Felipe Fidalgo
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Explore the profile of Felipe Fidalgo including associated specialties, affiliations and a list of published articles.
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10
Citations
55
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Recent Articles
1.
Soares de Sa B, Moredo L, Torrezan G, Fidalgo F, de Araujo E, Formiga M, et al.
Int J Mol Sci
. 2023 Nov;
24(21).
PMID: 37958811
Increased genetic risk for melanoma can occur in the context of germline pathogenic variants in high-penetrance genes, such as and , risk variants in low- to moderate-penetrance genes ( and...
2.
Fidalgo F, Torrezan G, Soares de Sa B, Barros B, Moredo L, Valieris R, et al.
PLoS One
. 2022 Jan;
17(1):e0262419.
PMID: 35085295
Genetic predisposition accounts for nearly 10% of all melanoma cases and has been associated with a dozen moderate- to high-penetrance genes, including CDKN2A, CDK4, POT1 and BAP1. However, in most...
3.
Soares de Sa B, Macedo M, Torrezan G, Braga J, Fidalgo F, Moredo L, et al.
BMC Cancer
. 2019 Nov;
19(1):1077.
PMID: 31706282
Background: BRCA1 associated-protein 1 (BAP1) tumor predisposition syndrome is associated with an increased risk for malignant mesotheliomas, uveal and cutaneous melanomas, renal cell carcinomas, and singular cutaneous lesions. The latter...
4.
Mariano F, Fidalgo F, Casarim A, Martins A, Scarini J, Souza R, et al.
Oral Surg Oral Med Oral Pathol Oral Radiol
. 2019 Oct;
129(1):59-64.
PMID: 31607675
Objective: As the genetic changes in recurrent pleomorphic adenoma (RPA) have not yet been investigated, the aim of this study was to assess the genomic profile of somatic copy number...
5.
Mariano F, Egal E, Pramio D, Fidalgo F, Sara E, Costa A, et al.
Oral Surg Oral Med Oral Pathol Oral Radiol
. 2016 Aug;
122(3):322-31.
PMID: 27544395
Objective: The progression of pleomorphic adenoma (PA) to carcinoma ex-pleomorphic adenoma (CXPA) encompasses several genomic alterations involving complex pathways. Tumor suppressor genes seem to play important roles in the tumorigenesis...
6.
Fidalgo F, Rodrigues T, Silva A, Facure L, Soares de Sa B, Duprat J, et al.
Future Oncol
. 2016 Mar;
12(11):1345-57.
PMID: 27020340
Aim: This work evaluates a possible causative role for germline copy number variants (CNVs) in melanoma predisposition. Patients & Methods: A total of 41 melanoma-prone Brazilian patients were investigated for...
7.
Rodrigues T, Fidalgo F, da Costa C, Ferreira E, da Cunha I, Carraro D, et al.
Future Oncol
. 2014 Dec;
10(15):2449-57.
PMID: 25525853
Aim: Cytogenetic data of hepatoblastomas, a rare embryonal tumor of the liver, mostly consist of descriptions of whole-chromosome aneuploidies and large chromosome alterations. High-resolution cytogenetics may provide clues to hepatoblastoma...
8.
Fidalgo F, Rodrigues T, Pinilla M, Silva A, Maciel M, Rosenberg C, et al.
Tumour Biol
. 2014 Nov;
36(3):1835-48.
PMID: 25391423
Lymphovascular invasion (LVI) and histologic grade are clinical parameters of high prognostic value in breast cancer and indicate the level of tumor aggressiveness. Many studies have focused on the association...
9.
Cappi C, Hounie A, Mariani D, Diniz J, Silva A, Reis V, et al.
PLoS One
. 2014 Oct;
9(10):e110198.
PMID: 25303678
Copy number variations (CNVs) have been previously associated with several different neurodevelopmental psychiatric disorders, such as autism, schizophrenia, and attention deficit hyperactivity disorder (ADHD). The present study consisted of a...
10.
Fidalgo F, Gomes E, Moredo Facure L, DA Silva F, Carraro D, Soares de Sa B, et al.
Exp Mol Pathol
. 2014 Jul;
97(1):144-7.
PMID: 24984283
Melanoma and pancreatic cancer are two low frequency types of cancer. In this study, three patients who developed both melanoma and intraepithelial neoplasia of the pancreas were tested for CDKN2A...