Item Type | Name |
Concept
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Chromosomes, Human, Pair 11
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Concept
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Chromosomes, Human, Pair 2
|
Concept
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Chromosomes, Human, Pair 6
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Concept
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Chromosomes, Human, Pair 8
|
Concept
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Chromosomes, Human, Pair 1
|
Concept
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Chromosomes, Human, Pair 15
|
Concept
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Chromosomes, Human, Pair 3
|
Concept
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Chromosomes, Human, Pair 12
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Concept
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Chromosomes, Human, Pair 14
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Concept
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Chromosomes, Human, Pair 13
|
Concept
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Chromosomes, Human, Pair 4
|
Concept
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Chromosomes, Human, Pair 5
|
Concept
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Chromosomes, Human, Pair 10
|
Concept
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Chromosomes, Human, Pair 17
|
Concept
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Chromosomes, Human, Pair 19
|
Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Human, Pair 18
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Academic Article
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Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.
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Academic Article
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Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
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Academic Article
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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
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Academic Article
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A genome scan in 260 inflammatory bowel disease-affected relative pairs.
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Academic Article
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A common cortactin gene variation confers differential susceptibility to severe asthma.
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Academic Article
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Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.
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Academic Article
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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
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Academic Article
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Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
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Academic Article
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Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors.
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Academic Article
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Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
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Academic Article
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Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease.
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Academic Article
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Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
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Academic Article
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Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans.
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Academic Article
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Rhinovirus wheezing illness and genetic risk of childhood-onset asthma.
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Academic Article
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Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.
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Academic Article
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Genome-wide association study of recalcitrant atopic dermatitis in Korean children.
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Academic Article
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An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos.
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Academic Article
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Role of local CpG DNA methylation in mediating the 17q21 asthma susceptibility gasdermin B (GSDMB)/ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) expression quantitative trait locus.
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Academic Article
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A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle.
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Academic Article
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Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.
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Academic Article
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Expression quantitative trait locus fine mapping of the 17q12-21 asthma locus in African American children: a genetic association and gene expression study.
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Academic Article
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Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood.
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