Concepedia

Jordi Minguillón

JM

Statistics

Publications

14

Citations

772

H-Index

12

Active since

2005

Affiliations

Centre for Biomedical Network Research on Rare Diseases(Current)

Universitat Autònoma de Barcelona

Hospital de Sant Pau

Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas

Instituto de Salud Carlos III

Jordi Minguillón is an author at Centre for Biomedical Network Research on Rare Diseases specializing in life sciences, molecular biology, and molecular oncology.

ORCID

Publications per year

2005–2025

14

Publications

14

Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker et al. · The American Journal of Human Genetics · 2013 · 308 citations · Full text

, , +11

Gene expression induced by Toll-like receptors in macrophages requires the transcription factor NFAT5

Maria Buxadé, Giulia Lunazzi, Jordi Minguillón et al. · The Journal of Experimental Medicine · 2012 · 154 citations · Full text

, , +17

Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1

Gonzalo Hernández, Jordi Minguillón, Paco Quiles et al. · Nature Communications · 2018 · 47 citations · Full text

, , +17

Gefitinib and Afatinib Show Potential Efficacy for Fanconi Anemia–Related Head and Neck Cancer

Helena Montanuy, Águeda Martínez‐Barriocanal, José Antonio Casado et al. · Clinical Cancer Research · 2020 · 45 citations

, , +11

Analysis of the transcriptional activity of endogenous NFAT5 in primary cells using transgenic NFAT-luciferase reporter mice

Beatriz Morancho, Jordi Minguillón, Jeffery D. Molkentin et al. · BMC Molecular Biology · 2008 · 44 citations · Full text

, , +13

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