Atchara Tunteeratum

Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma

W. Chantratita, Weenita Pipitprapat, Chutintorn Sriphrapradang, 2021, Annals of medicine.

Characteristics of breast cancer patients tested for germline BRCA1/2 mutations by next‐generation sequencing in Ramathibodi Hospital, Mahidol University

T. Sukarayothin, N. Iemwimangsa, Atchara Tunteeratum, 2021, Cancer reports.

Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method

V. Viprakasit, T. Sura, P. Vathesatogkit, 2007, Annals of Hematology.

Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of Duchenne muscular dystrophy with duplication of dystrophin gene.

T. Sura, J. Eu-ahsunthornwattana, R. Witoonpanich, 2009, Journal of clinical neuromuscular disease.

Carrier frequency of spinal muscular atrophy in Thailand

P. Sritara, T. Sura, W. Stitchantrakul, 2019, Neurological Sciences.

Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history?

T. Sura, J. Eu-ahsunthornwattana, S. Theerasasawat, 2009, Journal of Human Genetics.