"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 |
|---|
| 1995 | 6 | 1 | 7 |
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 2 | 3 |
| 1998 | 4 | 2 | 6 |
| 1999 | 2 | 1 | 3 |
| 2000 | 2 | 1 | 3 |
| 2001 | 7 | 5 | 12 |
| 2002 | 3 | 7 | 10 |
| 2003 | 8 | 5 | 13 |
| 2004 | 11 | 6 | 17 |
| 2005 | 4 | 5 | 9 |
| 2006 | 13 | 16 | 29 |
| 2007 | 23 | 7 | 30 |
| 2008 | 16 | 14 | 30 |
| 2009 | 9 | 14 | 23 |
| 2010 | 20 | 10 | 30 |
| 2011 | 19 | 22 | 41 |
| 2012 | 23 | 19 | 42 |
| 2013 | 16 | 24 | 40 |
| 2014 | 15 | 15 | 30 |
| 2015 | 31 | 16 | 47 |
| 2016 | 18 | 11 | 29 |
| 2017 | 14 | 18 | 32 |
| 2018 | 23 | 18 | 41 |
| 2019 | 16 | 18 | 34 |
| 2020 | 16 | 15 | 31 |
| 2021 | 13 | 19 | 32 |
| 2022 | 14 | 5 | 19 |
| 2023 | 8 | 5 | 13 |
| 2024 | 9 | 13 | 22 |
| 2025 | 0 | 6 | 6 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
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DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders. Am J Hum Genet. 2025 Feb 06; 112(2):394-413.
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Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource. Am J Hum Genet. 2025 Feb 06; 112(2):215-223.
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Small variant benchmark from a complete assembly of X and Y chromosomes. Nat Commun. 2025 Jan 08; 16(1):497.
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Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage. Clin Chem. 2025 Jan 03; 71(1):141-154.
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Characterizing features affecting local ancestry inference performance in admixed populations. Am J Hum Genet. 2025 Feb 06; 112(2):224-234.
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A reference quality, fully annotated diploid genome from a Saudi individual. Sci Data. 2024 Nov 23; 11(1):1278.
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 Nov 20; 34(11):2061-2073.
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Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps. Genome Res. 2024 Nov 20; 34(11):1785-1797.
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The "genetic test request": A genomic stewardship intervention for inpatient exome and genome orders at a tertiary pediatric hospital. Genet Med. 2025 Feb; 27(2):101330.