Chromosomes, Human, Pair 15
"Chromosomes, Human, Pair 15" 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 specific pair of GROUP D CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002884
|
| MeSH Number(s) |
A11.284.187.520.300.370.385 G05.360.162.520.300.370.385
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 15".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 13-15 [A11.284.187.520.300.370]
- Chromosomes, Human, Pair 15 [A11.284.187.520.300.370.385]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 13-15 [G05.360.162.520.300.370]
- Chromosomes, Human, Pair 15 [G05.360.162.520.300.370.385]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 15".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 15" by people in this website by year, and whether "Chromosomes, Human, Pair 15" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2014 | 0 | 2 | 2 |
| 2016 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Chromosomes, Human, Pair 15" by people in Profiles.
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. JAMA Psychiatry. 2020 04 01; 77(4):420-430.
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Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene. PLoS Genet. 2016 Mar; 12(3):e1005914.
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16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet. 2014 Nov 15; 23(22):6069-80.
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Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):493-8.
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'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate. Bioinformatics. 2012 Dec 01; 28(23):3027-33.
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Nonsense mutations in AAGAB cause punctate palmoplantar keratoderma type Buschke-Fischer-Brauer. Am J Hum Genet. 2012 Oct 05; 91(4):754-9.
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Parental origin and functional relevance of a de novo UBE3A variant. Eur J Med Genet. 2011 Jan-Feb; 54(1):19-24.
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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet. 2009 Feb; 41(2):160-2.
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A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome. Eur J Hum Genet. 2009 May; 17(5):582-90.
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Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura. Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 05; 147B(1):37-41.
MeSH information
