Associated Papers
Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population.
Goljan E et al.
Human Genomics, 2024
A gene risk score using missense variants in SLCO1B1 is associated with earlier onset statin intolerance.
Bigossi M et al.
European Heart Journal. Cardiovascular Pharmacotherapy, 2023
37253618 (PubMed )
Supplement: pvad040_supplemental_file.docx
Clinical pharmacogenetic analysis in 5,001 individuals with diagnostic Exome Sequencing data.
Lanillos J et al.
Npj Genomic Medicine, 2022
35181665 (PubMed )
Supplement: 41525_2022_283_MOESM4_ESM.xlsx › Novel_Previously_described_var.
SLCO1B1: Application and Limitations of Deep Mutational Scanning for Genomic Missense Variant Function.
Zhang L et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals, 2021
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