Author

Joséphine Henry

InsermORCID 0000-0002-3343-4505Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Assay:GWAS summary statistics· 3 Research Focus:GWAS / association mapping· 2 Approach:Bayesian inference· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Nabila Bouatia‐NajiiD· 4 shared Adrien B. GeorgesiD· 3 shared Takiy-Eddine BerrandouiD· 3 shared Lu LiuiD· 2 shared Adam S. ButterworthiD· 1 shared Amy WeintraubiD· 1 shared Anna BaranowskaiD· 1 shared Anne L. MaitlandiD· 1 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Nabila Bouatia‐NajiORCID

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4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 19, 2025

Complex Genetics and Regulatory Drivers of Hypermobile Ehlers-Danlos Syndrome: Insights from Genome-Wide Association Study Meta-analysis

Taylor Petrucci, Sacha Guilhaumou, Takiy-Eddine Berrandou…·Russell A. Norris

This study identifies two genome-wide significant loci associated with hypermobile Ehlers-Danlos syndrome, implicating neuroimmune and pain signaling pathways and highlighting genetic correlations with multiple comorbid conditions.

4 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineJournal of the American Heart AssociationPeer-reviewedApr 10, 2025

Blood pressure, cardiometabolic traits and cardiovascular events in women with uterine fibroids: a genetic correlation and Mendelian randomization study

Joséphine Henry, Takiy-Eddine Berrandou, Lizzy M. Brewster, Nabila Bouatia‐Naji

This study investigates genetic correlations and causal relationships between uterine fibroids and cardiometabolic traits using genetic data and Mendelian randomization.

3 citations

humanGWAS summary statistics

𝕏 PostBluesky

Molecular BiologybioRxivPreprintMay 9, 2023

Regulatory mechanisms in multiple vascular diseases locus LRP1 involve repression by SNAIL and extracellular matrix remodeling

Lu Liu, Joséphine Henry, Yingwei Liu…·Nabila Bouatia‐Naji

This study identifies rs11172113 as the causal variant in LRP1 for vascular diseases and shows SNAIL represses LRP1 expression, leading to extracellular matrix remodeling through TGF-β signaling.

2 citations

humanbulk RNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 5, 2022

Genome-wide association meta-analysis of spontaneous coronary artery dissection reveals common variants and genes related to artery integrity and tissue-mediated coagulation

David Adlam, Takiy-Eddine Berrandou, Adrien B. Georges…·Nabila Bouatia‐Naji

This study identifies 17 genetic risk loci for spontaneous coronary artery dissection (SCAD), including 12 new ones, and highlights genes related to artery integrity and coagulation.

5 citations

humanGWAS summary statistics

𝕏 PostBluesky