Associated Papers
Meta-analysis of genomic variants in power and endurance sports to decode the impact of genomics on athletic performance and success.
Psatha A et al.
Human Genomics, 2024
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota.
Lopes GS et al.
The Pharmacogenomics Journal, 2022
Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection.
Scott SA et al.
Clinical and Translational Science, 2021
32931151 (PubMed )
Supplement: CTS-14-204-s001.xlsx › Table_S1
Added Value of Clinical Sequencing: WGS-Based Profiling of Pharmacogenes.
Caspar SM et al.
International Journal of Molecular Sciences, 2020
32225115 (PubMed )
Supplement: ijms-21-02308-s001.zip › Caspar_et_al_Supplementary_Table_S1.xlsx › DPWG_Variants
Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi-Bickel Syndrome.
Eghbali M et al.
Frontiers in Genetics, 2020
CYP2D6 allele frequencies, copy number variants, and tandems in the population of Hong Kong.
Chan W et al.
Journal of Clinical Laboratory Analysis, 2019
Limited predictive value of achieving beneficial plasma (Z)-endoxifen threshold level by CYP2D6 genotyping in tamoxifen-treated Polish women with breast cancer.
Hennig EE et al.
Bmc Cancer, 2015
26232141 (PubMed )
Supplement: 12885_2015_1575_MOESM1_ESM.xlsx › Table_S1
High prevalence of CYP2D6*41 (G2988A) allele in Saudi Arabians.
Al-Dosari MS et al.
Environmental Toxicology and Pharmacology, 2013
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