 Homozygote
"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
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| MeSH Number(s) |
G05.380.554
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| Concept/Terms |
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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 |
|---|
| 1995 | 0 | 2 | 2 | | 1996 | 0 | 1 | 1 | | 1997 | 0 | 1 | 1 | | 1998 | 0 | 2 | 2 | | 1999 | 0 | 4 | 4 | | 2000 | 0 | 3 | 3 | | 2001 | 0 | 4 | 4 | | 2003 | 0 | 7 | 7 | | 2004 | 0 | 2 | 2 | | 2005 | 1 | 4 | 5 | | 2006 | 0 | 3 | 3 | | 2007 | 0 | 3 | 3 | | 2008 | 3 | 6 | 9 | | 2009 | 0 | 4 | 4 | | 2010 | 0 | 7 | 7 | | 2011 | 1 | 8 | 9 | | 2012 | 2 | 6 | 8 | | 2013 | 1 | 6 | 7 | | 2014 | 1 | 7 | 8 | | 2015 | 3 | 7 | 10 | | 2016 | 0 | 7 | 7 | | 2017 | 0 | 14 | 14 | | 2018 | 3 | 6 | 9 | | 2019 | 0 | 5 | 5 | | 2020 | 2 | 4 | 6 | | 2021 | 0 | 7 | 7 | | 2022 | 0 | 3 | 3 | | 2023 | 0 | 2 | 2 | | 2024 | 0 | 1 | 1 | | 2025 | 0 | 2 | 2 |
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Below are the most recent publications written about "Homozygote" by people in Profiles.
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Cline N, Merlo D, Frater S, Pollock NR, Mayor NP, Turner TR, Walsh L, Vivers S, Norman PJ. The Case of a Missing HLA-B Gene. HLA. 2025 Mar; 105(3):e70114.
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Pascual MG, Cox HC, Larson A, Bruckner AL. Phenotypic Characteristics of a Patient Cohort With Recessive Dystrophic Epidermolysis Bullosa and the Pathogenic Variant c.7485+5G>A in Intron 98 of COL7A1. Am J Med Genet A. 2025 Jul; 197(7):e64032.
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Ardon M, Nguyen L, Chen R, Rogers J, Stout T, Thomasy S, Moshiri A. Onset and Progression of Disease in Nonhuman Primates With PDE6C Cone Disorder. Invest Ophthalmol Vis Sci. 2024 Dec 02; 65(14):16.
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Sohail M, Palma-Martínez MJ, Chong AY, Quinto-Cortés CD, Barberena-Jonas C, Medina-Muñoz SG, Ragsdale A, Delgado-Sánchez G, Cruz-Hervert LP, Ferreyra-Reyes L, Ferreira-Guerrero E, Mongua-Rodríguez N, Canizales-Quintero S, Jimenez-Kaufmann A, Moreno-Macías H, Aguilar-Salinas CA, Auckland K, Cortés A, Acuña-Alonzo V, Gignoux CR, Wojcik GL, Ioannidis AG, Fernández-Valverde SL, Hill AVS, Tusié-Luna MT, Mentzer AJ, Novembre J, García-García L, Moreno-Estrada A. Mexican Biobank advances population and medical genomics of diverse ancestries. Nature. 2023 10; 622(7984):775-783.
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Colbert SMC, Wendt FR, Pathak GA, Helmer DA, Hauser ER, Keller MC, Polimanti R, Johnson EC. Declining autozygosity over time: An exploration in over 1 million individuals from three diverse cohorts. Am J Hum Genet. 2023 06 01; 110(6):1008-1014.
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Colbert SM, Keller MC, Agrawal A, Johnson EC. Exploring the Relationships Between Autozygosity, Educational Attainment, and Cognitive Ability in a Contemporary, Trans-Ancestral American Sample. Behav Genet. 2022 11; 52(6):315-323.
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Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Çelik T, Narli N, Bianca S, Murphy D, De Carvalho Moreira FM, Petree C, Huang K, Monastiri K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano P, Sahin Y, Al-Gazali L, Abi Warde MT, Gerard B, Zifarelli G, Beetz C, Fortuna S, Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H. A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease. Genet Med. 2022 10; 24(10):2194-2203.
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O'Connor MJ, Schroeder P, Huerta-Chagoya A, Cortés-Sánchez P, Bonàs-Guarch S, Guindo-Martínez M, Cole JB, Kaur V, Torrents D, Veerapen K, Grarup N, Kurki M, Rundsten CF, Pedersen O, Brandslund I, Linneberg A, Hansen T, Leong A, Florez JC, Mercader JM. Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes. Diabetes. 2022 03 01; 71(3):554-565.
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Tsai JW, Lee JC, Hsieh TH, Huang SC, Lee PH, Liu TT, Kao YC, Chang CD, Weng TF, Li CF, Lin JC, Liang CW, Su YL, Chang IY, Wang YT, Chang NY, Yu SC, Wang JC, Huang HY. Adult NTRK-rearranged spindle cell neoplasms of the viscera: with an emphasis on rare locations and heterologous elements. Mod Pathol. 2022 07; 35(7):911-921.
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Theodoridi A, Dinarello A, Badenetti L, Pavlidis M, Dalla Valle L, Tsalafouta A. Knockout of the hsd11b2 Gene Extends the Cortisol Stress Response in Both Zebrafish Larvae and Adults. Int J Mol Sci. 2021 Nov 20; 22(22).
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