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Japanese Journal of Ophthalmology|February 13, 2010
Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisisLa-ongsri Atchaneeyasakul, Adisak Trinavarat, Auengporn Pituksung, et al.
American Journal of Medical Genetics. Part A|September 27, 2006
Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletionPiranit N Kantaputra, Chanin Limwongse, Chintana Tochareontanaphol, et al.
European Journal of Clinical Pharmacology|May 28, 2022
Association study identifies genetic determinants and non-genetic factors on steady-state plasma and therapeutic outcome of galantamine in mixed dementiaThitipon Yaowaluk, Vorapun Senanarong, Chanin Limwongse, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|June 27, 2014
Effects of PCSK1 genetic variants on obesity among Thai children and their family members: in relation to health risk, and biochemical and anthropometric parametersSirikul Kulanuwat, Benjaluck Phonrat, Anchalee Tungtrongchitr, et al.
Gene|December 28, 2014
Common variations in the FTO gene and obesity in Thais: a family-based studyWanida Chuenta, Benjaluck Phonrat, Anchalee Tungtrongchitr, et al.
Asian Pacific Journal of Allergy and Immunology|October 7, 2019
Effect of gene polymorphisms in ADAM33, TGFβ1, VEGFA, and PLAUR on asthma in Thai populationTorpong Thongngarm, Aree Jameekornrak, Nachol Chaiyaratana, et al.
European Journal of Clinical Pharmacology|April 10, 2017
Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactionsKittika Yampayon, Chonlaphat Sukasem, Chanin Limwongse, et al.
Clinical and Translational Science|January 30, 2026
Prevalence of Severe Thalassemia and Performance of Prenatal Screening Tests Among Pregnant Women at Siriraj Thalassemia Center in ThailandKwandao Malasai, Usa Chaikledkaew, Pattarawalai Talungchit, et al.
American Journal of Medical Genetics. Part A|March 16, 2012
A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disabilityAnunchai Assawamakin, Duangrurdee Wattanasirichaigoon, Chintana Tocharoentanaphol, et al.
Diagnostics (Basel, Switzerland)|March 4, 2020
Pathogenic PSEN1 Glu184Gly Mutation in a Family from Thailand with Probable Autosomal Dominant Early Onset Alzheimer's DiseaseVorapun Senanarong, Seong Soo A An, Giau Vo Van, et al.
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