1 - 25 of 39 results for author:"Vieira A.R." in Literature citations
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| Tooth agenesis association with self-reported family history of cancer. Kuchler E.C., Lips A., Tannure P.N., Ho B., Costa M.C., Granjeiro J.M., Vieira A.R. J. Dent. Res. 92:149-155(2013) · Mapped (9) |
| Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate. Letra A., Fakhouri W., Fonseca R.F., Menezes R., Kempa I., Prasad J.L., McHenry T.G., Lidral A.C., Moreno L., Murray J.C. et al. PLoS ONE 7:e45441-e45441(2012) · Mapped (20) |
| MMP13 polymorphism decreases risk for dental caries. Tannure P.N., Kuchler E.C., Falagan-Lotsch P., Amorim L.M., Raggio Luiz R., Costa M.C., Vieira A.R., Granjeiro J.M. Caries Res. 46:401-407(2012) · Mapped (9) |
| MMP3 and TIMP1 variants contribute to chronic periodontitis and may be implicated in disease progression. Letra A., Silva R.M., Rylands R.J., Silveira E.M., de Souza A.P., Wendell S.K., Garlet G.P., Vieira A.R. J. Clin. Periodontol. 39:707-716(2012) · Mapped (7) |
| Genetic susceptibility to periapical disease: conditional contribution of MMP2 and MMP3 genes to the development of periapical lesions and healing response. Menezes-Silva R., Khaliq S., Deeley K., Letra A., Vieira A.R. J Endod 38:604-607(2012) · Mapped (4) |
| Association of AXIN2 with non-syndromic oral clefts in multiple populations. Letra A., Bjork B., Cooper M.E., Szabo-Rogers H., Deleyiannis F.W., Field L.L., Czeizel A.E., Ma L., Garlet G.P., Poletta F.A. et al. J. Dent. Res. 91:473-478(2012) · Mapped (4) |
| Genetic variation in MMP20 contributes to higher caries experience. Tannure P.N., Kuchler E.C., Lips A., Costa M.d.e. C., Luiz R.R., Granjeiro J.M., Vieira A.R. J Dent 40:381-386(2012) · Mapped (1) |
| Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin. Lace B., Kempa I., Piekuse L., Grinfelde I., Klovins J., Pliss L., Krumina A., Vieira A.R. Eur. J. Oral Sci. 119:413-417(2011) · Mapped (7) |
| MMP1 and MMP20 contribute to tooth agenesis in humans. Kuchler E.C., Menezes R., Callahan N., Costa M.C., Modesto A., Meira R., Patir A., Seymen F., Paiva K.B., Nunes F.D. et al. Arch. Oral Biol. 56:506-511(2011) · Mapped (13) |
| Studies with Wnt genes and nonsyndromic cleft lip and palate. Menezes R., Letra A., Kim A.H., Kuchler E.C., Day A., Tannure P.N., Gomes da Motta L., Paiva K.B., Granjeiro J.M., Vieira A.R. Birth Defects Res. Part A Clin. Mol. Teratol. 88:995-1000(2010) · Mapped (12) |
| CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip With or Without Cleft Palate. Letra A., Menezes R., Cooper M.E., Fonseca R.F., Tropp S., Govil M., Granjeiro J.M., Imoehl S.R., Mansilla M.A., Murray J.C. et al. Cleft Palate Craniofac. J. 48:363-370(2011) · Mapped (2) |
| Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate. Letra A., Menezes R., Govil M., Fonseca R.F., McHenry T., Granjeiro J.M., Castilla E.E., Orioli I.M., Marazita M.L., Vieira A.R. Am. J. Med. Genet. A 152A:1701-1710(2010) · Mapped (84) |
| Novel cleft susceptibility genes in chromosome 6q. Letra A., Menezes R., Fonseca R.F., Govil M., McHenry T., Murphy M.J., Hennebold J.D., Granjeiro J.M., Castilla E.E., Orioli I.M. et al. J. Dent. Res. 89:927-932(2010) · Mapped (16) |
| A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Beaty T.H., Murray J.C., Marazita M.L., Munger R.G., Ruczinski I., Hetmanski J.B., Liang K.Y., Wu T., Murray T., Fallin M.D. et al. Nat. Genet. 42:525-529(2010) · Mapped (17) |
| The antimicrobial peptide DEFB1 is associated with caries. Ozturk A., Famili P., Vieira A.R. J. Dent. Res. 89:631-636(2010) · Mapped (2) |
| Studies of palatine rugae and interferon regulatory factor 6 variations in a group of families with sporadic hypodontia. Murdoch A.M., Patir A., Seymen F., Vieira A.R. J Oral Sci 51:521-526(2009) · Mapped (3) |
| Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. Suzuki S., Marazita M.L., Cooper M.E., Miwa N., Hing A., Jugessur A., Natsume N., Shimozato K., Ohbayashi N., Suzuki Y. et al. Am. J. Hum. Genet. 84:406-411(2009) · UniProtKB (1) · Mapped (1) |
| Transforming growth factor-alfa gene (TGFA), human tooth agenesis, and evidence of segmental uniparental isodisomy. Callahan N., Modesto A., Deeley K., Meira R., Vieira A.R. Eur. J. Oral Sci. 117:20-26(2009) · Mapped (8) |
| AXIS inhibition protein 2, orofacial clefts and a family history of cancer. Menezes R., Marazita M.L., Goldstein McHenry T., Cooper M.E., Bardi K., Brandon C., Letra A., Martin R.A., Vieira A.R. J Am Dent Assoc 140:80-84(2009) · Mapped (4) |
| The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P. Choi S.J., Marazita M.L., Hart P.S., Sulima P.P., Field L.L., McHenry T.G., Govil M., Cooper M.E., Letra A., Menezes R. et al. Eur. J. Hum. Genet. 17:774-784(2009) · Mapped (4) |
| Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts. Vieira A.R., McHenry T.G., Daack-Hirsch S., Murray J.C., Marazita M.L. Genet. Med. 10:668-674(2008) · Mapped (209) |
| Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts. Vieira A.R., Howe A., Murray J.C. Am. J. Med. Genet. A 146A:2828-2830(2008) · Mapped (8) |
| Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis. Callahan N., Modesto A., Meira R., Seymen F., Patir A., Vieira A.R. Arch. Oral Biol. 54:45-49(2009) · Mapped (4) |
| Enamel formation genes are associated with high caries experience in Turkish children. Patir A., Seymen F., Yildirim M., Deeley K., Cooper M.E., Marazita M.L., Vieira A.R. Caries Res. 42:394-400(2008) · Mapped (18) |
| AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts. Letra A., Menezes R., Granjeiro J.M., Vieira A.R. Birth Defects Res. Part A Clin. Mol. Teratol. 85:169-173(2009) · Mapped (10) |