Mark Hermann

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

W. V. van IJcken, Y. Crow, T. Goldmann, 2016, The Journal of experimental medicine.

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

J. Jankovic, A. Bowcock, K. Bhatia, 2012, Cell reports.

ISG15: In Sickness and in Health.

D. Bogunovic, Mark Hermann, 2017, Trends in immunology.

ISG15 deficiency and increased viral resistance in humans but not mice

O. Sanal, I. Tezcan, A. García-Sastre, 2016, Nature Communications.