Maximilian Seidl

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

Desirée Schubert, Claudia Bode, Rupert Kenefeck et al. · Nature Medicine · 2014 · 805 citations · Full text

Immunogenetics, Autoimmune Disease, Immunodeficiencies +12

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects

Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich et al. · Journal of Allergy and Clinical Immunology · 2018 · 423 citations · Full text

Clinical Immunology, Allergy, Lymphocyte Development +12

Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2

Christian Klemann, Nadezhda Camacho-Ordóñez, Linlin Yang et al. · Frontiers in Immunology · 2019 · 143 citations · Full text

The TH1 phenotype of follicular helper T cells indicates an IFN-γ–associated immune dysregulation in patients with CD21low common variable immunodeficiency

Susanne Unger, Maximilian Seidl, Pauline A. van Schouwenburg et al. · Journal of Allergy and Clinical Immunology · 2017 · 129 citations · Full text

Clinical Immunology, Immunodeficiencies, Immune Regulation +17

DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas

Laura Herrtwich, Indrajit Nanda, Konstantinos Evangelou et al. · Cell · 2016 · 125 citations · Full text

Cell Division, Granulocyte, Immunology +5