"Trisomy" 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.
The possession of a third chromosome of any one type in an otherwise diploid cell.
| Descriptor ID |
D014314
|
| MeSH Number(s) |
C23.550.210.050.750 C23.550.210.182.500 G05.365.590.175.050.750 G05.365.590.175.183.500 G05.700.131.750
|
| Concept/Terms |
Trisomy- Trisomy
- Trisomies
- Chromosomal Triplication
- Chromosomal Triplications
Partial Trisomy- Partial Trisomy
- Partial Trisomies
- Trisomies, Partial
- Trisomy, Partial
|
Below are MeSH descriptors whose meaning is more general than "Trisomy".
Below are MeSH descriptors whose meaning is more specific than "Trisomy".
This graph shows the total number of publications written about "Trisomy" by people in this website by year, and whether "Trisomy" 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 |
|---|
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Trisomy" by people in Profiles.
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Siegelmann R, Siegelmann HT. Meta-Analytic Operation of Threshold-independent Filtering (MOTiF) reveals sub-threshold genomic robustness in trisomy: The J?rmungandr Effect. Biochem Biophys Res Commun. 2024 Dec 10; 737:150802.
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Gupta K, Czerminski JT, Lawrence JB. Trisomy silencing by XIST: translational prospects and challenges. Hum Genet. 2024 Jul; 143(7):843-855.
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Torres EM. Consequences of gaining an extra chromosome. Chromosome Res. 2023 08 25; 31(3):24.
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Moon JE, Lawrence JB. Chromosome silencing in?vitro reveals trisomy 21 causes cell-autonomous deficits in angiogenesis and early dysregulation in Notch signaling. Cell Rep. 2022 08 09; 40(6):111174.
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Hwang S, Cavaliere P, Li R, Zhu LJ, Dephoure N, Torres EM. Consequences of aneuploidy in human fibroblasts with trisomy 21. Proc Natl Acad Sci U S A. 2021 02 09; 118(6).
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Chiang JC, Jiang J, Newburger PE, Lawrence JB. Trisomy silencing by XIST normalizes Down syndrome cell pathogenesis demonstrated for hematopoietic defects in vitro. Nat Commun. 2018 12 05; 9(1):5180.
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Shaaya EA, Pollack SF, Boronat S, Davis-Cooper S, Zella GC, Thibert RL. Gastrointestinal problems in 15q duplication syndrome. Eur J Med Genet. 2015 Mar; 58(3):191-3.
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Rea G, Stallings RL, Mullarkey M, McKinstry CS, McManus D, Morrison PJ. Subcortical white matter abnormalities because of previously undescribed de-novo 14q12-q13.1 triplication. Clin Dysmorphol. 2013 Apr; 22(2):71-72.
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Lyons MJ, Fuller JD, Montoya Mdel C, DuPont BR, Holden KR. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays. J Child Neurol. 2013 Apr; 28(4):524-6.
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Laus AC, Baratela WA, Laureano LA, Santos SA, Huber J, Ramos ES, Rebelo CC, Squire JA, Martelli L. Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature. Am J Med Genet A. 2012 Apr; 158A(4):821-7.