Author

Audrey Labalme

Hospices Civils de LyonORCID 0009-0006-4523-6836Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Ada HamoshiD· 1 shared Alan H. BeggsiD· 1 shared Alessandro Brandulas CammarataiD· 1 shared Alice PoissoniD· 1 shared Anamaria NecşuleaiD· 1 shared André ReisiD· 1 shared Anita M. RauchiD· 1 shared Anne Blomhoff· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ada HamoshORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintAug 3, 2023

Transposable element expression with variation in sex chromosome number: insights into a toxic Y effect on human longevity

Jordan Teoli, Miriam Merenciano, Marie Fablet…·Ingrid Plotton

The paper investigates the association between transposable element expression and Y chromosome number in humans, suggesting a toxic Y effect on male longevity.

5 citations

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedMar 3, 2021

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny F. Lai…·Timothy W. Yu

The paper identifies RFX3, RFX4, and RFX7 mutations as causes of neurodevelopmental disorders including autism, ADHD, and intellectual disability, and links these genes to ASD risk genes through bioinformatic analysis.

84 citationstop 3%

humanbulk RNA-seq

𝕏 PostBluesky