Francisco Barros

Head of Laboratory

Spain

Research Interests

Explore related searches

Professors in Spain Professors in Medical Science Medical Science professors in Spain

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Francisco Barros is the Head of Laboratory at Fundación Pública Galega de Medicina Xenómica in Spain. His research areas include pharmacogenetics, cancer genetics, and neurodevelopmental disorders, as indicated by his recent publications. Notable works include studies on genetic variants in relation to thiopurine-related pancreatitis and the population frequencies of DPYD variants in Galicians. He is actively involved in projects addressing rare diseases and the genetic underpinnings of various health conditions.

Articles (12)

Year:

2025

Year:

2025

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Collaborators (23)

Angel Campos-Barros

Head of the Molecular Endocrinology Division

La Paz University Hospital

SPAIN

Francisco Barros

Research Interests

Explore related searches

Contact this professor

About

Articles (12)

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

Differences in <i>DPYD</i> Population Frequencies Observed in Galicians Compared to Europeans and Spanish from PhotoDPYD Study

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

Genetic linkage analysis of head and neck cancer in a Spanish family

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

Late-onset sporadic nemaline myopathy presenting as hypercapnic respiratory failure.

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

CIBERER: Spanish National Network for Research on Rare Diseases: a highly productive collaborative initiative.

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

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

Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I.

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

Collaborators (23)

Angel Campos-Barros

Manuel Van Domselaar

Pilar Rodríguez-Pombo

Elena Martín-Hernández

Lucía Martínez-Santamaría

Goretti Durán

María Tubío Fungueiriño

Noèlia Fernàndez-Castillo

Cintia Chamorro

Joana Fort

Ana Latorre-Pellicer

Raquel Rabionet

Abel García-García

Juan Andres Jimenez Estrada

Carlos Santos Ocaña

Esteban Guitián Fernández

Mario Pérez Sayáns

Alberto Marina

Saoud Tahsin Swafiri Swafiri

Leandro Sastre

María José Escámez

Mercedes Gil-Campos

Cristina Ugalde

Make your next move.