"Mosaicism" 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 occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote.
Descriptor ID |
D009030
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MeSH Number(s) |
G05.365.590.175.595
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Mosaicism".
Below are MeSH descriptors whose meaning is more specific than "Mosaicism".
This graph shows the total number of publications written about "Mosaicism" by people in this website by year, and whether "Mosaicism" 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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1995 | 0 | 1 | 1 |
1996 | 1 | 0 | 1 |
1997 | 0 | 2 | 2 |
2000 | 2 | 3 | 5 |
2001 | 1 | 1 | 2 |
2002 | 1 | 0 | 1 |
2003 | 1 | 1 | 2 |
2004 | 1 | 0 | 1 |
2005 | 2 | 0 | 2 |
2006 | 1 | 1 | 2 |
2007 | 1 | 1 | 2 |
2008 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2010 | 1 | 1 | 2 |
2011 | 1 | 0 | 1 |
2012 | 0 | 1 | 1 |
2013 | 1 | 1 | 2 |
2015 | 2 | 0 | 2 |
2016 | 2 | 0 | 2 |
2017 | 0 | 3 | 3 |
2018 | 1 | 0 | 1 |
2019 | 2 | 1 | 3 |
2021 | 1 | 3 | 4 |
2023 | 1 | 0 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mosaicism" by people in Profiles.
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Determinants of mosaic chromosomal alteration fitness. Nat Commun. 2024 May 07; 15(1):3800.
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Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. Nat Genet. 2023 Nov; 55(11):1912-1919.
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The first post-natal clinical description of true mosaic complete tetrasomy 21: A case report. Am J Med Genet A. 2021 11; 185(11):3507-3509.
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Abortive intussusceptive angiogenesis causes multi-cavernous vascular malformations. Elife. 2021 05 20; 10.
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Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function. Blood. 2021 05 06; 137(18):2450-2462.
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Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey. Mol Genet Genomic Med. 2021 07; 9(7):e1665.
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Detection and characterization of mosaicism in autosomal dominant polycystic kidney disease. Kidney Int. 2020 02; 97(2):370-382.
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Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nat Genet. 2019 10; 51(10):1438-1441.
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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. Elife. 2019 09 24; 8.
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First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report. BMC Med Genet. 2018 09 15; 19(1):170.