Pernilla Stridh
Team Leader Functional Genomics of Neurodegeneration at Karolinska Institutet
Based in Stockholm, Sweden
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Stockholm
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Higher Education
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9.6K
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Background
About Pernilla Stridh
I am an assistant professor in Genetic Epidemiology of Multiple Sclerosis at the Department of Clinical Neuroscience. My scientific work aims to understand the pathological mechanisms that are involved in multiple Sclerosis (MS), by identifying the genetic architecture and understanding how genetic variants contribute to disease. I have trained in sequence-based analysis to identify causative genetic variants (Wellcomme Trust Center for Human Genetics), and am experienced and skilled in human genetics. I have trained in advanced genetic analyses during three research visits to deCODE Genetics, Iceland, and have identified MS-risk variants by developing approaches that go beyond traditional genome-wide association. Since 2018, I have extended the human genetic MS studies to include low-frequency and rare variants and quantitative traits describing severity and progression of MS. My work is funded by Horizon2020 MultipleMS, the Margaretha af Ugglas Foundation, and Neurofonden. ORCID: Google Scholar: https://scholar.google.com/citations?hl=en & & view_op=list_works & sortby=pubdate
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