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
|
| MeSH Number(s) |
E05.393.385
|
| 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
|
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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 0 | 1 | 1 |
| 2009 | 2 | 2 | 4 |
| 2010 | 5 | 9 | 14 |
| 2011 | 6 | 14 | 20 |
| 2012 | 3 | 16 | 19 |
| 2013 | 11 | 9 | 20 |
| 2014 | 2 | 14 | 16 |
| 2015 | 6 | 18 | 24 |
| 2016 | 10 | 17 | 27 |
| 2017 | 6 | 5 | 11 |
| 2018 | 5 | 9 | 14 |
| 2019 | 9 | 12 | 21 |
| 2020 | 3 | 13 | 16 |
| 2021 | 5 | 8 | 13 |
| 2022 | 1 | 0 | 1 |
| 2023 | 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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BRASS: Permutation methods for binary traits in genetic association studies with structured samples. PLoS Genet. 2023 Nov; 19(11):e1011020.
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Gene-based association study of rare variants in children of diverse ancestries implicates TNFRSF21 in the development of allergic asthma. J Allergy Clin Immunol. 2024 Mar; 153(3):809-820.
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Protein prediction for trait mapping in diverse populations. PLoS One. 2022; 17(2):e0264341.
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Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes. Genes (Basel). 2021 10 22; 12(11).
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A cross-population atlas of genetic associations for 220 human phenotypes. Nat Genet. 2021 10; 53(10):1415-1424.
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Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. Eur J Paediatr Neurol. 2021 Nov; 35:27-34.
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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Genome Med. 2021 08 26; 13(1):136.
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Expanding the KIF4A-associated phenotype. Am J Med Genet A. 2021 12; 185(12):3728-3739.
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Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics data. Neurobiol Aging. 2021 12; 108:207-209.
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High-resolution HLA allele and haplotype frequencies in several unrelated populations determined by next generation sequencing: 17th International HLA and Immunogenetics Workshop joint report. Hum Immunol. 2021 Jul; 82(7):505-522.