Jesus Mates

Girona, CT, Spain

Last Updated: 09/26/2026

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Found 25 publications

The Selectivity for Tumor Cells of Nuclear-Directed Cytotoxic RNases Is Mediated by the Nuclear/Cytoplasmic Distribution of p27KIP1.

The Selectivity for Tumor Cells of Nuclear-Directed Cytotoxic RNases Is Mediated by the Nuclear/Cytoplasmic Distribution of p27KIP1.

Journal: Molecules (Basel, Switzerland)

Published: October 26, 2020

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants.

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants.

Journal: Cell reports. Medicine

Published: September 29, 2020

Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

Journal: Forensic science international. Genetics

Published: October 12, 2019

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants.

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants.

Journal: Journal of clinical medicine

Published: June 08, 2019

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.

Journal: Frontiers in genetics

Published: January 13, 2019

Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.

Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.

Journal: Human mutation

Published: December 02, 2018

Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients.

Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients.

Journal: PloS one

Published: May 09, 2018

Molecular autopsy in a cohort of infants died suddenly at rest.

Molecular autopsy in a cohort of infants died suddenly at rest.

Journal: Forensic science international. Genetics

Published: May 05, 2018

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.

Journal: Biology

Published: November 24, 2017

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.

Journal: PloS one

Published: September 15, 2017

Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice.

Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice.

Journal: European journal of human genetics : EJHG

Published: July 25, 2017

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.

Journal: PloS one

Published: March 22, 2017

Showing 1-12 of 25

Last Updated: 09/26/2026