Quantitative Trait, Heritable
"Quantitative Trait, Heritable" 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.
A characteristic showing quantitative inheritance such as SKIN PIGMENTATION in humans. (From A Dictionary of Genetics, 4th ed)
| Descriptor ID |
D019655
|
| MeSH Number(s) |
G05.420.720
|
| Concept/Terms |
Quantitative Trait, Heritable- Quantitative Trait, Heritable
- Heritable Quantitative Trait
- Heritable Quantitative Traits
- Quantitative Traits, Heritable
- Trait, Heritable Quantitative
- Traits, Heritable Quantitative
|
Below are MeSH descriptors whose meaning is more general than "Quantitative Trait, Heritable".
Below are MeSH descriptors whose meaning is more specific than "Quantitative Trait, Heritable".
This graph shows the total number of publications written about "Quantitative Trait, Heritable" by people in this website by year, and whether "Quantitative Trait, Heritable" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 3 | 1 | 4 |
| 1998 | 1 | 1 | 2 |
| 1999 | 3 | 0 | 3 |
| 2000 | 0 | 1 | 1 |
| 2001 | 3 | 5 | 8 |
| 2002 | 3 | 3 | 6 |
| 2003 | 3 | 0 | 3 |
| 2004 | 3 | 1 | 4 |
| 2005 | 1 | 1 | 2 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 2 | 3 |
| 2008 | 0 | 2 | 2 |
| 2009 | 0 | 2 | 2 |
| 2010 | 1 | 5 | 6 |
| 2011 | 1 | 3 | 4 |
| 2012 | 2 | 4 | 6 |
| 2013 | 6 | 0 | 6 |
| 2014 | 2 | 3 | 5 |
| 2016 | 2 | 2 | 4 |
| 2017 | 4 | 0 | 4 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 1 | 2 | 3 |
| 2021 | 3 | 2 | 5 |
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Below are the most recent publications written about "Quantitative Trait, Heritable" by people in Profiles.
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Distinct effect of prenatal and postnatal brain expression across 20 brain disorders and anthropometric social traits: a systematic study of spatiotemporal modularity. Brief Bioinform. 2021 11 05; 22(6).
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Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments. Nat Genet. 2021 09; 53(9):1322-1333.
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The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
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CSEA-DB: an omnibus for human complex trait and cell type associations. Nucleic Acids Res. 2021 01 08; 49(D1):D862-D870.
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Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. EBioMedicine. 2021 Jan; 63:103157.
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Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits. Nat Commun. 2020 11 03; 11(1):5562.
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A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. Am J Hum Genet. 2020 11 05; 107(5):849-863.
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Efficient gene-environment interaction tests for large biobank-scale sequencing studies. Genet Epidemiol. 2020 11; 44(8):908-923.
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TSEA-DB: a trait-tissue association map for human complex traits and diseases. Nucleic Acids Res. 2020 01 08; 48(D1):D1022-D1030.
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome. Hum Mutat. 2020 01; 41(1):150-168.