"Homozygote" 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 in which both alleles at a given locus are identical.
Descriptor ID |
D006720
|
MeSH Number(s) |
G05.380.554
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Homozygote".
Below are MeSH descriptors whose meaning is more specific than "Homozygote".
This graph shows the total number of publications written about "Homozygote" by people in this website by year, and whether "Homozygote" 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 | 5 | 5 |
1995 | 0 | 2 | 2 |
1996 | 0 | 2 | 2 |
1997 | 1 | 1 | 2 |
1998 | 0 | 1 | 1 |
1999 | 0 | 8 | 8 |
2001 | 0 | 4 | 4 |
2002 | 0 | 1 | 1 |
2003 | 0 | 2 | 2 |
2004 | 1 | 2 | 3 |
2005 | 0 | 3 | 3 |
2006 | 0 | 2 | 2 |
2008 | 0 | 5 | 5 |
2009 | 0 | 4 | 4 |
2010 | 0 | 3 | 3 |
2011 | 0 | 1 | 1 |
2012 | 1 | 3 | 4 |
2013 | 0 | 2 | 2 |
2014 | 0 | 1 | 1 |
2015 | 1 | 1 | 2 |
2016 | 0 | 4 | 4 |
2017 | 1 | 3 | 4 |
2019 | 0 | 4 | 4 |
2020 | 0 | 2 | 2 |
2022 | 0 | 2 | 2 |
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Below are the most recent publications written about "Homozygote" by people in Profiles.
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Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus. Ann Rheum Dis. 2022 Dec; 81(12):1712-1721.
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Intact mitochondrial substrate efflux is essential for prevention of tubular injury in a sex-dependent manner. JCI Insight. 2022 04 08; 7(7).
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An Ig ? Marker Genotype Is a Strong Risk Factor for Alzheimer Disease, Independent of Apolipoprotein E e4 Genotype. J Immunol. 2020 09 01; 205(5):1318-1322.
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Filling in the gaps on FILS syndrome: A case report and literature review. Pediatr Dermatol. 2020 Sep; 37(5):915-917.
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Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome. Kidney Int. 2019 10; 96(4):883-889.
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Vitamin D-Binding Protein Deficiency and Homozygous Deletion of the GC Gene. N Engl J Med. 2019 06 27; 380(26):2583-2584.
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Does MHC heterozygosity influence microbiota form and function? PLoS One. 2019; 14(5):e0215946.
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Immunoglobulin Genes and Immunity to HSV1 in Alzheimer's Disease. J Alzheimers Dis. 2019; 70(3):917-924.
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First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination. Pediatr Dev Pathol. 2018 Nov-Dec; 21(6):561-567.
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COPD in individuals with the PiMZ alpha-1 antitrypsin genotype. Eur Respir Rev. 2017 Dec 31; 26(146).