"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 |
---|
1998 | 0 | 3 | 3 |
2001 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2007 | 0 | 3 | 3 |
2008 | 0 | 2 | 2 |
2009 | 0 | 3 | 3 |
2010 | 0 | 3 | 3 |
2011 | 0 | 1 | 1 |
2012 | 0 | 7 | 7 |
2013 | 0 | 4 | 4 |
2014 | 1 | 5 | 6 |
2015 | 0 | 2 | 2 |
2016 | 0 | 9 | 9 |
2017 | 2 | 8 | 10 |
2018 | 1 | 5 | 6 |
2019 | 1 | 6 | 7 |
2020 | 0 | 4 | 4 |
2021 | 0 | 4 | 4 |
2022 | 0 | 3 | 3 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Heterozygote" by people in Profiles.
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Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival. Cancer Med. 2023 08; 12(15):16142-16162.
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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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The megabase-scale crossover landscape is largely independent of sequence divergence. Nat Commun. 2022 07 02; 13(1):3828.
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Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants. J Clin Oncol. 2022 05 10; 40(14):1529-1541.
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TP63-related disorders: two case reports and a brief review of the literature. Dermatol Online J. 2021 Nov 15; 27(11).
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun. 2021 06 07; 12(1):3417.
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Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ. Genes (Basel). 2021 05 13; 12(5).
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Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains. Clin Epigenetics. 2021 02 04; 13(1):30.
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Gamete binning: chromosome-level and haplotype-resolved genome assembly enabled by high-throughput single-cell sequencing of gamete genomes. Genome Biol. 2020 12 29; 21(1):306.
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HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence. J Clin Endocrinol Metab. 2020 07 01; 105(7).