B. D. F. Barros

发表

Assessment of somatic mutations in urine and plasma of Wilms tumor patients

S. D. de Souza, D. Carraro, I. Cunha, 2020, Cancer medicine.

Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors

P. Grundy, M. Maschietto, D. Carraro, 2016, Molecular Cytogenetics.

Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families

S. D. de Souza, D. Carraro, R. Valieris, 2022, PloS one.

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

P. Grundy, D. Carraro, I. Cunha, 2014, Nature Communications.

BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation

Dirce Maria Carraro, D. Carraro, V. Andrade, 2018, Breast Cancer Research and Treatment.

Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

J. Ragoussis, F. Couch, P. Tonin, 2020, Human mutation.

A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease

S. D. de Souza, D. Carraro, A. Lopes, 2016, Human Genomics.

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer

S. D. de Souza, D. Carraro, J. E. D. de Souza, 2018, Front. Genet..

Does the Addition of Mutations of CTNNB1 S45F to Clinical Factors Allow Prediction of Local Recurrence in Patients With a Desmoid Tumor? A Local Recurrence Risk Model

D. Carraro, A. Lopes, I. Cunha, 2023, Clinical orthopaedics and related research.

A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease

S. D. de Souza, D. Carraro, A. Lopes, 2016, Human Genomics.

BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation

D. Carraro, V. Andrade, E. N. Ferreira, 2018, Breast Cancer Research and Treatment.