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Molecular Genetics & Genomic Medicine|May 31, 2021
Identification of novel mutation in RANKL by whole-exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosisPongtawat Lertwilaiwittaya, Bhoom Suktitipat, Phongphak Khongthon, et al.
Case Reports in Dermatology|September 10, 2015
Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis CongenitaBenjaporn Panichareon, Thanawat Seedapan, Wanna Thongnoppakhun, et al.
Case Reports in Neurology|April 8, 2014
A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with InflammationJantima Tanboon, Kanjana Rongsa, Manop Pithukpakorn, et al.
BMC Cancer|February 25, 2025
Comprehensive genomic analysis in sporadic early-onset colorectal adenocarcinoma patientsBen Ponvilawan, Phuwanat Sakornsakolpat, Ananya Pongpaibul, et al.
Bioinformatics Advances|May 13, 2024
GLIMMERS: glioma molecular markers exploration using long-read sequencingWichayapat Thongrattana, Tantip Arigul, Bhoom Suktitipat, et al.
Pharmacogenomics and Personalized Medicine|December 26, 2014
Mycophenolic acid AUC in Thai kidney transplant recipients receiving low dose mycophenolate and its association with UGT2B7 polymorphismsManop Pithukpakorn, Tiwat Tiwawanwong, Yupaporn Lalerd, et al.
Plos One|April 26, 2019
Clinical outcome and laboratory markers for predicting disease activity in patients with disseminated opportunistic infections associated with anti-interferon-γ autoantibodiesNasikarn Angkasekwinai, Yupin Suputtamongkol, Pakpoom Phoompoung, et al.
Scientific Reports|May 3, 2026
Genomic profiling and therapeutic targets of Thai melanoma revealed by next-generation sequencingKornyok Kamdee, Manop Pithukpakorn, Panitta Sitthinamsuwan, et al.
BMC Cancer|July 13, 2026
Distinct genomic landscape of colorectal signet ring cell carcinoma reveals frequent KMT2 family alterations and SMAD4 inactivationKrittiya Korphaisarn, Jirapat Aiamsophon, Nuttapong Ngamphaiboon, et al.
European Journal of Medical Genetics|November 2, 2010
Six novel ATP7B mutations in Thai patients with Wilson diseaseBenjaporn Panichareon, Krailerk Taweechue, Wanna Thongnoppakhun, et al.
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