Victor J. Asensio

Health Research Institute Of The Balearic Islands
Palma, PM, Spain

Last Updated: 09/26/2026

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Found 15 publications

Analytical and Clinical Validation of Action PharmaKitDx: A Comprehensive NGS Panel for the Identification of Pharmacogenetic Variants in Diverse Populations.

Analytical and Clinical Validation of Action PharmaKitDx: A Comprehensive NGS Panel for the Identification of Pharmacogenetic Variants in Diverse Populations.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: February 19, 2026

Maternal Genotype and Dietary Vitamin A Modify Aortic Arch Phenotypes in a Mouse Model of 22q11DS.

Maternal Genotype and Dietary Vitamin A Modify Aortic Arch Phenotypes in a Mouse Model of 22q11DS.

Journal: International journal of molecular sciences

Published: September 29, 2025

Hypokalemic periodic paralysis associated with the atypical CACNA1S c.2690G>A (p.Arg897Lys) variant: description of 14 affected individuals from five families.

Hypokalemic periodic paralysis associated with the atypical CACNA1S c.2690G>A (p.Arg897Lys) variant: description of 14 affected individuals from five families.

Journal: Neuromuscular disorders : NMD

Published: March 30, 2025

New genomic technologies and their application in pediatric care.

New genomic technologies and their application in pediatric care.

Journal: Anales de pediatria

Published: November 20, 2024

Role of PATJ in stroke prognosis by modulating endothelial to mesenchymal transition through the Hippo/Notch/PI3K axis.

Role of PATJ in stroke prognosis by modulating endothelial to mesenchymal transition through the Hippo/Notch/PI3K axis.

Journal: Cell death discovery

Published: October 17, 2023

NOTCH1 Gene as a Novel Cause of Thoracic Aortic Aneurysm in Patients with Tricuspid Aortic Valve: Two Cases Reported.

NOTCH1 Gene as a Novel Cause of Thoracic Aortic Aneurysm in Patients with Tricuspid Aortic Valve: Two Cases Reported.

Journal: International journal of molecular sciences

Published: March 31, 2023

Screening for Prognostic microRNAs Associated with Treatment Failure in Diffuse Large B Cell Lymphoma.

Screening for Prognostic microRNAs Associated with Treatment Failure in Diffuse Large B Cell Lymphoma.

Journal: Cancers

Published: January 14, 2022

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.

Journal: Frontiers in genetics

Published: October 29, 2020

Detection of the EGFR G719S Mutation in Non-small Cell Lung Cancer Using Droplet Digital PCR.

Detection of the EGFR G719S Mutation in Non-small Cell Lung Cancer Using Droplet Digital PCR.

Journal: Frontiers in medicine

Published: August 14, 2020

Eosinophilic COPD Patients Display a Distinctive Serum miRNA Profile From Asthma and Non-eosinophilic COPD.

Eosinophilic COPD Patients Display a Distinctive Serum miRNA Profile From Asthma and Non-eosinophilic COPD.

Journal: Archivos de bronconeumologia

Published: July 05, 2019

Corrigendum to: "Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients" Stem Cell Res. 2018 May; 29:1-5.

Corrigendum to: "Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients" Stem Cell Res. 2018 May; 29:1-5.

Journal: Stem cell research

Published: January 27, 2019

Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients.

Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients.

Journal: Stem cell research

Published: December 20, 2017

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Last Updated: 09/26/2026