Author

Gonzalo Núñez‐Moreno

Genmab (Netherlands)ORCID 0000-0001-5982-570XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Organism:non-human primate· 1

Frequent Co-Authors

Marta CortóniD· 2 shared Pablo MíngueziD· 2 shared Alejandra DamiániD· 1 shared Alejandra Tamayo· 1 shared Almudena Ávila‐Fernández· 1 shared Anna DahlmaniD· 1 shared Anna WojtuszkiewicziD· 1 shared Attila CsalaiD· 1 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Marta CortónORCID

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3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintMar 19, 2026

A Cross-Study Multi-Organ Cell Atlas ofMacaca fascicularis Informed by Human Foundation Model Annotation: A Resource for Translational Target Assessment

Terezinha Maria de Souza, Joshua T. Gamse, Leandro F. Moreno…·Iris C. R. M. Kolder

This paper creates a cross-species single-cell atlas of Macaca fascicularis using human reference labels to improve target qualification and toxicity interpretation in preclinical research.

DOI 10.64898/2026.03.17.711997

non-human primatescRNA-seq

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Genetic & Genomic MedicineInternational Journal of Molecular SciencesPeer-reviewedJul 29, 2022

Aggregated genomic data as cohort-specific allelic frequencies can boost variants and genes prioritization in non-solved cases of inherited retinal dystrophies

Ionut-Florin Iancu, Irene Perea‐Romero, Gonzalo Núñez‐Moreno…·Pablo Mínguez

The paper builds a cohort-specific allelic frequency database to prioritize variants and genes in non-solved inherited retinal dystrophies, identifying 8 potential causative variants and 18 genes for further study.

10 citations

humanwhole-exome sequencing

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BioinformaticsbioRxivPreprintMar 1, 2022

VIsoQLR: an interactive tool for the detection, quantification and fine-tuning of isoforms using long-read sequencing

Gonzalo Núñez‐Moreno, Alejandra Tamayo, Carolina Ruiz‐Sánchez…·Pablo Mínguez

VIsoQLR is a tool for identifying, quantifying, and fine-tuning mRNA isoforms using long-read sequencing data in low-throughput splicing assays.

1 citation

humanlong-read sequencing

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