Gregor Dueckers

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

Desirée Schubert, Claudia Bode, Rupert Kenefeck et al. · Nature Medicine · 2014 · 822 citations · Full text

Life Sciences, Genetics, Immunology +14

Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

Derek Neilson, Mark D. Adams, Caitlin M.D. Orr et al. · The American Journal of Human Genetics · 2009 · 355 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Increasing Mixed Chimerism Is an Important Prognostic Factor for Unfavorable Outcome in Children With Acute Lymphoblastic Leukemia After Allogeneic Stem-Cell Transplantation: Possible Role For Pre-Emptive Immunotherapy?

Peter Bader, Hermann Kreyenberg, W Hoelle et al. · Journal of Clinical Oncology · 2004 · 251 citations

Medicine, Hematology, Immunology +16

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Karin R. Engelhardt, Michael E. Gertz, Sevgi Keleş et al. · Journal of Allergy and Clinical Immunology · 2015 · 193 citations · Full text

Life Sciences, Immunology, Clinical Immunology +12

ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation

Eric J. R. Jansen, Sharita Timal, Margret Ryan et al. · Nature Communications · 2016 · 150 citations · Full text

Life Sciences, Genetics, Molecular Biology +13