Bernat Del Olmo

Institut D'Investigació Biomedica De Girona Dr. Josep Trueta
Girona, CT, Spain

Last Updated: 09/26/2026

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Found 30 publications

Identification of a Novel Genetic Variant Responsible for Familial Atrial Fibrillation.

Identification of a Novel Genetic Variant Responsible for Familial Atrial Fibrillation.

Journal: The Canadian journal of cardiology

Published: March 09, 2026

Identification of a Novel Genetic Variant responsible for Familial Atrial Fibrillation.

Identification of a Novel Genetic Variant responsible for Familial Atrial Fibrillation.

Journal: The Canadian journal of cardiology

Published: March 09, 2026

The STAT3/TIMP1 inhibitor silibinin overcomes secondary immunoresistance to pembrolizumab in brain metastases from METex14 skipping mutated non-small cell lung cancer: a case report.

The STAT3/TIMP1 inhibitor silibinin overcomes secondary immunoresistance to pembrolizumab in brain metastases from METex14 skipping mutated non-small cell lung cancer: a case report.

Journal: Frontiers in medicine

Published: April 15, 2025

Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.

Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.

Journal: International journal of molecular sciences

Published: May 03, 2024

Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.

Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.

Journal: International journal of molecular sciences

Published: February 19, 2024

LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation.

LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation.

Journal: Frontiers in genetics

Published: December 31, 2022

Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.

Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.

Journal: International journal of legal medicine

Published: October 20, 2022

Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples.

Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples.

Journal: International journal of molecular sciences

Published: August 31, 2022

Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.

Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.

Journal: Journal of personalized medicine

Published: January 07, 2022

Post-mortem toxicology analysis in a young sudden cardiac death cohort.

Post-mortem toxicology analysis in a young sudden cardiac death cohort.

Journal: Forensic science international. Genetics

Published: December 21, 2021

Epidemiology and Molecular Profile of Mucosal Melanoma: A Population-Based Study in Southern Europe.

Epidemiology and Molecular Profile of Mucosal Melanoma: A Population-Based Study in Southern Europe.

Journal: Cancers

Published: November 29, 2021

Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations.

Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations.

Journal: Forensic science international. Genetics

Published: October 29, 2021

Showing 1-12 of 30

Last Updated: 09/26/2026