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The common variants/multiple disease hypothesis of common complex genetic disorders
scientific article published on 01 January 2004
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
title
The common variants/multiple disease hypothesis of common complex genetic disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
author name string
Kevin G Becker
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
publication date
1 January 2004
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
published in
Medical Hypotheses
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
volume
62
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
page(s)
309-317
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
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A single nucleotide polymorphism in the proximal IFN-gamma promoter alters control of gene transcription.
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Autoimmune disease in first-degree relatives of patients with multiple sclerosis. A UK survey
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Familial occurrence of autoimmune diseases and autoantibodies in a Caucasian population of patients with systemic lupus erythematosus
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Asthma hospitalization trends in Charleston, South Carolina, 1956 to 1997: twenty-fold increase among black children during a 30-year period
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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.
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QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing Il2
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Polyspecificity of autoimmune responses in type 1 (autoimmune) diabetes
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Identification of four new quantitative trait loci regulating arthritis severity and one new quantitative trait locus regulating autoantibody production in rats with collagen-induced arthritis
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A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases
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The comorbidity of ADHD in the general population of Swedish school-age children.
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A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.
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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
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The new genomics: global views of biology
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Chromosome 22 workshop.
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Autoimmune disease: why and where it occurs.
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Susceptibility gene discovery for common metabolic and endocrine traits
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Suggestive Evidence for Association of Human Chromosome 18q12-q21 and Its Orthologue on Rat and Mouse Chromosome 18 With Several Autoimmune Diseases
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Coincidence of immune-mediated diseases driven by Th1 and Th2 subsets suggests a common aetiology. A population-based study using computerized general practice data.
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1 reference
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7 January 2021
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inferred from DOI database lookup
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inferred from DOI database lookup
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0306-9877(03)00332-3
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
PubMed ID
14962646
1 reference
stated in
Europe PubMed Central
PubMed ID
14962646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14962646%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 November 2019
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