"Anticipation, Genetic" 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 apparent tendency of certain diseases to appear at earlier AGE OF ONSET and with increasing severity in successive generations. (Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed)
| Descriptor ID |
D020132
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| MeSH Number(s) |
C23.550.291.687.500.500 G05.420.040
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Anticipation, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Anticipation, Genetic".
This graph shows the total number of publications written about "Anticipation, Genetic" by people in this website by year, and whether "Anticipation, Genetic" was a major or minor topic of these publications.
Below are the most recent publications written about "Anticipation, Genetic" by people in Profiles.
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Ascertainment bias causes false signal of anticipation in genetic prion disease. Am J Hum Genet. 2014 Oct 02; 95(4):371-82.
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Relationship of neuroticism and laboratory pain in healthy children: does anxiety sensitivity play a role? Pain. 2013 Jan; 154(1):103-109.
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Bayesian modeling for genetic anticipation in presence of mutational heterogeneity: a case study in Lynch syndrome. Biometrics. 2011 Dec; 67(4):1627-37.
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A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome. Genet Epidemiol. 2010 Nov; 34(7):756-68.
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Fahr's disease - a model of neuropsychiatric illness with cognitive and psychotic symptoms. Acta Psychiatr Scand. 2010 Jan; 121(1):78.
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Anticipation in lynch syndrome: still waiting for the answer. J Clin Oncol. 2009 Jan 20; 27(3):326-7.
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SCA2 may present as levodopa-responsive parkinsonism. Mov Disord. 2003 Apr; 18(4):425-9.
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Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet. 1999 Sep; 65(3):764-72.
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The mutation properties of spinal and bulbar muscular atrophy disease alleles. Neurogenetics. 1998 Aug; 1(4):249-52.