Manuel Comabella

7PUBLICATIONS
12CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Medical bacteriologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Mar 21, 2024
No evidence for association between rs10191329 severity locus and longitudinal disease severity in 1813 relapse-onset multiple sclerosis patients from the MSBase registry.

Maria Pia Campagna, Eva Kubala Havrdova, Dana Horakova

|Nov 30, 2022
Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity.

Vilija G Jokubaitis, Maria Pia Campagna, Omar Ibrahim

|Oct 27, 2022
Polymorphisms in ARNTL/BMAL1 and CLOCK Are Not Associated with Multiple Sclerosis in Spanish Population.

Isabel de Rojas, César Martin-Montero, Maria Fedetz

|Jul 28, 2022
Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation.

Adela González-Jiménez, Pilar López-Cotarelo, Teresa Agudo-Jiménez

|Jan 28, 2022
Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis.

Antonio Alcina, Maria Fedetz, Isabel Vidal-Cobo

|Mar 01, 2020
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells.

Elia Gil-Varea, Maria Fedetz, Herena Eixarch

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