"Genome, Human" 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 complete genetic complement contained in the DNA of a set of CHROMOSOMES in a HUMAN. The length of the human genome is about 3 billion base pairs.
| Descriptor ID |
D015894
|
| MeSH Number(s) |
G05.360.340.350
|
| Concept/Terms |
Genome, Human- Genome, Human
- Human Genome
- Genomes, Human
- Human Genomes
|
Below are MeSH descriptors whose meaning is more general than "Genome, Human".
Below are MeSH descriptors whose meaning is more specific than "Genome, Human".
This graph shows the total number of publications written about "Genome, Human" by people in this website by year, and whether "Genome, Human" 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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 2 | 2 | 4 |
| 1998 | 4 | 2 | 6 |
| 1999 | 2 | 1 | 3 |
| 2000 | 2 | 1 | 3 |
| 2001 | 7 | 5 | 12 |
| 2002 | 3 | 7 | 10 |
| 2003 | 9 | 6 | 15 |
| 2004 | 12 | 7 | 19 |
| 2005 | 3 | 5 | 8 |
| 2006 | 13 | 15 | 28 |
| 2007 | 24 | 6 | 30 |
| 2008 | 14 | 15 | 29 |
| 2009 | 8 | 14 | 22 |
| 2010 | 21 | 11 | 32 |
| 2011 | 20 | 24 | 44 |
| 2012 | 24 | 21 | 45 |
| 2013 | 14 | 24 | 38 |
| 2014 | 16 | 15 | 31 |
| 2015 | 32 | 17 | 49 |
| 2016 | 19 | 13 | 32 |
| 2017 | 14 | 17 | 31 |
| 2018 | 23 | 19 | 42 |
| 2019 | 18 | 17 | 35 |
| 2020 | 16 | 16 | 32 |
| 2021 | 15 | 22 | 37 |
| 2022 | 14 | 5 | 19 |
| 2023 | 8 | 5 | 13 |
| 2024 | 13 | 14 | 27 |
| 2025 | 11 | 12 | 23 |
| 2026 | 7 | 6 | 13 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Polymorphic CGG repeats in gene regulation and disease. Am J Hum Genet. 2026 Jun 04; 113(6):1131-1158.
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MARRVEL-MCP: An agentic interface for Mendelian disease discovery via tool-augmented context engineering. Am J Hum Genet. 2026 Jun 04; 113(6):1194-1213.
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ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
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VISDB 2.0: A manually curated resource of viral integration sites and their regulatory maps in human diseases. Sci Data. 2026 Mar 17; 13(1).
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Specification of frequency criteria for secondary findings genes to improve variant classification concordance. Genet Med. 2026 May; 28(5):102552.
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications. Genome Res. 2026 Mar 02; 36(3):460-471.
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Comparison of variant callers using 60?532 multi-ancestry whole genome sequences. Brief Bioinform. 2026 Mar 01; 27(2).
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Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes. Nature. 2026 04; 652(8110):675-685.
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Expression spectrum of TE-driven transcripts in human adult tissues. Genome Biol. 2026 Jan 27; 27(1).
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Using the linear references from the pangenome to discover missing autism variants. Nat Commun. 2026 Jan 23; 17(1):1681.