Foxp3 Deficiency
FOXP3 Deficiency is a molecular pathogenic condition characterized by loss-of-function mutations in the FOXP3 gene, a master transcriptional regulator of regulatory T cell development and function, leading to unchecked immune activation and autoimmune manifestations.
568
Publications
82K
Citations
4K
Authors
988
Institutions
Publications per year
2017–2026
136
568
A function for interleukin 2 in Foxp3-expressing regulatory T cells
Jason D. Fontenot, Jeffrey P. Rasmussen, Marc A. Gavin et al. · Nature Immunology · 2005 · 1.8K citations
1–5 of 568
4K
Howard Hughes Medical Institute, United States
18 publications · 13.9K citations
18
h-index
Center for Experimental and Clinical Infection Research, Germany
15 publications · 2.4K citations
15
h-index
15
h-index
14
h-index
The San Raffaele Telethon Institute for Gene Therapy, Italy
13 publications · 1.4K citations
13
h-index
1–5 of 4K
988
Harvard University
Cambridge, United States
31 h-index
150 publications
20.6K citations
University of Washington
Seattle, United States
30 h-index
81 publications
52K citations

Howard Hughes Medical Institute
Chevy Chase, United States
21 h-index
47 publications
40.9K citations
Inserm
Paris, France
20 h-index
168 publications
12.7K citations
National Institutes of Health
Bethesda, United States
18 h-index
104 publications
23K citations
University of Pennsylvania
Philadelphia, United States
17 h-index
84 publications
9.7K citations

Brigham and Women's Hospital
Boston, United States
17 h-index
69 publications
13.8K citations
Center for Experimental and Clinical Infection Research
Hanover, Germany
14 h-index
41 publications
3.6K citations
1–8 of 988
JI · 53 publications · 6K citations
37
h-index
20 publications · 3.8K citations
20
h-index
20 publications · 4.8K citations
19
h-index
PNAS · 18 publications · 3.4K citations
17
h-index
15 publications · 868 citations
14
h-index
1–5