日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Genetic Variants in DVL3 are Associated With Root Maldevelopment, Tooth Agenesis, Mesiodens, and Oral Exostoses

DVL3基因变异与牙根发育不良、牙齿缺失、正中牙和口腔骨疣有关

期刊:International Dental Journal
影响因子:3.7
doi:10.1016/j.identj.2025.104019
Kantaputra, Piranit; Bunpiem, Narumon; Guven, Yeliz; Tripuwabhrut, Kanich; Kalayci, Tugba; Imren, Ebru; Sengtae, Nuttaporn; Pianmee, Chawalid; Pruksametanan, Apitchaya; Tongsima, Sissades; Ngamphiw, Chumpol; Kawasaki, Katsushige; Ohazama, Atsushi; Cairns, James R Ketudat
发育与干细胞
发表日期：2026
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Clinical and molecular spectrum of inherited epidermolysis bullosa in a Thai cohort: A 12-year retrospective study

泰国人群中遗传性大疱性表皮松解症的临床和分子谱：一项为期12年的回顾性研究

期刊:
影响因子:
doi:10.1016/j.jdin.2026.02.010
Supsrisunjai, Chavalit; Tirachaimongkol, Nuanjutha; Bunnag, Thareena; Sengtae, Nuttaporn; Tongsima, Sissades; Ngamphiw, Chumpol; Komkhong, Wanchanida; Kootiratrakarn, Tanawatt; Wessagowit, Vesarat; Kantaputra, Piranit
发表日期：2026
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Correction: Kularbkaew et al. Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. Int. J. Mol. Sci. 2024, 25, 8867

更正：Kularbkaew 等人，《TBC1D2B 基因的遗传变异与拉蒙综合征和遗传性牙龈纤维瘤病相关》，《国际分子科学杂志》，2024 年，25 卷，8867 页。

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms26073228
Kularbkaew, Thatphicha; Thongmak, Tipaporn; Sandeth, Phan; Daroontum, Teerada; Durward, Callum S; Vittayakittipong, Pichai; Duke, Paul; Iamaroon, Anak; Kintarak, Sompid; Intachai, Worrachet; Ngamphiw, Chumpol; Tongsima, Sissades; Jatooratthawichot, Peeranat; Cox, Timothy C; Ketudat Cairns, James R; Kantaputra, Piranit
发表日期：2025
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Heimler Syndrome With Tooth Agenesis, Abnormal Enamel and Dentin Mineralization, Root Maldevelopment, and PEX1 Mutation

海姆勒综合征伴牙齿缺失、牙釉质和牙本质矿化异常、牙根发育不良和PEX1基因突变

期刊:International Dental Journal
影响因子:3.7
doi:10.1016/j.identj.2025.04.002
Kantaputra, Piranit N; Apivatthakakul, Atitaya; Kaewgahya, Massupa; Tongsima, Sissades; Ngamphiw, Chumpol; Sastraruji, Thanapat; Sukantamala, Panwarit; Carlson, Bruce M; Kawasaki, Katsushige; Ketudat Cairns, James R; Sonsuwan, Nuntigar; Ohazama, Atsushi
发育与干细胞
发表日期：2025
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A Novel KDF1 Variant is Associated With Multiple Natal Teeth, Tooth Agenesis, and Root Maldevelopment

一种新型KDF1变异与多发性先天性牙齿、牙齿缺失和牙根发育不良有关

期刊:International Dental Journal
影响因子:3.7
doi:10.1016/j.identj.2025.100860
Graham, John M Jr; Sanchez-Lara, Pedro A; Ohazama, Atsushi; Kawasaki, Katsushige; Arold, Stefan T; Kantaputra, Piranit Nik
发育与干细胞
发表日期：2025
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Genetic Variants in KIF7 May Contribute to Supernumerary Tooth Formation

KIF7基因变异可能导致多生牙的形成

期刊:International Dental Journal
影响因子:3.7
doi:10.1016/j.identj.2025.100928
Chainaphaphorn, Phohathai; Ngamphiw, Chumpol; Tongsima, Sissades; Chintakanon, Kanoknart; Kawasaki, Katsushige; Cox, Timothy C; Ohazama, Atsushi; Ketudat Cairns, James R; Kantaputra, Piranit Nik
发表日期：2025
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Stuck Below: Failure of Tooth Eruption and Hereditary Enamel Defects

牙齿萌出障碍和遗传性牙釉质缺陷

期刊:International Dental Journal
影响因子:3.7
doi:10.1016/j.identj.2025.100942
Kantaputra, Piranit Nik; Sirikrai, Thamon; Green, Jeremy
发表日期：2025
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Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians

罕见丝聚蛋白变异体与亚洲人的脓疱性皮肤病相关

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms25126466
Lo Piccolo, Luca; Wongkummool, Wasinee; Jantaree, Phatcharida; Daroontum, Teerada; Chaowattanapanit, Suteeraporn; Choonhakarn, Charoen; Amornpinyo, Warayuwadee; Chaiwarith, Romanee; Kiratikanon, Salin; Rujiwetpongstorn, Rujira; Tovanabutra, Napatra; Chiewchanvit, Siri; Ngamphiw, Chumpol; Intachai, Worrachet; Kantaputra, Piranit; Chuamanochan, Mati
发表日期：2024
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Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain

罕见 Plec 变异的纯合子状态提示其可能在先天性痛觉缺失中发挥作用

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms25126358
Kantaputra, Piranit; Daroontum, Teerada; Kitiyamas, Kantapong; Piyakhunakorn, Panat; Kawasaki, Katsushige; Sathienkijkanchai, Achara; Wasant, Pornswan; Vatanavicharn, Nithiwat; Yasanga, Thippawan; Kaewgahya, Massupa; Tongsima, Sissades; Cox, Timothy C; Arold, Stefan T; Ohazama, Atsushi; Ngamphiw, Chumpol
发表日期：2024
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Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis

TBC1D2B基因的遗传变异与拉蒙综合征和遗传性牙龈纤维瘤病相关。

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms25168867
Kularbkaew, Thatphicha; Thongmak, Tipaporn; Sandeth, Phan; Daroontum, Teerada; Durward, Callum S; Vittayakittipong, Pichai; Duke, Paul; Iamaroon, Anak; Kintarak, Sompid; Intachai, Worrachet; Ngamphiw, Chumpol; Tongsima, Sissades; Jatooratthawichot, Peeranat; Cox, Timothy C; Ketudat Cairns, James R; Kantaputra, Piranit
发表日期：2024
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