Chromosomes, Human, Pair 18
"Chromosomes, Human, Pair 18" 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 E CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002887
|
MeSH Number(s) |
A11.284.187.520.300.415.430 G05.360.162.520.300.415.430
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 18".
- 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, 16-18 [A11.284.187.520.300.415]
- Chromosomes, Human, Pair 18 [A11.284.187.520.300.415.430]
- 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, 16-18 [G05.360.162.520.300.415]
- Chromosomes, Human, Pair 18 [G05.360.162.520.300.415.430]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 18".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 18" by people in this website by year, and whether "Chromosomes, Human, Pair 18" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 1 | 0 | 1 |
1999 | 1 | 0 | 1 |
2001 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2004 | 1 | 2 | 3 |
2010 | 1 | 0 | 1 |
2011 | 1 | 1 | 2 |
2012 | 0 | 1 | 1 |
2014 | 0 | 2 | 2 |
2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 18" by people in Profiles.
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Infants with Trisomy 18 and Complex Congenital Heart Defects Should Not Undergo Open Heart Surgery. J Law Med Ethics. 2016 06; 44(2):286-91.
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Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. PLoS Genet. 2014 Sep; 10(9):e1004606.
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Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18. Pediatrics. 2014 Feb; 133(2):226-35.
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Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: the VON charts. Am J Med Genet A. 2012 Feb; 158A(2):322-32.
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Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network. J Pediatr. 2012 May; 160(5):774-780.e11.
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A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3. Hum Mol Genet. 2011 Nov 01; 20(21):4282-9.
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A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet. 2010 Nov; 42(11):978-84.
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Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23. Arthritis Rheum. 2004 Oct; 50(10):3203-10.
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Effectiveness of cardiac surgery in trisomies 13 and 18 (from the Pediatric Cardiac Care Consortium). Am J Cardiol. 2004 Mar 15; 93(6):801-3.
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Trisomy 16 in a pigtailed macaque (M. nemestrina) with multiple anomalies and developmental delays. Am J Ment Retard. 2004 Jan; 109(1):9-20.