"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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3D genome topology distinguishes molecular subgroups of medulloblastoma. Am J Hum Genet. 2024 12 05; 111(12):2720-2734.
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The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation. Genet Med. 2025 Jan; 27(1):101228.
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TULIPs decorate the three-dimensional genome of PFA ependymoma. Cell. 2024 Sep 05; 187(18):4926-4945.e22.
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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 06; 26(6):101115.
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Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proc Natl Acad Sci U S A. 2021 12 21; 118(51).
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Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Res. 2021 06 15; 81(12):3162-3173.
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High-depth African genomes inform human migration and health. Nature. 2020 10; 586(7831):741-748.
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Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects. Hum Genet. 2020 Oct; 139(10):1299-1314.
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De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population. Proc Natl Acad Sci U S A. 2020 02 04; 117(5):2560-2569.
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Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease. Nat Commun. 2019 09 19; 10(1):4267.