(Q33645905)

28 July 2017

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene (English)

1 reference

genome-wide association study

28 July 2017

0 references

0 references

27

Aarno Palotie

1 reference

28 July 2017

22

Ludwig Kappos

1 reference

28 July 2017

26

Mark J Daly

1 reference

28 July 2017

25

David A Hafler

1 reference

28 July 2017

Leena Peltonen-Palotie

29

object named as

Leena Peltonen

1 reference

28 July 2017

19

Stacey B Gabriel

1 reference

28 July 2017

24

Philip L De Jager

1 reference

28 July 2017

28

Janna Saarela

1 reference

28 July 2017

21

Stephen L Hauser

1 reference

28 July 2017

17

Hanne F Harbo

1 reference

28 July 2017

20

Daniel B Mirel

1 reference

28 July 2017

15

Annette Bang Oturai

1 reference

28 July 2017

3

Anna-Maija Sulonen

1 reference

28 July 2017

23

Chris Polman

1 reference

28 July 2017

7

Shaun Purcell

1 reference

28 July 2017

1

Eveliina Jakkula

1 reference

28 July 2017

Virpi Leppä

2

1 reference

28 July 2017

Teppo Varilo

4

1 reference

28 July 2017

Suvi Kallio

5

1 reference

28 July 2017

Anu Kemppinen

6

1 reference

28 July 2017

Keijo Koivisto

8

1 reference

28 July 2017

Pentti Tienari

9

1 reference

28 July 2017

Marja-Liisa Sumelahti

10

1 reference

28 July 2017

Irina Elovaara

11

1 reference

28 July 2017

Tuula Pirttilä

12

1 reference

28 July 2017

Mauri Reunanen

13

1 reference

28 July 2017

Arpo Aromaa

14

1 reference

28 July 2017

Helle Bach Søndergaard

16

1 reference

28 July 2017

Inger-Lise Mero

18

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 2010

1 reference

American Journal of Human Genetics

28 July 2017

7

0 references

published in

1 reference

28 July 2017

86

1 reference

28 July 2017

285-291

1 reference

28 July 2017

2

1 reference

describes a project that uses

28 July 2017

genome-wide association study

1 reference

CD4+ regulatory T cells control TH17 responses in a Stat3-dependent manner.

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

STAT3 in CD4+ T helper cell differentiation and inflammatory diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Signals of recent positive selection in a worldwide sample of human populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The role of the CD58 locus in multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The genome-wide patterns of variation expose significant substructure in a founder population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The expanding genetic overlap between multiple sclerosis and type I diabetes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Loss of STAT3 in CD4+ T cells prevents development of experimental autoimmune diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

STAT3 mutations in the hyper-IgE syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Risk alleles for multiple sclerosis identified by a genomewide study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Identification of dystroglycan as a second laminin receptor in oligodendrocytes, with a role in myelination

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

A second major histocompatibility complex susceptibility locus for multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

PRKCA and multiple sclerosis: association in two independent populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Characterization of a neural-specific splicing form of the human neuregulin 3 gene involved in oligodendrocyte survival

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Haploview: analysis and visualization of LD and haplotype maps

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Genetic susceptibility to MS: a second stage analysis in Canadian MS families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Regulation of neuregulin signaling by PSD-95 interacting with ErbB4 at CNS synapses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Genomewide scan of multiple sclerosis in Finnish multiplex families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Genetic epidemiology of multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The British Isles survey of multiple sclerosis in twins

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Histocompatibility (HL-A) antigens associated with multiple sclerosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Studies on the clustering of multiple sclerosis in Finland I: Comparison between the domiciles and places of birth in selected subpopulations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Differential expression, and genetic association, of CD58 in Swedish multiple sclerosis patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

The SH2D2A gene and susceptibility to multiple sclerosis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Multiple sclerosis in western Finland: evidence for a founder effect.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

CNS integrins switch growth factor signalling to promote target-dependent survival

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2820168

Multiple susceptibility loci for multiple sclerosis

30 October 2018

1 reference

12 December 2020

Regional and temporal variation in the incidence of multiple sclerosis in Finland 1979-1993

1 reference

12 December 2020

Increasing prevalence of multiple sclerosis in Finland

1 reference

12 December 2020

Studies on the clustering of multiple sclerosis in Finland II: microepidemiology in one high-risk county with special reference to familial cases

1 reference

12 December 2020

Reappraisal of HLA in multiple sclerosis: close linkage in multiplex families

1 reference

12 December 2020

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

1 reference

12 December 2020

Fine mapping of the multiple sclerosis susceptibility locus on 5p14–p12

1 reference

12 December 2020

Genetic association analysis of the interleukin 7 gene (IL7) in multiple sclerosis

1 reference

12 December 2020

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24

1 reference

12 December 2020

10.1016/J.AJHG.2010.01.017

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

1 reference