Hereditary cancer syndromes: opportunities and challenges

por Ashton-Prolla, Patricia
Publicado 2013

Prevalence and impact of founder mutations in hereditary breast cancer in Latin America

por Ashton-Prolla, Patricia, Vargas, Fernando Regla
Publicado 2014

The Brazilian Hereditary Cancer Network: historical aspects and challenges for clinical cancer genetics in the public health care system in Brazil

por Ashton-Prolla, Patricia, Seuanez, Hector N.
Publicado 2016

miRNAs As Diagnostic and Prognostic Biomarkers in Pancreatic Ductal Adenocarcinoma and Its Precursor Lesions: A Review

por Alemar, Bárbara, Gregório, Cleandra, Ashton-Prolla, Patricia
Publicado 2015

Reviewing the characteristics of BRCA and PALB2-related cancers in the precision medicine era

por Macedo, Gabriel S., Alemar, Barbara, Ashton-Prolla, Patricia
Publicado 2019

TSC1 and TSC2 gene mutations and their implications for treatment in Tuberous Sclerosis Complex: a review

por Rosset, Clévia, Netto, Cristina Brinckmann Oliveira, Ashton-Prolla, Patricia
Publicado 2017

TULP3: A potential biomarker in colorectal cancer?

por Sartor, Ivaine Taís Sauthier, Recamonde-Mendoza, Mariana, Ashton-Prolla, Patricia
Publicado 2019

Analysis of the interval between submission and publication in genetics journals

por Zimmer, Rafael Leal, Mancuso, Aline Castello Branco, Matte, Ursula, Ashton-Prolla, Patricia
Publicado 2023

Influence of CYP19A1 polymorphisms on the treatment of breast cancer with aromatase inhibitors: a systematic review and meta-analysis

por Artigalás, Osvaldo, Vanni, Tazio, Hutz, Mara Helena, Ashton-Prolla, Patricia, Schwartz, Ida Vanessa
Publicado 2015

Costs of genetic testing: Supporting Brazilian Public Policies for the incorporating of molecular diagnostic technologies

por Schlatter, Rosane Paixão, Matte, Ursula, Polanczyk, Carisi Anne, Koehler-Santos, Patrícia, Ashton-Prolla, Patricia
Publicado 2015

The Role of Co-Deleted Genes in Neurofibromatosis Type 1 Microdeletions: An Evolutive Approach

por Brussa Reis, Larissa, Turchetto-Zolet, Andreia Carina, Fonini, Maievi, Ashton-Prolla, Patricia, Rosset, Clévia
Publicado 2019

Systems Biology Approaches Reveal Potential Phenotype-Modifier Genes in Neurofibromatosis Type 1

por Woycinck Kowalski, Thayne, Brussa Reis, Larissa, Finger Andreis, Tiago, Ashton-Prolla, Patricia, Rosset, Clévia
Publicado 2020

The paradox of autophagy in Tuberous Sclerosis Complex

por Reis, Larissa Brussa, Filippi-Chiela, Eduardo C., Ashton-Prolla, Patricia, Visioli, Fernanda, Rosset, Clévia
Publicado 2021

Complete Response to Immunotherapy in a Patient with MUTYH-Associated Polyposis and Gastric Cancer: A Case Report

por Mathias-Machado, Maria Cecilia, Peixoto, Renata D., Ashton-Prolla, Patricia, Da Silva, Leonard Medeiros, Dienstmann, Rodrigo
Publicado 2023

The TP53 fertility network

por Paskulin, Diego d’Avila, Paixão-Côrtes, Vanessa Rodrigues, Hainaut, Pierre, Bortolini, Maria Cátira, Ashton-Prolla, Patricia
Publicado 2012

Genetic variants involved in specialized DNA replication and their relation with breast cancer risk, disease progression and patient prognosis

por Brandalize, Ana PC, Minozzo, Roberto, Schüller-Faccini, Lavínia, Hoffman, Jean-Sebastien, Cazaux, Christophe, Ashton-Prolla, Patricia
Publicado 2013

Recommendations for Advancing the Diagnosis and Management of Hereditary Breast and Ovarian Cancer in Brazil

por Achatz, Maria Isabel, Caleffi, Maira, Guindalini, Rodrigo, Marques, Renato Moretti, Nogueira-Rodrigues, Angelica, Ashton-Prolla, Patricia
Publicado 2020

ESR1 rs9340799 Is Associated with Endometriosis-Related Infertility and In Vitro Fertilization Failure

por Paskulin, Diego Davila, Cunha-Filho, João Sabino, Paskulin, Livia Davila, Souza, Carlos Augusto Bastos, Ashton-Prolla, Patricia
Publicado 2013

A DNA repair variant in POLQ (c.-1060A > G) is associated to hereditary breast cancer patients: a case–control study

por Brandalize, Ana Paula Carneiro, Schüler-Faccini, Lavínia, Hoffmann, Jean-Sébastien, Caleffi, Maira, Cazaux, Christophe, Ashton-Prolla, Patricia
Publicado 2014

Genomic rearrangements in BRCA1 and BRCA2: A literature review

por Ewald, Ingrid Petroni, Ribeiro, Patricia Lisboa Izetti, Palmero, Edenir Inêz, Cossio, Silvia Liliana, Giugliani, Roberto, Ashton-Prolla, Patricia
Publicado 2009