"Homozygote" 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.
An individual in which both alleles at a given locus are identical.
| Descriptor ID |
D006720
|
| MeSH Number(s) |
G05.380.554
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Homozygote".
Below are MeSH descriptors whose meaning is more specific than "Homozygote".
This graph shows the total number of publications written about "Homozygote" by people in this website by year, and whether "Homozygote" 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 |
|---|
| 1994 | 0 | 4 | 4 |
| 1995 | 0 | 13 | 13 |
| 1996 | 0 | 13 | 13 |
| 1997 | 0 | 8 | 8 |
| 1998 | 2 | 6 | 8 |
| 1999 | 0 | 13 | 13 |
| 2000 | 0 | 12 | 12 |
| 2001 | 1 | 12 | 13 |
| 2002 | 1 | 13 | 14 |
| 2003 | 2 | 22 | 24 |
| 2004 | 0 | 14 | 14 |
| 2005 | 2 | 15 | 17 |
| 2006 | 0 | 13 | 13 |
| 2007 | 1 | 16 | 17 |
| 2008 | 5 | 12 | 17 |
| 2009 | 0 | 19 | 19 |
| 2010 | 3 | 11 | 14 |
| 2011 | 0 | 14 | 14 |
| 2012 | 0 | 15 | 15 |
| 2013 | 1 | 16 | 17 |
| 2014 | 1 | 6 | 7 |
| 2015 | 5 | 7 | 12 |
| 2016 | 1 | 14 | 15 |
| 2017 | 1 | 10 | 11 |
| 2018 | 5 | 12 | 17 |
| 2019 | 3 | 12 | 15 |
| 2020 | 1 | 12 | 13 |
| 2021 | 1 | 12 | 13 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 7 | 7 |
| 2024 | 3 | 7 | 10 |
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Below are the most recent publications written about "Homozygote" by people in Profiles.
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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia. Am J Hum Genet. 2024 Nov 07; 111(11):2566-2581.
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 Jan; 197(1):e63845.
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Prognostic value of DNA methylation subclassification, aneuploidy, and CDKN2A/B homozygous deletion in predicting clinical outcome of IDH mutant astrocytomas. Neuro Oncol. 2024 Jun 03; 26(6):1042-1051.
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It is Time to Screen for Homozygous Familial Hypercholesterolemia in the United States. Glob Heart. 2024; 19(1):43.
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Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Med Genomics. 2024 04 16; 17(1):85.
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DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations. Genet Med. 2024 Jul; 26(7):101126.
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Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma. Genet Med. 2024 Jul; 26(7):101125.
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HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data. Nucleic Acids Res. 2024 Feb 28; 52(4):e18.
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Phenotypic Analysis: Assessing Timing of Recessive Prenatal Lethality in Mice. Cold Spring Harb Protoc. 2024 01 02; 2024(1):107970.
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Strategies for Maintaining Mouse Mutations. Cold Spring Harb Protoc. 2024 01 02; 2024(1):107960.