Rogatto SR - Search Results

1

TP53 Pathogenic Variants in Early-Onset Breast Cancer Patients Fulfilling Hereditary Breast and Ovary Cancer and Li-Fraumeni-like Syndromes.

da Silva PFF, Goveia RM, Teixeira TB, Gamba BF, de Lima AP, Rogatto SR, Silveira-Lacerda EP. da Silva PFF, et al. Among authors: rogatto sr. Biomolecules. 2022 Apr 27;12(5):640. doi: 10.3390/biom12050640. Biomolecules. 2022. PMID: 35625568 Free PMC article.

2

Germline large genomic alterations on 7q in patients with multiple primary cancers.

Villacis RA, Basso TR, Canto LM, Nóbrega AF, Achatz MI, Rogatto SR. Villacis RA, et al. Among authors: rogatto sr. Sci Rep. 2017 Jan 31;7:41677. doi: 10.1038/srep41677. Sci Rep. 2017. PMID: 28139749 Free PMC article.

3

Germline variants in DNA repair genes are associated with young-onset head and neck cancer.

Cury SS, Miranda PM, Marchi FA, Canto LMD, Chulam TC, Petersen AH, Aagaard MM, Pinto CAL, Kowalski LP, Rogatto SR. Cury SS, et al. Among authors: rogatto sr. Oral Oncol. 2021 Nov;122:105545. doi: 10.1016/j.oraloncology.2021.105545. Epub 2021 Sep 28. Oral Oncol. 2021. PMID: 34598035 Free article.

4

The repertoire of germline variants in patients with early-onset rectal cancer.

Beltrami CM, do Canto LM, Villacis RAR, Petersen AH, Aagaard MM, Cury SS, Formiga MNDC, Junior SA, Rogatto SR. Beltrami CM, et al. Among authors: rogatto sr. Cancer Commun (Lond). 2022 May;42(5):481-485. doi: 10.1002/cac2.12262. Epub 2022 Jan 14. Cancer Commun (Lond). 2022. PMID: 35029067 Free PMC article. No abstract available.

5

Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients.

Côrtes L, Basso TR, Villacis RAR, Souza JDS, Jørgensen MMA, Achatz MI, Rogatto SR. Côrtes L, et al. Among authors: rogatto sr. Genes (Basel). 2023 Aug 3;14(8):1580. doi: 10.3390/genes14081580. Genes (Basel). 2023. PMID: 37628631 Free PMC article.

6

Genomic profile of a Li-Fraumeni-like syndrome patient with a 45,X/46,XX karyotype, presenting neither mutations in TP53 nor clinical stigmata of Turner syndrome.

Basso TR, Villacis RA, Canto LM, Alves VM, Lapa RM, Nóbrega AF, Achatz MI, Rogatto SR. Basso TR, et al. Among authors: rogatto sr. Cancer Genet. 2015 Jun;208(6):341-4. doi: 10.1016/j.cancergen.2015.03.004. Epub 2015 Mar 19. Cancer Genet. 2015. PMID: 25935441

7

DNA methylation patterns of candidate genes regulated by thymine DNA glycosylase in patients with TP53 germline mutations.

Fortes FP, Kuasne H, Marchi FA, Miranda PM, Rogatto SR, Achatz MI. Fortes FP, et al. Among authors: rogatto sr. Braz J Med Biol Res. 2015 Jul;48(7):610-5. doi: 10.1590/1414-431X20154026. Epub 2015 Apr 28. Braz J Med Biol Res. 2015. PMID: 25945745 Free PMC article.

8

Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.

Villacis RAR, Basso TR, Canto LM, Pinheiro M, Santiago KM, Giacomazzi J, de Paula CAA, Carraro DM, Ashton-Prolla P, Achatz MI, Rogatto SR. Villacis RAR, et al. Among authors: rogatto sr. J Mol Med (Berl). 2017 May;95(5):523-533. doi: 10.1007/s00109-017-1507-7. Epub 2017 Jan 16. J Mol Med (Berl). 2017. PMID: 28093616

9

HABP2 p.G534E variant in patients with family history of thyroid and breast cancer.

Pinheiro M, Drigo SA, Tonhosolo R, Andrade SCS, Marchi FA, Jurisica I, Kowalski LP, Achatz MI, Rogatto SR. Pinheiro M, et al. Among authors: rogatto sr. Oncotarget. 2017 Jun 20;8(25):40896-40905. doi: 10.18632/oncotarget.16639. Oncotarget. 2017. PMID: 28402931 Free PMC article.

10

Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients.

Santiago KM, Castro LP, Neto JPD, de Nóbrega AF, Pinto CAL, Ashton-Prolla P, Pinto E Vairo F, de Medeiros PFV, Ribeiro EM, Ribeiro BFR, do Valle FF, Doriqui MJR, Leite CHB, Rocha RM, Moura LMS, Munford V, Galante PAF, Menck CFM, Rogatto SR, Achatz MI. Santiago KM, et al. Among authors: rogatto sr. J Eur Acad Dermatol Venereol. 2020 Oct;34(10):2392-2401. doi: 10.1111/jdv.16405. Epub 2020 May 21. J Eur Acad Dermatol Venereol. 2020. PMID: 32239545

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