Francisco M. Barros

Santiago De Compostela, GA 15706, Spain

Last Updated: 09/26/2026

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Found 28 publications

A Lack of Complete Linkage Disequilibrium Between c.1236G>A and c.1129-5923C>G HapB3 Variants of DPYD: A Call to Revise European Pharmacogenetic Guidelines.

A Lack of Complete Linkage Disequilibrium Between c.1236G>A and c.1129-5923C>G HapB3 Variants of DPYD: A Call to Revise European Pharmacogenetic Guidelines.

Journal: International journal of molecular sciences

Published: July 05, 2025

Differences in DPYD Population Frequencies Observed in Galicians Compared to Europeans and Spanish from PhotoDPYD Study.

Differences in DPYD Population Frequencies Observed in Galicians Compared to Europeans and Spanish from PhotoDPYD Study.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: February 27, 2025

Balance of care activity after EMA recommendation for DPYD gene testing in Galicia.

Balance of care activity after EMA recommendation for DPYD gene testing in Galicia.

Journal: Frontiers in pharmacology

Published: November 06, 2024

Evaluation of Genetic Variants Associated with the Risk of Thiopurine-Related Pancreatitis: A Case Control Study from ENEIDA Registry.

Evaluation of Genetic Variants Associated with the Risk of Thiopurine-Related Pancreatitis: A Case Control Study from ENEIDA Registry.

Journal: Digestive diseases (Basel, Switzerland)

Published: September 13, 2023

Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders.

Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders.

Journal: Cytogenetic and genome research

Published: July 19, 2023

Deletion of the CYP2D6 gene as a likely explanation for the serious side effects of the antipsychotic drug pimozide: a case report.

Deletion of the CYP2D6 gene as a likely explanation for the serious side effects of the antipsychotic drug pimozide: a case report.

Journal: Frontiers in pharmacology

Published: June 09, 2023

Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability.

Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability.

Journal: European journal of human genetics : EJHG

Published: November 29, 2021

Schuurs-Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review.

Schuurs-Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review.

Journal: Genes

Published: April 08, 2021

Predictive value of ERCC2, ABCC2 and MMP2 of response and long-term survival in locally advanced head and neck cancer patients treated with chemoradiotherapy.

Predictive value of ERCC2, ABCC2 and MMP2 of response and long-term survival in locally advanced head and neck cancer patients treated with chemoradiotherapy.

Journal: Cancer chemotherapy and pharmacology

Published: March 18, 2021

Efficacy and toxicity of adjuvant chemotherapy on colorectal cancer patients: how much influence from the genetics?

Efficacy and toxicity of adjuvant chemotherapy on colorectal cancer patients: how much influence from the genetics?

Journal: Journal of chemotherapy (Florence, Italy)

Published: May 23, 2020

Molecular and Clinical Characterization of a Novel Nonsense Variant in Exon 1 of the UPF3B Gene Found in a Large Spanish Basque Family (MRX82).

Molecular and Clinical Characterization of a Novel Nonsense Variant in Exon 1 of the UPF3B Gene Found in a Large Spanish Basque Family (MRX82).

Journal: Frontiers in genetics

Published: July 24, 2019

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children.

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children.

Journal: Scientific reports

Published: February 08, 2019

Showing 1-12 of 28

Last Updated: 09/26/2026