Genomewide linkage analysis of celiac disease in Finnish families (Q40751383)

23 September 2017

Genomewide linkage analysis of celiac disease in Finnish families (English)

1 reference

23 September 2017

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Jukka Partanen

12

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Jianjun Liu

1

object named as

Jianjun Liu

1 reference

23 September 2017

10

Markku Mäki

1 reference

23 September 2017

9

Kirsi Mustalahti

1 reference

23 September 2017

3

Päivi Holopainen

1 reference

23 September 2017

Suh-Hang Juo

2

1 reference

23 September 2017

Joseph Terwilliger

4

1 reference

23 September 2017

Xiaomei Tong

5

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23 September 2017

Adina Grunn

6

1 reference

23 September 2017

Miguel Brito

7

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23 September 2017

Peter Green

8

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23 September 2017

T Conrad Gilliam

11

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23 September 2017

language of work or name

English

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publication date

19 November 2001

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American Journal of Human Genetics

23 September 2017

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23 September 2017

70

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23 September 2017

1

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23 September 2017

51-59

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The first large population based twin study of coeliac disease.

23 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

A genomewide screen for autism susceptibility loci

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Candidate gene regions and genetic heterogeneity in gluten sensitivity

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Molecular basis of celiac disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Contribution of the MHC region to the familial risk of coeliac disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Molecular genetics of the Finnish disease heritage.

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

HLA-DQ2-negative celiac disease in Finland and Spain.

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Genome search in celiac disease.

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Faster sequential genetic linkage computations

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Disease gene mapping in isolated human populations: the example of Finland

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

LABMAN and LINKMAN: a data management system specifically designed for genome searches of complex diseases

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

HLA-DR phenotypes in Spanish coeliac children: their contribution to the understanding of the genetics of the disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Assessing the role of HLA-linked and unlinked determinants of disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Celiac disease risk in the USA: high prevalence of antiendomysium antibodies in healthy blood donors

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Genetic contribution of the HLA region to the familial clustering of coeliac disease.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Measuring the genetic contribution of a single locus to a multilocus disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

HLA-DR and -DQ genotypes of celiac disease patients serologically typed to be non-DR3 or non-DR5/7.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

Estimation of pairwise relationships in the presence of genotyping errors

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

A genome-wide family-based linkage study of coeliac disease

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders

4 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study

4 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

4 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384903

2 December 2018

1 reference

12 December 2020

Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group

1 reference

12 December 2020

Demographic history and linkage disequilibrium in human populations

1 reference

12 December 2020

A pedigree-based linkage study of coeliac disease: failure to replicate previous positive findings

1 reference

12 December 2020

A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease

1 reference

12 December 2020

Search for coeliac disease susceptibility loci on 7q11.23 candidate region: absence of association with the ELN17 microsatellite marker

1 reference

12 December 2020

Concordance of dermatitis herpetiformis and celiac disease in monozygous twins

1 reference

12 December 2020

A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22

1 reference

12 December 2020

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

1 reference

12 December 2020

Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families

1 reference

12 December 2020

Susceptibility to develop celiac disease is primarily associated with HLA-DQ alleles

1 reference

12 December 2020

Serological markers and HLA genes among healthy first-degree relatives of patients with coeliac disease

1 reference

12 December 2020

[Williams-Beuren syndrome in combination with celiac disease]

1 reference

12 December 2020

Williams syndrome and coeliac disease

1 reference

12 December 2020

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping

1 reference

12 December 2020

[Williams-Beuren syndrome and celiac disease]

1 reference

12 December 2020

Linkage analysis of candidate regions for coeliac disease genes

1 reference

12 December 2020

Identifiers

DOI

10.1086/338453

1 reference

23 September 2017

1 reference

23 September 2017

PubMed publication ID

11715113

1 reference