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Marguerite Neerman-Arbez

Full Professor

University of Geneva, Faculty of Medicine

Switzerland

Research Interests

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Professors in Switzerland Professors in Biostatistics Biostatistics professors in Switzerland

About

Marguerite Neerman-Arbez is a Full Professor at the University of Geneva Faculty of Medicine in Switzerland. Her research primarily focuses on congenital fibrinogen disorders, with recent publications exploring genetic analyses, physiological implications during pregnancy, and novel genetic variants associated with fibrinogen storage diseases. She contributes significantly to the understanding of rare bleeding disorders through her work in both clinical and genetic contexts.

Articles (14)

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2025

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2025

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2024

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2023

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2022

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2022

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2020

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2020

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2020

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2020

Collaborators (9)

Jean‐Luc Reny

Head of division

SWITZERLAND

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Alessandro Casini

Senior attending

University Hospital of Geneva

SWITZERLAND

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Océane Pécheux

Dre

University Hospital of Geneva

SWITZERLAND

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Rosanna Asselta

Full Professor in Medical Genetics

Humanitas University

ITALY

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Paul Billoir

Rouen University Hospital

FRANCE

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Stéphane Durual

Professor - Head of biomaterials

University of Geneva

SWITZERLAND

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Aurélien Lebreton

Université Clermont Auvergne

FRANCE

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Tomas Simurda

SLOVAKIA

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Jordan A. Shavit

University of Michigan

UNITED STATES

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Marguerite Neerman-Arbez

Research Interests

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About

Articles (14)

Congenital Fibrinogen Deficiencies: Not So Rare

Erratum to: Congenital Fibrinogen Deficiencies: Not So Rare

A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database

Physiological correction of hereditary mild hypofibrinogenemia during pregnancy

Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster

When fibrin(ogen) is too loud, silence it!

Afibrinogenemia with two compound heterozygous mutations in FGA gene

Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders

Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis

Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A

MicroRNA-126 is a regulator of platelet-supported thrombin generation

Collaborators (9)

Jean‐Luc Reny

Alessandro Casini

Océane Pécheux

Rosanna Asselta

Paul Billoir

Stéphane Durual

Aurélien Lebreton

Tomas Simurda

Jordan A. Shavit

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