Author

Ursula Houessou

Centre National de la Recherche ScientifiqueORCID 0009-0002-8716-3007Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:GWAS summary statistics· 1 Research Focus:polygenic risk· 1

Frequent Co-Authors

Aïda Eslami· 1 shared Amélie PitoniD· 1 shared Angélique QuartieriD· 1 shared Arnaud S. GirardiD· 1 shared Arthur SorliniD· 1 shared Audrey PutouxiD· 1 shared Benoît J. ArsenaultiD· 1 shared Brigitte Gilbert‐DussardieriD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aïda Eslami

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicineAtherosclerosisPeer-reviewedDec 5, 2024

Association of Genetically Predicted Levels of Circulating Blood Lipids with Coronary Artery Disease Incidence

Hasanga D. Manikpurage, Jasmin Ricard, Ursula Houessou…·Sébastien Thériault

This paper evaluates polygenic risk scores (PRS) for CAD and blood lipids to predict CAD incidence in UK Biobank participants.

6 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsMolecular PsychiatryPeer-reviewedNov 29, 2023

Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome

Jérémie Courraud, Camille Engel, Angélique Quartier…·Amélie Piton

This study investigates the molecular consequences of PQBP1 deficiency in Renpenning syndrome by analyzing gene expression and protein interactions, identifying dysregulated genes and a novel UPF3B isoform.

10 citations

humanbulk RNA-seq

𝕏 PostBluesky