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.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 1 | 2 |
1996 | 1 | 0 | 1 |
1997 | 3 | 1 | 4 |
1998 | 1 | 0 | 1 |
1999 | 0 | 2 | 2 |
2000 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2004 | 0 | 1 | 1 |
2005 | 2 | 1 | 3 |
2006 | 4 | 0 | 4 |
2007 | 2 | 0 | 2 |
2008 | 6 | 1 | 7 |
2009 | 5 | 2 | 7 |
2010 | 10 | 2 | 12 |
2011 | 6 | 3 | 9 |
2012 | 6 | 1 | 7 |
2013 | 1 | 1 | 2 |
2014 | 1 | 2 | 3 |
2015 | 2 | 0 | 2 |
2016 | 2 | 4 | 6 |
2017 | 0 | 2 | 2 |
2018 | 2 | 2 | 4 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 15" by people in Profiles.
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Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis. J Hum Genet. 2019 Mar; 64(3):253-255.
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Genome-wide association study of familial lung cancer. Carcinogenesis. 2018 09 21; 39(9):1135-1140.
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Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nat Commun. 2018 08 13; 9(1):3221.
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Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. Am J Hum Genet. 2018 02 01; 102(2):296-308.
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Functional Consequences of CHRNA7 Copy-Number Alterations in Induced Pluripotent Stem Cells and Neural Progenitor Cells. Am J Hum Genet. 2017 Dec 07; 101(6):874-887.
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Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins. Am J Med Genet A. 2017 Sep; 173(9):2451-2455.
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome. Am J Hum Genet. 2016 09 01; 99(3):555-566.
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The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genet Med. 2017 01; 19(1):45-52.
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Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung Cancer. 2016 08; 98:33-42.
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Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome. J Autism Dev Disord. 2016 Apr; 46(4):1455-63.