"Aneuploidy" 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 chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1).
| Descriptor ID |
D000782
|
| MeSH Number(s) |
C23.550.210.050 G05.365.590.175.050 G05.700.131
|
| Concept/Terms |
Aneuploidy- Aneuploidy
- Aneuploidies
- Aneuploid
- Aneuploids
Aneuploid Cell- Aneuploid Cell
- Aneuploid Cells
- Cell, Aneuploid
- Cells, Aneuploid
|
Below are MeSH descriptors whose meaning is more general than "Aneuploidy".
Below are MeSH descriptors whose meaning is more specific than "Aneuploidy".
This graph shows the total number of publications written about "Aneuploidy" by people in this website by year, and whether "Aneuploidy" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 1 | 2 |
| 1999 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 3 | 1 | 4 |
| 2020 | 0 | 1 | 1 |
| 2022 | 0 | 4 | 4 |
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Below are the most recent publications written about "Aneuploidy" by people in Profiles.
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Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2023 02; 25(2):100336.
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Apoptotic qPCR gene expression array analysis demonstrates proof-of-concept for rapid blastocoel fluid-conditioned media molecular prediction. J Assist Reprod Genet. 2022 Jul; 39(7):1515-1522.
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SWAN pathway-network identification of common aneuploidy-based oncogenic drivers. Nucleic Acids Res. 2022 04 22; 50(7):3673-3692.
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The expression of pregnancy-associated plasma protein-A (PAPP-A) in human blastocoel fluid-conditioned media: a proof of concept study. J Assist Reprod Genet. 2022 Feb; 39(2):389-394.
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Single-cell analysis of copy-number alterations in serous ovarian cancer reveals substantial heterogeneity in both low- and high-grade tumors. Cell Cycle. 2020 11; 19(22):3154-3166.
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Polysomy is associated with poor outcome in 1p/19q codeleted oligodendroglial tumors. Neuro Oncol. 2019 09 06; 21(9):1164-1174.
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Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia. Pediatr Hematol Oncol. 2019 Oct; 36(7):432-437.
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What are the cost considerations for preimplantation genetic testing for aneuploidy? Fertil Steril. 2019 06; 111(6):1115-1116.
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Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations. Genet Med. 2019 10; 21(10):2285-2292.
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Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics. Genet Med. 2016 10; 18(10):1056-65.