.pdf

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An assessment of CETP sequence variation in relation to cognitive decline and dementia risk.

International Journal Of Molecular Epidemiology And Genetics

Reynolds, Chandra A CA; Gatz, Margaret M; Pedersen, Nancy L NL; Prince, Jonathan A JA

Publication Date: 2011

Variant appearance in text: rs12720898

PubMed Link: 21686126

Variant Present in the following documents:

• Main text

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