"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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2013 | 1 | 2 | 3 |
| 2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Inheritance Patterns" by people in Profiles.
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Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies. Am J Med Genet B Neuropsychiatr Genet. 2015 Jun; 168B(4):247-57.
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Maternal inheritance of an inactive type III deiodinase gene allele affects mouse pancreatic ?-cells and disrupts glucose homeostasis. Endocrinology. 2014 Aug; 155(8):3160-71.
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. 2013 Sep; 45(9):984-94.
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Principal components methods for narrow-sense heritability in the analysis of multidimensional longitudinal cognitive phenotypes. Am J Med Genet B Neuropsychiatr Genet. 2013 Oct; 162B(7):770-8.
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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles. Am J Med Genet A. 2013 Apr; 161A(4):771-8.
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Identification of genomic regions contributing to etoposide-induced cytotoxicity. Hum Genet. 2009 Mar; 125(2):173-80.
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Chiari in the family: inheritance of the Chiari I malformation. Pediatr Neurol. 2006 Jun; 34(6):481-5.
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Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene. Acta Neuropathol. 2005 Sep; 110(3):298-305.