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Multiple sclerosis genetics
scientific article published on 19 May 2014
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
title
Multiple sclerosis genetics
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
main subject
multiple sclerosis
1 reference
based on heuristic
inferred from title
author
Stephen Sawcer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
Robin Franklin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
author name string
Maria Ban
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
publication date
19 May 2014
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
published in
Lancet Neurology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
volume
13
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
issue
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
page(s)
700-709
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
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7 January 2021
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7 January 2021
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What role for genetics in the prediction of multiple sclerosis?
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7 January 2021
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Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting
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7 January 2021
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Risk for Relatives of Patients with Multiple Sclerosis in Central Sardinia, Italy
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7 January 2021
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The mystery of missing heritability: Genetic interactions create phantom heritability
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7 January 2021
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Modelling the effects of penetrance and family size on rates of sporadic and familial disease
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7 January 2021
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Genome-wide association studies: theoretical and practical concerns
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7 January 2021
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The future of genetic studies of complex human diseases
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7 January 2021
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A genome-wide scan in forty large pedigrees with multiple sclerosis
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7 January 2021
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Genome-wide linkage screen of a consanguineous multiple sclerosis kinship
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7 January 2021
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A linkage study in two families with multiple sclerosis and healthy members with oligoclonal CSF immunopathy
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7 January 2021
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A genome scan in a single pedigree with a high prevalence of multiple sclerosis
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7 January 2021
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HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation
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7 January 2021
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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
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7 January 2021
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A high-density screen for linkage in multiple sclerosis
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Multiple Sclerosis: Association with HL—A3
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Histocompatibility determinants in multiple sclerosis, with special reference to clinical course
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7 January 2021
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Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project
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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
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HLA*IMP--an integrated framework for imputing classical HLA alleles from SNP genotypes
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A statistical method for predicting classical HLA alleles from SNP data
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7 January 2021
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Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects
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Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis
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based on heuristic
inferred from DOI database lookup
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis.
1 reference
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Crossref
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7 January 2021
based on heuristic
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A second major histocompatibility complex susceptibility locus for multiple sclerosis
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
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7 January 2021
based on heuristic
inferred from DOI database lookup
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis
1 reference
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based on heuristic
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Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis
1 reference
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7 January 2021
based on heuristic
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Risk alleles for multiple sclerosis identified by a genomewide study
1 reference
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based on heuristic
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
1 reference
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based on heuristic
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Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
1 reference
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7 January 2021
based on heuristic
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Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
1 reference
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7 January 2021
based on heuristic
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Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association study in progressive multiple sclerosis
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk.
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pervasive sharing of genetic effects in autoimmune disease
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Promise and pitfalls of the Immunochip
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
An integrated encyclopedia of DNA elements in the human genome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Bayesian refinement of association signals for 14 loci in 3 common diseases
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Refining genetic associations in multiple sclerosis
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
The complex genetics of multiple sclerosis: pitfalls and prospects
1 reference
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https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Common SNPs explain a large proportion of the heritability for human height
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
A method and server for predicting damaging missense mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Predicting the functional effect of amino acid substitutions and indels
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Chromatin marks identify critical cell types for fine mapping complex trait variants
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rare variants create synthetic genome-wide associations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synthetic associations are unlikely to account for many common disease genome-wide association signals
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Five years of GWAS discovery
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Soluble IL-2RA levels in multiple sclerosis subjects and the effect of soluble IL-2RA on immune responses
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
The role of the CD58 locus in multiple sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial effects on the clinical course of multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MGAT5 alters the severity of multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study of severity in multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association study of brain lesion distribution in multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sustained activation of ERK1/2 MAPK in oligodendrocytes and schwann cells enhances myelin growth and stimulates oligodendrocyte progenitor expansion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inflammation stimulates myelination by transplanted oligodendrocyte precursor cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functionally defective germline variants of sialic acid acetylesterase in autoimmunity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A map of human genome variation from population-scale sequencing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rare variants in the CYP27B1 gene are associated with multiple sclerosis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for a role of rareCYP27B1functional variations in multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prediction and interaction in complex disease genetics: experience in type 1 diabetes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk in complex genetics: "all models are wrong but some are useful".
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sick individuals and sick populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A High-Density Admixture Map for Disease Gene Discovery in African Americans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970041-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1474-4422(14)70041-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
PubMed publication ID
24852507
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24852507
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24852507%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
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