"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 | 0 | 3 | 3 |
| 1995 | 0 | 1 | 1 |
| 1997 | 0 | 2 | 2 |
| 1998 | 1 | 1 | 2 |
| 1999 | 1 | 2 | 3 |
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 2 | 2 |
| 2002 | 0 | 3 | 3 |
| 2003 | 0 | 3 | 3 |
| 2004 | 1 | 4 | 5 |
| 2005 | 0 | 7 | 7 |
| 2006 | 0 | 4 | 4 |
| 2007 | 0 | 3 | 3 |
| 2008 | 0 | 8 | 8 |
| 2009 | 1 | 3 | 4 |
| 2010 | 0 | 5 | 5 |
| 2011 | 2 | 5 | 7 |
| 2012 | 1 | 4 | 5 |
| 2013 | 4 | 11 | 15 |
| 2014 | 2 | 7 | 9 |
| 2015 | 1 | 3 | 4 |
| 2016 | 0 | 8 | 8 |
| 2017 | 0 | 4 | 4 |
| 2018 | 0 | 7 | 7 |
| 2019 | 1 | 4 | 5 |
| 2020 | 0 | 3 | 3 |
| 2021 | 1 | 1 | 2 |
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Below are the most recent publications written about "Heterozygote" by people in Profiles.
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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism. Am J Hum Genet. 2021 06 03; 108(6):1138-1150.
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Different posterior hippocampus and default mode network modulation in young APOE e4 carriers: a functional connectome-informed phenotype longitudinal study. Mol Neurobiol. 2021 Jun; 58(6):2757-2769.
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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report. Genet Med. 2021 04; 23(4):705-712.
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Hydrocephaly associated with compound heterozygous alterations in TRAPPC12. Birth Defects Res. 2020 08; 112(13):1028-1034.
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Genome Editing As an Approach to the Study of in Vivo Transcription Reprogramming. Dokl Biochem Biophys. 2020 Jan; 490(1):43-46.
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Does MHC heterozygosity influence microbiota form and function? PLoS One. 2019; 14(5):e0215946.
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A Novel Case of Compound Heterozygous Type 3 Von Willebrand Disease. Ann Clin Lab Sci. 2019 May; 49(3):393-394.
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Venous endothelin modulates responsiveness of cardiac sympathetic axons to arterial semaphorin. Elife. 2019 02 08; 8.
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Are BRCA1 and BRCA2 gene mutation patients underscreened for pancreatic adenocarcinoma? J Surg Oncol. 2019 May; 119(6):777-783.
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Immunoglobulin Genes and Immunity to HSV1 in Alzheimer's Disease. J Alzheimers Dis. 2019; 70(3):917-924.