Momenilandi, Mana
Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Human Genetic of Infectious Diseases · Institut des Maladies Génétiques Imagine
2 papers on CoChatORCID 0000-0002-5340-2762
Most cited papers
- Verified
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
- Verified
Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy
Béziat, V., Rapaport, F., Hu, J., Titeux, M., Bonnet des Claustres, M., Bourgey, M., Griffin, H., Bandet, É., Ma, C. S., Sherkat, R., et al. (2021) · Cell
T-cell and B-cell ImmunologyCervical Cancer and HPV Research
Cited by 95
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