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BERNAT DEL OLMO CABASTRÉ

Firma
BERNAT DEL OLMO-CABASTRÉ
Posició
Investigador/a Post-doctoral – R2
Investigadors/es Post-doctorals – R2

Publicacions

Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, Cesar S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol V, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O

Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.

Journal of Personalized Medicine, 2021, 11, 162 dx.doi.org/10.3390/jpm11030162

Pinsach-Abuin ML, Del Olmo B, Pérez-Agustin A, Mates J, Allegue C, Iglesias A, Ma Q, Merkurjev D, Konovalov S, Zhang J, Sheikh F, Telenti A, Brugada J, Brugada R, Gymrek M, di Iulio J, Garcia-Bassets I, Pagans S

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

Cell Reports. Medicine, 2021, 2, 100250-100250 dx.doi.org/10.1016/j.xcrm.2021.100250

Campuzano O, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Coll M, Fiol V, Iglesias A, Perez-Serra A, Mates J, Del Olmo B, Ferrer C, Alcalde M, Puigmulé M, Mademont-Soler I, Pico F, Lopez L, Tiron C, Brugada J, Brugada R

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

Frontiers in Genetics, 2019, 10, 450-450 dx.doi.org/10.3389/fgene.2019.00450

Campuzano O, Fernandez-Falgueras A, Lemus X, Sarquella-Brugada G, Cesar S, Coll M, Mates J, Arbelo E, Jordà P, Perez-Serra A, Del Olmo B, Ferrer-Costa C, Iglesias A, Fiol V, Puigmulé M, Lopez L, Pico F, Brugada J, Brugada R

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

Journal of Clinical Medicine, 2019, 8, 1035 dx.doi.org/10.3390/jcm8071035

Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Coll M, Mates J, Arbelo E, Perez-Serra A, Del Olmo B, Jordá P, Fiol V, Iglesias A, Puigmulé M, Lopez L, Pico F, Brugada J, Brugada R

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

HUMAN MUTATION, 2019, 40, 749-764 dx.doi.org/10.1002/humu.23730

Campuzano O, Beltramo P, Fernandez A, Iglesias A, García L, Allegue C, Sarquella-Brugada G, Coll M, Perez-Serra A, Mademont-Soler I, Mates J, Del Olmo B, Rodríguez Á, Maciel N, Puigmulé M, Pico F, Cesar S, Brugada J, Cuesta A, Gutierrez C, Brugada R

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

FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2018, 37, 54-63 dx.doi.org/10.1016/j.fsigen.2018.07.023

Mates J, Mademont-Soler I, Del Olmo B, Ferrer-Costa C, Coll M, Pérez-Serra A, Picó F, Allegue C, Fernandez-Falgueras A, Álvarez P, Yotti R, Espinosa MA, Sarquella-Brugada G, Cesar S, Carro E, Brugada J, Arbelo E, Garcia-Pavia P, Borregan M, Tizzano E, López-Granados A, Mazuelos F, Díaz de Bustamante A, Darnaude MT, González-Hevia JI, Díaz-Flores F, Trujillo F, Iglesias A, Fernandez-Aviles F, Campuzano O, Brugada R

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

EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26, 1014-1025 dx.doi.org/10.1038/s41431-018-0119-1

Campuzano O, Sanchez-Molero O, Fernandez A, Mademont-Soler I, Coll M, Perez-Serra A, Mates J, Del Olmo B, Pico F, Nogue-Navarro L, Sarquella-Brugada G, Iglesias A, Cesar S, Carro E, Borondo JC, Brugada J, Castellà J, Medallo J, Brugada R

Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis.

SPORTS MEDICINE, 2017, 47, 2101-2115 dx.doi.org/10.1007/s40279-017-0705-3

Coll M, Pérez-Serra A, Mates J, Del Olmo B, Puigmulé M, Fernandez-Falgueras A, Iglesias A, Picó F, Lopez L, Brugada R, Campuzano O

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

BIOLOGY-BASEL, 2017, 7, 3 dx.doi.org/10.3390/biology7010003

Coll M, Striano P, Ferrer-Costa C, Campuzano O, Matés J, Del Olmo B, Iglesias A, Pérez-Serra A, Mademont I, Picó F, Oliva A, Brugada R

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

Plos One, 2017, 12, e0189618 dx.doi.org/10.1371/journal.pone.0189618

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