(Q37192690)

18 August 2017

A follow-up study of chromosome 19q13 in multiple sclerosis susceptibility (English)

1 reference

18 August 2017

0 references

Leena Peltonen-Palotie

8

object named as

Leena Peltonen

1 reference

18 August 2017

Alessandro Bonetti

1

1 reference

18 August 2017

Keijo Koivisto

2

1 reference

18 August 2017

Tuula Pirttilä

3

1 reference

18 August 2017

Irina Elovaara

4

1 reference

18 August 2017

Mauri Reunanen

5

1 reference

18 August 2017

Mikko Laaksonen

6

1 reference

18 August 2017

Juhani Ruutiainen

7

1 reference

18 August 2017

Terhi Rantamäki

9

1 reference

18 August 2017

Pentti J Tienari

10

1 reference

18 August 2017

4 February 2009

1 reference

Journal of Neuroimmunology

18 August 2017

6

0 references

published in

1 reference

18 August 2017

208

1 reference

18 August 2017

1-2

1 reference

18 August 2017

119-124

1 reference

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

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Risk alleles for multiple sclerosis identified by a genomewide study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

PRKCA and multiple sclerosis: association in two independent populations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Use of population isolates for mapping complex traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Genomewide scan of multiple sclerosis in Finnish multiplex families

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

High plasma insulin is associated with lower LDL cholesterol in elderly individuals.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Multiple sclerosis in western Finland: evidence for a founder effect

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Association of protein kinase C alpha (PRKCA) gene with multiple sclerosis in a UK population

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Refining the analysis of a whole genome linkage disequilibrium association map: the United Kingdom results

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

A genome screen for multiple sclerosis in Italian families.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Meta-analysis of genome searches

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families

3 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

20 October 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

EVI5 is a risk gene for multiple sclerosis

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

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

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

A full genome search in multiple sclerosis

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682252

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

4 December 2018

1 reference

12 December 2020

An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population

1 reference

12 December 2020

Linkage analysis in multiple sclerosis of chromosomal regions syntenic to experimental autoimmune disease loci

1 reference

12 December 2020

The value of isolated populations

1 reference

12 December 2020

A genome screen for multiple sclerosis in Sardinian multiplex families

1 reference

12 December 2020

Linkage and association analysis of chromosome 19q13 in multiple sclerosis

1 reference

12 December 2020

Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study

1 reference

12 December 2020

Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3.

1 reference

12 December 2020

Multiple susceptibility loci for multiple sclerosis

1 reference

12 December 2020

Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland

1 reference

12 December 2020

A genome-wide screen for linkage disequilibrium in Australian HLA-DRB1*1501 positive multiple sclerosis patients

1 reference

12 December 2020

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms

1 reference

12 December 2020

Association of multiple sclerosis with ILT6 deficiency

1 reference

12 December 2020

A linkage study in two families with multiple sclerosis and healthy members with oligoclonal CSF immunopathy

1 reference

12 December 2020

10.1016/J.JNEUROIM.2009.01.003

Identifiers

DOI

1 reference

release_dk6xwdliqjh6vgmyobrs5422xi

18 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dk6xwdliqjh6vgmyobrs5422xi

24 November 2022

mapped directly with Wikidata item

1 reference

18 August 2017

1 reference