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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Marjolein Peters
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320
Publications
6,787
Citation Statements Received
10,148
Citation Statements Given
How they've been cited
6,953
308
6,410
69
How they cite others
9,036
363
9,658
127
Affiliations
Emma Kinderziekenhuis
,
Academic Medical Center
Publications
Order By: Most citations
Venous thromboembolism in childhood: A prospective two-year registry in The Netherlands
van Ommen
1
,
Heijboer
2
,
Büller
3
et al.
2001
The Journal of Pediatrics
712
29
546
13
Get access via publisher
Add to collection
Cite
Mortality and causes of death in patients with hemophilia, 1992–2001: a prospective cohort study
Plug
1
,
van der Bom
2
,
Peters
3
et al.
2006
Journal of Thrombosis and Haemostasis
Abstract
Show
271
12
333
1
Get access via publisher
Add to collection
Cite
Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A
Eckhardt
1
,
van Velzen
2
,
Peters
3
et al.
2013
Abstract
Show
223
5
302
6
1
Get access via publisher
Add to collection
Cite
Rivaroxaban compared with standard anticoagulants for the treatment of acute venous thromboembolism in children: a randomised, controlled, phase 3 trial
Male
1
,
Lensing
2
,
Palumbo
3
et al.
2020
The Lancet Haematology
Abstract
Show
350
8
285
0
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Cite
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura
Breunis
1
,
van Mirre
2
,
Bruin
3
et al.
2008
Abstract
Show
206
23
258
1
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Add to collection
Cite
Efficacy and safety of recombinant factor VIIa for treatment of severe bleeding: A systematic review
Levi
1
,
Peters
2
,
Büller
3
2005
Critical Care Medicine
Abstract
Show
309
6
186
2
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Add to collection
Cite
Primary postpartum haemorrhage in women with von Willebrand disease or carriership of haemophilia despite specialised care: a retrospective survey
Stoof
1
,
van Steenbergen
2
,
Zwagemaker
3
et al.
2015
Haemophilia
Abstract
Show
107
8
136
5
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Cite
Intensive peri-operative use of factor VIII and the Arg593→Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A
Eckhardt
1
,
Menke
2
,
van Ommen
3
et al.
2009
Journal of Thrombosis and Haemostasis
Abstract
Show
96
4
133
3
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Add to collection
Cite
1
2
3
4