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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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Autosomal Dominant Myopathy: Missense Mutation (Gly-706 → Lys) in the Myosin Heavy Chain IIa Gene

Proceedings of the National Academy of Sciences - PNAS, 2000-12, Vol.97 (26), p.14614-14619

2000

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Psoriasis susceptibility locus in chromosome region 3q21 identified in patients from southwest Sweden

European journal of human genetics : EJHG, 1999-10, Vol.7 (7), p.783-790

1999

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Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

Genes chromosomes & cancer, 2007-03, Vol.46 (3), p.302-309

2007

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Searching for genes influencing a complex disease: the case of coeliac disease

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.542-553

2008

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PDE4D plays a critical role in the control of airway smooth muscle contraction

The FASEB journal, 2003-10, Vol.17 (13), p.1831-1841

2003

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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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Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL

Brain (London, England : 1878), 2007-02, Vol.130 (2), p.357-367

2007

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Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from western Sweden

Familial cancer, 2007, Vol.6 (1), p.35-41

2007

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Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age

Neurology, 2002-03, Vol.58 (5), p.780

2002

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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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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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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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The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.787-793

2001

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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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A population genetic study of psoriasis

British journal of dermatology (1951), 1994-07, Vol.131 (1), p.32-39

1994

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Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis

Journal of rheumatology, 2004-11, Vol.31 (11), p.2230

2004

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PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

Human mutation, 2000-11, Vol.16 (5), p.395-400

2000

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Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

European journal of human genetics : EJHG, 2000, Vol.8 (12), p.918-922

2000

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A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques

Familial cancer, 2005-01, Vol.4 (2), p.89-96

2005

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Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patients

Archives of Dermatological Research, 2000-11, Vol.292 (11), p.525-530

2000

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Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes

International journal of molecular medicine, 2004-01, Vol.13 (1), p.47

2004

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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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Fine Mapping of the Gene for Carbohydrate-Deficient Glycoprotein Syndrome, Type I (CDG1): Linkage Disequilibrium and Founder Effect in Scandinavian Families

Genomics (San Diego, Calif.), 1997-02, Vol.39 (3), p.247-253

1997

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

Autosomal Dominant Myopathy: Missense Mutation (Gly-706 → Lys) in the Myosin Heavy Chain IIa Gene

Psoriasis susceptibility locus in chromosome region 3q21 identified in patients from southwest Sweden

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

Searching for genes influencing a complex disease: the case of coeliac disease

PDE4D plays a critical role in the control of airway smooth muscle contraction

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

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL

Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from western Sweden

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age

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

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

Meta and pooled analysis of European coeliac disease data

The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

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

A population genetic study of psoriasis

Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques

Stronger association with HLA-Cw6 than with corneodesmosin (S-gene) polymorphisms in Swedish psoriasis patients

Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes

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

Fine Mapping of the Gene for Carbohydrate-Deficient Glycoprotein Syndrome, Type I (CDG1): Linkage Disequilibrium and Founder Effect in Scandinavian Families

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