All Stories

  1. From toothed dinosaurs to toothless birds: evolutionary clues from people with missing teeth.

    Article • Proceedings of the National Academy of Sciences, October 2026, Proceedings of the National Academy of Sciences

    Piranit Kantaputra

  2. Genetic regulatory pathways of split-hand/foot malformation

    Article • Clinical Genetics, September 2018, Wiley

    Piranit Kantaputra

  3. Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation

    Article • American Journal of Medical Genetics Part A, August 2018, Wiley

    Professor James R Ketudat Cairns, Piranit Kantaputra

  4. Making extra teeth: Lessons from aTRPS1mutation

    Article • American Journal of Medical Genetics Part A, October 2016, Wiley

    Piranit Kantaputra

  5. Syndromes with supernumerary teeth

    Article • American Journal of Medical Genetics Part A, June 2016, Wiley

    Piranit Kantaputra

  6. All enamel is not created equal:Supports from a novelFAM83Hmutation

    Article • American Journal of Medical Genetics Part A, October 2015, Wiley

    Piranit Kantaputra

  7. Preaxial polydactyly associated with aMSX1mutation and report of two novel mutations

    Article • American Journal of Medical Genetics Part A, October 2015, Wiley

    Piranit Kantaputra

  8. Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novelFBLN5mutation

    Article • American Journal of Medical Genetics Part A, June 2014, Wiley

    Dr Karen W Gripp, Piranit Kantaputra

  9. Enamel-Renal-Gingival syndrome, hypodontia, and a novelFAM20Amutation

    Article • American Journal of Medical Genetics Part A, April 2014, Wiley

    Piranit Kantaputra

  10. Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novelARSBmutations

    Article • American Journal of Medical Genetics Part A, March 2014, Wiley

    Piranit Kantaputra

  11. Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations

    Article • American Journal of Medical Genetics Part A, January 2014, Wiley

    Piranit Kantaputra

  12. Clinical Correlate: CLCN7 ‐Associated Autosomal Recessive Osteopetrosis

    Article • May 2012, Wiley

    Piranit Kantaputra