Takol Chareonsirisuthigul

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2014-2023
Publications (10 Years): 5

Top Topics

Top Venues

Journal of pediatric genetics

Case reports in genetics

BioMed research international

This page only lists publications with an associated author ORCID identifier.

Publications

Yanisa Rattanapan, Sodsai Narkpetch, Takol Chareonsirisuthigul
Upregulation of miR-20a-5p as the Potential MicroRNA Marker in Red Blood Cell Storage Lesion. BioMed research international 2023 (2023)
Chanita Prapasrat, Preyaporn Onsod, Veerawat Korkiatsakul, Budsaba Rerkamnuaychoke, Duangrurdee Wattanasirichaigoon, Takol Chareonsirisuthigul
The Utilization of MS-MLPA as the First-Line Test for the Diagnosis of Prader-Willi Syndrome in Thai Patients. Journal of pediatric genetics 12 (4) (2022)
Jirawan Panachan, Napat Rojsirikulchai, Nutkridta Pongsakul, Ladawan Khowawisetsut, Pongpak Pongphitcha, Teerapong Siriboonpiputtana, Takol Chareonsirisuthigul, Pitichai Phornsarayuth, Nisakorn Klinkulab, Natini Jinawath, Wararat Chiangjong, Usanarat Anurathapan, Kovit Pattanapanyasat, Suradej Hongeng, Somchai Chutipongtanate
Extracellular Vesicle-Based Method for Detecting MYCN Amplification Status of Pediatric Neuroblastoma. Cancers 14 (11) (2022)
Chanita Prapasrat, Preyaporn Onsod, Veerawat Korkiatsakul, Budsaba Rerkamnuaychoke, Duangrurdee Wattanasirichaigoon, Takol Chareonsirisuthigul
The Utilization of MS-MLPA as the First-Line Test for the Diagnosis of Prader-Willi Syndrome in Thai Patients. Journal of pediatric genetics 12 (4) (2022)
Kitiwan Rojnueangnit, Thanitchet Khetkham, Preyaporn Onsod, Takol Chareonsirisuthigul
Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing. Journal of pediatric genetics 11 (1) (2020)
Takol Chareonsirisuthigul, Suchin Worawichawong, Rachanee Parinayok, Patama Promsonthi, Budsaba Rerkamnuaychoke
Intrauterine growth retardation fetus with trisomy 16 mosaicism. Case reports in genetics 2014 (2014)