| Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds J Yang, SK Wang, M Choi, BM Reid, Y Hu, YL Lee, CR Herzog, ... Molecular genetics & genomic medicine 3 (1), 40-58, 2015 | 115 | 2015 |
| STIM1 and SLC24A4 Are Critical for Enamel Maturation S Wang, M Choi, AS Richardson, BM Reid, F Seymen, M Yildirim, E Tuna, ... Journal of dental research 93 (7_suppl), 94S-100S, 2014 | 113 | 2014 |
| FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS) SK Wang, P Aref, Y Hu, RN Milkovich, JP Simmer, M El-Khateeb, ... PLoS genetics 9 (2), e1003302, 2013 | 107 | 2013 |
| ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta SK Wang, M Choi, AS Richardson, BM Reid, BP Lin, SJ Wang, JW Kim, ... Human molecular genetics 23 (8), 2157-2163, 2014 | 70 | 2014 |
| FAM20A Mutations Associated with Enamel Renal Syndrome SK Wang, BM Reid, SL Dugan, JA Roggenbuck, L Read, P Aref, ... Journal of dental research 93 (1), 42-48, 2014 | 68 | 2014 |
| Novel KLK4 and MMP20 Mutations Discovered by Whole-exome Sequencing SK Wang, Y Hu, JP Simmer, F Seymen, N Estrella, S Pal, BM Reid, ... Journal of dental research 92 (3), 266-271, 2013 | 68 | 2013 |
| Altered enamelin phosphorylation site causes amelogenesis imperfecta HC Chan, L Mai, A Oikonomopoulou, HL Chan, AS Richardson, SK Wang, ... Journal of dental research 89 (7), 695-699, 2010 | 60 | 2010 |
| Critical roles for WDR 72 in calcium transport and matrix protein removal during enamel maturation SK Wang, Y Hu, J Yang, CE Smith, SM Nunez, AS Richardson, S Pal, ... Molecular genetics & genomic medicine 3 (4), 302-319, 2015 | 51 | 2015 |
| Fam83h null mice support a neomorphic mechanism for human ADHCAI SK Wang, Y Hu, J Yang, CE Smith, AS Richardson, Y Yamakoshi, YL Lee, ... Molecular genetics & genomic medicine 4 (1), 46-67, 2016 | 45 | 2016 |
| Potential contribution of neural crest cells to dental enamel formation SK Wang, Y Komatsu, Y Mishina Biochemical and biophysical research communications 415 (1), 114-119, 2011 | 43 | 2011 |
| Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities SK Wang, HC Chan, I Makovey, JP Simmer, JCC Hu PLoS One 7 (12), e51533, 2012 | 40 | 2012 |
| Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families SK Wang, HC Chan, S Rajderkar, RN Milkovich, KA Uston, JW Kim, ... European journal of oral sciences 119, 158-167, 2011 | 38 | 2011 |
| AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue … T Liang, Y Hu, CE Smith, AS Richardson, H Zhang, J Yang, B Lin, ... Molecular Genetics & Genomic Medicine 7 (9), e929, 2019 | 29 | 2019 |
| FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta SK Wang, H Zhang, CY Hu, JF Liu, S Chadha, JW Kim, JP Simmer, ... Journal of Dental Research 100 (3), 293-301, 2021 | 27 | 2021 |
| A genetic model for the secretory stage of dental enamel formation JP Simmer, JCC Hu, Y Hu, S Zhang, T Liang, SK Wang, JW Kim, ... Journal of structural biology 213 (4), 107805, 2021 | 23 | 2021 |
| The Enamel Phenotype in Homozygous Fam83h Truncation Mice SK Wang, Y Hu, CE Smith, J Yang, C Zeng, JW Kim, JCC Hu, JP Simmer Molecular Genetics & Genomic Medicine 7 (6), e724, 2019 | 22 | 2019 |
| Ameloblast transcriptome changes from secretory to maturation stages JP Simmer, AS Richardson, SK Wang, BM Reid, Y Bai, Y Hu, JCC Hu Connective tissue research 55 (sup1), 29-32, 2014 | 22 | 2014 |
| FAM20C functions intracellularly within both ameloblasts and odontoblasts in vivo SK Wang, AC Samann, JCC Hu, JP Simmer Journal of Bone and Mineral Research 28 (12), 2508-2511, 2013 | 19 | 2013 |
| Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis KY Chu, YL Wang, YR Chou, JT Chen, YP Wang, JP Simmer, JCC Hu, ... Journal of Personalized Medicine 11 (11), 1217, 2021 | 18 | 2021 |
| ENAM mutations and digenic inheritance H Zhang, Y Hu, F Seymen, M Koruyucu, Y Kasimoglu, SK Wang, ... Molecular Genetics & Genomic Medicine 7 (10), e00928, 2019 | 16 | 2019 |
Murim ChoiSeoul National UniversityDirección de correo verificada de snu.ac.kr
