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.
MeSH Number(s)
A11.284.187.520.300.505.515
G05.360.162.520.300.505.515
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 Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, Pair 22" 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 |
|---|
| 1994 | 3 | 1 | 4 |
| 1995 | 6 | 6 | 12 |
| 1996 | 9 | 4 | 13 |
| 1997 | 9 | 3 | 12 |
| 1998 | 5 | 2 | 7 |
| 1999 | 5 | 4 | 9 |
| 2000 | 6 | 4 | 10 |
| 2001 | 3 | 2 | 5 |
| 2002 | 1 | 2 | 3 |
| 2003 | 2 | 3 | 5 |
| 2004 | 6 | 3 | 9 |
| 2005 | 9 | 7 | 16 |
| 2006 | 5 | 2 | 7 |
| 2007 | 3 | 4 | 7 |
| 2008 | 5 | 8 | 13 |
| 2009 | 3 | 3 | 6 |
| 2010 | 4 | 1 | 5 |
| 2011 | 5 | 2 | 7 |
| 2012 | 1 | 2 | 3 |
| 2013 | 1 | 7 | 8 |
| 2014 | 2 | 5 | 7 |
| 2015 | 0 | 2 | 2 |
| 2016 | 0 | 5 | 5 |
| 2017 | 0 | 8 | 8 |
| 2018 | 0 | 2 | 2 |
| 2019 | 0 | 2 | 2 |
| 2020 | 0 | 2 | 2 |
| 2021 | 0 | 3 | 3 |
| 2022 | 0 | 3 | 3 |
| 2023 | 0 | 2 | 2 |
Below are the most recent publications written about "Chromosomes, Human, Pair 22" by people in Profiles.
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Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage. Gene. 2023 Dec 15; 887:147737.
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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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Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium. Hum Mol Genet. 2022 02 21; 31(4):625-637.
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Zinc deficiency and supplementation in autism spectrum disorder and Phelan-McDermid syndrome. J Neurosci Res. 2022 Apr; 100(4):970-978.
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A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome. Mol Autism. 2022 01 29; 13(1):6.
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Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome. J Neurodev Disord. 2021 11 05; 13(1):53.
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Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome. PLoS One. 2021; 16(7):e0253859.
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Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome. Mol Autism. 2021 04 28; 12(1):29.
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Psychometric Study of the Social Responsiveness Scale in Phelan-McDermid Syndrome. Autism Res. 2020 08; 13(8):1383-1396.
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Neural and behavioral measures suggest that cognitive and affective functioning interactions mediate risk for psychosis-proneness symptoms in youth with chromosome 22q11.2 deletion syndrome. Am J Med Genet A. 2020 07; 182(7):1615-1630.