Wichittra Tassaneeyakul
Khon Kaen, 40002, Thailand
Last Updated: 09/26/2026
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Found 59 publications
Genetic Variants Associated with Non-Steroidal Anti-Inflammatory Drug-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.
Journal: Medical sciences (Basel, Switzerland)
Published: January 16, 2026
HLA-B alleles confer susceptibility to sulfasalazine-induced severe cutaneous adverse reactions.
Journal: The Journal of allergy and clinical immunology
Published: December 05, 2025
Development of a non-genetic risk prediction model for allopurinol-induced severe cutaneous adverse drug reactions: a multicenter retrospective observational study.
Journal: Clinical rheumatology
Published: October 26, 2025
Genetic Determinants of Hematopoietic Toxicity Risk in Thai Pediatric Patients Undergoing 6-Mercaptopurine Treatment.
Journal: Clinical and translational science
Published: August 12, 2025
Dual approaches in pharmacogenetics: Developing PCR-SSP and RT-PCR methods for HLA-B*13:01 screening to prevent dapsone and Co-trimoxazole SCARs.
Journal: Heliyon
Published: February 12, 2024
Complete mitochondrial genomes of patients from Thailand with cardiovascular diseases.
Journal: PloS one
Published: January 27, 2024
Cost-effectiveness analysis of HLA-B*13:01 screening for the prevention of co-trimoxazole-induced severe cutaneous adverse reactions among HIV-infected patients in Thailand.
Journal: Journal of medical economics
Published: October 13, 2023
Association between HLA alleles and beta-lactam antibiotics-related severe cutaneous adverse reactions.
Journal: Frontiers in pharmacology
Published: June 27, 2023
Development of label-free electrochemical impedance spectroscopy for the detection of HLA-B*15:02 and HLA-B*15:21 for the prevention of carbamazepine-induced Stevens-Johnson syndrome.
Journal: Analytical biochemistry
Published: August 08, 2022
Associations of HLA and drug-metabolizing enzyme genes in co-trimoxazole-induced severe cutaneous adverse reactions.
Journal: Drug metabolism and pharmacokinetics
Published: May 11, 2022
Meta-Analysis of NUDT15 Genetic Polymorphism on Thiopurine-Induced Myelosuppression in Asian Populations.
Journal: Frontiers in pharmacology
Published: September 28, 2021
NUDT15 is a key genetic factor for prediction of hematotoxicity in pediatric patients who received a standard low dosage regimen of 6-mercaptopurine.
Journal: Drug metabolism and pharmacokinetics
Published: August 16, 2021
Last Updated: 09/26/2026