公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
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 | 45 | 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 |