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Role of proneurotensin as marker of paediatric coeliac disease

Clinical and experimental immunology, 2016-12, Vol.186 (3), p.387-392

2016

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The angiotensin-converting enzyme gene insertion polymorphism: a higher risk for psoriasis in male patients

British journal of dermatology (1951), 2016-10, Vol.175 (4), p.824-826

2016

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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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Characterisation of a Swedish cohort with orofacial granulomatosis with or without Crohn's disease

Oral diseases, 2015-01, Vol.21 (1), p.e98-e104

2015

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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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Heredity of nasal polyps

Rhinology, 2015-03, Vol.53 (1), p.25-28

2015

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Heredity of nasal polyps

Rhinology, 2015-03, Vol.53 (1), p.25-28

2015

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Single nucleotide polymorphisms in fatty acid desaturases is associated with cord blood long chain PUFA proportions and development of allergy

Allergy, 2015, Vol.70 (special issue 101), p.402

2015

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Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease

Annals of human genetics, 2002-03, Vol.66 (2), p.125-137

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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Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease

Annals of human genetics, 2002-03, Vol.66 (2), p.125-137

2002

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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

Tissue antigens, 2000-10, Vol.56 (4), p.350-355

2000

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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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The associations between ADHD, pain, inflammation, and quality of life in children and adolescents-a clinical study protocol

PloS one, 2022-09, Vol.17 (9), p.e0273653

2022

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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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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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Transcriptomics unravels molecular changes associated with cilia and COVID-19 in chronic rhinosinusitis with nasal polyps

Scientific reports, 2023-04, Vol.13 (1), p.6592-6592, Article 6592

2023

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Decreased Risk of Parkinson's Disease After Rheumatoid Arthritis Diagnosis: A Nested Case-Control Study with Matched Cases and Controls

Journal of Parkinson's disease, 2021-01, Vol.11 (2), p.821-832

2021

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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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Different DRB103:01‐DQB102:01 haplotypes confer different risk for celiac disease

HLA, 2017-08, Vol.90 (2), p.95-101

2017

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Genome-wide association study identifies five loci associated with lung function

Nature genetics, 2010-01, Vol.42 (1), p.36-44

2010

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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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haplotype in the inducible T-cell tyrosine kinase is a risk factor for seasonal allergic rhinitis

Allergy (Copenhagen), 2009-09, Vol.64 (9), p.1286-1291

2009

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Inverse relation between nasal fluid Clara Cell Protein 16 levels and symptoms and signs of rhinitis in allergen-challenged patients with intermittent allergic rhinitis

Allergy, 2007-02, Vol.62 (2), p.178-183

2007

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Meta and pooled analysis of European coeliac disease data

European journal of human genetics : EJHG, 2003-11, Vol.11 (11), p.828-834

2003

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Role of proneurotensin as marker of paediatric coeliac disease

The angiotensin-converting enzyme gene insertion polymorphism: a higher risk for psoriasis in male patients

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

Characterisation of a Swedish cohort with orofacial granulomatosis with or without Crohn's disease

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

Heredity of nasal polyps

Heredity of nasal polyps

Single nucleotide polymorphisms in fatty acid desaturases is associated with cord blood long chain PUFA proportions and development of allergy

Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease

The IL12B gene does not confer susceptibility to coeliac disease

Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease

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

Intestinal gluconeogenesis is downregulated in pediatric patients with celiac disease

The associations between ADHD, pain, inflammation, and quality of life in children and adolescents-a clinical study protocol

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

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

Transcriptomics unravels molecular changes associated with cilia and COVID-19 in chronic rhinosinusitis with nasal polyps

Decreased Risk of Parkinson's Disease After Rheumatoid Arthritis Diagnosis: A Nested Case-Control Study with Matched Cases and Controls

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

Different DRB103:01‐DQB102:01 haplotypes confer different risk for celiac disease

Genome-wide association study identifies five loci associated with lung function

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

haplotype in the inducible T-cell tyrosine kinase is a risk factor for seasonal allergic rhinitis

Inverse relation between nasal fluid Clara Cell Protein 16 levels and symptoms and signs of rhinitis in allergen-challenged patients with intermittent allergic rhinitis

Meta and pooled analysis of European coeliac disease data

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