"Heterozygote" 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 having different alleles at one or more loci regarding a specific character.
| Descriptor ID |
D006579
|
| MeSH Number(s) |
G05.380.383
|
| Concept/Terms |
Genetic Carriers- Genetic Carriers
- Carrier, Genetic
- Genetic Carrier
- Carriers, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Heterozygote".
Below are MeSH descriptors whose meaning is more specific than "Heterozygote".
This graph shows the total number of publications written about "Heterozygote" by people in this website by year, and whether "Heterozygote" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 21 | 21 |
| 1996 | 4 | 28 | 32 |
| 1997 | 5 | 34 | 39 |
| 1998 | 4 | 30 | 34 |
| 1999 | 4 | 23 | 27 |
| 2000 | 3 | 23 | 26 |
| 2001 | 4 | 27 | 31 |
| 2002 | 4 | 40 | 44 |
| 2003 | 6 | 45 | 51 |
| 2004 | 6 | 42 | 48 |
| 2005 | 5 | 44 | 49 |
| 2006 | 5 | 47 | 52 |
| 2007 | 12 | 62 | 74 |
| 2008 | 5 | 41 | 46 |
| 2009 | 6 | 44 | 50 |
| 2010 | 8 | 43 | 51 |
| 2011 | 17 | 50 | 67 |
| 2012 | 11 | 56 | 67 |
| 2013 | 12 | 63 | 75 |
| 2014 | 7 | 53 | 60 |
| 2015 | 14 | 60 | 74 |
| 2016 | 7 | 46 | 53 |
| 2017 | 6 | 52 | 58 |
| 2018 | 9 | 50 | 59 |
| 2019 | 15 | 47 | 62 |
| 2020 | 3 | 65 | 68 |
| 2021 | 7 | 35 | 42 |
| 2022 | 0 | 18 | 18 |
| 2023 | 1 | 13 | 14 |
| 2024 | 12 | 27 | 39 |
| 2025 | 0 | 5 | 5 |
Below are the most recent publications written about "Heterozygote" by people in Profiles.
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Involvement of the Cerebellar Peduncles in FMR1 Premutation Carriers: A Pictorial Review of Their Anatomy, Imaging, and Pathology. Int J Mol Sci. 2025 May 06; 26(9).
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Heterozygous NTHL1 variant in a breast cancer survivor with malignant pleural effusion revealing metastatic colon adenocarcinoma. BMJ Case Rep. 2025 Apr 30; 18(4).
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Longitudinal associations between lipid panel and cognitive decline modified by APOE 4 carrier status in biracial community-dwelling older adults: Findings from the Chicago health and aging project. Arch Gerontol Geriatr. 2025 Jul; 134:105825.
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Impacts of reproductive systems on grapevine genome and breeding. Nat Commun. 2025 Mar 03; 16(1):2031.
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Monoallelic expression can govern penetrance of inborn errors of immunity. Nature. 2025 Jan; 637(8048):1186-1197.
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Heterozygous de novo variants in HSPD1 cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation. J Med Genet. 2024 Dec 31; 62(1):15-24.
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Thymic and T-cell intrinsic critical roles associated with severe combined immunodeficiency and Omenn syndrome due to a heterozygous variant (G201R) in PSMB10. J Allergy Clin Immunol. 2025 Apr; 155(4):1378-1385.e2.
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Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability. Am J Hum Genet. 2025 Jan 02; 112(1):75-86.
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Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0. Am J Hum Genet. 2025 Jan 02; 112(1):181-195.
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Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C). J Exp Med. 2024 Dec 02; 221(12).