Rossi BM - Search Results

1

Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report.

Torrezan GT, da Silva FC, Krepischi AC, Santos ÉM, Ferreira Fde O, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: rossi bm. BMC Med Genet. 2011 Sep 30;12:128. doi: 10.1186/1471-2350-12-128. BMC Med Genet. 2011. PMID: 21962078 Free PMC article.

2

Mismatch repair genes in Lynch syndrome: a review.

Silva FC, Valentin MD, Ferreira Fde O, Carraro DM, Rossi BM. Silva FC, et al. Among authors: rossi bm. Sao Paulo Med J. 2009 Jan;127(1):46-51. doi: 10.1590/s1516-31802009000100010. Sao Paulo Med J. 2009. PMID: 19466295 Free PMC article. Review.

3

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: rossi bm. Fam Cancer. 2011 Dec;10(4):641-7. doi: 10.1007/s10689-011-9461-y. Fam Cancer. 2011. PMID: 21681552

4

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: rossi bm. BMC Cancer. 2012 Feb 9;12:64. doi: 10.1186/1471-2407-12-64. BMC Cancer. 2012. PMID: 22321913 Free PMC article.

5

A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype.

Torrezan GT, da Silva FC, Krepischi AC, dos Santos EM, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: rossi bm. BMC Med Genet. 2012 Jul 16;13:55. doi: 10.1186/1471-2350-13-55. BMC Med Genet. 2012. PMID: 22799487 Free PMC article.

6

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: rossi bm. Anticancer Res. 2012 Oct;32(10):4347-51. Anticancer Res. 2012. PMID: 23060557

7

Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.

Torrezan GT, da Silva FC, Santos EM, Krepischi AC, Achatz MI, Aguiar S Jr, Rossi BM, Carraro DM. Torrezan GT, et al. Among authors: rossi bm. Orphanet J Rare Dis. 2013 Apr 5;8:54. doi: 10.1186/1750-1172-8-54. Orphanet J Rare Dis. 2013. PMID: 23561487 Free PMC article.

8

Mutation spectrum in South American Lynch syndrome families.

Dominguez-Valentin M, Nilbert M, Wernhoff P, López-Köstner F, Vaccaro C, Sarroca C, Palmero EI, Giraldo A, Ashton-Prolla P, Alvarez K, Ferro A, Neffa F, Caris J, Carraro DM, Rossi BM. Dominguez-Valentin M, et al. Among authors: rossi bm. Hered Cancer Clin Pract. 2013 Dec 18;11(1):18. doi: 10.1186/1897-4287-11-18. Hered Cancer Clin Pract. 2013. PMID: 24344984 Free PMC article.

9

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.

Silva FC, Lisboa BC, Figueiredo MC, Torrezan GT, Santos EM, Krepischi AC, Rossi BM, Achatz MI, Carraro DM. Silva FC, et al. Among authors: rossi bm. BMC Med Genet. 2014 May 15;15:55. doi: 10.1186/1471-2350-15-55. BMC Med Genet. 2014. PMID: 24884479 Free PMC article.

10

ROBO1 deletion as a novel germline alteration in breast and colorectal cancer patients.

Villacis RA, Abreu FB, Miranda PM, Domingues MA, Carraro DM, Santos EM, Andrade VP, Rossi BM, Achatz MI, Rogatto SR. Villacis RA, et al. Among authors: rossi bm. Tumour Biol. 2016 Mar;37(3):3145-53. doi: 10.1007/s13277-015-4145-0. Epub 2015 Oct 1. Tumour Biol. 2016. PMID: 26427657

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