| Item Type | Name |
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Academic Article
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Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
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Academic Article
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Genome-wide search for atopy susceptibility genes in Dutch families with asthma.
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Academic Article
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Mapping susceptibility genes for allergic diseases.
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Academic Article
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Genome screen for asthma and bronchial hyperresponsiveness: interactions with passive smoke exposure.
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Academic Article
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Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.
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Academic Article
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Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.
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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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Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
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Academic Article
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Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy.
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Academic Article
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Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population.
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Academic Article
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Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus.
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Academic Article
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Genetics of allergy and bronchial hyperresponsiveness.
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Academic Article
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Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
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Academic Article
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Major genes regulating total serum immunoglobulin E levels in families with asthma.
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Academic Article
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Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.
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Academic Article
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Fine mapping of an IgE-controlling gene on chromosome 2q: Analysis of CTLA4 and CD28.
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Academic Article
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Identification of polymorphisms in the human glucocorticoid receptor gene (NR3C1) in a multi-racial asthma case and control screening panel.
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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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Genomewide screen for pulmonary function in 200 families ascertained for asthma.
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Academic Article
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Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
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Academic Article
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Identification of PCDH1 as a novel susceptibility gene for bronchial hyperresponsiveness.
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Academic Article
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COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.
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Academic Article
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Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome.
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Academic Article
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D20S213, a microsatellite polymorphism near the D20S16 locus.
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Academic Article
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Physical and genetic mapping of the muscle phosphofructokinase gene (PFKM): reassignment to human chromosome 12q.
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Academic Article
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Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.
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Academic Article
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A physical map of the 20q12-q13.1 region associated with type 2 diabetes.
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Academic Article
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Mapping susceptibility genes for asthma and allergy.
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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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Physical Chromosome Mapping
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Concept
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Chromosomes, Human, Pair 11
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Concept
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Chromosomes, Human, Pair 1
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Concept
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Chromosomes, Human, Pair 3
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Concept
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Chromosomes, Human, Pair 20
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Concept
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Chromosomes, Human
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Concept
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Chromosomes, Artificial, Yeast
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Concept
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Chromosomes, Human, Pair 4
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Concept
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Chromosomes, Human, Pair 10
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Concept
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Chromosomes, Human, Pair 7
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Concept
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Chromosomes, Human, Pair 6
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Chromosomes, Human, Pair 22
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Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Bacterial
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Concept
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Chromosomes, Human, Pair 5
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Concept
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Chromosome Mapping
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Concept
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Chromosome Deletion
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Concept
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Chromosomes, Human, Pair 2
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Academic Article
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Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
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Academic Article
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Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
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Academic Article
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Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.
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Academic Article
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Allele-specific methylation in the FADS genomic region in DNA from human saliva, CD4+ cells, and total leukocytes.
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Academic Article
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Intrinsic DNA topology as a prioritization metric in genomic fine-mapping studies.
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