Garrigue, Alexandrine
Hôpital Necker-Enfants Malades · Inserm · Institut Necker Enfants Malades · Institut des Maladies Génétiques Imagine
2 papers on CoChatORCID 0000-0002-2660-3681
Most cited papers
- Verified
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1
Hacein-Bey-Abina, S., Garrigue, A., Wang, G. P., Soulier, J., Lim, A., Morillon, E., Clappier, E., Caccavelli, L., Delabesse, E., Beldjord, K., et al. (2008) · Journal of Clinical Investigation
Virus-based gene therapy researchCAR-T cell therapy research
Cited by 1,854
- Verified
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency
Lagresle-Peyrou, C., Olichon, A., Sadek, H., Roche, P., Tardy, C., Silva, C. D., Garrigue, A., Fischer, A., Moshous, D., Collette, Y., et al. (2020) · Haematologica
Immunodeficiency and Autoimmune DisordersBlood disorders and treatments
Cited by 35
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