"Genomics" 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 systematic study of the complete DNA sequences (GENOME) of organisms.
| Descriptor ID |
D023281
|
| MeSH Number(s) |
H01.158.273.180.350 H01.158.273.343.350
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Genomics".
Below are MeSH descriptors whose meaning is more specific than "Genomics".
This graph shows the total number of publications written about "Genomics" by people in this website by year, and whether "Genomics" 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 |
|---|
| 2003 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2012 | 1 | 3 | 4 |
| 2013 | 1 | 0 | 1 |
| 2014 | 3 | 0 | 3 |
| 2015 | 1 | 4 | 5 |
| 2016 | 2 | 1 | 3 |
| 2017 | 3 | 0 | 3 |
| 2018 | 2 | 0 | 2 |
| 2019 | 2 | 0 | 2 |
| 2020 | 4 | 3 | 7 |
| 2021 | 1 | 1 | 2 |
| 2022 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Genomics" by people in Profiles.
-
Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans. Transl Vis Sci Technol. 2024 Sep 03; 13(9):4.
-
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network. Sci Rep. 2023 Feb 03; 13(1):1971.
-
Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts. Perm J. 2022 06 29; 26(2):28-39.
-
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nat Commun. 2022 Jun 14; 13(1):3428.
-
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions. BMC Med Inform Decis Mak. 2022 01 28; 22(1):23.
-
Neptune: an environment for the delivery of genomic medicine. Genet Med. 2021 10; 23(10):1838-1846.
-
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Nat Genet. 2021 07; 53(7):962-971.
-
Preferences of biobank participants for receiving actionable genomic test results: results of a recontacting study. Genet Med. 2021 06; 23(6):1163-1166.
-
Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model. Patient Educ Couns. 2021 05; 104(5):969-978.
-
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility. Cancer Res. 2021 04 01; 81(7):1695-1703.