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Anne-Sophie Pulcrano-Nicolas
Anne-Sophie Pulcrano-Nicolas
University of Paris
Biomarker (medicine)
Medicine
Diabetes mellitus
Whole blood
Subarachnoid hemorrhage
5
Papers
22
Citations
0
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A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.
2021
PLOS Genetics
Pierre-Emmanuel Morange
Franck Peiretti
Lénaïck Gourhant
Carole Proust
Omar Soukarieh
Anne-Sophie Pulcrano-Nicolas
Ganapathi Varma Saripella
Luca Stefanucci
Romaric Lacroix
Manal Ibrahim-Kosta
Catherine A. Lemarié
Mattia Frontini
Marie-Christine Alessi
David-Alexandre Trégouët
Francis Couturaud
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Citations (1)
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
2020
medRxiv
Pierre-Emmanuel Morange
Franck Peiretti
L. Gourhant
Carole Proust
G. Sapirella
Anne-Sophie Pulcrano-Nicolas
L. Stefanucci
R. Lacroix
Manal Ibrahim-Kosta
C Lemarie
M Frontini
Marie-Christine Alessi
D. A. Tregouet
Francis Couturaud
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Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage
2019
Journal of Neurosurgery
Anne-Sophie Pulcrano-Nicolas
A Jacquens
Carole Proust
Frédéric Clarençon
Claire Perret
Eimad Shotar
L. Puybasset
Wilfried Le Goff
Vincent Degos
David-Alexandre Trégouët
Sophie Garnier
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A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process
2019
Journal of Thrombosis and Haemostasis
Florian Thibord
Lise M Hardy
Manal Ibrahim-Kosta
Noémie Saut
Anne-Sophie Pulcrano-Nicolas
Louisa Goumidi
Mete Civelek
Per Eriksson
Jean-François Deleuze
Wilfried Le Goff
David-Alexandre Trégouët
Pierre-Emmanuel Morange
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Citations (2)
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