Chantal Lagresle‐Peyrou

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

Chantal Lagresle‐Peyrou, Emmanuelle Six, Capucine Pïcard et al. · Nature Genetics · 2008 · 234 citations · Full text

Health Sciences, Profound Hematopoietic Defect, Physiology +7

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

Tangui Le Guen, Fabien Touzot, Isabelle André‐Schmutz et al. · Journal of Allergy and Clinical Immunology · 2015 · 110 citations

Hematological Malignancy, Immunogenetics, Medicine +8

Plerixafor enables safe, rapid, efficient mobilization of hematopoietic stem cells in sickle cell disease patients after exchange transfusion

Chantal Lagresle‐Peyrou, François Lefrère, Elisa Magrin et al. · Haematologica · 2018 · 107 citations · Full text

DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transfer

Gary P. Wang, Alexandrine Garrigue, Angela Ciuffi et al. · Nucleic Acids Research · 2008 · 100 citations · Full text

In Vivo Gene Therapy, Genetics, Immunodeficiencies +21

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Karin Pike‐Overzet, Mark Rodijk, Y-Y Ng et al. · Leukemia · 2011 · 90 citations

Primary Immunodeficiency, Immunogenetics, Genetics +7