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European Journal of Oral Sciences|February 19, 2022
Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9Narin Intarak, Thanakorn Theerapanon, Thantrira Porntaveetus, et al.
American Journal of Medical Genetics. Part A|August 1, 2018
Cole-Carpenter syndrome in a patient from ThailandThantrira Porntaveetus, Thanakorn Theerapanon, Chalurmpon Srichomthong, et al.
Journal of Translational Medicine|March 21, 2021
MBTPS2, a membrane bound protease, underlying several distinct skin and bone disordersNatarin Caengprasath, Thanakorn Theerapanon, Thantrira Porntaveetus, et al.
Oral Diseases|June 28, 2018
Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cellsNunthawan Nowwarote, Thanakorn Theerapanon, Thanaphum Osathanon, et al.
Genes & Diseases|December 14, 2019
Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and <i>FAM83H</i> 1261G>T mutationNunthawan Nowwarote, Thanaphum Osathanon, Kiattipan Kanjana, et al.
Molecular Genetics and Genomics : MGG|March 20, 2019
Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disordersNarin Intarak, Thanakorn Theerapanon, Sermporn Thaweesapphithak, et al.
BDJ Open|April 11, 2023
Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literatureKanokwan Sriwattanapong, Thanakorn Theerapanon, Lawan Boonprakong, et al.
Journal of Applied Oral Science : Revista FOB|June 8, 2022
Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestationsSermporn Thaweesapphithak, Jirawat Saengsin, Wuttichart Kamolvisit, et al.
International Journal of Neonatal Screening|February 10, 2021
Compound Heterozygosity for a Novel Frameshift Variant Causing Fatal Infantile Liver Failure and Genotype-Phenotype Correlation of <i>POLG</i> c.3286C>T VariantKanokwan Sriwattanapong, Kitiwan Rojnueangnit, Thanakorn Theerapanon, et al.
Genes & Diseases|June 14, 2019
A novel mutation in <i>COL1A2</i> leads to osteogenesis imperfecta/Ehlers-Danlos overlap syndrome with brachydactylyThunyaporn Budsamongkol, Narin Intarak, Thanakorn Theerapanon, et al.
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