Marguerite Neerman‐Arbez

4.8k citations

109 papers · 3.0k indexed · h-index 32

Pulmonary and Respiratory Medicine top 1%
Hematology top 0.5%
Physiology top 5%
Molecular Biology
Genetics top 5%

Co-authors: Philippe de Moerloose Alessandro Casini Richard J. Fish Stylianos E. Antonarakis Michael A. Morris R. Vilar Philippe A. Halban Dũng Chí Vũ
Topics: Blood properties and coagulation (80 papers)Erythrocyte Function and Pathophysiology (30 papers)Platelet Disorders and Treatments (22 papers)
Cited by: Hematology Pulmonary and Respiratory Medicine Internal Medicine
Journals: Journal of Biological Chemistry Journal of Clinical Investigation Blood
Partner nations: Switzerland United States France

In The Last Decade

Marguerite Neerman‐Arbez

106 papers receiving 2.9k citations

Peers

Countries citing papers authored by Marguerite Neerman‐Arbez

Since Specialization

Citations

This map shows the geographic impact of Marguerite Neerman‐Arbez's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marguerite Neerman‐Arbez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marguerite Neerman‐Arbez more than expected).

Fields of papers citing papers by Marguerite Neerman‐Arbez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marguerite Neerman‐Arbez. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marguerite Neerman‐Arbez. The network helps show where Marguerite Neerman‐Arbez may publish in the future.

Co-authorship network of co-authors of Marguerite Neerman‐Arbez

This figure shows the co-authorship network connecting the top 25 collaborators of Marguerite Neerman‐Arbez. A scholar is included among the top collaborators of Marguerite Neerman‐Arbez based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marguerite Neerman‐Arbez. Marguerite Neerman‐Arbez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database 2025 ·Research and Practice in Thrombosis and Haemostasis ·(unknown),Roberta Palla,Marzia Menegatti,(unknown),Simona Maria Siboni,Marguerite Neerman‐Arbez,Mehran Karimi,(unknown),Rosanna Asselta,Danijela Miković,(unknown),(unknown),(unknown),Amy D. Shapiro,(unknown),Michael Makris,Alessandro Casini,Flora Peyvandi	0
2	A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec 2024 ·Haemophilia ·Marie‐Claude Pelland‐Marcotte,(unknown),(unknown),Christine Demers,Julie Castilloux,Julie Gauthier,Marguerite Neerman‐Arbez,Alessandro Casini,Georges‐Étienne Rivard	1
3	Physiological correction of hereditary mild hypofibrinogenemia during pregnancy 2023 ·Haemophilia ·Rita Marchi,Stéphane Durual,(unknown),Marguerite Neerman‐Arbez,Alessandro Casini	2
4	PB0045 SEM and 3D Reconstruction of ex-vivo Arterial Thrombi: A Pilot Study 2023 ·Research and Practice in Thrombosis and Haemostasis ·(unknown),Frederick L. Glauser,Stéphane Noble,Pierre Fontana,Rita Marchi,Marguerite Neerman‐Arbez,Alessandro Casini	0
5	Impact of Fibrinogen Infusion on Thrombin Generation and Fibrin Clot Structure in Patients with Inherited Afibrinogenemia 2022 ·Thrombosis and Haemostasis ·Claudia Djambas Khayat,Rita Marchi,Stéphane Durual,Thomas Lecompte,Marguerite Neerman‐Arbez,Alessandro Casini	5
6	A series of Polish patients with congenital fibrinogen disorders: 2 new mutations in fibrinogen gamma chain, Fibrinogen Kostrzyn and Fibrinogen Łódź II 2022 ·Polskie Archiwum Medycyny Wewnętrznej ·(unknown),Anna Klukowska,Marguerite Neerman‐Arbez,Jacek Treliński,Anetta Undas,Ewa Wypasek	0
7	A homozygous duplication of the <I>FGG</i> exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family 2021 ·Haematologica ·Michel Guipponi,Frédéric G. Masclaux,Frédérique Sloan‐Béna,(unknown),Namık Yaşar Özbek,Flora Peyvandi,Marzia Menegatti,Alessandro Casini,Barış Malbora,Marguerite Neerman‐Arbez	2
8	Chemical Modulators of Fibrinogen Production and Their Impact on Venous Thrombosis 2020 ·Thrombosis and Haemostasis ·R. Vilar,Samuel W. Lukowski,Marco Garieri,(unknown),Marguerite Neerman‐Arbez,Richard J. Fish	7
9	A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype 2020 ·Biomedicines ·Tomáš Šimurda,R. Vilar,Jana Žolková,(unknown),Zuzana Kolková,Dušan Loderer,Marguerite Neerman‐Arbez,Alessandro Casini,(unknown),Ingrid Škorňová,Miroslava Dobrotová,Marian Grendár,Ján Staško,Peter Kubisz	28
10	Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review 2019 ·Haemophilia ·(unknown),Justine Hugon‐Rodin,Pierre Fontana,Marguerite Neerman‐Arbez,Alessandro Casini	18
11	Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia 2017 ·Haemophilia ·Alessandro Casini,R. Vilar,(unknown),Deniz Aslan,Katrien Devreese,Veerle Mondelaers,Lorenzo Alberio,(unknown),Philippe de Moerloose,Marguerite Neerman‐Arbez	14
12	Thromboembolism in patients with congenital afibrinogenaemia 2016 ·Thrombosis and Haemostasis ·Michael Nagler,Lorenzo Alberio,(unknown),Hendrik von Tengg‐Kobligk,Daniel Lottaz,Marguerite Neerman‐Arbez,Bernhard Lämmle,Johanna A. Kremer Hovinga	31
13	In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes 2014 ·Journal of Thrombosis and Haemostasis ·Deborah Stroka,Adrian Keogh,Dũng Chí Vũ,Alexandre Fort,Michael Stoffel,(unknown),(unknown),Vanessa Banz,Franziska Demarmels Biasiutti,Bernhard Lämmle,Daniel Candinas,Marguerite Neerman‐Arbez	4
14	A novel regulatory element between the human FGA and FGG genes 2012 ·Thrombosis and Haemostasis ·Richard J. Fish,Marguerite Neerman‐Arbez	11
15	Developmental expression and organisation of fibrinogen genes in the zebrafish 2011 ·Thrombosis and Haemostasis ·(unknown),Frédérique Béna,Alexandre Fort,Richard J. Fish,Marguerite Neerman‐Arbez	21
16	A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream 2009 ·Blood Coagulation & Fibrinolysis ·Helia Robert‐Ebadi,Philippe de Moerloose,M. El Khorassani,(unknown),Marguerite Neerman‐Arbez	6
17	Treatment of congenital fibrinogen disorders 2008 ·Expert Opinion on Biological Therapy ·Philippe de Moerloose,Marguerite Neerman‐Arbez	25
18	Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes 2001 ·Human Genetics ·Marguerite Neerman‐Arbez,Philippe de Moerloose,(unknown),(unknown),(unknown),Christine A. Biron,Jeanne‐Yvonne Borg,Stefan Eber,Esther Meili,(unknown),Laurent Ripoll,C. Vervel,(unknown),Philippe Staeger,Stylianos E. Antonarakis,Michael A. Morris	56
19	Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia. 2000 ·Blood ·Marguerite Neerman‐Arbez,Philippe de Moerloose,Claire Bridel,(unknown),(unknown),Colette Rossier,Kathelijne Peerlinck,S. Claeyssens,(unknown),Roseline d’Oiron,Marie Dreyfus,(unknown),(unknown),Stylianos E. Antonarakis,Michael A. Morris	77
20	The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster 1999 ·European Journal of Human Genetics ·Marguerite Neerman‐Arbez,Stylianos E. Antonarakis,(unknown),Michael A. Morris	23

About Marguerite Neerman‐Arbez

Marguerite Neerman‐Arbez is a scholar working on Hematology, Pulmonary and Respiratory Medicine and Genetics, having authored 109 papers that have together received 3.0k indexed citations. Recurring topics across this work include Blood properties and coagulation (80 papers), Erythrocyte Function and Pathophysiology (30 papers) and Platelet Disorders and Treatments (22 papers). The work is most often cited by research in Hematology (1.1k citations), Pulmonary and Respiratory Medicine (1.7k citations) and Internal Medicine (158 citations). Marguerite Neerman‐Arbez has collaborated with scholars based in Switzerland, United States and France. Frequent co-authors include Philippe de Moerloose, Alessandro Casini, Richard J. Fish, Stylianos E. Antonarakis, Michael A. Morris, R. Vilar, Philippe A. Halban, Dũng Chí Vũ, Françoise Boehlen and Alexandre Fort. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact