Publications by authors named "Amanda Nobrega"

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Whole-body magnetic resonance imaging of Li-Fraumeni syndrome patients: observations from a two rounds screening of Brazilian patients.
Daniele Paixão, Marcos Duarte Guimarães, Kelvin César de Andrade, Amanda França Nóbrega, Rubens Chojniak

Cancer Imaging· August 2018

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Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
Giovana T Torrezan, Fernanda G Dos Santos R de Almeida, Márcia C P Figueiredo, Bruna D de Figueiredo Barros, Cláudia A A de Paula

Front Genet· May 2018

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Level Of Knowledge Use Survey (LOKUS): A validated instrument for tracking knowledge uptake and use.
Joseph P Lane, Vathsala I Stone, Amanda Nobrega, Machiko Tomita

Stud Health Technol Inform· April 2017

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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.
Kelvin C Andrade, Karina M Santiago, Fernanda P Fortes, Lisley I Mambelli, Amanda F Nóbrega

Genet Mol Biol· May 2016

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Development of a measure of knowledge use by stakeholders in rehabilitation technology.
Vathsala I Stone, Amanda R Nobrega, Joseph P Lane, Machiko R Tomita, Douglas J Usiak

SAGE Open Med· January 2016

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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.
Tatiane R Basso, Rolando A R Villacis, Luisa M Canto, Vinicius M F Alves, Rainer M L Lapa

Cancer Genet· June 2015

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(18)F-FDG PET-CT for Surveillance of Brazilian Patients with Li-Fraumeni Syndrome.
Sonia Tereza Santos Nogueira, Eduardo Nóbrega Pereira Lima, Amanda França Nóbrega, Ivone Do Carmo Gonçalves Torres, Marcelo Cavicchioli

Front Oncol· March 2015

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Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.
Alexandre Leon Ribeiro de Ávila, Ana Cristina Victorino Krepischi, Luciana Facure Moredo, Talita Ferreira Marques Aguiar, Felipe Carneiro da Silva

Fam Cancer· December 2014

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Age at cancer onset in germline TP53 mutation carriers: association with polymorphisms in predicted G-quadruplex structures.
Charlotte Sagne, Virginie Marcel, Maria Bota, Ghyslaine Martel-Planche, Amanda Nobrega

Carcinogenesis· April 2014

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Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.
Amanda Gonçalves Silva, Ingrid Petroni Ewald, Marina Sapienza, Manuela Pinheiro, Ana Peixoto

BMC Cancer· June 2012

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Germline DNA copy number variation in familial and early-onset breast cancer.
Ana Cv Krepischi, Maria Isabel W Achatz, Erika Mm Santos, Silvia S Costa, Bianca Cg Lisboa

Breast Cancer Res· February 2012

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