Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips (Q60689186)

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9 January 2020

title

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips (English)

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9 January 2020

12

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9 January 2020

author name string

René Gödde

1

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9 January 2020

Klaus Rohde

2

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9 January 2020

Christian Becker

3

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9 January 2020

Patricia Entz

5

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9 January 2020

Anita Suk

6

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9 January 2020

Norbert Müller

7

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9 January 2020

Eckhart Sindern

8

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9 January 2020

Michael Haupts

9

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9 January 2020

Sebastian Schimrigk

10

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9 January 2020

Peter Nürnberg

11

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9 January 2020

Mahammad R Toliat

4

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9 January 2020

publication date

16 March 2005

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Journal of Molecular Medicine

9 January 2020

published in

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volume

83

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9 January 2020

issue

6

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9 January 2020

page(s)

486-494

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The usefulness of different density SNP maps for disease association studies of common variants

9 January 2020

cites work

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12 December 2020

Mapping complex disease loci in whole-genome association studies

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12 December 2020

HapMap: Building a Database with Blocks

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A high-throughput SNP typing system for genome-wide association studies

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Genetic predisposition to multiple sclerosis as revealed by immunoprinting

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Genomics. Consensus emerges on HapMap strategy

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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

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12 December 2020

Genetics of multiple sclerosis--how could disease-associated HLA-types contribute to pathogenesis?

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

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12 December 2020

A meta-analysis of whole genome linkage screens in multiple sclerosis

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Genetics of multiple sclerosis: determinants of autoimmunity and neurodegeneration

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Immunological update on multiple sclerosis

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

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A simple salting out procedure for extracting DNA from human nucleated cells

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Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

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12 December 2020

The structure of haplotype blocks in the human genome

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12 December 2020

Genetic analysis of multiple sclerosis in Europeans: French data

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12 December 2020

Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

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12 December 2020

High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise

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12 December 2020

High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)

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12 December 2020

HLA typing in the United Kingdom multiple sclerosis genome screen

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12 December 2020

Prognosis of multiple sclerosis: environmental factors

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12 December 2020

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

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12 December 2020

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

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12 December 2020

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

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12 December 2020

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease

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HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

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Haplotype blocks and linkage disequilibrium in the human genome

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

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A population-based study of multiple sclerosis in twins

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An integrated system for high throughput TaqManTM based SNP genotyping

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High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

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Is there a future for TNF promoter polymorphisms?

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New diagnostic criteria for multiple sclerosis: guidelines for research protocols

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Seeking genes for MS: big risks for big gains

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12 December 2020

A whole genome screen for association in Polish multiple sclerosis patients

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12 December 2020

From genotypes to genes: doubling the sample size

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12 December 2020

HLA-DMB gene and HLA-DRA promoter region polymorphisms in Australian multiple sclerosis patients

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12 December 2020

High-throughput SNP analysis for genetic association studies.

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12 December 2020

Linkage disequilibrium patterns of the human genome across populations

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12 December 2020

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

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12 December 2020

DASH-2: flexible, low-cost, and high-throughput SNP genotyping by dynamic allele-specific hybridization on membrane arrays

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12 December 2020

The International HapMap Project

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12 December 2020

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course

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12 December 2020

High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers

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12 December 2020

Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.

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12 December 2020

10.1007/S00109-005-0650-8

Identifiers

DOI

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9 January 2020

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