Author

Álvaro Muñoz-Morales

Universitat Internacional de CatalunyaORCID 0009-0003-7580-3756Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Agustı́n RuiziD· 2 shared Amanda C. CanoiD· 2 shared Berta CalmiD· 2 shared Clàudia OlivéiD· 2 shared Itziar de RojasiD· 2 shared Laura MontrrealiD· 2 shared Maria Eugenia SáeziD· 2 shared Marta MarquiéiD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Agustı́n RuizORCID

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2 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedJun 30, 2026

Landscape of copy number variants in Spanish People with Dementia

Itziar de Rojas, Pablo García‐González, Clàudia Olivé…·Maria-Dolores Alonso

The paper analyzes copy number variants in a Spanish dementia cohort and identifies potential novel genes associated with ADRD but finds no genome-wide significant associations.

DOI 10.1038/s41525-026-00589-6

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintMar 25, 2025

Long-read sequencing reveals two common APOE ϵ3 and ϵ4 intragenic haplotypes in the Spanish population

Pablo García‐González, Raquel Puerta, Álvaro Muñoz-Morales…·Agustı́n Ruiz

The paper uses long-read sequencing to identify and characterize APOE haplotypes in a Spanish cohort, finding associations between specific haplotypes and reduced risk of Alzheimer's disease progression.

DOI 10.1101/2025.03.25.25324541

humanwhole-genome sequencing

𝕏 PostBluesky