Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
---|---|---|---|---|---|---|
2010 | Altered enamelin phosphorylation site causes amelogenesis imperfecta | Chan H.-C.; Mai L.; Oikonomopoulou A.; Chan H.L.; Richardson A.S.; SHIH-KAI WANG ; Simmer J.P.; Hu J.C.-C. | Journal of Dental Research | 43 | 39 | |
2014 | Ameloblast transcriptome changes from secretory to maturation stages | Simmer J.P.; Richardson A.S.; SHIH-KAI WANG ; Reid B.M.; Bai Y.; Hu Y.; Hu J.C.-C. | Connective Tissue Research | 16 | 14 | |
2015 | Critical roles for wdr72 in calcium transport and matrix protein removal during enamel maturation | SHIH-KAI WANG ; Hu Y.; Yang J.; Smith C.E.; Nunez S.M.; Richardson A.S.; Pal S.; Samann A.C.; Hu J.C.-C.; Simmer J.P. | Molecular Genetics and Genomic Medicine | 40 | 39 | |
2011 | Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families | SHIH-KAI WANG ; Chan H.-C.; Rajderkar S.; Milkovich R.N.; Uston K.A.; Kim J.-W.; Simmer J.P.; Hu J.C.-C. | European Journal of Oral Sciences | 25 | 23 | |
2014 | FAM20A mutations associated with enamel renal syndrome | SHIH-KAI WANG ; Reid B.M.; Dugan S.L.; Roggenbuck J.A.; Read L.; Aref P.; Taheri A.P.H.; Yeganeh M.Z.; Simmer J.P.; Hu J.C.-C. | Journal of Dental Research | 50 | 50 | |
2013 | FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS) | SHIH-KAI WANG ; Aref P.; Hu Y.; Milkovich R.N.; Simmer J.P.; El-Khateeb M.; Daggag H.; Baqain Z.H.; Hu J.C.-C. | PLoS Genetics | 73 | 78 | |
2013 | FAM20C functions intracellularly within both ameloblasts and odontoblasts in vivo | SHIH-KAI WANG ; Samann A.C.; Hu J.C.-C.; Simmer J.P. | Journal of Bone and Mineral Research | 17 | 15 | |
2016 | Fam83h null mice support a neomorphic mechanism for human ADHCAI | SHIH-KAI WANG ; Hu Y.; Yang J.; Smith C.E.; Richardson A.S.; Yamakoshi Y.; YUAN-LING LEE ; Seymen F.; Koruyucu M.; Gencay K.; Lee M.; Choi M.; Kim J.-W.; Hu J.C.-C.; Simmer J.P. | Molecular Genetics and Genomic Medicine | 33 | 36 | |
2014 | ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta | SHIH-KAI WANG ; Choi M.; Richardson A.S.; Reid B.M.; Lin B.P.; Wang S.J.; Kim J.; Simmer J.P.; Hu J.C.-C. | Human Molecular Genetics | 43 | 41 | |
2013 | Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing | SHIH-KAI WANG ; Hu Y.; Simmer J.P.; Seymen F.; Estrella N.M.R.P.; Pal S.; Reid B.M.; Yildirim M.; Bayram M.; Bartlett J.D.; Hu J.C.-C. | Journal of Dental Research | 46 | 43 | |
2012 | Novel PAX9 and COL1A2 Missense Mutations Causing Tooth Agenesis and OI/DGI without Skeletal Abnormalities | SHIH-KAI WANG ; Chan H.-C.; Makovey I.; Simmer J.P.; Hu J.C.-C. | PLoS ONE | 26 | 14 | |
2015 | Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC) | Vieira A.R.; Lee M.; Vairo F.; Loguercio Leite J.C.; Munerato M.C.; Visioli F.; D'?vila S.R.; SHIH-KAI WANG ; Choi M.; Simmer J.P.; Hu J.C.-C. | Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology | 11 | 9 | |
2015 | Taurodontism, variations in tooth number, and misshapened crowns in wnt10a null mice and human kindreds | Yang J.; SHIH-KAI WANG ; Choi M.; Reid B.M.; Hu Y.; YUAN-LING LEE ; Herzog C.R.; Kim-Berman H.; Lee M.; Benke P.J.; Kent Lloyd K.C.; Simmer J.P.; Hu J.C.-C. | Molecular Genetics and Genomic Medicine | 82 | 74 |