日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Development and Validation of a Multigene Panel for Pharmacogenomics Testing Using Next-Generation Sequencing for Routine Clinical Practice

利用新一代测序技术开发和验证用于常规临床实践的药物基因组学检测多基因检测组合

Hongkaew, Yaowaluck; Kunadirek, Pattapon; Sangtian, Montinee; Pateetin, Prangwan; Bunlungsup, Srichan; Panmontha, Wipa; Kawprasertsri, Sornsawan; Khunlertkit, Tanawat

Association of UGT1A1*6, UGT1A1*28, or ABCC2 c.3972C>T genetic polymorphisms with irinotecan-induced toxicity in Asian cancer patients: Meta-analysis

UGT1A1*6、UGT1A1*28 或 ABCC2 c.3972C>T 基因多态性与亚洲癌症患者伊立替康诱导毒性的相关性:荟萃分析

Atasilp, Chalirmporn; Biswas, Mohitosh; Jinda, Pimonpan; Nuntharadthanaphong, Nutthan; Rachanakul, Jiratha; Hongkaew, Yaowaluck; Vanwong, Natchaya; Saokaew, Surasak; Sukasem, Chonlaphat

Pharmacogenomics Factors Influencing the Effect of Risperidone on Prolactin Levels in Thai Pediatric Patients With Autism Spectrum Disorder

影响利培酮对泰国自闭症谱系障碍患儿催乳素水平影响的药物基因组学因素

Hongkaew, Yaowaluck; Gaedigk, Andrea; Wilffert, Bob; Gaedigk, Roger; Kittitharaphan, Wiranpat; Ngamsamut, Nattawat; Limsila, Penkhae; Puangpetch, Apichaya; Sukprasong, Rattanaporn; Sukasem, Chonlaphat

Relationship between CYP2D6 genotype, activity score and phenotype in a pediatric Thai population treated with risperidone

利培酮治疗的泰国儿科人群中CYP2D6基因型、活性评分和表型之间的关系

Hongkaew, Yaowaluck; Gaedigk, Andrea; Wilffert, Bob; Ngamsamut, Nattawat; Kittitharaphan, Wiranpat; Limsila, Penkhae; Sukasem, Chonlaphat

Associations of the SREBF2 Gene and INSIG2 Polymorphisms with Obesity and Dyslipidemia in Thai Psychotic Disorder Patients Treated with Risperidone

SREBF2 基因和 INSIG2 多态性与接受利培酮治疗的泰国精神病患者的肥胖和血脂异常的关联

Natchaya Vanwong, Chonlaphat Sukasem, Weerapon Unaharassamee, Napa Jiratjintana, Chalitpon Na Nakorn, Yaowaluck Hongkaew, Apichaya Puangpetch

Resolving discordant CYP2D6 genotyping results in Thai subjects: platform limitations and novel haplotypes

解决泰国受试者不一致的 CYP2D6 基因分型结果:平台限制和新单倍型

Yaowaluck Hongkaew, Wendy Y Wang, Roger Gaedigk, Chonlaphat Sukasem, Andrea Gaedigk

Clinically relevant genetic variants of drug-metabolizing enzyme and transporter genes detected in Thai children and adolescents with autism spectrum disorder.

在患有自闭症谱系障碍的泰国儿童和青少年中检测到与药物代谢酶和转运蛋白基因相关的临床遗传变异

Medhasi Sadeep, Pasomsub Ekawat, Vanwong Natchaya, Ngamsamut Nattawat, Puangpetch Apichaya, Chamnanphon Montri, Hongkaew Yaowaluck, Limsila Penkhae, Pinthong Darawan, Sukasem Chonlaphat

CYP2D6 polymorphisms and their influence on risperidone treatment

CYP2D6多态性及其对利培酮治疗的影响

Puangpetch, Apichaya; Vanwong, Natchaya; Nuntamool, Nopphadol; Hongkaew, Yaowaluck; Chamnanphon, Monpat; Sukasem, Chonlaphat

HLA-B allele and haplotype diversity among Thai patients identified by PCR-SSOP: evidence for high risk of drug-induced hypersensitivity

通过PCR-SSOP鉴定的泰国患者HLA-B等位基因和单倍型多样性:药物诱发超敏反应高风险的证据

Puangpetch, Apichaya; Koomdee, Napatrupron; Chamnanphol, Montri; Jantararoungtong, Thawinee; Santon, Siwalee; Prommas, Santirhat; Hongkaew, Yaowaluck; Sukasem, Chonlaphat

Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand

泰国疟疾流行区泰国人和缅甸人中葡萄糖-6-磷酸脱氢酶 (G6PD) 变异体的流行率和分布

Phompradit, Papichaya; Kuesap, Jiraporn; Chaijaroenkul, Wanna; Rueangweerayut, Ronnatrai; Hongkaew, Yaowaluck; Yamnuan, Rujira; Na-Bangchang, Kesara