Maria Fedetz
Granada, AN 18016, Spain
Last Updated: 09/26/2026
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Found 18 publications
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis.
Journal: Human molecular genetics
Published: July 29, 2021
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells.
Journal: Journal of clinical medicine
Published: January 16, 2020
Splice-site variant in ACSL5: a marker promoting opposing effect on cell viability and protein expression.
Journal: European journal of human genetics : EJHG
Published: June 11, 2018
SP140 regulates the expression of immune-related genes associated with multiple sclerosis and other autoimmune diseases by NF-κB inhibition.
Journal: Human molecular genetics
Published: June 01, 2018
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
Journal: G3 (Bethesda, Md.)
Published: May 20, 2016
A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria.
Journal: European journal of human genetics : EJHG
Published: December 21, 2015
Genome-wide significant association with seven novel multiple sclerosis risk loci.
Journal: Journal of medical genetics
Published: August 06, 2015
The multiple sclerosis-associated regulatory variant rs10877013 affects expression of CYP27B1 and VDR under inflammatory or vitamin D stimuli.
Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: May 13, 2015
A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.
Journal: Human molecular genetics
Published: March 01, 2015
A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands.
Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: April 01, 2014
Last Updated: 09/26/2026