"Inheritance Patterns" 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 different ways GENES and their ALLELES interact during the transmission of genetic traits that effect the outcome of GENE EXPRESSION.
| Descriptor ID |
D040582
|
| MeSH Number(s) |
G05.420
|
| Concept/Terms |
Inheritance Patterns- Inheritance Patterns
- Inheritance Pattern
- Pattern, Inheritance
- Patterns, Inheritance
|
Below are MeSH descriptors whose meaning is more general than "Inheritance Patterns".
Below are MeSH descriptors whose meaning is more specific than "Inheritance Patterns".
This graph shows the total number of publications written about "Inheritance Patterns" by people in this website by year, and whether "Inheritance Patterns" 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 |
|---|
| 2005 | 3 | 1 | 4 |
| 2008 | 1 | 2 | 3 |
| 2009 | 1 | 5 | 6 |
| 2010 | 0 | 3 | 3 |
| 2012 | 2 | 2 | 4 |
| 2013 | 1 | 2 | 3 |
| 2014 | 3 | 1 | 4 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 2 | 3 |
| 2018 | 1 | 3 | 4 |
| 2019 | 5 | 3 | 8 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 1 | 2 |
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Below are the most recent publications written about "Inheritance Patterns" by people in Profiles.
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Stochastic models of Mendelian and reverse transcriptional inheritance in state-structured cancer populations. Sci Rep. 2022 07 29; 12(1):13079.
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021 04 19; 13(1):63.
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Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach. PLoS Genet. 2021 03; 17(3):e1009413.
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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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Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblings. Exp Mol Pathol. 2020 08; 115:104471.
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Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings. Genomics. 2020 09; 112(5):2937-2941.
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Evaluation of liver failure in a pediatric transplant recipient of a liver allograft with inherited chromosomally integrated HHV-6B. J Med Virol. 2020 02; 92(2):241-250.
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TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease. Hum Mutat. 2020 01; 41(1):182-195.
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Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations. Hum Genet. 2019 Oct; 138(10):1155-1169.
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Heritability analysis of nontraditional glycemic biomarkers in the Atherosclerosis Risk in Communities Study. Genet Epidemiol. 2019 10; 43(7):776-785.