"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 | 3 | 5 |
| 2013 | 1 | 2 | 3 |
| 2014 | 3 | 1 | 4 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 2 | 2 |
| 2017 | 0 | 2 | 2 |
| 2018 | 2 | 4 | 6 |
| 2019 | 5 | 3 | 8 |
| 2020 | 0 | 1 | 1 |
| 2021 | 2 | 1 | 3 |
| 2023 | 0 | 1 | 1 |
| 2026 | 1 | 0 | 1 |
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Below are the most recent publications written about "Inheritance Patterns" by people in Profiles.
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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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TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. Genet Med. 2019 07; 21(7):1548-1558.
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Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder. Genome Med. 2018 09 28; 10(1):74.
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De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder. Am J Hum Genet. 2018 06 07; 102(6):1195-1203.
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A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell. 2014 Sep 25; 159(1):200-214.
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No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles. Prenat Diagn. 2013 Dec; 33(13):1242-7.
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Propagation of obesity across generations: the roles of differential realized fertility and assortative mating by body mass index. Hum Hered. 2013; 75(2-4):204-12.
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Maximum-likelihood estimation of recent shared ancestry (ERSA). Genome Res. 2011 May; 21(5):768-74.