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Dental malformations associated with biallelic MMP20 mutations.
Wang SK, Zhang H, Chavez MB, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Colvin CD, Kolli TN, Tan MH, Wang YL, Lu PY, Kim JW, Foster BL, Bartlett JD, Simmer JP, Hu JC. Wang SK, et al. Among authors: zhang h. Mol Genet Genomic Med. 2020 Aug;8(8):e1307. doi: 10.1002/mgg3.1307. Epub 2020 Jun 3. Mol Genet Genomic Med. 2020. PMID: 32495503 Free PMC article.
ENAM mutations and digenic inheritance.
Zhang H, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Wang SK, Wright JT, Havel MW, Zhang C, Kim JW, Simmer JP, Hu JC. Zhang H, et al. Among authors: zhang c. Mol Genet Genomic Med. 2019 Oct;7(10):e00928. doi: 10.1002/mgg3.928. Epub 2019 Sep 2. Mol Genet Genomic Med. 2019. PMID: 31478359 Free PMC article.
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations.
Liang T, Wang SK, Smith C, Zhang H, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Kim JW, Zhang C, Saunders TL, Simmer JP, Hu JC. Liang T, et al. Among authors: zhang c, zhang h. Sci Rep. 2022 Oct 1;12(1):16477. doi: 10.1038/s41598-022-20684-9. Sci Rep. 2022. PMID: 36183038 Free PMC article.
Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.
Seymen F, Kim YJ, Lee YJ, Kang J, Kim TH, Choi H, Koruyucu M, Kasimoglu Y, Tuna EB, Gencay K, Shin TJ, Hyun HK, Kim YJ, Lee SH, Lee ZH, Zhang H, Hu JC, Simmer JP, Cho ES, Kim JW. Seymen F, et al. Among authors: zhang h. Am J Hum Genet. 2016 Nov 3;99(5):1199-1205. doi: 10.1016/j.ajhg.2016.09.018. Epub 2016 Oct 27. Am J Hum Genet. 2016. PMID: 27843125 Free PMC article.
Mouse Dspp frameshift model of human dentinogenesis imperfecta.
Liang T, Hu Y, Zhang H, Xu Q, Smith CE, Zhang C, Kim JW, Wang SK, Saunders TL, Lu Y, Hu JC, Simmer JP. Liang T, et al. Among authors: zhang c, zhang h. Sci Rep. 2021 Oct 19;11(1):20653. doi: 10.1038/s41598-021-00219-4. Sci Rep. 2021. PMID: 34667213 Free PMC article.
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
Parry DA, Smith CE, El-Sayed W, Poulter JA, Shore RC, Logan CV, Mogi C, Sato K, Okajima F, Harada A, Zhang H, Koruyucu M, Seymen F, Hu JC, Simmer JP, Ahmed M, Jafri H, Johnson CA, Inglehearn CF, Mighell AJ. Parry DA, et al. Among authors: zhang h. Am J Hum Genet. 2016 Oct 6;99(4):984-990. doi: 10.1016/j.ajhg.2016.08.020. Epub 2016 Sep 29. Am J Hum Genet. 2016. PMID: 27693231 Free PMC article.
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia.
Lee Y, Zhang H, Seymen F, Koruyucu M, Kasimoglu Y, Lee ZH, Hu JC, Simmer JP, Kim JW. Lee Y, et al. Among authors: zhang h. Oral Dis. 2022 Apr;28(3):843-845. doi: 10.1111/odi.13921. Epub 2021 Jun 9. Oral Dis. 2022. PMID: 34028942 Free PMC article. No abstract available.
Analyses of oligodontia phenotypes and genetic etiologies.
Zhou M, Zhang H, Camhi H, Seymen F, Koruyucu M, Kasimoglu Y, Kim JW, Kim-Berman H, Yuson NMR, Benke PJ, Wu Y, Wang F, Zhu Y, Simmer JP, Hu JC. Zhou M, et al. Among authors: zhang h. Int J Oral Sci. 2021 Sep 30;13(1):32. doi: 10.1038/s41368-021-00135-3. Int J Oral Sci. 2021. PMID: 34593752 Free PMC article.
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