"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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1994 | 0 | 4 | 4 |
1995 | 7 | 1 | 8 |
1996 | 1 | 4 | 5 |
1997 | 2 | 2 | 4 |
1998 | 5 | 1 | 6 |
1999 | 4 | 2 | 6 |
2000 | 2 | 2 | 4 |
2001 | 14 | 8 | 22 |
2002 | 7 | 8 | 15 |
2003 | 13 | 7 | 20 |
2004 | 17 | 10 | 27 |
2005 | 11 | 11 | 22 |
2006 | 18 | 23 | 41 |
2007 | 28 | 16 | 44 |
2008 | 29 | 29 | 58 |
2009 | 17 | 26 | 43 |
2010 | 32 | 22 | 54 |
2011 | 25 | 33 | 58 |
2012 | 41 | 29 | 70 |
2013 | 24 | 41 | 65 |
2014 | 23 | 24 | 47 |
2015 | 36 | 25 | 61 |
2016 | 24 | 22 | 46 |
2017 | 17 | 26 | 43 |
2018 | 27 | 27 | 54 |
2019 | 23 | 22 | 45 |
2020 | 21 | 23 | 44 |
2021 | 18 | 25 | 43 |
2022 | 16 | 6 | 22 |
2023 | 9 | 6 | 15 |
2024 | 4 | 3 | 7 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Unveiling novel genetic variants in 370 challenging medically relevant genes using the long read sequencing data of 41 samples from 19 global populations. Mol Genet Genomics. 2024 Jul 07; 299(1):65.
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MethPhaser: methylation-based long-read haplotype phasing of human genomes. Nat Commun. 2024 Jun 22; 15(1):5327.
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Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder loci. Cell Genom. 2024 Jul 10; 4(7):100590.
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Genome-wide DNA methylation changes in human spermatogenesis. Am J Hum Genet. 2024 06 06; 111(6):1125-1139.
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Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project. Hum Genomics. 2024 Apr 29; 18(1):44.
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Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Med Genomics. 2024 Apr 16; 17(1):85.
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Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis. Genet Med. 2024 Jun; 26(6):101115.
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Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. Nat Genet. 2023 Nov; 55(11):1912-1919.
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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation. Nat Methods. 2023 10; 20(10):1483-1492.
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Structural underpinnings of mutation rate variations in the human genome. Nucleic Acids Res. 2023 08 11; 51(14):7184-7197.