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Amanda França de Nóbrega

Observed names: A. F. Nóbrega, A. Nóbrega, A.F. de Nóbrega, Amanda Aparecida França de Nobrega, Amanda F Nóbrega, Amanda F. Nobrega, Amanda F. Nóbrega, Amanda F. de Nóbrega, Amanda Franca Nobrega, Amanda França Nóbrega, Amanda França Nóbrega, Amanda Nobrega, Amanda Nóbrega, Nóbrega, Amanda
Institution: AC Camargo Hospital
Observed institution: AC Camargo Hospital
ORCID: 0000-0002-6470-5881
Observed ORCID: 0000-0002-6470-5881
OpenAlex ID: A5028726402
Germline DNA copy number variation in familial and early-onset breast cancer
2012 · Ana CV Krepischi, Maria Isabel W Achatz, et al. · Breast Cancer Research · 86
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Whole-body magnetic resonance imaging of Li-Fraumeni syndrome patients: observations from a two rounds screening of Brazilian patients
2018 · Daniele Paixão, Marcos Duarte Guimarães, et al. · Cancer Imaging · 30
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Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion
2012 · Amanda Gonçalves Silva, Ingrid Petroni Ewald, et al. · BMC Cancer · 28
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Early-onset breast cancer patients in the South and Southeast of Brazil should be tested for the TP53 p.R337H mutation
2016 · Kelvin C. Andrade, Karina M. Santiago, et al. · Genetics and Molecular Biology · 26
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Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer
2018 · Giovana T. Torrezan, Fernanda G. dos Santos R. de Almeida, et al. · Frontiers in Genetics · 25
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Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients
2020 · K.M. Santiago, L.P. Castro, et al. · Journal of the European Academy of Dermatology and Venereology · 24
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Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma
2014 · Alexandre Leon Ribeiro de Ávila, Ana Cristina Victorino Krepischi, et al. · Familial Cancer · 23
18F-FDG PET-CT for Surveillance of Brazilian Patients with Li-Fraumeni Syndrome
2015 · Sonia Tereza Santos Nogueira, Eduardo Nóbrega Pereira Lima, et al. · Frontiers in Oncology · 19
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Xeroderma Pigmentosum: Low Prevalence of Germline XPA Mutations in a Brazilian XP Population
2015 · Karina Santiago, Amanda França de Nóbrega, et al. · International Journal of Molecular Sciences · 12
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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
2015 · Tatiane R. Basso, Rolando A.R. Villacis, et al. · Cancer Genetics · 7
Germline large genomic alterations on 7q in patients with multiple primary cancers
2017 · R. A. R. Villacis, T. R. Basso, et al. · Scientific Reports · 3
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Research nurses contributions to research practice: an oncology nursing experience in Brazil
2018 · Bruna Tirapelli, Silvana Soares dos Santos, et al. · Applied cancer research/Applied Cancer Research · 2
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Abstract A37: Complex landscape of germline variants in hereditary and early-onset breast cancer ascertained through whole exome sequencing
2018 · Giovana T. Torrezan, Fernanda GSR Almeida, et al. · Clinical Cancer Research · 2
Evaluation of rapid whole-body magnetic resonance as screening strategy for early cancer detection in 57 Brazilian Li-Fraumeni syndrome patients.
2015 · Daniele Paixao, Marcos Duarte Guimaraes, et al. · Journal of Clinical Oncology · 2
Prevalence of germline TP53 p.R337H mutation in Brazilian young breast cancer patients.
2017 · Fernanda Paschoal Fortes, Renata Tonhosolo, et al. · Journal of Clinical Oncology · 1
Molecular and clinical profile of Li-Fraumeni Syndrome in a Brazilian cohort.
2015 · Maria Nirvana Cruz Formiga, Amanda Franca Nobrega, et al. · Journal of Clinical Oncology · 1
Avaliacao Do Impacto Do Suporte Familiar E Da Espiritualidade No Aconselhamento Genetico De Portadores Da Sindrome De Li- Fraumeni E Li-fraumeni Like
2014 · Christina Haas Tarabay, Antônio Prudente, et al. · 1
Abstract A20: Identification of new promising germline variants in melanoma-prone patients
2018 · Felipe Fidalgo, Luciana Facure, et al. · Clinical Cancer Research
Identification of new promising germline variants in melanoma-prone patients
2018 · Felipe Fidalgo, Luciana Facure, et al. · Clinical Cancer Research
SILENCING OF GENES MAPPED ON 7q ARE CANDIDATES TO BE ASSOCIATED WITH MULTIPLE PRIMARY TUMORS INCLUDING TRIPLE NEGATIVE BREAST CANCER
2016 · Sílvia Regina Rogatto, Rolando André Rios Villacis, et al. · University of Southern Denmark Research Portal (University of Southern Denmark)
3311 Germline mutations and rare copy number variations in melanoma-prone patients
2015 · F. Fidalgo, T. Rodrigues, et al. · European Journal of Cancer
Abstract 2753: The germline TP53 p.R337H mutation: a putative selective advantage
2015 · Kelvin César Andrade, Ana Carolina Leite, et al. · Cancer Research
Abstract 3418: Rare germline copy number variations in hereditary cutaneous melanoma
2014 · Felipe Fidalgo, Tatiane Rodrigues, et al. · Cancer Research
Abstract 1836: Distinct tumor spectrum and age of onset in a Brazilian cohort of p.R337H TP53 mutation carriers
2011 · Hadrien Hainaut, Sonia Nogueira, et al. · Cancer Research
Works count: 26
Citation count: 292
H-index: 9
I10-index: 9
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