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Frontiers in Genetics|June 4, 2019
Personalized Interpretation and Clinical Translation of Genetic Variants Associated With CardiomyopathiesOscar Campuzano, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, et al.
International Journal of Molecular Sciences|May 13, 2023
Clinical and Translational Applications of Serological and Histopathological Biomarkers in Metastatic Breast Cancer: A Comprehensive ReviewLeonel Pekarek, Alicia Sánchez Cendra, Eduardo D Roberts Cervantes, et al.
Medicina (Kaunas, Lithuania)|January 23, 2024
Exploring Biomarkers in Breast Cancer: Hallmarks of Diagnosis, Treatment, and Follow-Up in Clinical PracticeLaura Lopez-Gonzalez, Alicia Sanchez Cendra, Cristina Sanchez Cendra, et al.
Human Genetics|September 21, 2021
Clinical impact of rare variants associated with inherited channelopathies: a 5-year updateGeorgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.
Orphanet Journal of Rare Diseases|August 11, 2021
The GoodHope Ehlers Danlos Syndrome Clinic: development and implementation of the first interdisciplinary program for multi-system issues in connective tissue disorders at the Toronto General HospitalNimish Mittal, Daniel Santa Mina, Laura McGillis, et al.
Medical Sciences (Basel, Switzerland)|July 27, 2026
Late-Onset Preeclampsia Is Linked to Extensive Remodeling of the Placental Extracellular MatrixCielo García-Montero, Tatiana Pekarek, Óscar Fraile-Martinez, et al.
European Journal of Cell Biology|January 7, 2026
The role of the LOX family in cancerDiego Liviu Boaru, Diego De Leon-Oliva, Oscar Fraile-Martinez, et al.
Journal of Personalized Medicine|March 3, 2021
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years LaterMarta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, et al.
International Journal of Legal Medicine|January 24, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohortEstefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, et al.
Forensic Science International. Genetics|April 6, 2020
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, et al.
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