Browsing by Author Bjorn Olsen
Showing results 1 to 11 of 11
| Issue Date | Title | Author(s) |
| 1-Nov-2020 | Are dental anomalies associated with Tietz syndrome? | Piranit Nik Kantaputra; Worrachet Intachai; Bruce Carlson; Bjorn Olsen; Saisinee Ngaohirunphat; Jitprapa Sri-Oon; James R. Ketudat Cairns; Janejit Choovuthayakorn |
| 1-Feb-2022 | Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation | Piranit Nik Kantaputra; Nutsuchar Wangtiraumnuay; Chumpol Ngamphiw; Bjorn Olsen; Worrachet Intachai; Abigail S. Tucker; Sissades Tongsima |
| 1-Jan-2022 | Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome | Piranit Kantaputra; Yeliz Guven; Tugba Kalayci; Pelin Karaca Özer; Wannakamon Panyarak; Worrachet Intachai; Bjorn Olsen; Bruce M. Carlson; Oranud Praditsap; Sissades Tongsima; Chumpol Ngamphiw; Peeranat Jatooratthawichot; Abigail S. Tucker; James R. Ketudat Cairns |
| 1-Jan-2020 | Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation | Napaporn Tananuvat; Rak Tananuvat; Wattana Chartapisak; Pongsak Mahanupab; Chananya Hokierti; Metawee Srikummool; Jatupol Kampuansai; Worrachet Intachai; Bjorn Olsen; James R. Ketudat Cairns; Piranit Kantaputra |
| 1-Nov-2020 | Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2 | Piranit Nik Kantaputra; Prapai Dejkhamron; Sissades Tongsima; Chumpol Ngamphiw; Worrachet Intachai; Lukana Ngiwsara; Phannee Sawangareetrakul; Jisnuson Svasti; Bjorn Olsen; James R.Ketudat Cairns; Kanokkan Bumroongkit |
| 1-Feb-2021 | Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2 | Piranit Nik Kantaputra; Prapai Dejkhamron; Worrachet Intachai; Chumpol Ngamphiw; Katsushige Kawasaki; Atsushi Ohazama; Suttichai Krisanaprakornkit; Bjorn Olsen; Sissades Tongsima; Jame R. Ketudat Cairns |
| 1-Oct-2022 | Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses | Piranit Nik Kantaputra; Yeliz Guven; Kanich Tripuwabhrut; Ploy Adisornkanj; Athiwat Hatsadaloi; Massupa Kaewgahya; Bjorn Olsen; Chumpol Ngamphiw; Peeranat Jatooratthawichot; Sissades Tongsima; James R. Ketudat Cairns |
| 1-Oct-2022 | Mutations in LRP6 highlight the role of WNT signaling in oral exostoses and dental anomalies | Piranit Kantaputra; Peeranat Jatooratthawichot; Kanoknart Chintakanon; Worrachet Intachai; Prapat Pradermdutsadeeporn; Ploy Adisornkanj; Sissades Tongsima; Chumpol Ngamphiw; Bjorn Olsen; Abigail S. Tucker; James R. Ketudat Cairns |
| 1-Jan-2022 | Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites | Piranit Kantaputra; Peeranat Jatooratthawichot; Oranuch Tantachamroon; Kamonporn Nanekrungsan; Worrachet Intachai; Bjorn Olsen; Sissades Tongsima; Chumpol Ngamphiw; James R.Ketudat Cairns |
| 1-Dec-2021 | A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomalies | Piranit Nik Kantaputra; Prapai Dejkhamron; Worrachet Intachai; Chumpol Ngamphiw; James R. Ketudat Cairns; Katsushige Kawasaki; Atsushi Ohazama; Bjorn Olsen; Sissades Tongsima; Salita Angkurawaranon |
| 1-May-2022 | WNT10A variant and severe scoliosis? | Piranit Kantaputra; Bjorn Olsen; John A. McGrath |
