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Celiac disease confers a 1.6-fold increased risk of asthma: A nationwide population-based cohort study

Journal of allergy and clinical immunology, 2011-04, Vol.127 (4), p.1071-1073.e4

2011

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Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan

Behavior genetics, 2011, Vol.41 (1), p.43-49

2011

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Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Alimentary pharmacology & therapeutics, 2011-03, Vol.33 (6), p.689-696

2011

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Essential fatty acid deficiency in relation to genotype in patients with cystic fibrosis

The Journal of pediatrics, 2001-11, Vol.139 (5), p.650-655

2001

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Predicting the drug interaction potential of AMG 853, a dual antagonist of the D-prostanoid and chemoattractant receptor-homologous molecule expressed on T helper 2 cells receptors

Drug metabolism and disposition, 2012-12, Vol.40 (12), p.2239

2012

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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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Collecting a set of psoriasis family material through a patient organisation; clinical characterisation and presence of additional disorders

BMC dermatology, 2005-10, Vol.5 (1), p.10-10, Article 10

2005

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Chromosomes in Anorexia Nervosa. A Study of 47 Cases Including a Population-Based Group: A Research Note

Journal of child psychology and psychiatry, 1991-05, Vol.32 (4), p.695-701

1991

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Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls

Journal of neurology, 2000-08, Vol.247 (8), p.616-622

2000

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Utilizing Physiologically Based Pharmacokinetic Modeling to Inform Formulation and Clinical Development for a Compound with pH-Dependent Solubility

Journal of pharmaceutical sciences, 2015-04, Vol.104 (4), p.1522-1532

2015

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Leber's hereditary optic neuropathy and complex I deficiency in muscle

Annals of neurology, 1991-11, Vol.30 (5), p.701-708

1991

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Anticipation in Swedish families with bipolar affective disorder

Journal of medical genetics, 1994-09, Vol.31 (9), p.686-689

1994

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A candidate region for Asperger syndrome defined by two 17p breakpoints

European journal of human genetics : EJHG, 2003-02, Vol.11 (2), p.189-195

2003

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Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

Acta neuropathologica, 2000-07, Vol.100 (1), p.23-28

2000

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Genetic Analysis of Mosaicism in 53 Women with Turner Syndrome

Hereditas, 2001-01, Vol.134 (2), p.153-159

2001

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Dilated cardiomyopathy and the dystrophin gene: an illustrated review

British Heart Journal, 1994-10, Vol.72 (4), p.344-348

1994

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CHROMOSOME ABNORMALITIES IN INFANTILE AUTISM AND OTHER CHILDHOOD PSYCHOSES: A POPULATION STUDY OF 66 CASES

Developmental medicine and child neurology, 1985-06, Vol.27 (3), p.293-304

1985

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Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11q

European journal of human genetics : EJHG, 1999-04, Vol.7 (3), p.339-344

1999

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Coeliac disease and risk of sarcoidosis

Sarcoidosis, vasculitis, and diffuse lung diseases, 2007-09, Vol.24 (2), p.121

2007

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Rett syndrome: potential gene sources - phenotypical variability

Clinical genetics, 1995-10, Vol.48 (4), p.169-172

1995

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Infantile autism and the fragile X. A swedish multicenter study

American journal of medical genetics, 1986-01, Vol.23 (1-2), p.403-408

1986

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TEENAGE PSYCHOSES-EPIDEMIOLOGY, CLASSIFICATION AND REDUCED OPTIMALITY IN THE PRE-, PERI-AND NEONATAL PERIODS

Journal of child psychology and psychiatry, 1986-01, Vol.27 (1), p.87-98

1986

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The Syndromes Described by Kanner and Rett‐Hagberg: Overlap in an Extended Family

Developmental medicine and child neurology, 1990-03, Vol.32 (3), p.258-261

1990

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Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family

Clinical genetics, 1994-02, Vol.45 (2), p.97-103

1994

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Frequency of the fragile X syndrome in infantile autism. A swedish multicenter study

Clinical genetics, 1985-01, Vol.27 (2), p.113-117

1985

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Celiac disease confers a 1.6-fold increased risk of asthma: A nationwide population-based cohort study

Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan

Risk of tuberculosis in a large sample of patients with coeliac disease – a nationwide cohort study

Essential fatty acid deficiency in relation to genotype in patients with cystic fibrosis

Predicting the drug interaction potential of AMG 853, a dual antagonist of the D-prostanoid and chemoattractant receptor-homologous molecule expressed on T helper 2 cells receptors

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

Collecting a set of psoriasis family material through a patient organisation; clinical characterisation and presence of additional disorders

Chromosomes in Anorexia Nervosa. A Study of 47 Cases Including a Population-Based Group: A Research Note

Incidence of CSF abnormalities in siblings of multiple sclerosis patients and unrelated controls

Utilizing Physiologically Based Pharmacokinetic Modeling to Inform Formulation and Clinical Development for a Compound with pH-Dependent Solubility

Leber's hereditary optic neuropathy and complex I deficiency in muscle

Anticipation in Swedish families with bipolar affective disorder

A candidate region for Asperger syndrome defined by two 17p breakpoints

Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

Genetic Analysis of Mosaicism in 53 Women with Turner Syndrome

Dilated cardiomyopathy and the dystrophin gene: an illustrated review

CHROMOSOME ABNORMALITIES IN INFANTILE AUTISM AND OTHER CHILDHOOD PSYCHOSES: A POPULATION STUDY OF 66 CASES

Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11q

Coeliac disease and risk of sarcoidosis

Rett syndrome: potential gene sources - phenotypical variability

Infantile autism and the fragile X. A swedish multicenter study

TEENAGE PSYCHOSES-EPIDEMIOLOGY, CLASSIFICATION AND REDUCED OPTIMALITY IN THE PRE-, PERI-AND NEONATAL PERIODS

The Syndromes Described by Kanner and Rett‐Hagberg: Overlap in an Extended Family

Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family

Frequency of the fragile X syndrome in infantile autism. A swedish multicenter study

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