Marta Balada-Rodriguez
Reus, CT, Spain
Last Updated: 09/26/2026
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Found 11 publications
Metabolomic-driven prediction of the mutational status of healthy individuals with a family history of hereditary breast and ovarian cancer syndrome: the HRRmet study.
Journal: Scientific reports
Published: August 05, 2025
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.
Journal: Database : the journal of biological databases and curation
Published: April 02, 2024
Opportunistic genetic screening increases the diagnostic yield and is medically valuable for care of patients and their relatives with hereditary cancer.
Journal: Journal of medical genetics
Published: May 10, 2023
Utility of ctDNA Liquid Biopsies from Cancer Patients: An Institutional Study of 285 ctDNA Samples.
Journal: Cancers
Published: November 16, 2022
Immunohistochemical Algorithm for the Classification of Muscle-Invasive Urinary Bladder Carcinoma with Lymph Node Metastasis: An Institutional Study.
Journal: Journal of clinical medicine
Published: October 31, 2022
Identification of germline pathogenic variants in DNA damage repair genes by a next-generation sequencing multigene panel in BRCAX patients.
Journal: Clinical biochemistry
Published: August 01, 2019
Germline promoter hypermethylation in BRCA1 and BRCA2 genes is not present in hereditary breast cancer patients.
Journal: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
Published: September 28, 2017
In silico, in vitro and case-control analyses as an effective combination for analyzing BRCA1 and BRCA2 unclassified variants in a population-based sample.
Journal: Cancer genetics
Published: June 03, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026