Cristina Brinckmann Oliveira Netto
Overview
Explore the profile of Cristina Brinckmann Oliveira Netto including associated specialties, affiliations and a list of published articles.
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17
Citations
192
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Recent Articles
1.
Andreis T, de Souza K, Vieira I, Alemar B, Sinigaglia M, Rocha Y, et al.
Gene
. 2023 Feb;
862:147281.
PMID: 36775216
In the context of cancer predisposition syndromes, it is widely known that the correct interpretation of germline variants identified in multigene panel testing is essential for adequate genetic counseling and...
2.
Rosset C, da Cunha Jaeger M, Filippi-Chiela E, Reis L, Sartor I, Oliveira Netto C, et al.
Genet Mol Biol
. 2021 Oct;
44(4):e20200475.
PMID: 34609442
Tuberous sclerosis complex (TSC) is an autosomal dominant cancer predisposition disorder caused by heterozygous mutations in TSC1 or TSC2 genes and characterized by mTORC1 hyperactivation. TSC-associated tumors develop after loss...
3.
Reis L, Konzen D, Oliveira Netto C, Braghini P, Prolla G, Ashton-Prolla P
BMC Gastroenterol
. 2020 Nov;
20(1):394.
PMID: 33225890
Background: Tuberous Sclerosis Complex (TSC) is a complex and heterogeneous genetic disease that has well-established clinical diagnostic criteria. These criteria do not include gastrointestinal tumors. Case Presentation: We report a...
4.
Vianna F, Giacomazzi J, Oliveira Netto C, Nunes L, Caleffi M, Ashton-Prolla P, et al.
Genet Mol Biol
. 2019 Jun;
42(1 suppl 1):232-237.
PMID: 31170278
Breast cancer (BC) risk assessment models base their estimations on different aspects of a woman's personal and familial history. The Gail and Tyrer-Cuzick models are the most commonly used, and...
5.
Hahn E, Bittar C, Vianna F, Oliveira Netto C, Biazus J, Cericatto R, et al.
PLoS One
. 2019 Jan;
13(12):e0209934.
PMID: 30596752
Premenopausal breast cancer (BC) is a core tumor of Li-Fraumeni (LFS) and Li-Fraumeni-like (LFL) Syndromes, predisposition disorders caused by germline mutations in TP53 gene. In the Southern and Southeastern regions...
6.
Felicio P, Alemar B, Coelho A, Berardinelli G, Melendez M, van Helvoort Lengert A, et al.
Cancer Genet
. 2018 Dec;
228-229:93-97.
PMID: 30553478
Portuguese immigration to Brazil occurred in several waves and greatly contributed to the genetic composition of current Brazilian population. In this study, we evaluated the frequency of a Portuguese founder...
7.
Alemar B, Gregorio C, Herzog J, Bittar C, Oliveira Netto C, Artigalas O, et al.
PLoS One
. 2018 May;
13(5):e0197529.
PMID: 29750819
[This corrects the article DOI: 10.1371/journal.pone.0187630.].
8.
Rosset C, Vairo F, Bandeira I, Fonini M, Oliveira Netto C, Ashton-Prolla P
Expert Rev Mol Diagn
. 2018 Apr;
18(6):577-586.
PMID: 29685074
Objectives: Neurofibromatoses (type 1: NF1; type 2: NF2) are autosomal dominant tumor predisposition syndromes mostly caused by loss-of-function mutations in the tumor suppressor genes NF1 and NF2, respectively. Genotyping is...
9.
Alemar B, Gregorio C, Herzog J, Bittar C, Oliveira Netto C, Artigalas O, et al.
PLoS One
. 2017 Nov;
12(11):e0187630.
PMID: 29161300
Background: Germline pathogenic variants in BRCA1 and BRCA2 (BRCA) are the main cause of Hereditary Breast and Ovarian Cancer syndrome (HBOC). Methods: In this study we evaluated the mutational profile...
10.
Rosset C, Vairo F, Bandeira I, Correia R, Goes F, Da Silva R, et al.
PLoS One
. 2017 Oct;
12(10):e0185713.
PMID: 28968464
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem disorder characterized by the development of multiple hamartomas in many organs and tissues. It occurs due to inactivating mutations in either...