"Meta-Analysis as Topic" 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.
A quantitative method of combining the results of independent studies (usually drawn from the published literature) and synthesizing summaries and conclusions which may be used to evaluate therapeutic effectiveness, plan new studies, etc., with application chiefly in the areas of research and medicine.
| Descriptor ID |
D015201
|
| MeSH Number(s) |
E05.318.780.500 E05.581.500.501 N05.715.360.780.515 N06.850.520.445.500
|
| Concept/Terms |
Meta-Analysis as Topic- Meta-Analysis as Topic
- Meta Analysis as Topic
- Data Pooling
- Data Poolings
- Overviews, Clinical Trial
- Clinical Trial Overviews
- Clinical Trial Overview
- Overview, Clinical Trial
|
Below are MeSH descriptors whose meaning is more general than "Meta-Analysis as Topic".
Below are MeSH descriptors whose meaning is more specific than "Meta-Analysis as Topic".
This graph shows the total number of publications written about "Meta-Analysis as Topic" by people in this website by year, and whether "Meta-Analysis as Topic" 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 |
| 2010 | 0 | 3 | 3 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 3 | 3 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 3 | 3 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 2 | 2 |
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click here.
Below are the most recent publications written about "Meta-Analysis as Topic" by people in Profiles.
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Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits. Nat Commun. 2020 11 03; 11(1):5562.
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Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study. Nutrients. 2020 Jul 28; 12(8).
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Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Mutagenesis. 2019 12 19; 34(4):323-330.
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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat Genet. 2018 11; 50(11):1505-1513.
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Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat Genet. 2017 May; 49(5):789-794.
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Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015 Sep; 56(9):e129-33.
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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor. Hum Mol Genet. 2015 Sep 15; 24(18):5345-55.
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nat Genet. 2015 Apr; 47(4):373-80.
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A genome-wide association study of anorexia nervosa. Mol Psychiatry. 2014 Oct; 19(10):1085-94.
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Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet. 2014 May; 22(5):675-80.
MeSH information
