Chromosomes, Human, Pair 10
"Chromosomes, Human, Pair 10" 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 C CHROMOSOMES of the human chromosome classification.
MeSH Number(s)
A11.284.187.520.300.325.350
G05.360.162.520.300.325.350
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 10".
- 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, 6-12 and X [A11.284.187.520.300.325]
- Chromosomes, Human, Pair 10 [A11.284.187.520.300.325.350]
- 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, 6-12 and X [G05.360.162.520.300.325]
- Chromosomes, Human, Pair 10 [G05.360.162.520.300.325.350]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 10".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 10" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, Pair 10" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1992 | 2 | 0 | 2 |
| 1993 | 7 | 0 | 7 |
| 1994 | 1 | 1 | 2 |
| 1995 | 2 | 1 | 3 |
| 1996 | 1 | 2 | 3 |
| 1997 | 5 | 2 | 7 |
| 1998 | 4 | 4 | 8 |
| 1999 | 6 | 6 | 12 |
| 2000 | 1 | 1 | 2 |
| 2001 | 3 | 7 | 10 |
| 2002 | 1 | 2 | 3 |
| 2003 | 2 | 3 | 5 |
| 2004 | 2 | 2 | 4 |
| 2005 | 0 | 2 | 2 |
| 2006 | 4 | 4 | 8 |
| 2007 | 4 | 2 | 6 |
| 2008 | 3 | 4 | 7 |
| 2009 | 3 | 2 | 5 |
| 2010 | 4 | 7 | 11 |
| 2011 | 1 | 7 | 8 |
| 2012 | 1 | 7 | 8 |
| 2013 | 1 | 0 | 1 |
| 2014 | 0 | 2 | 2 |
| 2015 | 2 | 0 | 2 |
| 2017 | 1 | 1 | 2 |
| 2018 | 0 | 3 | 3 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
Below are the most recent publications written about "Chromosomes, Human, Pair 10" by people in Profiles.
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Not All Genes Are Created Equal in Age-Related Macular Degeneration. JAMA Ophthalmol. 2022 03 01; 140(3):260-261.
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Genome-wide enhancer maps link risk variants to disease genes. Nature. 2021 05; 593(7858):238-243.
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Detecting fitness epistasis in recently admixed populations with genome-wide data. BMC Genomics. 2020 Jul 11; 21(1):476.
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Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion. Childs Nerv Syst. 2020 07; 36(7):1367-1377.
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A novel missense mutation in TFAP2B associated with Char syndrome and central diabetes insipidus. Am J Med Genet A. 2019 07; 179(7):1299-1303.
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ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition. Am J Hum Genet. 2018 10 04; 103(4):612-620.
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Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations. Nature. 2018 07; 559(7714):350-355.
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A Hematogenous Route for Medulloblastoma Leptomeningeal Metastases. Cell. 2018 02 22; 172(5):1050-1062.e14.
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Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15. Can J Ophthalmol. 2017 12; 52(6):e203-e205.
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Specific correlation between the major chromosome 10q26 haplotype conferring risk for age-related macular degeneration and the expression of HTRA1. Mol Vis. 2017; 23:318-333.