(Q30665913)

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A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

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1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes (English)

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

type-1 diabetes

0 references

Heather Cordell

object named as

Heather J Cordell

1

1 reference

ORCID Public Data File 2021

author name string

David G Clayton

2

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

language of work or name

0 references

publication date

21 November 2001

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

70

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

1

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

124-141

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

A permutation procedure for the haplotype method for identification of disease-predisposing variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Unbiased application of the transmission/disequilibrium test to multilocus haplotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Sequence organisation of the class II region of the human MHC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

The critical region for Behçet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Tests for linkage and association in nuclear families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Detecting disease-predisposing variants: the haplotype method

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

General score tests for associations of genetic markers with disease using cases and their parents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Mapping disease genes: family-based association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

14 July 2018

The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/ disequilibrium test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

25 November 2018

Variation in HLA-associated risks of childhood insulin-dependent diabetes in the Finnish population: II. Haplotype effects. DiMe Study Group. Childhood Diabetes in Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

25 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384883

25 November 2018

Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1, -DRB1 disease loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On estimating HLA/disease association with application to a study of aplastic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography, chromosome recombination frequency and selection

1 reference

https://pubmed.ncbi.nlm.nih.gov/11719900

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

ResearchGate publication ID

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