Stefan Pinkert

Multiple sclerosis Molecular mimicry of an antimyelin HLA class I restricted T-cell receptor

R. Hohlfeld, Maria Kalemanov, I. Antes, 2022 .

Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy

M. Schlesner, C. Evers, C. Bartram, 2016, American journal of medical genetics. Part A.

Melanocyte antigen triggers autoimmunity in human psoriasis

S. Krebs, M. Spannagl, J. Prinz, 2015, The Journal of experimental medicine.

Multiple sclerosis

R. Hohlfeld, Maria Kalemanov, I. Antes, 2016, Neurology: Neuroimmunology & Neuroinflammation.

Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline.

R. Eils, M. Schlesner, P. Bauer, 2015, Molecular and cellular probes.