Trisomy
"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
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| 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
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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 UAMS Profiles 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 |
|---|
| 2025 | 0 | 1 | 1 | | 2017 | 0 | 2 | 2 | | 2015 | 2 | 1 | 3 | | 2014 | 2 | 1 | 3 | | 2013 | 1 | 0 | 1 | | 2011 | 0 | 1 | 1 | | 2008 | 1 | 0 | 1 | | 2007 | 2 | 0 | 2 | | 2006 | 2 | 2 | 4 | | 2005 | 1 | 1 | 2 | | 2004 | 2 | 1 | 3 | | 2003 | 0 | 1 | 1 | | 1998 | 1 | 0 | 1 |
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Below are the most recent publications written about "Trisomy" by people in Profiles over the past ten years.
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Maura F, Kaddoura M, Poos AM, Baughn LB, Ziccheddu B, B?rtsch MA, Cirrincione A, Maclachlan K, Chojnacka M, Diamond B, Papadimitriou M, Blaney P, John L, Reichert P, Huhn S, Gagler D, Zhang Y, Dogan A, Lesokhin AM, Davies F, Goldschmidt H, Fenk R, Weisel KC, Mai EK, Korde N, Morgan GJ, Rajkumar SV, Kumar S, Usmani S, Landgren O, Raab MS, Weinhold N. Temporal genomic dynamics shape clinical trajectory in multiple myeloma. Nat Genet. 2025 Sep; 57(9):2203-2214.
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Kosiv KA, Gossett JM, Bai S, Collins RT. Congenital Heart Surgery on In-Hospital Mortality in Trisomy 13 and 18. Pediatrics. 2017 Nov; 140(5).
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Sharma R, Harris VM, Cavett J, Kurien BT, Liu K, Koelsch KA, Fayaaz A, Chaudhari KS, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Alarc?n-Riquelme M, Mariette X, Lessard CJ, Harley JB, Ng WF, Rasmussen A, Sivils KL, Scofield RH. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sj?gren's Syndrome. Arthritis Rheumatol. 2017 11; 69(11):2187-2192.
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Sandoval-Sus JD, Chavez JC, Dalia S, Naqvi SMH, Talati C, Nodzon L, Kharfan-Dabaja MA, Pinilla-Ibarz J. Association between immunoglobulin heavy-chain variable region mutational status and isolated favorable baseline genomic aberrations in chronic lymphocytic leukemia. Leuk Lymphoma. 2018 01; 59(1):59-68.
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Rush ET, Schaefer GB, Sanger WG, Coccia PF. Aplastic Anemia in Two Patients with Sex Chromosome Aneuploidies. Cytogenet Genome Res. 2015; 147(1):31-4.
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