Vorasuk Shotelersuk

37PUBLICATIONS
209CO-AUTHORS
Disease surveillanceNanomedicineEpigenetics (incl. genome methylation and epigenomics)Craniofacial biologyOral implantology
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Publications (37)

|Apr 27, 2026
Long-read genome sequencing increases diagnostic yield in a short-read sequencing unsolved developmental epileptic encephalopathy (DEE) cohort.

|Apr 12, 2026
Development of the PICCOTEAM Reference Case for Economic Evaluation of Precision Medicine.

Wenjia Chen, Dimple Butani, Yi Wang

|Mar 24, 2026
Pentanucleotide repeat instability and transmission in benign adult familial myoclonic epilepsy types 1, 4, and 8.

Supphakorn Rakwongkhachon, Monnat Pongpanich, Chalurmpon Srichomthong

|Feb 11, 2026
A missense variant in ASCL5 leads to lobodontia.

Thanakorn Theerapanon, Narin Intarak, Khanti Rattanapornsompong

|Aug 05, 2025
A comparison of DNA methylation detection between HiFi sequencing and whole genome bisulfite sequencing in monozygotic twins with Down syndrome.

Kanyanee Promsawan, Chalurmpon Srichomthong, Monnat Pongpanich

|Jul 22, 2025
FAM20A Deficiency Drives Transcriptomic Dysregulation and Functional Impairment in Gingival Fibroblasts.

Kanokwan Sriwattanapong, Sermporn Thaweesapphithak, Chompak Khamwachirapitak

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Frequent Collaborators

11 joint publications

Thantrira Porntaveetus

6 joint publications

Thanakorn Theerapanon

5 joint publications

Kanya Suphapeetiporn

5 joint publications

Monnat Pongpanich