Chumpol Ngamphiw
10PUBLICATIONS
29CO-AUTHORS
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Publications (10)
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|Apr 17, 2025
Correction: Kularbkaew et al. Genetic Variants in the <i>TBC1D2B</i> Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. <i>Int. J. Mol. Sci.</i> 2024, <i>25</i>, 8867.Thatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth
|Aug 29, 2024
Genetic Variants in the <i>TBC1D2B</i> Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.Thatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth
|Jun 27, 2024
Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians.Luca Lo Piccolo, Wasinee Wongkummool, Phatcharida Jantaree
|Jun 27, 2024
Homozygosity for a Rare <i>Plec</i> Variant Suggests a Contributory Role in Congenital Insensitivity to Pain.Piranit Kantaputra, Teerada Daroontum, Kantapong Kitiyamas
|May 25, 2024
Genetic Variants in <i>KCTD1</i> Are Associated with Isolated Dental Anomalies.Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin
|Mar 29, 2023
Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation.Ploy Adisornkanj, Rajit Chanprasit, Steven Eliason
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Frequent Collaborators
9 joint publications
Piranit Nik Kantaputra
6 joint publications
Timothy C Cox
4 joint publications
Peeranat Jatooratthawichot
4 joint publications
James R Ketudat Cairns
3 joint publications
Worrachet Intachai
3 joint publications
Teerada Daroontum
2 joint publications
Callum S Durward
2 joint publications
Sompid Kintarak
2 joint publications
Sissades Tongsima
2 joint publications
Ploy Adisornkanj
