Author

Alfonso Ambrós

Hospital General Universitario de Ciudad Real

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Approach:benchmark study· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Almudena CorralesiD· 3 shared Aurelio RodrígueziD· 3 shared Beatriz Guillén‐GuíoiD· 3 shared Carlos FloresiD· 3 shared David DomíngueziD· 3 shared Demetrio CarriedoiD· 3 shared Elena Espinosa· 3 shared Elena González-Higueras· 3 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Almudena CorralesORCID

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3 papers

Recent·Most cited

Rare genetic variant risks in patients with sepsis-associated acute respiratory distress syndrome

Eva Tosco-Herrera, Luis A. Rubio‐Rodríguez, Adrián Muñoz‐Barrera, David Jáspez, Eva Suarez-Pajes, Almudena Corrales, Aitana Alonso-González, Miryam Prieto-González, Aurelio Rodríguez, Demetrio Carriedo, Jesus Blanco, Alfonso Ambrós, Leonardo Lorente, M. Almudena Sánchez Martín, Jordi Solé‐Violán, , Carlos Flores

The paper identifies rare genetic variants associated with sepsis-associated ARDS using whole-exome sequencing and network-based clustering analysis.

Respiratory Research · Feb 25, 2026Peer-reviewedGenetic & Genomic Medicine

Genetic regulation of the vascular endothelial growth factor receptor 1 during sepsis and association with ARDS susceptibility

Eva Suarez-Pajes, Nick R. G. Shrine, Eva Tosco-Herrera, Tamara Hernández-Beeftink, Luis A. Rubio‐Rodríguez, M. Isabel García-Laorden, Almudena Corrales, Miryam Prieto-González, Aurelio Rodríguez, Demetrio Carriedo, Jesús Blanco, Alfonso Ambrós, Elena González-Higueras, Elena Espinosa, Arturo Muriel-Bombín, , Carlos Flores

This study identifies pQTLs of sVEGFR1 levels during sepsis and links them to ARDS susceptibility and mortality using GWAS, colocalisation, and Mendelian randomisation.

medRxiv · Jan 30, 2025 · PreprintGenetic & Genomic Medicine

A Genome-Wide Association Study of Survival in Patients with Sepsis

Tamara Hernández-Beeftink, Beatriz Guillén‐Guío, Jose Miguel Lorenzo-Salazar, Almudena Corrales, Eva Suarez-Pajes, Rui Feng, Luis A. Rubio‐Rodríguez, Megan L. Paynton, Raquel Cruz, M. Isabel García-Laorden, Miryam Prieto-González, Aurelio Rodríguez, Demetrio Carriedo, Jesús Blanco, Alfonso Ambrós, , the Genetics of Sepsis (GEN-SEP) Network

This paper conducts a genome-wide association study (GWAS) to identify genetic variants associated with 28-day survival in sepsis patients, finding three novel variants linked to reduced survival.

Critical Care · Nov 5, 2022Peer-reviewedGenetic & Genomic Medicine