"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 |
|---|
| 2015 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
| 2024 | 1 | 2 | 3 |
| 2025 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Databases, Genetic" by people in Profiles.
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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants. Am J Hum Genet. 2025 Oct 02; 112(10):2266-2280.
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Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS. Am J Hum Genet. 2024 Nov 07; 111(11):2427-2443.
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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants. Am J Hum Genet. 2024 Nov 07; 111(11):2411-2426.
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Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel. Am J Hum Genet. 2024 Sep 05; 111(9):2044-2058.
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Comparison of critical biomarkers in 2 erectile dysfunction models based on GEO and NOS-cGMP-PDE5 pathway. Medicine (Baltimore). 2021 Oct 15; 100(41):e27508.
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet Neurol. 2019 12; 18(12):1091-1102.
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A Portal to Visualize Transcriptome Profiles in Mouse Models of Neurological Disorders. Genes (Basel). 2019 09 26; 10(10).
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Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and a-synuclein mechanisms. Mov Disord. 2019 06; 34(6):866-875.
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Gene-specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel. Hum Mutat. 2018 11; 39(11):1581-1592.
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Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar. Genet Med. 2017 10; 19(10):1096-1104.