"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 | 13 | 26 |
| 2007 | 24 | 6 | 30 |
| 2008 | 14 | 15 | 29 |
| 2009 | 8 | 14 | 22 |
| 2010 | 20 | 11 | 31 |
| 2011 | 20 | 23 | 43 |
| 2012 | 24 | 21 | 45 |
| 2013 | 14 | 24 | 38 |
| 2014 | 16 | 15 | 31 |
| 2015 | 29 | 17 | 46 |
| 2016 | 18 | 13 | 31 |
| 2017 | 14 | 17 | 31 |
| 2018 | 23 | 19 | 42 |
| 2019 | 18 | 17 | 35 |
| 2020 | 16 | 14 | 30 |
| 2021 | 14 | 21 | 35 |
| 2022 | 14 | 5 | 19 |
| 2023 | 8 | 5 | 13 |
| 2024 | 13 | 14 | 27 |
| 2025 | 11 | 12 | 23 |
| 2026 | 11 | 9 | 20 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Charting the silent variation within us. Cell. 2026 Oct 15; 189(21):6589-6593.
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Curating the Fetal Genome: Experience of the ClinGen Prenatal Gene Curation Expert Panel (GCEP). Prenat Diagn. 2026 Oct; 46(11):1703-1710.
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Mapping long-read sequences to a complete reference genome reveals uncaptured variants across the ?-Globin cluster in Africans with sickle cell disease. HGG Adv. 2026 Oct 08; 7(4):100669.
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Human nuclear ribomes reveal DNA-embedded ribonucleotides as epigenetic modulators of transcription-associated DNA supercoiling. Cell. 2026 Oct 15; 189(21):6648-6665.e11.
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A complete diploid human genome benchmark for personalized genomics. Cell. 2026 Aug 06; 189(16):4857-4875.e31.
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Multi-genome benchmark for simple and complex genome inversion detection. Genome Biol. 2026 Aug 01; 27(1).
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Harmonizing standards and resources for the medical genome. Nature. 2026 Jul; 655(8121):47-58.
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Structural variant calling using Sniffles2. Nat Protoc. 2026 Oct; 21(10):4926-4938.
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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.