Author

CHARGE Hemostasis working group

Inserm

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Anne BolandiD· 2 shared Astrid van Hylckama VliegiD· 2 shared David‐Alexandre TrégouëtiD· 2 shared Frits Richard RosendaaliD· 2 shared Gaëlle MunschiD· 2 shared Jean‐François DeleuzeiD· 2 shared Maria Sabater‐LlealiD· 2 shared Marine GermainiD· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Anne BolandORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genomic Landscape of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes

Gaëlle Munsch, Florian Thibord, Ohanna Cavalcanti de Lima Bezerra, Jennifer A. Brody, Astrid van Hylckama Vlieg, Lénaïck Gourhant, Ming‐Huei Chen, Marine Germain, Ilana Caro, Pierre Suchon, Robert Olaso, Kerri L. Wiggins, Noémie Saut, Céline Besse, Louisa Goumidi, , David‐Alexandre Trégouët

The paper identifies genetic loci and proteins associated with venous thromboembolism recurrence risk using GWAS and subgroup analyses across different thrombotic subtypes.

medRxiv · Dec 2, 2024 · PreprintGenetic & Genomic Medicine

A genome wide search for non-additive allele effects identifies PSKH2 as involved in the variability of Factor V activity.

Blandine Gendre, Ángel Martínez-Pérez, Marcus Edi Kleber, Astrid van Hylckama Vlieg, Anne Boland, Robert Olaso, Marine Germain, Gaëlle Munsch, Angela P. Moissl, Pierre Suchon, Juan Carlos Souto, José Manuel Soria, CHARGE Hemostasis working group, Jean‐François Deleuze, Winfried März, , David‐Alexandre Trégouët

The paper identifies PSKH2 as a gene influencing variability in Factor V plasma activity through genome-wide analysis of non-additive allele effects.

bioRxiv · Feb 8, 2024 · PreprintGenetics

Elucidating mechanisms of genetic cross-disease associations: an integrative approach implicates protein C as a causal pathway in arterial and venous diseases

David Stacey, Lingyan Chen, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess, Stephen G. MacDonald, Jonathan Langdown, Harriet McKinney, Kate Downes, Neda Farahi, James E. Peters, Saonli Basu, James S. Pankow, Nathan Pankratz, Weihong Tang, , Dirk S. Paul

The paper identifies a genetic variant in PROCR that influences protein C and factor VII levels, linking it to both reduced coronary artery disease risk and increased venous thromboembolism risk through opposing inflammatory and thrombotic mechanisms.

medRxiv · Mar 16, 2020 · PreprintGenetic & Genomic Medicine