"Databases, Genetic" 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.
Databases devoted to knowledge about specific genes and gene products.
Descriptor ID |
D030541
|
MeSH Number(s) |
L01.313.500.750.300.188.400.325 L01.470.750.750.325
|
Concept/Terms |
Databases, Genetic- Databases, Genetic
- Database, Genetic
- Genetic Database
- Genetic Information Databases
- Database, Genetic Information
- Databases, Genetic Information
- Genetic Information Database
- Information Database, Genetic
- Information Databases, Genetic
- Genetic Databanks
- Databank, Genetic
- Databanks, Genetic
- Genetic Databank
- Genetic Databases
- Genetic Data Banks
- Bank, Genetic Data
- Banks, Genetic Data
- Data Bank, Genetic
- Data Banks, Genetic
- Genetic Data Bank
- Genetic Data Bases
- Data Base, Genetic
- Data Bases, Genetic
- Genetic Data Base
Genetic Sequence Databases- Genetic Sequence Databases
- Database, Genetic Sequence
- Databases, Genetic Sequence
- Genetic Sequence Database
- Sequence Database, Genetic
- Sequence Databases, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Databases, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Databases, Genetic".
This graph shows the total number of publications written about "Databases, Genetic" by people in this website by year, and whether "Databases, Genetic" 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 |
---|
2013 | 0 | 1 | 1 |
2014 | 1 | 1 | 2 |
2015 | 0 | 1 | 1 |
2016 | 1 | 0 | 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 "Databases, Genetic" by people in Profiles.
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A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer. J Natl Cancer Inst. 2020 10 01; 112(10):1003-1012.
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Protein-altering germline mutations implicate novel genes related to lung cancer development. Nat Commun. 2020 05 11; 11(1):2220.
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Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. PLoS Genet. 2020 03; 16(3):e1008684.
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Functional informed genome-wide interaction analysis of body mass index, diabetes and colorectal cancer risk. Cancer Med. 2020 05; 9(10):3563-3573.
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. PLoS Genet. 2019 12; 15(12):e1008500.
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LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. 2018 10 23; 138(17):1839-1849.
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Gene expression imputation identifies candidate genes and susceptibility loci associated with cutaneous squamous cell carcinoma. Nat Commun. 2018 10 15; 9(1):4264.
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Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. Nat Commun. 2018 02 08; 9(1):556.
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Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network. Clin Pharmacol Ther. 2016 08; 100(2):160-9.
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A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. Pharmacogenomics J. 2016 06; 16(3):231-7.