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NPJ Genomic Medicine|November 21, 2025
Transferability of polygenic risk scores for metabolic and cardiovascular traits in an underrepresented populationPhongthana Pasookhush, Apinya Surawit, Sophida Suta, et al.
International Journal of Molecular Sciences|March 11, 2023
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary TeethChomchanok Panyarat, Siriruk Nakornchai, Kanoknart Chintakanon, et al.
European Journal of Orthodontics|April 8, 2020
Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2Piranit Nik Kantaputra, Prapai Dejkhamron, Worrachet Intachai, et al.
Scientific Reports|July 31, 2023
A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented populationJohn Mauleekoonphairoj, Sissades Tongsima, Apichai Khongphatthanayothin, et al.
Clinical Genetics|January 5, 2023
DKK1 is a strong candidate for mesiodens and taurodontismPiranit Kantaputra, Peeranat Jatooratthawichot, Naomi Kottege, et al.
Journal of Personalized Medicine|November 27, 2021
PharmVIP: A Web-Based Tool for Pharmacogenomic Variant Analysis and InterpretationJittima Piriyapongsa, Chanathip Sukritha, Pavita Kaewprommal, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|March 19, 2021
A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomaliesPiranit Nik Kantaputra, Prapai Dejkhamron, Worrachet Intachai, et al.
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