Genetic Association Studies
"Genetic Association Studies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The analysis of a sequence such as a region of a chromosome, a haplotype, a gene, or an allele for its involvement in controlling the phenotype of a specific trait, metabolic pathway, or disease.
Descriptor ID |
D056726
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MeSH Number(s) |
E05.393.385
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Concept/Terms |
Genetic Association Studies- Genetic Association Studies
- Association Studies, Genetic
- Association Study, Genetic
- Genetic Association Study
- Studies, Genetic Association
- Study, Genetic Association
Genotype-Phenotype Associations- Genotype-Phenotype Associations
- Association, Genotype-Phenotype
- Associations, Genotype-Phenotype
- Genotype Phenotype Associations
- Genotype-Phenotype Correlation
- Genotype Phenotype Correlation
- Genotype-Phenotype Correlations
- Correlation, Genotype-Phenotype
- Correlations, Genotype-Phenotype
- Genotype Phenotype Correlations
- Genotype-Phenotype Association
- Genotype Phenotype Association
Candidate Gene Analysis- Candidate Gene Analysis
- Analyses, Candidate Gene
- Analysis, Candidate Gene
- Candidate Gene Analyses
- Gene Analyses, Candidate
- Gene Analysis, Candidate
Candidate Gene Identification- Candidate Gene Identification
- Gene Identification, Candidate
- Identification, Candidate Gene
- Candidate Gene Association Study
- Gene Discovery
- Discovery, Gene
- Candidate Gene Association Studies
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Below are MeSH descriptors whose meaning is more general than "Genetic Association Studies".
Below are MeSH descriptors whose meaning is more specific than "Genetic Association Studies".
This graph shows the total number of publications written about "Genetic Association Studies" by people in this website by year, and whether "Genetic Association Studies" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2013 | 0 | 2 | 2 |
2014 | 2 | 0 | 2 |
2015 | 0 | 1 | 1 |
2018 | 1 | 0 | 1 |
2019 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genetic Association Studies" by people in Profiles.
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Identification of a novel allele, HLA-DPB1*34:01:01:03, in Black South African individuals. HLA. 2019 12; 94(6):547-549.
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Identification of a novel recombinant allele, HLA-DPB1*835:01:01:02, in Black South African individuals. HLA. 2019 12; 94(6):549-551.
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Mutations of FAM111B gene are not associated with Systemic Sclerosis. Sci Rep. 2018 10 30; 8(1):15988.
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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct; 168(7):573-85.
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Intrafamilial aggregation and heritability of office-day blood pressure difference in a community of African ancestry: implications for genetic association studies. Blood Press Monit. 2014 Dec; 19(6):346-52.
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New insights into genotype-phenotype correlation for GLI3 mutations. Eur J Hum Genet. 2015 Jan; 23(1):92-102.
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The elusive gene for keratolytic winter erythema. S Afr Med J. 2013 Oct 11; 103(12 Suppl 1):961-5.
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A polymorphism in IL4 may associate with sensory neuropathy in African HIV patients. Mol Immunol. 2013 Oct; 55(3-4):197-9.