Author

Teresa Requena

Roslin InstituteORCID 0000-0001-8355-6028Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alvaro Gallego‐MartineziD· 1 shared Amy S. FindlayiD· 1 shared Anna RaperiD· 1 shared Brian Ho Ching Chan· 1 shared Dominique MeunieriD· 1 shared Holly HardyiD· 1 shared Jason IoannidisiD· 1 shared Joe RaingeriD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenomics

Alvaro Gallego‐MartinezORCID

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2 papers

Recent·Most cited

Developmental BiologybioRxivPreprintOct 1, 2024

A stable Netrin-1 fluorescent reporter chicken reveals cell-specific molecular signaturesduring optic fissure closure.

Brian Ho Ching Chan, Holly Hardy, Teresa Requena…·Joe Rainger

The paper generates a Netrin-1 fluorescent reporter chicken line to study molecular signatures during optic fissure closure and identifies new markers and pathways for developmental tissue fusion.

DOI 10.1101/2024.10.01.616014

experimental assaycell type annotation

𝕏 PostBluesky

GenomicsFrontiers in GeneticsPeer-reviewedFeb 15, 2019

Excess of rare missense variants in hearing loss genes in sporadic Meniere disease

Alvaro Gallego‐Martinez, Teresa Requena, Pablo Román-Naranjo, Jose Antonio Lopez-Escamez

This study identifies an excess of rare missense variants in SNHL genes in sporadic Meniere disease patients compared to controls.

59 citations

humanwhole-exome sequencing

𝕏 PostBluesky