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Journal of Medical Genetics|November 20, 2012
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosisAntonio Alcina, Maria Fedetz, Oscar Fernández, et al.Cells|January 16, 2020
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple SclerosisPaloma Gómez-Fernández, Aitzkoa Lopez de Lapuente Portilla, Ianire Astobiza, et al.Human Molecular Genetics|July 9, 2015
A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosisFuencisla Matesanz, Victor Potenciano, Maria Fedetz, et al.G3 (Bethesda, Md.)|May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis PatientsA Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.Journal of Medical Genetics|October 18, 2015
Genome-wide significant association with seven novel multiple sclerosis risk lociChristina M Lill, Felix Luessi, Antonio Alcina, et al.Pageof 4