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Expression of the multiple sclerosis-associated MHC class II Allele HLA-DRB11501 is regulated by vitamin D

PLoS genetics, 2009-02, Vol.5 (2), p.e1000369-e1000369

2009

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Enhanced astrocyte responses are driven by a genetic risk allele associated with multiple sclerosis

Nature communications, 2018-12, Vol.9 (1), p.5337-9, Article 5337

2018

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Pearls & Oy-sters: Homozygous Complement Factor I Deficiency Presenting as Fulminant Relapsing Complement-Mediated CNS Vasculitis

Neurology, 2023-07, Vol.101 (2), p.e220

2023

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Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility

Proceedings of the National Academy of Sciences - PNAS, 2009-05, Vol.106 (18), p.7542-7547

2009

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Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance

Human molecular genetics, 2005-07, Vol.14 (14), p.2019-2026

2005

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The inheritance of resistance alleles in multiple sclerosis

PLoS genetics, 2007-09, Vol.3 (9), p.1607-1613

2007

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HLA class I alleles tag HLA-DRB11501 haplotypes for differential risk in multiple sclerosis susceptibility

Proceedings of the National Academy of Sciences - PNAS, 2008-09, Vol.105 (35), p.13069-13074

2008

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Type I interferon transcriptional network regulates expression of coinhibitory receptors in human T cells

Nature immunology, 2022-04, Vol.23 (4), p.632

2022

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Vitamin D as disease-modifying therapy for multiple sclerosis?

Expert review of clinical immunology, 2021-07, Vol.17 (7), p.691-693

2021

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A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution

Genome research, 2010-10, Vol.20 (10), p.1352

2010

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Epigenetic fine-mapping: identification of causal mechanisms for autoimmunity

Current opinion in immunology, 2020-12, Vol.67, p.50-56

2020

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Chronic cerebrospinal venous insufficiency and multiple sclerosis

Annals of neurology, 2010-08, Vol.68 (2), p.270-270

2010

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Clinical Reasoning: A 34-year-old man with headache, diplopia, and hemiparesis

Neurology, 2016-01, Vol.86 (3), p.e24

2016

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A multiple sclerosis-protective coding variant reveals an essential role for HDAC7 in regulatory T cells

Science translational medicine, 2022-12, Vol.14 (675), p.eabl3651

2022

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Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis

The American journal of clinical nutrition, 2008-08, Vol.88 (2), p.441-447

2008

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PRKCA and multiple sclerosis: association in two independent populations

PLoS genetics, 2006-03, Vol.2 (3), p.e42-e42

2006

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Of mice and men: experimental autoimmune encephalitis and multiple sclerosis

European journal of clinical investigation, 2011-11, Vol.41 (11), p.1254-1258

2011

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Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex

Human molecular genetics, 2009-01, Vol.18 (2), p.261-266

2009

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Teaching neuroimages: large vagal nerve schwannoma presenting with hemorrhage and respiratory failure

Neurology, 2014-03, Vol.82 (10), p.e89

2014

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

Neurology, 2012-07, Vol.79 (5), p.406

2012

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Robert Whytt, Benjamin Franklin, and the first probable case of multiple sclerosis

Annals of neurology, 2012-09, Vol.72 (3), p.307-311

2012

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Methylation of class II transactivator gene promoter IV is not associated with susceptibility to multiple sclerosis

BMC medical genetics, 2008-07, Vol.9 (1), p.63-63, Article 63

2008

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Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis

Human molecular genetics, 2010-09, Vol.19 (18), p.3679-3689

2010

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Parental transmission of HLA-DRB115 in multiple sclerosis

Human genetics, 2008, Vol.122 (6), p.661-663

2008

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Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium

Human molecular genetics, 2007-08, Vol.16 (16), p.1951-1958

2007

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Expression of the multiple sclerosis-associated MHC class II Allele HLA-DRB11501 is regulated by vitamin D

Enhanced astrocyte responses are driven by a genetic risk allele associated with multiple sclerosis

Pearls & Oy-sters: Homozygous Complement Factor I Deficiency Presenting as Fulminant Relapsing Complement-Mediated CNS Vasculitis

Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility

Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance

The inheritance of resistance alleles in multiple sclerosis

HLA class I alleles tag HLA-DRB11501 haplotypes for differential risk in multiple sclerosis susceptibility

Type I interferon transcriptional network regulates expression of coinhibitory receptors in human T cells

Vitamin D as disease-modifying therapy for multiple sclerosis?

A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution

Epigenetic fine-mapping: identification of causal mechanisms for autoimmunity

Chronic cerebrospinal venous insufficiency and multiple sclerosis

Clinical Reasoning: A 34-year-old man with headache, diplopia, and hemiparesis

A multiple sclerosis-protective coding variant reveals an essential role for HDAC7 in regulatory T cells

Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis

PRKCA and multiple sclerosis: association in two independent populations

Of mice and men: experimental autoimmune encephalitis and multiple sclerosis

Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex

Teaching neuroimages: large vagal nerve schwannoma presenting with hemorrhage and respiratory failure

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

Robert Whytt, Benjamin Franklin, and the first probable case of multiple sclerosis

Methylation of class II transactivator gene promoter IV is not associated with susceptibility to multiple sclerosis

Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis

Parental transmission of HLA-DRB115 in multiple sclerosis

Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium

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