Duangrurdee Wattanasirichaigoon

25PUBLICATIONS
46CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseaseCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Cancer genetics
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (25)

|May 04, 2026
Prenatal Whole-Genome Sequencing for Fetal Anomalies: Diagnostic Performance, Challenges, and Clinical Implications.

|Mar 16, 2026
Impacts and Economic Burden of Pompe Disease on Patients and Families in Thailand: A Mixed Method Study.

Sitaporn Youngkong, Montarat Thavorncharoensap, Usa Chaikledkaew

|Feb 27, 2026
Application of Prenatal Whole Exome Sequencing for Congenital Heart Anomalies.

Threebhorn Kamlungkuea, Fuanglada Tongprasert, Duangrurdee Wattanasirichaigoon

|Aug 13, 2025
New patients with duplication of the pituitary gland-plus syndrome, including a PTCH2 variant and a literature review.

Kochakorn Buasri, Pattima Pakhathirathien, Thiparom Sananmuang

|Jul 23, 2025
Expanding the clinical and molecular spectrum of TBC1D32-related ciliopathy: case reports and literature Review.

Wongsathorn Eiumtrakul, Thipwimol Tim-Aroon, Wadakarn Wuthisiri

|Jun 23, 2025
HMG-CoA Synthase-2 Deficiency: Neonatal Hyperammonemic Coma and Abnormal Metabolic Screening Resembling Maple Syrup Urine Disease.

Hathaipat Vaseenon, Thipwimol Tim-Aroon, Vitchayaporn Emarach Saengow

Pageof 5

Frequent Collaborators

8 joint publications

Thipwimol Tim-Aroon

2 joint publications

Threebhorn Kamlungkuea

2 joint publications

Achara Sathienkijkanchai

2 joint publications

Fuanglada Tongprasert