| A genetic association study between growth differentiation factor 5 (GDF 5) polymorphism and knee osteoarthritis in Thai population T Tawonsawatruk, T Changthong, S Pingsuthiwong, O Trachoo, T Sura, ... Journal of orthopaedic surgery and research 6, 1-5, 2011 | 54 | 2011 |
| Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis E Mukda, O Trachoo, E Pasomsub, R Tiyasirichokchai, N Iemwimangsa, ... International Journal of Hematology 106, 282-290, 2017 | 29 | 2017 |
| Fine‐Needle Aspiration Cytology of Parathyroid Carcinoma Mimic Hürthle Cell Thyroid Neoplasm C Sriphrapradang, P Sornmayura, N Chanplakorn, O Trachoo, ... Case Reports in Endocrinology 2014 (1), 680876, 2014 | 29 | 2014 |
| 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 … T Sura, O Trachoo, V Viprakasit, P Vathesatogkit, A Tunteeratum, ... Annals of hematology 86, 659-663, 2007 | 26 | 2007 |
| Amelioration of osteogenesis in iPSC-derived mesenchymal stem cells from osteogenesis imperfecta patients by endoplasmic reticulum stress inhibitor T Duangchan, T Tawonsawatruk, C Angsanuntsukh, O Trachoo, ... Life Sciences 278, 119628, 2021 | 18 | 2021 |
| Chromosome 20p inverted duplication deletion identified in a Thai female adult with mental retardation, obesity, chronic kidney disease and characteristic facial features O Trachoo, M Assanatham, N Jinawath, A Nongnuch European journal of medical genetics 56 (6), 319-324, 2013 | 17 | 2013 |
| Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease T Sura, M Busabaratana, S Youngcharoen, R Wisedpanichkij, ... European journal of haematology 79 (3), 251-254, 2007 | 17 | 2007 |
| Association of Estrogen Receptor-alpha single-nucleotide polymorphism (codon 594 G/A) and Thai patients affected by knee osteoarthritis T Tawonsawatruk, O Trachoo, T Channoom, T Sura, ... J Med Assoc Thai 92 (Suppl 6), 45-50, 2009 | 14 | 2009 |
| Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a … C Satirapod, M Sukprasert, B Panthan, A Charoenyingwattana, ... PloS one 14 (11), e0225457, 2019 | 13 | 2019 |
| Screening of Fabry disease in patients with end-stage renal disease of unknown etiology: the first Thailand study O Trachoo, P Jittorntam, S Pibalyart, S Kajanachumphol, ... Journal of Biomedical Research 31 (1), 17, 2016 | 13 | 2016 |
| Chromosome 22q11. 2 deletion syndrome presenting as adult onset hypoparathyroidism: clues to diagnosis from dysmorphic facial features S Korpaisarn, O Trachoo, C Sriphrapradang Case Reports in Endocrinology 2013 (1), 802793, 2013 | 11 | 2013 |
| Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history? T Sura, J Eu-Ahsunthornwattana, S Youngcharoen, M Busabaratana, ... Journal of human genetics 54 (5), 284-288, 2009 | 11 | 2009 |
| Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand O Trachoo, T Sura, A Sakuntabhai, P Singhasivanon, S Krudsood, ... Hemoglobin 27 (2), 97-104, 2003 | 9 | 2003 |
| Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII PN Kantaputra, LJ Smith, ML Casal, C Kuptanon, YC Chang, ... American Journal of Medical Genetics Part A 179 (3), 486-493, 2019 | 8 | 2019 |
| First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration O Trachoo, C Satirapod, B Panthan, M Sukprasert, A Charoenyingwattana, ... Journal of assisted reproduction and genetics 34, 109-116, 2017 | 7 | 2017 |
| Angiotensin‐converting enzyme gene polymorphism in Thai patients with systemic lupus erythematosus U Pitipakorn, P Suwannalai, O Trachoo, S Rattanasiri, S Chitphuk, ... International Journal of Rheumatic Diseases 19 (7), 693-699, 2016 | 7 | 2016 |
| A novel mutation in thyroid peroxidase gene causing congenital goitrous hypothyroidism in a German-Thai patient C Sriphrapradang, Y Thewjitcharoen, S Chanprasertyothin, S Nakasatien, ... Journal of Clinical Research in Pediatric Endocrinology 8 (2), 241, 2016 | 7 | 2016 |
| A novel PRKAR1A mutation identified in a patient with isolated primary pigmented nodular adrenocortical disease S Korpaisarn, O Trachoo, B Panthan, R Aroonroch, R Suvikapakornkul, ... Case Reports in Oncology 10 (2), 769-776, 2017 | 6 | 2017 |
| Low oxygen saturation and severe anemia in compound heterozygous Hb Louisville [β42 (CD1) Phe→ Leu] and Hb La Desirade [β129 (H7) Ala→ Val] P Kamseng, S Trakulsrichai, O Trachoo, W Yimniam, B Panthan, ... Hematology 22 (2), 114-118, 2017 | 6 | 2017 |
| Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service O Trachoo, T Yingchoncharoen, T Ngernsritrakul, N Iemwimangsa, ... PloS one 17 (9), e0267770, 2022 | 5 | 2022 |
