Marguerite Neerman-Arbez (M Neerman-Arbez)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Venues

Haemophilia : the official journal of the World Federation of Hemophilia

Blood advances

International journal of molecular sciences

Biomedicines

University of Geneva Faculty of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Geneva Faculty of Medicine Dec 01 2013

Switzerland

Full Professor :: Dep. of Genetic Medicine and Development

Publications

Marie-Claude Pelland-Marcotte, Adelina-Teona Avram, Hélène Néron, Christine Demers, Julie Castilloux, Julie Gauthier, Marguerite Neerman-Arbez, Alessandro Casini, Georges-Etienne Rivard
A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec. Haemophilia : the official journal of the World Federation of Hemophilia 30 (3) (2024)
Marie-Claude Pelland-Marcotte, Adelina-Teona Avram, Hélène Néron, Christine Demers, Julie Castilloux, Julie Gauthier, Marguerite Neerman-Arbez, Alessandro Casini, Georges-Etienne Rivard
A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec. Haemophilia : the official journal of the World Federation of Hemophilia 30 (3) (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Marie-Claude Pelland-Marcotte, Adelina-Teona Avram, Hélène Néron, Christine Demers, Julie Castilloux, Julie Gauthier, Marguerite Neerman-Arbez, Alessandro Casini, Georges-Etienne Rivard
A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec. Haemophilia : the official journal of the World Federation of Hemophilia (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatný, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta A P Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steven Kenneth Austin, Amy D Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances (2024)
Rita Marchi, Stéphane Dural, Océane Pecheux, Marguerite Neerman-Arbez, Alessandro Casini
Physiological correction of hereditary mild hypofibrinogenemia during pregnancy. Haemophilia : the official journal of the World Federation of Hemophilia (2023)
Rita Marchi, Stéphane Durual, Océane Pecheux, Marguerite Neerman-Arbez, Alessandro Casini
Physiological correction of hereditary mild hypofibrinogenemia during pregnancy. Haemophilia : the official journal of the World Federation of Hemophilia (2023)
Marguerite Neerman-Arbez
When fibrin(ogen) is too loud, silence it! Blood 139 (9) (2022)
Alexander Couzens, Aurelien Lebreton, Frédéric Masclaux, Michel Guipponi, Céline Pebrel-Richard, Fanny Laffargue, Piotr Gembara, Alessandro Casini, Marguerite Neerman-Arbez
Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster. Haemophilia : the official journal of the World Federation of Hemophilia 28 (5) (2022)
Timea Szanto, Riitta Lassila, Marja Lemponen, Elina Lehtinen, Marguerite Neerman-Arbez, Alessandro Casini
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders. International journal of molecular sciences 22 (5) (2021)
Guillaume Feugray, Paul Billoir, Alessandro Casini, Marguerite Neerman-Arbez, Virginie Barbay, Pierre Chamouni, Pascale Schneider, Véronique Le Cam Duchez
Afibrinogenemia with two compound heterozygous mutations in FGA gene. Haemophilia : the official journal of the World Federation of Hemophilia 27 (5) (2021)
Richard J Fish, Cristina Freire, Corinne Di Sanza, Marguerite Neerman-Arbez
Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders. International journal of molecular sciences 22 (2) (2021)
Tomas Simurda, Rui Vilar, Jana Zolkova, Eliska Ceznerova, Zuzana Kolkova, Dusan Loderer, Marguerite Neerman-Arbez, Alessandro Casini, Monika Brunclikova, Ingrid Skornova, Miroslava Dobrotova, Marian Grendar, Jan Stasko, Peter Kubisz
A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype. Biomedicines 8 (12) (2020)
C Espitia Jaimes, Richard J Fish, Marguerite Neerman-Arbez
Local chromatin interactions contribute to expression of the fibrinogen gene cluster. Journal of thrombosis and haemostasis : JTH 16 (10) (2018)

Marguerite Neerman-Arbez.css-eqlu8i{font-size:small;padding-left:4px;} (M Neerman-Arbez)

Publication Activity (10 Years)

Top Topics

Top Venues

Marguerite Neerman-Arbez (M Neerman-Arbez)