Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLRBS16_het
APF2: an improved ensemble method for pharmacogenomic variant effect prediction.
Zhou Y et al.
The Pharmacogenomics Journal, 2024
38802404 (PubMed )
Supplement: 41397_2024_338_MOESM2_ESM.xlsx › Sheet1
Crosstalk between KIF1C and PRKAR1A in left atrial myxoma.
Zhou M et al.
Communications Biology, 2023
Functional Characterization of 21 Rare Allelic CYP1A2 Variants Identified in a Population of 4773 Japanese Individuals by Assessing Phenacetin O-Deethylation.
Kumondai M et al.
Journal of Personalized Medicine, 2021
Investigation of the major cytochrome P450 1A2 genetic variant in a healthy Tibetan population in China.
Ren Y et al.
Molecular Medicine Reports, 2017
Genetic polymorphism analysis of the drug-metabolizing enzyme CYP1A2 in a Uyghur Chinese population: a pilot study.
Geng T et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems, 2016
Structure, function, regulation and polymorphism and the clinical significance of human cytochrome P450 1A2.
Zhou SF et al.
Drug Metabolism Reviews, 2010
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