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Felix Luessi

Researcher at University of Mainz

Publications -  85
Citations -  3259

Felix Luessi is an academic researcher from University of Mainz. The author has contributed to research in topics: Multiple sclerosis & Medicine. The author has an hindex of 23, co-authored 70 publications receiving 2517 citations. Previous affiliations of Felix Luessi include Montreal Neurological Institute and Hospital & Technische Universität München.

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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Ashley Beecham, +206 more
- 01 Nov 2013 - 
TL;DR: This study enhances the catalog of multiple sclerosis risk variants and illustrates the value of fine mapping in the resolution of GWAS signals.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Ashley Beecham, +206 more
TL;DR: Using the ImmunoChip custom genotyping array, this article analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 potentially associated regions (P < 1.0 × 10(-4)).
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Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation

Till F. M. Andlauer, +93 more
- 01 Jun 2016 - 
TL;DR: A genome-wide association study on multiple sclerosis susceptibility in German cohorts with 4888 cases and 10,395 controls detected associations not found in larger, more heterogeneous cohorts, thus providing new clues regarding MS pathogenesis.
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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

Mitja Mitrovic, +133 more
- 29 Nov 2018 - 
TL;DR: This work identifies four novel genes driving MS risk independently of common-variant signals, highlighting key pathogenic roles for regulatory T cell homeostasis and regulation, IFNγ biology, and NFκB signaling.
Posted ContentDOI

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

Nikolaos A. Patsopoulos, +191 more
- 13 Jul 2017 - 
TL;DR: While MS is most likely initially triggered by perturbation of peripheral immune responses the functional responses of microglia and other brain cells are also altered and may have a role in targeting an autoimmune process to the central nervous system.