Associated Papers
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.
Li Z et al.
Jama, 2021
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Y-01A.domain
Korean, Japanese, and Chinese populations featured similar genes encoding drug-metabolizing enzymes and transporters: a DMET Plus microarray assessment.
Yi S et al.
Pharmacogenetics and Genomics, 2014
Genetic, anatomic, and clinical determinants of human serum sterol and vitamin D levels.
Stiles AR et al.
Proceedings of the National Academy of Sciences of the United States of America, 2014
Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.
O'Rawe JA et al.
Peerj, 2013
24109560 (PubMed )
Supplement: peerj-01-177-s012.xlsx › all_drug.csv
An SNP in CYP39A1 is associated with severe neutropenia induced by docetaxel.
Uchiyama T et al.
Cancer Chemotherapy and Pharmacology, 2012
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