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For: Mendoza G, Pemberton TJ, Lee K, Scarel-Caminaga R, Mehrian-Shai R, Gonzalez-Quevedo C, Ninis V, Hartiala J, Allayee H, Snead ML, Leal SM, Line SR, Patel PI. A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Hum Genet 2007;120:653-62. [PMID: 17024372 DOI: 10.1007/s00439-006-0246-6] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 1.2] [Reference Citation Analysis]
Number Citing Articles
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8 Haubek D, Gjørup H, Jensen LG, Juncker I, Nyegaard M, Børglum AD, Poulsen S, Hertz JM. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation. Int J Paediatr Dent 2011;21:407-12. [PMID: 21702852 DOI: 10.1111/j.1365-263X.2011.01142.x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 1.1] [Reference Citation Analysis]
9 Wang SK, Hu Y, Yang J, Smith CE, Richardson AS, Yamakoshi Y, Lee YL, Seymen F, Koruyucu M, Gencay K, Lee M, Choi M, Kim JW, Hu JC, Simmer JP. Fam83h null mice support a neomorphic mechanism for human ADHCAI. Mol Genet Genomic Med 2016;4:46-67. [PMID: 26788537 DOI: 10.1002/mgg3.178] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 3.5] [Reference Citation Analysis]
10 Dashash M, Bazrafshani MR, Poulton K, Jaber S, Naeem E, Blinkhorn AS. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families: Enamelin/ameloblastin gene polymorphisms. Journal of Investigative and Clinical Dentistry 2011;2:16-22. [DOI: 10.1111/j.2041-1626.2010.00038.x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
11 Chaudhary M, Dixit S, Singh A, Kunte S. Amelogenesis imperfecta: Report of a case and review of literature. J Oral Maxillofac Pathol 2009;13:70-7. [PMID: 21887005 DOI: 10.4103/0973-029X.57673] [Cited by in Crossref: 19] [Cited by in F6Publishing: 7] [Article Influence: 1.9] [Reference Citation Analysis]
12 Inoue A, Kiyoshima T, Yoshizaki K, Nakatomi C, Nakatomi M, Ohshima H, Shin M, Gao J, Tsuru K, Okabe K, Nakamura I, Honda H, Matsuda M, Takahashi I, Jimi E. Deletion of epithelial cell-specific p130Cas impairs the maturation stage of amelogenesis. Bone 2021;154:116210. [PMID: 34592494 DOI: 10.1016/j.bone.2021.116210] [Reference Citation Analysis]
13 Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta. Head Face Med 2007;3:8. [PMID: 17266769 DOI: 10.1186/1746-160X-3-8] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
14 Tachie-Menson T, Gázquez-Gutiérrez A, Fulcher LJ, Macartney TJ, Wood NT, Varghese J, Gourlay R, Soares RF, Sapkota GP. Characterisation of the biochemical and cellular roles of native and pathogenic amelogenesis imperfecta mutants of FAM83H. Cell Signal 2020;72:109632. [PMID: 32289446 DOI: 10.1016/j.cellsig.2020.109632] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
15 Li L, Shu Y, Lou B, Wu H. Candidate-gene exclusion in a family with inherited non-syndromic dental disorders. Gene 2012;511:420-6. [PMID: 23018043 DOI: 10.1016/j.gene.2012.09.042] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
16 Sriwattanapong K, Nitayavardhana I, Theerapanon T, Thaweesapphithak S, Chantarawaratit PO, Garuyakich R, Phokaew C, Porntaveetus T, Shotelersuk V. Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcified amelogenesis imperfecta. Oral Dis 2021. [PMID: 33486840 DOI: 10.1111/odi.13780] [Reference Citation Analysis]
17 Urzúa B, Ortega-pinto A, Farias DA, Franco E, Morales-bozo I, Moncada G, Escobar-pezoa N, Scholz U, Cifuentes V. A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families. Acta Odontologica Scandinavica 2011;70:7-14. [DOI: 10.3109/00016357.2011.574973] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
18 Lee SK, Hu JC, Bartlett JD, Lee KE, Lin BP, Simmer JP, Kim JW. Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification. Hum Mutat 2008;29:E95-9. [PMID: 18484629 DOI: 10.1002/humu.20789] [Cited by in Crossref: 47] [Cited by in F6Publishing: 44] [Article Influence: 4.3] [Reference Citation Analysis]
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