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A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease

PloS one, 2013-08, Vol.8 (8), p.e70174-e70174

2013

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Intestinal gluconeogenesis is downregulated in pediatric patients with celiac disease

BMC medicine, 2022-11, Vol.20 (1), p.1-440, Article 440

2022

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Altered peripheral amino acid profile indicate a systemic impact of active celiac disease and a possible role of amino acids in disease pathogenesis

PloS one, 2018-03, Vol.13 (3), p.e0193764-e0193764

2018

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Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases

PloS one, 2016-08, Vol.11 (8), p.e0159593-e0159593

2016

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FOXP3 polymorphisms in type 1 diabetes and coeliac disease

Journal of autoimmunity, 2006-09, Vol.27 (2), p.140-144

2006

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Validity of histology for the diagnosis of paediatric coeliac disease: a Swedish multicentre study

Scandinavian journal of gastroenterology, 2016, Vol.51 (4), p.427-433

2016

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Antibodies Against Deamidated Gliadin Peptides and Tissue Transglutaminase for Diagnosis of Pediatric Celiac Disease

Journal of pediatric gastroenterology and nutrition, 2012-12, Vol.55 (6), p.695-700

2012

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Questionnaire showed that Swedish paediatric clinics complied well with the revised European guidelines for diagnosing coeliac disease

Acta Paediatrica, 2019-06, Vol.108 (6), p.1140-1143

2019

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Genes involved in muscle contractility and nutrient signaling pathways within celiac disease risk loci show differential mRNA expression

BMC medical genetics, 2015-06, Vol.16 (1), p.44-44, Article 44

2015

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Association Between Genotypes and Phenotypes in Coeliac Disease

Journal of pediatric gastroenterology and nutrition, 2009-08, Vol.49 (2), p.165-169

2009

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A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish Norwegian celiac disease families

European journal of human genetics : EJHG, 2007-09, Vol.15 (9), p.980-987

2007

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Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

Human Immunology, 2006-04, Vol.67 (4), p.341-345

2006

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Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

European journal of human genetics : EJHG, 2001-12, Vol.9 (12), p.938-944

2001

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Journal of pediatric gastroenterology and nutrition, 2004-03, Vol.38 (3), p.338-342

2004

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Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles

Immunogenetics (New York), 2003-08, Vol.55 (5), p.339-343

2003

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A Possible Mechanism behind Autoimmune Disorders Discovered By Genome-Wide Linkage and Association Analysis in Celiac Disease. e70174

PloS one, 2013-08, Vol.8 (8)

2013

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Antibodies Against Deamidated Gliadin Peptides and Tissue Transglutaminase for Diagnosis of Pediatric Celiac Disease - Diagnostic Performance and Cost in Clinical Practice

Journal of pediatric gastroenterology and nutrition, 2012-06, Vol.55 (6), p.695

2012

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Journal of pediatric gastroenterology and nutrition, 2004-03, Vol.38 (3), p.338-342

2004

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Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families

Genes and immunity, 2008-06, Vol.9 (4), p.364-367

2008

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Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort

Genes and immunity, 2010-01, Vol.11 (1), p.79-86

2010

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Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32

Tissue antigens, 2008-01, Vol.71 (1), p.27-34

2008

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Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease

Tissue antigens, 2004-11, Vol.64 (5), p.593-599

2004

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HLA in coeliac disease families: A novel test of risk modification by the 'other' haplotype when at least one DQA105-DQB102 haplotype is carried

Tissue antigens, 2002-08, Vol.60 (2), p.147-154

2002

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The IL12B gene does not confer susceptibility to coeliac disease

Tissue antigens, 2002-01, Vol.59 (1), p.70-72

2002

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A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease

Intestinal gluconeogenesis is downregulated in pediatric patients with celiac disease

Altered peripheral amino acid profile indicate a systemic impact of active celiac disease and a possible role of amino acids in disease pathogenesis

Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases

FOXP3 polymorphisms in type 1 diabetes and coeliac disease

Validity of histology for the diagnosis of paediatric coeliac disease: a Swedish multicentre study

Antibodies Against Deamidated Gliadin Peptides and Tissue Transglutaminase for Diagnosis of Pediatric Celiac Disease

Questionnaire showed that Swedish paediatric clinics complied well with the revised European guidelines for diagnosing coeliac disease

Genes involved in muscle contractility and nutrient signaling pathways within celiac disease risk loci show differential mRNA expression

Association Between Genotypes and Phenotypes in Coeliac Disease

A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish Norwegian celiac disease families

Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles

A Possible Mechanism behind Autoimmune Disorders Discovered By Genome-Wide Linkage and Association Analysis in Celiac Disease. e70174

Antibodies Against Deamidated Gliadin Peptides and Tissue Transglutaminase for Diagnosis of Pediatric Celiac Disease - Diagnostic Performance and Cost in Clinical Practice

The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings

Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families

Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort

Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32

Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease

HLA in coeliac disease families: A novel test of risk modification by the 'other' haplotype when at least one DQA105-DQB102 haplotype is carried

The IL12B gene does not confer susceptibility to coeliac disease

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