"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 10 | 11 |
| 1995 | 1 | 23 | 24 |
| 1996 | 2 | 21 | 23 |
| 1997 | 3 | 20 | 23 |
| 1998 | 8 | 19 | 27 |
| 1999 | 2 | 9 | 11 |
| 2000 | 2 | 22 | 24 |
| 2001 | 1 | 21 | 22 |
| 2002 | 1 | 26 | 27 |
| 2003 | 2 | 20 | 22 |
| 2004 | 1 | 20 | 21 |
| 2005 | 1 | 17 | 18 |
| 2006 | 2 | 15 | 17 |
| 2007 | 1 | 15 | 16 |
| 2008 | 4 | 14 | 18 |
| 2009 | 3 | 11 | 14 |
| 2010 | 4 | 16 | 20 |
| 2011 | 4 | 14 | 18 |
| 2012 | 1 | 14 | 15 |
| 2013 | 3 | 13 | 16 |
| 2014 | 4 | 24 | 28 |
| 2015 | 8 | 18 | 26 |
| 2016 | 6 | 22 | 28 |
| 2017 | 0 | 15 | 15 |
| 2018 | 0 | 20 | 20 |
| 2019 | 6 | 25 | 31 |
| 2020 | 1 | 28 | 29 |
| 2021 | 3 | 12 | 15 |
| 2022 | 2 | 13 | 15 |
| 2023 | 0 | 5 | 5 |
| 2024 | 2 | 2 | 4 |
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Below are the most recent publications written about "Heterozygote" by people in Profiles.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. J Med Genet. 2024 May 21; 61(6):549-552.
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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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Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar; 143(3):279-291.
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Impact of Apolipoprotein E Genotype on Neurocognitive Function in Patients With Brain Metastases: An Analysis of NRG Oncology's RTOG 0614. Int J Radiat Oncol Biol Phys. 2024 Jul 01; 119(3):846-857.
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Autoantibodies against type I IFNs in humans with alternative NF-?B pathway deficiency. Nature. 2023 Nov; 623(7988):803-813.
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A mutation in TBXT causes congenital vertebral malformations in?humans and mice. J Genet Genomics. 2024 Apr; 51(4):433-442.
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Discordant calls across genotype discovery approaches elucidate variants with systematic errors. Genome Res. 2023 06; 33(6):999-1005.
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Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder. Eur J Hum Genet. 2023 09; 31(9):973-974.
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A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism. Am J Hum Genet. 2022 12 01; 109(12):2253-2269.