(Q34993579)

5 August 2017

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis (English)

1 reference

5 August 2017

0 references

11

J L Haines

1 reference

5 August 2017

8

J R Oksenberg

1 reference

5 August 2017

7

S L Hauser

1 reference

5 August 2017

J L McCauley

1

1 reference

5 August 2017

R L Zuvich

2

1 reference

5 August 2017

Y Bradford

3

1 reference

5 August 2017

S J Kenealy

4

1 reference

5 August 2017

N Schnetz-Boutaud

5

1 reference

5 August 2017

S G Gregory

6

1 reference

5 August 2017

D P Mortlock

9

1 reference

5 August 2017

M A Pericak-Vance

10

1 reference

5 August 2017

23 July 2009

1 reference

5 August 2017

1 reference

5 August 2017

10

1 reference

5 August 2017

7

1 reference

5 August 2017

624-630

1 reference

https://scigraph.springernature.com/pub.10.1038/gene.2009.53

5 August 2017

0 references

cites work

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Risk alleles for multiple sclerosis identified by a genomewide study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

FLOSS: flexible ordered subset analysis for linkage mapping of complex traits

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Efficiency and power in genetic association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A high-density screen for linkage in multiple sclerosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A second-generation genomic screen for multiple sclerosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Haploview: analysis and visualization of LD and haplotype maps

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Identification and characterization of multi-species conserved sequences

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

The structure of haplotype blocks in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Genome-wide screen for systemic lupus erythematosus susceptibility genes in multiplex families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Genomewide scan of multiple sclerosis in Finnish multiplex families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Faster sequential genetic linkage computations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

The number of families required to detect or exclude linkage heterogeneity

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A genome screen for multiple sclerosis in Italian families.

8 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

A full genome search in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

A whole genome screen for linkage in Turkish multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Whole-genome linkage analysis of rheumatoid arthritis susceptibility loci in 252 affected sibling pairs in the United Kingdom

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Spinal cord injury induces expression of RGS7 in microglia/macrophages in rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Avoiding recomputation in linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

Refining genetic associations in multiple sclerosis

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2765552

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis

26 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

Evidence for Linkage Disequilibrium Between HLA-DRB1 Gene and Multiple Sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

A genome screen for multiple sclerosis in Sardinian multiplex families

21 January 2018

1 reference

12 December 2020

Genetic basis for clinical expression in multiple sclerosis

1 reference

12 December 2020

A genome screen for linkage disequilibrium in HLA-DRB1*15-positive Germans with multiple sclerosis based on 4666 microsatellite markers

1 reference

12 December 2020

A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

1 reference

12 December 2020

A whole genome association study in Finnish multiple sclerosis patients with 3669 markers

1 reference

12 December 2020

Diagnostic criteria for multiple sclerosis research involving multiply affected families

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

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

Genetic Linkage Analysis of Complex Genetic Traits by Using Affected Sibling Pairs

1 reference

12 December 2020

Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44

1 reference

12 December 2020

The developing mosaic of autoimmune disease risk

1 reference

12 December 2020

A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.53

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/GENE.2009.53

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference

5 August 2017

1 reference