"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 |
|---|
| 1993 | 1 | 2 | 3 |
| 1995 | 1 | 1 | 2 |
| 1996 | 0 | 1 | 1 |
| 1997 | 1 | 3 | 4 |
| 1998 | 1 | 3 | 4 |
| 1999 | 1 | 1 | 2 |
| 2000 | 1 | 4 | 5 |
| 2001 | 0 | 7 | 7 |
| 2002 | 8 | 4 | 12 |
| 2003 | 16 | 2 | 18 |
| 2004 | 13 | 5 | 18 |
| 2005 | 8 | 7 | 15 |
| 2006 | 14 | 7 | 21 |
| 2007 | 19 | 11 | 30 |
| 2008 | 22 | 16 | 38 |
| 2009 | 17 | 17 | 34 |
| 2010 | 11 | 19 | 30 |
| 2011 | 18 | 15 | 33 |
| 2012 | 15 | 18 | 33 |
| 2013 | 16 | 10 | 26 |
| 2014 | 17 | 12 | 29 |
| 2015 | 15 | 11 | 26 |
| 2016 | 10 | 7 | 17 |
| 2017 | 10 | 10 | 20 |
| 2018 | 19 | 10 | 29 |
| 2019 | 4 | 12 | 16 |
| 2020 | 9 | 5 | 14 |
| 2021 | 6 | 7 | 13 |
| 2022 | 2 | 2 | 4 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Res. 2023 01 06; 51(D1):D1300-D1311.
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The sequences of 150,119 genomes in the UK Biobank. Nature. 2022 07; 607(7920):732-740.
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Acute lymphoblastic leukemia displays a distinct highly methylated genome. Nat Cancer. 2022 06; 3(6):768-782.
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Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types. Elife. 2022 02 10; 11.
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A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias. Genet Med. 2022 04; 24(4):931-954.
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Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods. Hum Mutat. 2022 08; 43(8):1097-1113.
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Benchmarking sequencing methods and tools that facilitate the study of alternative polyadenylation. Genome Biol. 2021 10 14; 22(1):291.
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A signature of Neanderthal introgression on molecular mechanisms of environmental responses. PLoS Genet. 2021 09; 17(9):e1009493.
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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Am J Hum Genet. 2021 10 07; 108(10):1836-1851.
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Parental relatedness through time revealed by runs of homozygosity in ancient DNA. Nat Commun. 2021 09 14; 12(1):5425.