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Neuropsychiatric Disease and Treatment|December 5, 2018
Identification of a novel mutation in <i>APP</i> gene in a Thai subject with early-onset Alzheimer's diseaseVo Van Giau, Vorapun Senanarong, Eva Bagyinszky, et al.
BMC Medical Genetics|March 17, 2004
Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP)Wanna Thongnoppakhun, Chanin Limwongse, Kriengsak Vareesangthip, et al.
Neurology. Genetics|February 3, 2026
Expanding the Genetic Landscape of Congenital Insensitivity to PainTheeraphong Pho-Iam, Pimchanok Kulsirichawaroj, Surachai Likasitwattanakul, et al.
Hematology (Amsterdam, Netherlands)|January 24, 2022
The efficacy of low-dose warfarin initiation (3 mg versus 5 mg) in newly diagnosed venous thromboembolism patients among a population with a high prevalence of warfarin-sensitive haplotype of the <i>VKORC1</i> gene: a randomized controlled trialBundarika Suwanawiboon, Wannaphorn Rotchanapanya, Komkrit Mahaprom, et al.
Clinical Chemistry|March 9, 2022
Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar AtaxiasMulias Lian, Chanin Limwongse, Chui-Sheun Yoon, et al.
International Journal of Data Mining and Bioinformatics|January 30, 2013
Small Ancestry Informative Marker panels for complete classification between the original four HapMap populationsDamrongrit Setsirichok, Theera Piroonratana, Anunchai Assawamakin, et al.
Ophthalmic Genetics|March 18, 2006
Novel and de-novo truncating PAX6 mutations and ocular phenotypes in Thai aniridia patientsLa-Ongsri Atchaneeyasakul, Adisak Trinavarat, Dhaivadee Dulayajinda, et al.
World Journal of Gastroenterology|January 28, 2015
Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancerKrittiya Korphaisarn, Ananya Pongpaibul, Chanin Limwongse, et al.
Annals of Medicine|June 16, 2025
Prevalence of genetic alterations in basal cell carcinoma patients resistant to Hedgehog pathway inhibitors: a systematic reviewSuvijak Untaaveesup, Pornteera Srichana, Gynna Techataweewan, et al.
Ophthalmic Genetics|September 4, 2008
Mutation analysis of the VMD2 gene in thai families with best macular dystrophyLa-ongsri Atchaneeyasakul, Worapoj Jinda, Natta Sakolsatayadorn, et al.
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