Gomy I - Search Results

1

Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndrome.

Valentin MD, Da Silva FC, Santos EM, Da Silva SD, De Oliveira Ferreira F, Aguiar Junior S, Gomy I, Vaccaro C, Redal MA, Della Valle A, Sarroca C, Rasmussen LJ, Carraro DM, Rossi BM. Valentin MD, et al. Among authors: gomy i. Anticancer Res. 2012 Oct;32(10):4347-51. Anticancer Res. 2012. PMID: 23060557

2

Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals.

Valentin MD, da Silva FC, dos Santos EM, Lisboa BG, de Oliveira LP, Ferreira Fde O, Gomy I, Nakagawa WT, Aguiar Junior S, Redal M, Vaccaro C, Valle AD, Sarroca C, Carraro DM, Rossi BM. Valentin MD, et al. Among authors: gomy i. Fam Cancer. 2011 Dec;10(4):641-7. doi: 10.1007/s10689-011-9461-y. Fam Cancer. 2011. PMID: 21681552

3

Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries.

Monteiro Santos EM, Valentin MD, Carneiro F, de Oliveira LP, de Oliveira Ferreira F, Junior SA, Nakagawa WT, Gomy I, de Faria Ferraz VE, da Silva Junior WA, Carraro DM, Rossi BM. Monteiro Santos EM, et al. Among authors: gomy i. BMC Cancer. 2012 Feb 9;12:64. doi: 10.1186/1471-2407-12-64. BMC Cancer. 2012. PMID: 22321913 Free PMC article.

4

Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes.

Villacis RA, Miranda PM, Gomy I, Santos EM, Carraro DM, Achatz MI, Rossi BM, Rogatto SR. Villacis RA, et al. Among authors: gomy i. Int J Cancer. 2016 Apr 15;138(8):1928-35. doi: 10.1002/ijc.29948. Epub 2015 Dec 28. Int J Cancer. 2016. PMID: 26620301 Free article.

5

Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.

Gomy I, Molfetta GA, de Andrade Barreto E, Ferreira CA, Zanette DL, Casali-da-Rocha JC, Silva WA Jr. Gomy I, et al. Fam Cancer. 2010 Dec;9(4):635-42. doi: 10.1007/s10689-010-9357-2. Fam Cancer. 2010. PMID: 20567917

6

Hereditary cancer risk assessment: insights and perspectives for the Next-Generation Sequencing era.

Gomy I, Diz Mdel P. Gomy I, et al. Genet Mol Biol. 2016 May 13;39(2):184-8. doi: 10.1590/1678-4685-GMB-2014-0346. Genet Mol Biol. 2016. PMID: 27192130 Free PMC article.

7

Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and PALB2 in a Tumor-Only Genomic Testing Program.

Bychkovsky BL, Li T, Sotelo J, Tayob N, Mercado J, Gomy I, Chittenden A, Kane S, Stokes S, Hughes ME, Kim JS, Umeton R, Awad MM, Konstantinopoulos PA, Yurgelun MB, Wolpin BM, Taplin ME, Newmark RE, Johnson BE, Lindeman NI, MacConaill LE, Garber JE, Lin NU. Bychkovsky BL, et al. Among authors: gomy i. Clin Cancer Res. 2022 Jun 1;28(11):2349-2360. doi: 10.1158/1078-0432.CCR-21-2861. Clin Cancer Res. 2022. PMID: 35363308 Free PMC article.

8

Hereditary cancer risk assessment: essential tools for a better approach.

Gomy I, Estevez Diz Mdel P. Gomy I, et al. Hered Cancer Clin Pract. 2013 Oct 28;11(1):16. doi: 10.1186/1897-4287-11-16. Hered Cancer Clin Pract. 2013. PMID: 24165150 Free PMC article.

9

Two new Brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights.

Gomy I, Heck B, Santos AC, Figueiredo MS, Martinelli CE Jr, Nogueira MP, Pina-Neto JM. Gomy I, et al. Am J Med Genet A. 2008 Mar 1;146A(5):649-57. doi: 10.1002/ajmg.a.32173. Am J Med Genet A. 2008. PMID: 18247421

10

Editorial: Hereditary Cancer Risk Assessment: New Perspectives and Challenges for the Next-Gen Sequencing Era.

Gomy I. Gomy I. Front Oncol. 2016 Jun 3;6:133. doi: 10.3389/fonc.2016.00133. eCollection 2016. Front Oncol. 2016. PMID: 27376026 Free PMC article. No abstract available.

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