"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 |
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1995 | 0 | 1 | 1 |
1998 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2002 | 1 | 0 | 1 |
2003 | 0 | 1 | 1 |
2004 | 0 | 3 | 3 |
2005 | 1 | 2 | 3 |
2006 | 2 | 0 | 2 |
2007 | 3 | 1 | 4 |
2008 | 2 | 4 | 6 |
2009 | 2 | 2 | 4 |
2010 | 4 | 0 | 4 |
2011 | 1 | 3 | 4 |
2012 | 3 | 5 | 8 |
2013 | 0 | 4 | 4 |
2014 | 3 | 3 | 6 |
2015 | 0 | 8 | 8 |
2016 | 3 | 5 | 8 |
2017 | 0 | 3 | 3 |
2018 | 4 | 3 | 7 |
2019 | 1 | 1 | 2 |
2020 | 1 | 2 | 3 |
2021 | 0 | 6 | 6 |
2022 | 0 | 2 | 2 |
2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Secondary structure of the human mitochondrial genome affects formation of deletions. BMC Biol. 2023 05 08; 21(1):103.
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CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online. Bioinformatics. 2023 05 04; 39(5).
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The Anglo-Saxon migration and the formation of the early English gene pool. Nature. 2022 10; 610(7930):112-119.
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DNA methylation changes associated with cannabis use and verbal learning performance in adolescents: an exploratory whole genome methylation study. Transl Psychiatry. 2022 08 06; 12(1):317.
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Biallelic variants in YRDC cause a developmental disorder with progeroid features. Hum Genet. 2021 Dec; 140(12):1679-1693.
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The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
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New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing. Am J Med Genet A. 2021 10; 185(10):3053-3056.
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nat Genet. 2021 06; 53(6):817-829.
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Integrative genomic analysis of pediatric T-cell lymphoblastic lymphoma reveals candidates of clinical significance. Blood. 2021 04 29; 137(17):2347-2359.
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Genome-wide study of a Neolithic Wartberg grave community reveals distinct HLA variation and hunter-gatherer ancestry. Commun Biol. 2021 01 25; 4(1):113.