Nareenart Iemwimangsa

Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations

Zeina N. Al-Mahayri, George P. Patrinos, Sukanya Wattanapokayakit et al. · Scientific Reports · 2020 · 37 citations · Full text

Medicine, Pharmacology, Human Genetics +12

Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm)

Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn et al. · Human Genome Variation · 2021 · 37 citations · Full text

Medicine, Genetics, Pharmacology +15

Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis

Ekchol Mukda, Objoon Trachoo, Ekawat Pasomsub et al. · International Journal of Hematology · 2017 · 29 citations

Medicine, Genetics, Molecular Genetics +16

DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

Kinnaree Sorapipatcharoen, Thipwimol Tim‐Aroon, Pat Mahachoklertwattana et al. · Endocrine Connections · 2020 · 18 citations · Full text

Medicine, Endocrinology, Genetics +17

Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma

Weenita Pipitprapat, Oraluck Pattanaprateep, Nareenart Iemwimangsa et al. · Annals of Medicine · 2021 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17