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Confounding Underlies the Apparent Month of Birth Effect in Multiple Sclerosis.
- Published in:
- Journal of Neurology, 2014, v. 261, n. 1, p. 714, doi. 10.1002/ana.23925
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- Publication type:
- Article
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome.
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- Movement Disorders, 2012, v. 27, n. 2, p. 312, doi. 10.1002/mds.24029
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- Publication type:
- Article
Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.
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- BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0220-7
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- Publication type:
- Article
The expanding genetic overlap between multiple sclerosis and type I diabetes.
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- Genes & Immunity, 2009, v. 10, n. 1, p. 11, doi. 10.1038/gene.2008.83
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- Publication type:
- Article
European multiple sclerosis risk variants in the south Asian population.
- Published in:
- Multiple Sclerosis Journal, 2016, v. 22, n. 12, p. 1536, doi. 10.1177/1352458515624270
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- Article
HLA associations in South Asian multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2016, v. 22, n. 1, p. 19, doi. 10.1177/1352458515581439
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- Publication type:
- Article
Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2012, v. 18, n. 1, p. 16, doi. 10.1177/1352458511415562
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- Publication type:
- Article
Evaluation of the established non-MHC multiple sclerosis loci in an Indian population.
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- Multiple Sclerosis Journal, 2011, v. 17, n. 2, p. 139, doi. 10.1177/1352458510384011
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- Publication type:
- Article
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.
- Published in:
- Nature Communications, 2015, v. 6, n. 2, p. 6326, doi. 10.1038/ncomms7326
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- Article
Recent advances and future challenges in the genetics of multiple sclerosis.
- Published in:
- Frontiers in Neurology, 2014, v. 5, p. 1, doi. 10.3389/fneur.2014.00130
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- Publication type:
- Article
Expression profiling of cerebrospinal fluid identifies dysregulated antiviral mechanisms in multiple sclerosis.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 2, p. 554, doi. 10.1093/brain/awad404
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- Publication type:
- Article
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
- Published in:
- 2018
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- Publication type:
- journal article
Confounding underlies the apparent month of birth effect in multiple sclerosis.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 6, p. 714, doi. 10.1002/ana.23925
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- Publication type:
- Article
No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 3, p. 430, doi. 10.1002/ana.23833
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- Publication type:
- Article
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis.
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- European Journal of Human Genetics, 2010, v. 18, n. 4, p. 502, doi. 10.1038/ejhg.2009.195
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- Publication type:
- Article
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.
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- European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1309, doi. 10.1038/ejhg.2009.41
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- Publication type:
- Article
No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis.
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- 2006
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- Publication type:
- Letter
Ultraconserved regions in multiple sclerosis.
- Published in:
- 2005
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- Publication type:
- Letter
Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
- Published in:
- Nature Genetics, 2015, v. 47, n. 8, p. 962, doi. 10.1038/ng0815-962c
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- Publication type:
- Article
Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
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- Nature Genetics, 2015, v. 47, n. 7, p. 839, doi. 10.1038/ng.3330
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- Publication type:
- Article
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.
- Published in:
- 2012
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- Publication type:
- Letter
Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 9, p. 1083, doi. 10.1038/ng2103
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- Publication type:
- Article
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
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- PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005272
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- Publication type:
- Article
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
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- PLoS Genetics, 2015, v. 11, n. 5, p. 1, doi. 10.1371/journal.pgen.1005272
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- Publication type:
- Article
Association of the 1513C polymorphism in the P2X7 gene with familial forms of chronic lymphocytic leukaemia.
- Published in:
- 2004
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- Publication type:
- Letter
5-HTTLPR and Early Childhood Adversities Moderate Cognitive and Emotional Processing in Adolescence.
- Published in:
- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048482
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- Publication type:
- Article
Investigation of the Role of Mitochondrial DNA in Multiple Sclerosis Susceptibility.
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- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002891
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- Publication type:
- Article
SEROTONIN TRANSPORTER LENGTH POLYMORPHISM, CHILDHOOD MALTREATMENT, AND CHRONIC DEPRESSION: A SPECIFIC GENE-ENVIRONMENT INTERACTION.
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- Depression & Anxiety (1091-4269), 2013, v. 30, n. 1, p. 5, doi. 10.1002/da.21982
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- Publication type:
- Article
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
- Published in:
- Nature, 2013, v. 498, n. 7453, p. 232, doi. 10.1038/nature12170
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- Publication type:
- Article
IL-21 drives secondary autoimmunity in patients with multiple sclerosis, following therapeutic lymphocyte depletion with alemtuzumab (Campath-1H).
- Published in:
- 2009
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- Publication type:
- journal article
Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.
- Published in:
- 2013
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- Publication type:
- Journal Article
Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 2, p. 392, doi. 10.1093/brain/aws318
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- Publication type:
- Article
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.
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- Brain: A Journal of Neurology, 2009, v. 132, n. 11, p. 2958, doi. 10.1093/brain/awp245
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- Publication type:
- Article
Polymorphisms in the neuromyelitis optica auto-antigen AQP4 and susceptibility to multiple sclerosis.
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- Journal of Neurology, 2007, v. 254, n. 3, p. 398, doi. 10.1007/s00415-006-0392-8
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- Publication type:
- Article
No evidence for association of the protein kinase C alpha gene with multiple sclerosis.
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- Journal of Neurology, 2005, v. 252, n. 5, p. 619, doi. 10.1007/s00415-005-0706-2
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- Publication type:
- Article
What role for genetics in the prediction of multiple sclerosis?
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- Annals of Neurology, 2010, v. 67, n. 1, p. 3, doi. 10.1002/ana.21911
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- Publication type:
- Article
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease.
- Published in:
- 2007
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- Publication type:
- journal article
Tau and α-synuclein in susceptibility to, and dementia in, Parkinson's disease.
- Published in:
- Annals of Neurology, 2007, v. 62, n. 2, p. 145, doi. 10.1002/ana.21192
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- Publication type:
- Article
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
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- Annals of Neurology, 2007, v. 61, n. 3, p. 228
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- Publication type:
- Article
Increased THEMIS First Exon Usage in CD4+ T-Cells Is Associated with a Genotype that Is Protective against Multiple Sclerosis.
- Published in:
- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158327
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- Publication type:
- Article