Luis A. Aguirre

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Publications

Citations

1.5K

H-Index

Active since

2005

Affiliations

Centre for Biomedical Network Research on Rare Diseases(Current)

Hospital Universitario La Paz

Hospital La Paz Institute for Health Research

Centro de Investigación en Red en Enfermedades Cardiovasculares

Centro de Investigación Biomédica en Red de Enfermedades Respiratorias

Luis A. Aguirre is an author at Centre for Biomedical Network Research on Rare Diseases specializing in immunology, life sciences, and infectious diseases.

ORCID

Publications per year

2005–2022

Publications

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss

Ángeles Mencía, Silvia Modamio‐Høybjør, Nick Redshaw et al. · Nature Genetics · 2009 · 555 citations

Life Sciences, Genetics, Molecular Genetics +14

Hypoxia-induced PD-L1/PD-1 crosstalk impairs T-cell function in sleep apnoea

Carolina Cubillos‐Zapata, José Avendaño‐Ortiz, Enrique Hernandez-Jimenez et al. · European Respiratory Journal · 2017 · 115 citations · Full text

Life Sciences, Immunology, Oncology +17

Nonsense Mutations in SMPX, Encoding a Protein Responsive to Physical Force, Result in X-Chromosomal Hearing Loss

Antje K. Huebner, Marta Gandía, Peter Frommolt et al. · The American Journal of Human Genetics · 2011 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

High prevalence of the <i>W24X</i> mutation in the gene encoding connexin‐26 (<i>GJB2</i>) in Spanish Romani (gypsies) with autosomal recessive non‐syndromic hearing loss

Araceli Álvarez, Ignacio del Castillo, Manuela Villamar et al. · American Journal of Medical Genetics Part A · 2005 · 81 citations

Life Sciences, Genetics, Molecular Genetics +17

Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP

Luis A. Aguirre, M. Eva Alonso, Claudio Badía-Careaga et al. · BMC Biology · 2015 · 63 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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