Genes expressed in dental enamel development are associated with molar-incisor hypomineralization F Jeremias, M Koruyucu, EC Küchler, M Bayram, EB Tuna, K Deeley, ... Archives of oral biology 58 (10), 1434-1442, 2013 | 298 | 2013 |
Enamel formation genes are associated with high caries experience in Turkish children. VAR Patir A, Seymen F, Yildirim M, Deeley K, Cooper ME, Marazita ML Caries Res 42 (5), 394-400., 2008 | 233 | 2008 |
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24. 2, 17q23 and 19q13 EJ Leslie, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ... Human molecular genetics 25 (13), 2862-2872, 2016 | 232 | 2016 |
A genome-wide association study of nonsyndromic cleft palate identifies an etiologic missense variant in GRHL3 EJ Leslie, H Liu, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ... The American Journal of Human Genetics 98 (4), 744-754, 2016 | 166 | 2016 |
Enamel formation genes influence enamel microhardness before and after cariogenic challenge T Shimizu, B Ho, K Deeley, J Briseno-Ruiz, IM Faraco Jr, BI Schupack, ... Public Library of Science 7 (9), e45022, 2012 | 154 | 2012 |
Prevalence and etiology of molar-incisor hypomineralization (MIH) in the city of Istanbul M Koruyucu, S Özel, EB Tuna Journal of dental sciences 13 (4), 318-328, 2018 | 124 | 2018 |
STIM1 and SLC24A4 Are Critical for Enamel Maturation. HJC Wang S, Choi M, Richardson AS, Reid BM, Seymen F, Yildirim M, Tuna E ... J Dent Res 12 (93), 94S-100S, 2014 | 117* | 2014 |
An assessment of antibacterial activity of three pulp capping materials on Enterococcus faecalis by a direct contact test: An in vitro study M Koruyucu, N Topcuoglu, EB Tuna, S Ozel, K Gencay, G Kulekci, ... European journal of dentistry 9 (02), 240-245, 2015 | 89 | 2015 |
LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta. HJC Kim JW, Seymen F, Lee KE, Ko J, Yildirim M, Tuna EB, Gencay K, Shin TJ ... J Dent Res. 92 (10), 899-904., 2013 | 83 | 2013 |
Mutations in the pH-sensing G-protein-coupled receptor GPR68 cause amelogenesis imperfecta DA Parry, CEL Smith, W El-Sayed, JA Poulter, RC Shore, CV Logan, ... The American Journal of Human Genetics 99 (4), 984-990, 2016 | 79 | 2016 |
Novel FAM20A mutations in hypoplastic amelogenesis imperfecta SH Cho, F Seymen, KE Lee, SK Lee, YS Kweon, KJ Kim, SE Jung, ... Human mutation 33 (1), 91-94, 2012 | 78 | 2012 |
Gene-environment interaction in molar-incisor hypomineralization M Bezamat, JF Souza, FMF Silva, EG Corrêa, AL Fatturi, JA Brancher, ... PloS one 16 (1), e0241898, 2021 | 75 | 2021 |
Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing. HJC Wang SK, Hu Y, Simmer JP, Seymen F, Estrella NM, Pal S, Reid BM ... J Dent Res. 92 (3), 266-71., 2013 | 70 | 2013 |
Craniofacial and dental characteristics of Goldenhar syndrome: a report of two cases EB Tuna, D Orino, K Ogawa, M Yildirim, F Seymen, K Gencay, T Maeda Journal of oral Science 53 (1), 121-124, 2011 | 68 | 2011 |
Mutations in RELT cause autosomal recessive amelogenesis imperfecta JW Kim, H Zhang, F Seymen, M Koruyucu, Y Hu, J Kang, YJ Kim, A Ikeda, ... Clinical genetics 95 (3), 375-383, 2019 | 65 | 2019 |
Fused teeth: a review of the treatment options EB Tuna, M Yildirim, F Seymen, K Gencay, M Ozgen Journal of Dentistry for Children 76 (2), 109-116, 2009 | 59 | 2009 |
Clinical findings and long-term managements of patients with amelogenesis imperfecta M Koruyucu, M Bayram, EB Tuna, K Gencay, F Seymen European journal of dentistry 8 (04), 546-552, 2014 | 56 | 2014 |
Analyses of oligodontia phenotypes and genetic etiologies M Zhou, H Zhang, H Camhi, F Seymen, M Koruyucu, Y Kasimoglu, ... International journal of oral science 13 (1), 32, 2021 | 55 | 2021 |
Recessive mutations in ACPT, encoding testicular acid phosphatase, cause hypoplastic amelogenesis imperfecta F Seymen, YJ Kim, YJ Lee, J Kang, TH Kim, H Choi, M Koruyucu, ... The American Journal of Human Genetics 99 (5), 1199-1205, 2016 | 55 | 2016 |
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay ML Weber, HY Hsin, E Kalay, DŠ Brožková, T Shimizu, M Bayram, ... BMC medical genetics 15, 1-10, 2014 | 55 | 2014 |