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

Authors

4K

  1. AY
    Alexander Y. Rudensky

    Howard Hughes Medical Institute, United States

    18 publications · 13.9K citations

    18

    h-index

  2. TS
    Tim Sparwasser

    Center for Experimental and Clinical Infection Research, Germany

    15 publications · 2.4K citations

    15

    h-index

  3. DM
    Diane Mathis

    Harvard University, United States

    15 publications · 1.5K citations

    15

    h-index

  4. CB
    Christophe Benoıst

    Harvard University, United States

    14 publications · 1.4K citations

    14

    h-index

  5. RB
    Rosa Bacchetta

    The San Raffaele Telethon Institute for Gene Therapy, Italy

    13 publications · 1.4K citations

    13

    h-index

1–5 of 4K

Venues

  1. The Journal of Immunology

    JI · 53 publications · 6K citations

    37

    h-index

  2. Blood

    20 publications · 3.8K citations

    20

    h-index

  3. The Journal of Experimental Medicine

    20 publications · 4.8K citations

    19

    h-index

  4. Proceedings of the National Academy of Sciences

    PNAS · 18 publications · 3.4K citations

    17

    h-index

  5. Frontiers in Immunology

    15 publications · 868 citations

    14

    h-index

1–5