(Q46084074)

19 December 2017

title

Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex (English)

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19 December 2017

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I Kockum

7

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Flemming Pociot

object named as

F Pociot

5

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Dag Undlien

10

object named as

D E Undlien

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19 December 2017

9

E Thorsby

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19 December 2017

8

A Cambon-Thomsen

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19 December 2017

author name string

M K Viken

1

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19 December 2017

A Blomhoff

2

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19 December 2017

M Olsson

3

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19 December 2017

H E Akselsen

4

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19 December 2017

J Nerup

6

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19 December 2017

B A Lie

11

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19 December 2017

publication date

19 March 2009

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19 December 2017

published in

Genes and Immunity

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19 December 2017

volume

10

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19 December 2017

issue

4

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19 December 2017

page(s)

323-333

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19 December 2017

https://scigraph.springernature.com/pub.10.1038/gene.2009.13

exact match

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cites work

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A diabetes-susceptible HLA haplotype is best defined by a combination of HLA-DR and -DQ alleles

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Genetic structure of IDDM1: two separate regions in the major histocompatibility complex contribute to susceptibility or protection. Belgian Diabetes Registry

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Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and –DRB1

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Association between D6S2223 and type I diabetes independent of HLA class II in Dutch families

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The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene

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Homozygous parent affected sib pair method for detecting disease predisposing variants: application to insulin dependent diabetes mellitus

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Extreme genetic risk for type 1A diabetes

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"Extended" A1, B8, DR3 haplotype shows remarkable linkage disequilibrium but is similar to nonextended haplotypes in terms of diabetes risk

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

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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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A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms

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HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?

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Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks

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Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes.

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Gene map of the extended human MHC.

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The immunoglobulin superfamily--domains for cell surface recognition

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Cloning and molecular characterization of a cross-homologous zinc finger locus ZNF204.

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Cloning of a novel MHC-encoded serine peptidase highly expressed by cortical epithelial cells of the thymus

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Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases

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Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease

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Extent and distribution of linkage disequilibrium in three genomic regions

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A survey of genetic and epigenetic variation affecting human gene expression

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Analysis of single nucleotide polymorphisms identifies major type 1A diabetes locus telomeric of the major histocompatibility complex

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Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

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Non-class II HLA gene associated with type 1 diabetes maps to the 240-kb region near HLA-B

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Human leukocyte antigen class I B and C loci contribute to Type 1 Diabetes (T1D) susceptibility and age at T1D onset

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

The cluster of BTN genes in the extended major histocompatibility complex

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

A 1.1-Mb transcript map of the hereditary hemochromatosis locus

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Extending the B7 (CD80) gene family

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

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Problems of reporting genetic associations with complex outcomes

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Fine mapping versus replication in whole-genome association studies

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Global variation in copy number in the human genome

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Strong association of de novo copy number mutations with autism

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7 January 2021

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Frequency of new copy number variation in humans

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Large-scale copy number polymorphism in the human genome

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome.

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

The DNA sequence and analysis of human chromosome 6

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

The International HapMap Project

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Maximum-likelihood estimation of haplotype frequencies in nuclear families

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https://api.crossref.org/works/10.1038%2FGENE.2009.13

7 January 2021

Identifiers

DOI

10.1038/GENE.2009.13

1 reference

19 December 2017

1 reference

19 December 2017