I focus on the role of genetic variants underlying a complex inflammatory disease, Multiple
Sclerosis (MS), and specifically on developing and applying genome‐wide and sequence-level approaches to identify and characterize genetic variants that modify progression and severity of disease. For publications see: https://scholar.google.se/citations?hl=en&user=tlg0XloAAAAJ

I work as an Assistant Professor in the Genetic Epidemiology of Multiple Sclerosis group at the Center for Molecular Medicine (CMM) in the Department of Clinical Neuroscience at Karolinska Institutet  (https://ki.se/personer/pernilla-strid).