 Genotype
"Genotype" 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.
The genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS.
| Descriptor ID |
D005838
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| MeSH Number(s) |
G05.380
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Genotype".
Below are MeSH descriptors whose meaning is more specific than "Genotype".
This graph shows the total number of publications written about "Genotype" by people in this website by year, and whether "Genotype" 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 |
|---|
| 1996 | 0 | 7 | 7 | | 1997 | 0 | 5 | 5 | | 1998 | 0 | 8 | 8 | | 1999 | 0 | 8 | 8 | | 2000 | 1 | 10 | 11 | | 2001 | 1 | 23 | 24 | | 2002 | 0 | 20 | 20 | | 2003 | 0 | 27 | 27 | | 2004 | 2 | 41 | 43 | | 2005 | 1 | 37 | 38 | | 2006 | 1 | 52 | 53 | | 2007 | 2 | 55 | 57 | | 2008 | 4 | 58 | 62 | | 2009 | 1 | 68 | 69 | | 2010 | 3 | 57 | 60 | | 2011 | 3 | 65 | 68 | | 2012 | 7 | 53 | 60 | | 2013 | 2 | 63 | 65 | | 2014 | 7 | 93 | 100 | | 2015 | 5 | 77 | 82 | | 2016 | 6 | 66 | 72 | | 2017 | 4 | 64 | 68 | | 2018 | 7 | 57 | 64 | | 2019 | 8 | 52 | 60 | | 2020 | 6 | 41 | 47 | | 2021 | 7 | 36 | 43 | | 2022 | 1 | 23 | 24 | | 2023 | 1 | 23 | 24 | | 2024 | 4 | 25 | 29 | | 2025 | 1 | 36 | 37 | | 2026 | 2 | 21 | 23 |
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Below are the most recent publications written about "Genotype" by people in Profiles.
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Gonzalez-Covarrubias V, Morales-Alfaro A, Bonilla-Jimenez O, Rodríguez-Dorantes M, Frías-Jimenez E, Soto-Perez-de-Celis E. Characterization of DPYD pharmacogenetic variation in Mexican patients with gastrointestinal malignancies. Cancer Chemother Pharmacol. 2026 Sep 17; 96(1).
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Hohsfield KR, Dong F, Waugh K, Steck AK, Buckner T, Johnson RK, Carry PM, Frohnert B, Rewers M, Norris JM. A Secular Increase in the Incidence of Islet Autoimmunity Among Colorado Children With Moderate-Risk HLA Genotypes. Diabetes Care. 2026 Sep 01; 49(9):1700-1704.
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Ingold M, Gao Q, Mandel JR, McNellie JP, Keepers KG, Barb JG, Burke JM, Rieseberg LH, Hulke BS. The stability of fatty acid composition in sunflower oil is dependent on environment and affected by structural variation. Theor Appl Genet. 2026 Aug 20; 139(9).
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Sadeeq SA, Leaton LA, Kichula KM, Farias TDJ, Font-Porterias N, Pollock NR, Collora CE, Castelli EC, Gignoux CR, Norman PJ. PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors. Hum Mol Genet. 2026 Aug 10; 35(17).
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Schneider K, Chowdhury M, Tepper M, Khan JB, Shortt JA, Gignoux C, Layer RM. Biobank-scale genotype similarity search and dynamic patient-matched cohort creation with GenoSiS. Genome Res. 2026 Aug 03; 36(8):1624-1636.
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Korch CT, Capes-Davis A, Shen C. Analytical Workflow for Determining the Authenticity of Human Cell Lines and Tissue Samples by Short Tandem Repeat (STR) Genotype Analysis. Curr Protoc. 2026 Aug; 6(8):e70439.
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Ridolfi F, Amorim G, Haas DW, Arriaga M, Staats C, Cordeiro-Santos M, Kritski AL, Figueiredo MC, Andrade BB, Sterling TR, Rolla VC, Benjamin A, Sant'Anna FM, Oliveira JG, Marin J, Rezende A, Carvalho AC, Rocha M, Nogueira B, Brito A, Spener R, Turner M. Determinants of HIV-1 virologic suppression in HIV-associated tuberculosis in Brazil. Mem Inst Oswaldo Cruz. 2026; 121:e250090.
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Richbourg H, Rangel Miller V, Khazaie Japalaghi O, AlSayed M, Baker PR, Daugherty S, Ekstein T, Grünert SC, Kiel MJ, Khan A, Kobayashi H, Korngut L, Monteleone SA, Schwartz IVD, Miller N, Vockley J. Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes. Hum Mutat. 2026; 2026:6864813.
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Korch CT. A Biomedical Researcher's Guide for Analyzing Short Tandem Repeat (STR) Genotypes of Human Cell Lines and in Vitro Tissue Samples Using Three Standard Authentication Algorithms. Curr Protoc. 2026 Jul; 6(7):e70387.
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Rossi F, Sportelli L, Kikidis GC, Grassi G, Di Camillo F, Bertolino A, Blasi G, Borcuk CJ, Fusco D, Hyde TM, Kleinman JE, Marnetto D, Pellegrini S, Rampino A, Vitiello B, Ripke S, Braun A, Kraft J, Belangero SI, Menezes PR, Arango C, Walters JTR, O'Donovan MC, Owen MJ, Braff D, Corvin A, Morris DW, Domenici E, van Os J, Atbasoglu E, Saka MC, Di Forti M, Baune BT, Pato CN, McQuillin A, Golimbet V, Kondratyev N, Escott-Price V, Gareeva A, Khusnutdinova E, Cervilla JA, Rivera M, Campion D, Laurent-Levinson C, Serretti A, Andreassen OA, St Clair D, Lencz T, Malhotra AK, McCarthy NS, Mowry BJ, Rujescu D, Giegling I, Hartmann AM, Konte B, Nöthen MM, Rietschel M, Kirov G, Sullivan PF, Petryshen TL, Werge T, McIntosh AM, Esko T, Jönsson EG, Ehrenreich H, Riley BP, Levinson DF, Buxbaum JD, Bramon E, Hultman CM, Ophoff RA, Adolfsson R, Stahl EA, Guloksuz S, Rutten BPF, Del-Ben CM, Thibaut F, Weinberger DR, Pergola G. Co-expression-based models improve eQTL predictions for transcriptome-wide association studies and highlight new schizophrenia-associated genes. Nat Genet. 2026 Jul; 58(7):1559-1572.
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