Author

Ferrán Casals

Instituto de Salud Carlos IIIORCID 0000-0002-8941-0369Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aina Medina-DolsiD· 1 shared Alba Tristán‐NogueroiD· 1 shared Alberto Fernández‐JaéniD· 1 shared Àlex BayésiD· 1 shared Alfons MacayaiD· 1 shared Alfons NadaliD· 1 shared Amaia Lasa‐AranzastiiD· 1 shared Amanda SoléiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aina Medina-DolsORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genotype-Phenotype Correlations and Putative Modifier Genes in SYNGAP1 Encephalopathy

Selena Aranda, Juliana Ribeiro‐Constante, Alba Tristán‐Noguero, Nerea Moreno‐Ruiz, C. Arenas, Fernando Francisco Martínez Calvo, Salvador Ibáñez‐Micó, José Luis Peña Segura, José Miguel Ramos‐Fernández, María del Carmen Moyano Chicano, Rafael Camino León, Victor Miguel Soto Insuga, Elena González Alguacil, Carlos Valera Dávila, Alberto Fernández‐Jaén, , Marina Mitjans

This study investigates genotype-phenotype correlations in SYNGAP1 Encephalopathy, finding that variant location and type, along with modifier genes, influence clinical severity and autistic traits.

Neurobiology of Disease · Mar 17, 2026Peer-reviewedGenetic & Genomic Medicine

Rare Variant Association Analysis Uncovers Involvement of VNN2 in Stroke Outcome

Estefanía Alcaide-Consuegra, Marina Mola-Caminal, Geòrgia Escaramís, Uxue Lazcano, Isabel Fernández Pérez, Jaume Reig‐Palou, Joan Jiménez-Baladó, Eva Giralt Steinhauer, Elisa Cuadrado‐Godia, Ángel Ois, Ana Rodríguez-Campello, Marta Vallverdú-Prats, Aina Medina-Dols, Carmen Jiménez, Sílvia Tur, , Raquel Rabionet

This study identifies rare variants in VNN2 associated with improved stroke recovery using exome sequencing and structural analysis.

Stroke · Jun 11, 2025Peer-reviewedGenetic & Genomic Medicine

Genome-wide postnatal changes in immunity following fetal inflammatory response

Daniel Costa, Núria Bonet, Amanda Solé, José Manuel González de Aledo‐Castillo, Eduard Sabidó, Ferrán Casals, Carlota Rovira, Alfons Nadal, José Luis Marı́n, Teresa Cobo, Robert Castelo

The paper identifies molecular changes in immunity postnatal in ELGANs with fetal inflammatory response, showing innate immune activation and adaptive immunity impairment.

FEBS Journal · Oct 2, 2020Peer-reviewedGenetic & Genomic Medicine