"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 |
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1994 | 0 | 10 | 10 |
1995 | 1 | 22 | 23 |
1996 | 2 | 19 | 21 |
1997 | 2 | 19 | 21 |
1998 | 7 | 16 | 23 |
1999 | 2 | 7 | 9 |
2000 | 2 | 18 | 20 |
2001 | 0 | 16 | 16 |
2002 | 1 | 14 | 15 |
2003 | 2 | 20 | 22 |
2004 | 1 | 21 | 22 |
2005 | 1 | 19 | 20 |
2006 | 2 | 16 | 18 |
2007 | 1 | 15 | 16 |
2008 | 4 | 15 | 19 |
2009 | 3 | 11 | 14 |
2010 | 6 | 17 | 23 |
2011 | 5 | 15 | 20 |
2012 | 2 | 16 | 18 |
2013 | 3 | 13 | 16 |
2014 | 4 | 25 | 29 |
2015 | 9 | 18 | 27 |
2016 | 6 | 22 | 28 |
2017 | 0 | 19 | 19 |
2018 | 1 | 21 | 22 |
2019 | 7 | 25 | 32 |
2020 | 1 | 30 | 31 |
2021 | 3 | 13 | 16 |
2022 | 2 | 11 | 13 |
2023 | 0 | 3 | 3 |
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Below are the most recent publications written about "Heterozygote" by people in Profiles.
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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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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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Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome. Brain. 2022 10 21; 145(10):3383-3390.
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Commun Biol. 2022 10 06; 5(1):1061.
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A validation of models for prediction of pathogenic variants in mismatch repair genes. Genet Med. 2022 10; 24(10):2155-2166.
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Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes. Cancer. 2022 10; 128(20):3709-3717.
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Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson's disease-associated GBA gene. Commun Biol. 2022 07 06; 5(1):670.
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Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes. Dig Dis Sci. 2023 01; 68(1):312-322.
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A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. Intern Med. 2023 Jan 01; 62(1):107-111.