Catarina Silveira
Lisbon, 1649028, Portugal
Last Updated: 09/26/2026
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Found 10 publications
Comprehensive Genomic Profiling of Cell-Free Circulating Tumor DNA Detects Response to Ribociclib Plus Letrozole in a Patient with Metastatic Breast Cancer.
Journal: Biomolecules
Published: November 04, 2022
Bi-allelic REN Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD.
Journal: Kidney international reports
Published: September 12, 2022
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Journal: The Lancet. Oncology
Published: July 17, 2022
Stromal MED12 exon 2 mutations in complex fibroadenomas of the breast.
Journal: Journal of clinical pathology
Published: August 26, 2020
Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations.
Journal: Kidney international reports
Published: March 31, 2020
Identification of recurrent FHL2-GLI2 oncogenic fusion in sclerosing stromal tumors of the ovary.
Journal: Nature communications
Published: May 15, 2019
PAX8-GLIS3 gene fusion is a pathognomonic genetic alteration of hyalinizing trabecular tumors of the thyroid.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: April 13, 2019
Genomic analysis of recurrences and high-grade forms of polymorphous adenocarcinoma.
Journal: Histopathology
Published: February 08, 2019
The Genomic Landscape of Mucinous Breast Cancer.
Journal: Journal of the National Cancer Institute
Published: August 03, 2018
A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A.
Journal: Hormones (Athens, Greece)
Published: February 16, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026