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Peerj|March 5, 2019
Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling geneSuvimol Niyomnaitham, Napa Parinyanitikul, Ekkapong Roothumnong, et al.
Molecular Vision|April 29, 2016
A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosaWorapoj Jinda, Naravat Poungvarin, Todd D Taylor, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Basic Science and PathogenesisVorapun Senanarong, Chatchawan Rattanabannakit, Natthamon Wongkom, et al.
Springerplus|May 8, 2014
An omnibus permutation test on ensembles of two-locus analyses can detect pure epistasis and genetic heterogeneity in genome-wide association studiesDamrongrit Setsirichok, Phuwadej Tienboon, Nattapong Jaroonruang, et al.
Muscle & Nerve|July 1, 2006
Mutation analysis of the GNE gene in distal myopathy with rimmed vacuoles (DMRV) patients in ThailandTeerin Liewluck, Theeraphong Pho-Iam, Chanin Limwongse, et al.
Journal of Neuromuscular Diseases|November 6, 2023
Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in ThailandPimchanok Kulsirichawaroj, Yanin Suksangkharn, Da Eun Nam, et al.
Clinical and Translational Science|December 19, 2025
Pharmacogenomic and Clinical Predictors of Deferasirox Response in Transfusion-Dependent Thalassemia Identified Using Whole-Genome SequencingKittika Yampayon, Watchara Sakares, Krittin Pitinanon, et al.
Plos Neglected Tropical Diseases|May 26, 2011
Orientia tsutsugamushi stimulates an original gene expression program in monocytes: relationship with gene expression in patients with scrub typhusWiwit Tantibhedhyangkul, Thanavadee Prachason, Duangdao Waywa, et al.
Pediatric Research|June 10, 2025
Next-generation sequencing for pediatric-onset neuromuscular disorders unresolved by conventional diagnostic methodsPimchanok Kulsirichawaroj, Mongkol Chanvanichtrakool, Pish Wattanadilokchatkun, et al.
Breast Cancer Research and Treatment|March 2, 2021
Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testingPongtawat Lertwilaiwittaya, Ekkapong Roothumnong, Panee Nakthong, et al.
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