Rachel Petermann
Paris, France
Last Updated: 09/26/2026
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Found 20 publications
Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity.
Journal: Prenatal diagnosis
Published: September 09, 2024
Author Correction: Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome.
Journal: Nature medicine
Published: August 09, 2022
Subamniotic Haemorrhage, a Possible New Presentation of Fetal and Neonatal Alloimmune Thrombocytopenia.
Journal: Fetal diagnosis and therapy
Published: May 15, 2022
Management of fetal and neonatal alloimmunization thrombocytopenia: About the Francophone working group on fetomaternal platelet alloimmunization.
Journal: Journal of gynecology obstetrics and human reproduction
Published: February 18, 2022
Stepwise GATA1 and SMC3 mutations alter megakaryocyte differentiation in a Down syndrome leukemia model.
Journal: The Journal of clinical investigation
Published: November 01, 2021
New αIIbβ3 variants in 28 Turkish Glanzmann patients; structural hypothesis for complex activation by residues variations in I-EGF domains.
Journal: Platelets
Published: July 19, 2021
Pathophysiology and Diagnosis of Drug-Induced Immune Thrombocytopenia.
Journal: Journal of clinical medicine
Published: June 25, 2020
A new efficient tool for non-invasive diagnosis of fetomaternal platelet antigen incompatibility.
Journal: British journal of haematology
Published: December 20, 2019
A mutation in the gene coding for the sialic acid transporter SLC35A1 is required for platelet life span but not proplatelet formation.
Journal: Haematologica
Published: August 18, 2018
Last Updated: 09/26/2026