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

by Ashton-Prolla,Patricia, Vargas,Fernando Regla
Published 2014

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

by Ashton-Prolla,Patricia, Seuanez,Hector N.
Published 2016

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

by Macedo,Gabriel S., Alemar,Barbara, Ashton-Prolla,Patricia
Published 2019

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

by Rosset,Clévia, Netto,Cristina Brinckmann Oliveira, Ashton-Prolla,Patricia
Published 2017

Hereditary non-polipomatous colorectal cancer: hereditary predisposition, diagnosis and prevention

by Coura,Renata dos Santos, Ashton-Prolla,Patricia, Prolla,João Carlos
Published 2005

CHEK2 1100DELC germline mutation: a frequency study in hereditary breast and colon cancer Brazilian families

by Abud,Jamile, Prolla,João Carlos, Koehler-Santos,Patrícia, Ashton-Prolla,Patricia
Published 2012

Pineal region hemangioblastoma in a patient with Von Hippel-Lindau disease

by Isolan,Gustavo Rassier, Ashton-Prolla,Patrícia, Reis,Marcelo Martins dos, Antunes,Ápio Cláudio Martins
Published 2011

Melanoma hereditário: prevalência de fatores de risco em um grupo de pacientes no Sul do Brasil

by Carvalho,Charles André, Cunha,Mauricio Estrela da, Giugliani,Roberto, Bakos,Lucio, Ashton-Prolla,Patrícia
Published 2004

The paradox of autophagy in Tuberous Sclerosis Complex

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

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

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

Effect of HFE gene polymorphism on sustained virological response in patients with chronic hepatitis C and elevated serum ferritin

by Coelho-Borges,Silvia, Cheinquer,Hugo, Wolff,Fernando Herz, Cheinquer,Nelson, Krug,Luciano, Ashton-Prolla,Patricia
Published 2012

The TP53 fertility network

by Paskulin,Diego d'Avila, Paixão-Côrtes,Vanessa Rodrigues, Hainaut,Pierre, Bortolini,Maria Cátira, Ashton-Prolla,Patricia
Published 2012

Polymorphic variation of mononucleotide microsatellites in healthy humans and its implication for microsatellite instability screening

by Cossio,Silvia Liliana, Coura,Renata dos Santos, Bortolini,Maria Cátira, Giugliani,Roberto, Ashton-Prolla,Patricia, Prolla,João Carlos
Published 2007

Knowledge about breast cancer and hereditary breast cancer among nurses in a public hospital

by Prolla,Carmen Maria Dornelles, Silva,Patrícia Santos da, Netto,Cristina Brinckmann Oliveira, Goldim,José Roberto, Ashton-Prolla,Patricia
Published 2015

Genomic rearrangements in BRCA1 and BRCA2: a literature review

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

The Development of the Study of Hereditary Cancer in South America

by Rossi,Benedito Mauro, Sarroca,Carlos, Vaccaro,Carlos, Lopez,Francisco, Ashton-Prolla,Patricia, Ferreira,Fabio de Oliveira, Santos,Erika Maria Monteiro
Published 2016

Comparison of multiple genotyping methods for the identification of the cancer predisposing founder mutation p.R337H in TP53

by Fitarelli-Kiehl,Mariana, Macedo,Gabriel S., Schlatter,Rosane Paixão, Koehler-Santos,Patricia, Matte,Ursula da Silveira, Ashton-Prolla,Patricia, Giacomazzi,Juliana
Published 2016

Performance of the Gail and Tyrer-Cuzick breast cancer risk assessment models in women screened in a primary care setting with the FHS-7 questionnaire

by Vianna,Fernanda Sales Luiz, Giacomazzi,Juliana, Oliveira Netto,Cristina Brinckmann, Nunes,Luciana Neves, Caleffi,Maira, Ashton-Prolla,Patricia, Camey,Suzi Alves
Published 2019

Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer

by Palmero,Edenir Inêz, Campacci,Natalia, Schüler-Faccini,Lavinia, Giugliani,Roberto, Rocha,José Claudio Casali da, Vargas,Fernando Regla, Ashton-Prolla,Patricia
Published 2020

Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer

by Gomes,Renan, Soares,Barbara Luisa, Felicio,Paula Silva, Michelli,Rodrigo, Netto,Cristina B. O., Alemar,Barbara, Ashton-Prolla,Patrícia, Palmero,Edenir Inêz, Moreira,Miguel Ângelo Martins
Published 2020