Chromosomes, Human, Pair 22
"Chromosomes, Human, Pair 22" 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 G CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002892
|
MeSH Number(s) |
A11.284.187.520.300.505.515 G05.360.162.520.300.505.515
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 22".
- 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, 21-22 and Y [A11.284.187.520.300.505]
- Chromosomes, Human, Pair 22 [A11.284.187.520.300.505.515]
- 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, 21-22 and Y [G05.360.162.520.300.505]
- Chromosomes, Human, Pair 22 [G05.360.162.520.300.505.515]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 22".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 22" by people in this website by year, and whether "Chromosomes, Human, Pair 22" 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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1994 | 2 | 0 | 2 |
1995 | 2 | 2 | 4 |
1996 | 0 | 2 | 2 |
1997 | 1 | 0 | 1 |
1998 | 1 | 0 | 1 |
1999 | 3 | 3 | 6 |
2000 | 6 | 3 | 9 |
2001 | 2 | 2 | 4 |
2002 | 1 | 3 | 4 |
2003 | 1 | 4 | 5 |
2004 | 0 | 1 | 1 |
2005 | 2 | 2 | 4 |
2006 | 1 | 1 | 2 |
2007 | 2 | 1 | 3 |
2008 | 5 | 2 | 7 |
2009 | 1 | 1 | 2 |
2010 | 3 | 2 | 5 |
2011 | 0 | 6 | 6 |
2012 | 1 | 3 | 4 |
2013 | 2 | 4 | 6 |
2014 | 1 | 0 | 1 |
2015 | 0 | 4 | 4 |
2016 | 0 | 1 | 1 |
2017 | 3 | 2 | 5 |
2018 | 0 | 2 | 2 |
2020 | 0 | 2 | 2 |
2021 | 1 | 0 | 1 |
2023 | 0 | 1 | 1 |
2024 | 2 | 1 | 3 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 22" by people in Profiles.
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Optical Genome Mapping for Detection of BCR::ABL1-Another Tool in Our Toolbox. Genes (Basel). 2024 Oct 22; 15(11).
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Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome. J Neurodev Disord. 2024 May 10; 16(1):25.
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Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science. 2024 05 03; 384(6695):584-590.
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Updated consensus guidelines on the management of Phelan-McDermid syndrome. Am J Med Genet A. 2023 08; 191(8):2015-2044.
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Translational pediatrics: clinical perspective for Phelan-McDermid syndrome and autism research. Pediatr Res. 2022 08; 92(2):373-377.
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Two Cases of Possible Familial Chronic Myeloid Leukemia in a Family with Extensive History of Cancer. Acta Haematol. 2021; 144(5):585-590.
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Chronic myeloid leukemia: 2020 update on diagnosis, therapy and monitoring. Am J Hematol. 2020 06; 95(6):691-709.
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Access to Multidisciplinary Care for Patients With 22q11.2 Deletion Syndrome: Identifying Breakdowns in the Screening Process. J Craniofac Surg. 2020 Mar/Apr; 31(2):428-431.
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Utility of copy number variants in the classification of intracranial ependymoma. Cancer Genet. 2020 01; 240:66-72.
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Heterozygous WNT1 variant causing a variable bone phenotype. Am J Med Genet A. 2018 11; 176(11):2419-2424.