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Low-Frequency Coding Variation Within GWAS Loci Illuminates New Genetic Contributors to Multiple Sclerosis: Evidence From Family Exomes and
Genetics
Low-Frequency Coding Variation Within GWAS Loci Illuminates New Genetic Contributors to Multiple Sclerosis: Evidence From Family Exomes and

09, Jan 2026

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Low-Frequency Coding Variation Within GWAS Loci Illuminates New Genetic Contributors to Multiple Sclerosis: Evidence From Family Exomes and
Genetics
A KCNA3 Promoter Variant and the Immunogenetics of Multiple Sclerosis Progression: Evidence Linking rs2821557 to Severe Disability Accumulat

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From Risk to Outcome: Longitudinal Genomics and the Biology of Multiple Sclerosis Severity

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Low-Frequency Coding Variants in Multiple Sclerosis: Quantifying Rare Genetic Risk and Refining Immune Mechanisms
Genetics
Low-Frequency Coding Variants in Multiple Sclerosis: Quantifying Rare Genetic Risk and Refining Immune Mechanisms

06, Jan 2026

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IL2RA Variants and Multiple Sclerosis Susceptibility
Genetics
IL2RA Variants and Multiple Sclerosis Susceptibility

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Categories:
Genetics
A KCNA3 Promoter Variant and the Immunogenetics of Multiple Sclerosis Progression: Evidence Linking rs2821557 to Severe Disability Accumulat
Genetics
A KCNA3 Promoter Variant and the Immunogenetics of Multiple Sclerosis Progression: Evidence Linking rs2821557 to Severe Disability Accumulat

08, Jan 2026

Low-Frequency Coding Variation Within GWAS Loci Illuminates New Genetic Contributors to Multiple Sclerosis: Evidence From Family Exomes and
Genetics
Low-Frequency Coding Variation Within GWAS Loci Illuminates New Genetic Contributors to Multiple Sclerosis: Evidence From Family Exomes and

09, Jan 2026