GREMLIN 2 Mutations and Dental Anomalies von Kantaputra, P.N., Kaewgahya, M., Hatsadaloi, A., Vogel, P., Kawasaki, K., Ohazama, A., Ketudat Cairns, J.R.

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A Mutation in ICACNA1S/I Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment von Kantaputra, Piranit, Leelaadisorn, Niramol, Hatsadaloi, Athiwat, Quarto, Natalina, Intachai, Worrachet, Tongsima, Sissades, Kawasaki, Katsushige, Ohazama, Atsushi, Ngamphiw, Chumpol, Wiriyakijja, Paswach

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Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis von Kantaputra, Piranit, Tripuwabhrut, Kanich, Jatooratthawichot, Peeranat, Adisornkanj, Ploy, Hatsadaloi, Athiwat, Porntrakoolsaree, Nop, Kaewgaya, Massupa, Olsen, Bjorn, Tongsima, Sissades, Ngamphiw, Chumpol, Ketudat Cairns, James R

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A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment von Kantaputra, Piranit, Leelaadisorn, Niramol, Hatsadaloi, Athiwat, Quarto, Natalina, Intachai, Worrachet, Tongsima, Sissades, Kawasaki, Katsushige, Ohazama, Atsushi, Ngamphiw, Chumpol, Wiriyakijja, Paswach

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Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies von Ruangchan, Cholaporn, Ngamphiw, Chumpol, Krasaesin, Annop, Intarak, Narin, Tongsima, Sissades, Kaewgahya, Massupa, Kawasaki, Katsushige, Mahawong, Phitsanu, Paripurana, Kullaya, Sookawat, Bussaneeya, Jatooratthawichot, Peeranat, Cox, Timothy C, Ohazama, Atsushi, Ketudat Cairns, James R, Porntaveetus, Thantrira, Kantaputra, Piranit

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Genetic Variants in IKCTD1/I Are Associated with Isolated Dental Anomalies von Ruangchan, Cholaporn, Ngamphiw, Chumpol, Krasaesin, Annop, Intarak, Narin, Tongsima, Sissades, Kaewgahya, Massupa, Kawasaki, Katsushige, Mahawong, Phitsanu, Paripurana, Kullaya, Sookawat, Bussaneeya, Jatooratthawichot, Peeranat, Cox, Timothy C, Ohazama, Atsushi, Ketudat Cairns, James R, Porntaveetus, Thantrira, Kantaputra, Piranit

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Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth von Panyarat, Chomchanok, Nakornchai, Siriruk, Chintakanon, Kanoknart, Leelaadisorn, Niramol, Intachai, Worrachet, Olsen, Bjorn, Tongsima, Sissades, Adisornkanj, Ploy, Ngamphiw, Chumpol, Cox, Timothy C, Kantaputra, Piranit

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Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans von Kantaputra, Piranit Nik, Jatooratthawichot, Peeranat, Adisornkanj, Ploy, Kitsadayurach, Panita, Kaewgahya, Massupa, Olsen, Bjorn, Ohazama, Atsushi, Ngamphiw, Chumpol, Tongsima, Sissades, Cox, Timothy C, Ketudat Cairns, James R

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Rare Genetic Variants in Human IAPC/I Are Implicated in Mesiodens and Isolated Supernumerary Teeth von Panyarat, Chomchanok, Nakornchai, Siriruk, Chintakanon, Kanoknart, Leelaadisorn, Niramol, Intachai, Worrachet, Olsen, Bjorn, Tongsima, Sissades, Adisornkanj, Ploy, Ngamphiw, Chumpol, Cox, Timothy C, Kantaputra, Piranit

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Genetic/Protein Association of Atopic Dermatitis and Tooth Agenesis von Ouyang, Wanlu, Goh, Charlene E, Ng, Wei Bo, Chew, Fook Tim, Yap, Eric Peng Huat, Hsu, Chin-Ying Stephen

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Rare Variants in ILRP4/I Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans von Kantaputra, Piranit Nik, Jatooratthawichot, Peeranat, Adisornkanj, Ploy, Kitsadayurach, Panita, Kaewgahya, Massupa, Olsen, Bjorn, Ohazama, Atsushi, Ngamphiw, Chumpol, Tongsima, Sissades, Cox, Timothy C, Ketudat Cairns, James R

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An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis von Sarkar, Tanmoy, Ranjan, Prashant, Kanathur, Smitha, Gupta, Ankush, Das, Parimal

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Heterozygous Variants in IFREM2/I Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas von Kantaputra, Piranit Nik, Tripuwabhrut, Kanich, Anthonappa, Robert P, Chintakanon, Kanoknart, Ngamphiw, Chumpol, Adisornkanj, Ploy, Porntrakulseree, Nop, Olsen, Bjorn, Intachai, Worrachet, Hennekam, Raoul C, Vieira, Alexandre R, Tongsima, Sissades

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Rethinking the Genetic Etiology of Nonsyndromic Tooth Agenesis von Letra, Ariadne

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miR-122–5p targets GREM2 to protect against glucocorticoid-induced endothelial damage through the BMP signaling pathway von Huang, Xianzhe, Jie, Shuo, Li, Wenzhao, Li, Hui, Ni, Jiangdong, Liu, Chan

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Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis von Du, Renqian, Dinckan, Nuriye, Song, Xiaofei, Coban-Akdemir, Zeynep, Jhangiani, Shalini N., Guven, Yeliz, Aktoren, Oya, Kayserili, Hulya, Petty, Lauren E., Muzny, Donna M., Below, Jennifer E., Boerwinkle, Eric, Wu, Nan, Gibbs, Richard A., Posey, Jennifer E., Lupski, James R., Letra, Ariadne, Uyguner, Z. Oya

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Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas von Kantaputra, Piranit Nik, Tripuwabhrut, Kanich, Anthonappa, Robert P, Chintakanon, Kanoknart, Ngamphiw, Chumpol, Adisornkanj, Ploy, Porntrakulseree, Nop, Olsen, Bjorn, Intachai, Worrachet, Hennekam, Raoul C, Vieira, Alexandre R, Tongsima, Sissades

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Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation von Adisornkanj, Ploy, Chanprasit, Rajit, Eliason, Steven, Fons, Juan M, Intachai, Worrachet, Tongsima, Sissades, Olsen, Bjorn, Arold, Stefan T, Ngamphiw, Chumpol, Amendt, Brad A, Tucker, Abigail S, Kantaputra, Piranit

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Novel LRP6 Mutations Causing Non-Syndromic Oligodontia von Lee, Yejin, Chae, Wonseon, Kim, Youn Jung, Kim, Jung-Wook

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A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis von Dinckan, Nuriye, Du, Renqian, Akdemir, Zeynep C., Bayram, Yavuz, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Guven, Yeliz, Aktoren, Oya, Kayserili, Hulya, Boerwinkle, Eric, Gibbs, Richard A., Posey, Jennifer E., Lupski, James R., Uyguner, Zehra O., Letra, Ariadne

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