C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients

Meta-analysis of the association of IL2RA polymorphisms rs2104286 and rs12722489 with multiple sclerosis risk

(2018) Xiao-Xiong Wang et al.   IMMUNOLOGICAL INVESTIGATIONS

Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family

(2018) Julia Y Mescheriakova et al.   Multiple Sclerosis Journal

Genetics of Multiple Sclerosis: An Overview and New Directions

(2018) Nikolaos A. Patsopoulos   Cold Spring Harbor Perspectives in Medicine

Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family

(2018) Julia Y Mescheriakova et al.   Multiple Sclerosis Journal

Coagulation Factor XII Levels and Intrinsic Thrombin Generation in Multiple Sclerosis

(2018) Nicole Ziliotto et al.   Frontiers in Neurology

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

(2018) Ming Zhang et al.   BRAIN

Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis

(2018) Giovanna Marchetti et al.   MOLECULAR MEDICINE

Multiple Sclerosis in Italy: A 40-Year Follow-Up of the Prevalence in Ferrara

(2018) Enrico Granieri et al.   NEUROEPIDEMIOLOGY

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

(2018) Mitja Mitrovič et al.   CELL

Analysis of NOD-like receptor NLRP1 in multiple sclerosis families

(2017) Cecily Q. Bernales et al.   IMMUNOGENETICS

Decitabine inhibits T cell proliferation via a novel TET2-dependent mechanism and exerts potent protective effect in mouse auto- and allo-immunity models

(2017) Xue Wang et al.   Oncotarget

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

(2017) Ales Maver et al.   Scientific Reports

Interactions between genetic, lifestyle and environmental risk factors for multiple sclerosis

(2016) Tomas Olsson et al.   Nature Reviews Neurology

Estimated prevalence of multiple sclerosis in Italy in 2015

(2016) Mario Alberto Battaglia et al.   NEUROLOGICAL SCIENCES

Publicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple Sclerosis

(2016) Eric Vallabh Minikel et al.   NEURON

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

(2016) Zhe Wang et al.   NEURON

An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants

(2016) Dario Balestra et al.   Molecular Therapy-Nucleic Acids

A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches

(2015) V. V. Bashinskaya et al.   HUMAN GENETICS

The Methylcytosine Dioxygenase Tet2 Promotes DNA Demethylation and Activation of Cytokine Gene Expression in T Cells

(2015) Kenji Ichiyama et al.   IMMUNITY

The immunogenetics of multiple sclerosis: A comprehensive review

(2015) Jill A. Hollenbach et al.   JOURNAL OF AUTOIMMUNITY

Prevalence of Multiple Sclerosis in Tuscany (Central Italy): A Study Based on Validated Administrative Data

(2015) Daiana Bezzini et al.   NEUROEPIDEMIOLOGY

Multiple Sclerosis between Genetics and Infections: Human Endogenous Retroviruses in Monocytes and Macrophages

(2015) Elena Morandi et al.   Frontiers in Immunology

Assessing the effects of multiple markers in genetic association studies

(2015) Xuefeng Wang et al.   Frontiers in Genetics

Soluble IL-2RA Levels in Multiple Sclerosis Subjects and the Effect of Soluble IL-2RA on Immune Responses

(2014) L. M. Maier et al.   JOURNAL OF IMMUNOLOGY

Pathogenesis of multiple sclerosis: insights from molecular and metabolic imaging

(2014) Olga Ciccarelli et al.   LANCET NEUROLOGY

Exome sequencing in single cells from the cerebrospinal fluid in multiple sclerosis

(2014) AK Kemppinen et al.   Multiple Sclerosis Journal

No evidence of association between mutant alleles of theCYP27B1gene and multiple sclerosis

(2012) Maria Ban et al.   ANNALS OF NEUROLOGY

Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

(2012) Donato Gemmati et al.   BMC Medical Genetics

TET2 promotes histone O-GlcNAcylation during gene transcription

(2012) Qiang Chen et al.   NATURE

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene

(2012) D. A. Dyment et al.   NEUROLOGY

Rare variants in the CYP27B1 gene are associated with multiple sclerosis

(2011) Sreeram V. Ramagopalan et al.   ANNALS OF NEUROLOGY

Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria

(2011) Chris H. Polman et al.   ANNALS OF NEUROLOGY

Comparative molecular analysis of therapy-related and de novo acute promyelocytic leukemia

(2011) T. Ottone et al.   LEUKEMIA RESEARCH

Association of IL2RA polymorphisms with susceptibility to multiple sclerosis is not explained by missense mutations in IL2RA

(2011) Marcelo Matiello et al.   Multiple Sclerosis Journal