N. König

Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

W. Schmidt, B. Plecko, M. Lee-Kirsch, 2017, Pediatric Rheumatology.

SAMHD1 prevents autoimmunity by maintaining genome stability

A. Shevchenko, M. C. Cardoso, J. Guck, 2014, Annals of the rheumatic diseases.

Familial chilblain lupus due to a gain-of-function mutation in STING

C. Fiehn, C. Günther, R. Goldbach-Mansky, 2016, Annals of the rheumatic diseases.

RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA

M. C. Cardoso, D. Wieczorek, T. Kurth, 2016, Nature Communications.

Typ-I-Interferonopathien

C. Günther, N. König, C. Günther, 2016, Zeitschrift für Rheumatologie.

Response to: ‘JAK inhibition in STING-associated interferonopathy’ by Crow et al

C. Fiehn, C. Günther, M. von der Hagen, 2016, Annals of the rheumatic diseases.

Familial chilblain lupus caused by an activating mutation in STING

C. Fiehn, H. Lorenz, N. König, 2015, Pediatric Rheumatology Online Journal.