Philippot, Quentin

Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Human Genetic of Infectious Diseases · Institut des Maladies Génétiques Imagine

1 paper on CoChatORCID 0000-0003-3429-9605

Most cited papers

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Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Sharma, M., Leung, D., Momenilandi, M., Jones, L. C. W., Pacillo, L., James, A. E., Murrell, J. R., Delafontaine, S., Maimaris, J., Vaseghi-Shanjani, M., et al. (2023) · Journal of Experimental Medicine
Immunodeficiency and Autoimmune DisordersAsthma and respiratory diseases
Cited by 125

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