Saisuda Noojarern

Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing

K. Rojnueangnit, D. Wattanasirichaigoon, Boonchu Sirichongkolthong, 2019, Pediatric Cardiology.

MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance

Asif Javed, L. T. Jensen, N. Jinawath, 2020, Scientific Reports.

Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome

S. Kaewsutthi, P. Lertrit, D. Wattanasirichaigoon, 2022, Frontiers in Pediatrics.

Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1

D. Wattanasirichaigoon, Thitiporn Junhasavasdikul, Parith Wongkittichote, 2022, Frontiers in Genetics.

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

W. Chantratita, Chutintorn Sriphrapradang, P. Mahachoklertwattana, 2020, Endocrine connections.

Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients

P. Charoenkwan, A. Tantiworawit, K. Suphapeetiporn, 2021, Orphanet Journal of Rare Diseases.