Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain
International Journal of Molecular Sciences.  2024.  25  (12):

Phenotypic and molecular features of Thai patients with primary carnitine deficiency
Pediatr Int.  2022. 

Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variants
Molecular Biology Reports.  2021. 

Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics.  2019.  181  (2): 155-165.

An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand
PLoS One.  2015.  10  (8):

Analysis of Novel Mutations and Methylmalonyl-CoA Mutase Levels in Thai Patients with Isolated Methylmalonic Acidemia
Biochem Genet.  2015.  53  (11): 310-318.

Clinical characteristics and mutation analysis of propionic acidemia in Thailand
World Journal of Pediatrics.  2014.  10  (1): 64-68.

Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response.
Brain Dev.  2014. 

Genetic counseling/consultation in South-East Asia: A report from the workshop at the 10th Asia pacific conference on human genetics
Journal of Genetic Counseling .  2013.  22  (6): 917-924.

Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region
Molecular Genetics and Metabolism.  2012.  107  (1-2): 136-144.