Author

Carlos Rodríguez‐Gallego

Hospital Universitario de Gran Canaria Doctor NegrínORCID 0000-0002-4344-8644Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexandre BolzeiD· 2 shared Carlos FloresiD· 2 shared Horst von BernuthiD· 2 shared Adem KarbuziD· 1 shared Adrian GervaisiD· 1 shared Adrián Muñoz‐BarreraiD· 1 shared Agatha SchlüteriD· 1 shared Ahmad N. Abou TayouniD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alexandre BolzeORCID

Mutual co-authors in cluster

Author profile →

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

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with critical COVID-19

Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jérémy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic, Adrian Gervais, Paul Bastard, Takaki Asano, Lucy Bizien, Federica Barzaghi, , Michel Vidaud

The paper identifies rare loss-of-function variants in type I IFN immunity genes associated with severe COVID-19, particularly in younger patients with recessive inheritance.

Genome Medicine · Apr 5, 2023Peer-reviewedGenetic & Genomic Medicine

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

Alexandre Bolze, Bertrand Boisson, Barbara Bosch, Alexander Antipenko, Matthieu Bouaziz, Paul E. Sackstein, Malik Chaker-Margot, Vincent Barlogis, Tracy Ann Briggs, Elena Colino, Aurora C. Elmore, Alain Fischer, Ferah Genel, Angela L. Hewlett, Maher Jedidi, , Jean‐Laurent Casanova

The paper reports new RPSA mutations causing isolated congenital asplenia, including 5-UTR mutations and incomplete penetrance in some cases.

Proceedings of the National Academy of Sciences · Aug 2, 2018Peer-reviewedGenetics