 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 |
|---|
| 1997 | 0 | 1 | 1 | | 1998 | 1 | 8 | 9 | | 1999 | 0 | 2 | 2 | | 2000 | 0 | 3 | 3 | | 2001 | 0 | 4 | 4 | | 2002 | 0 | 4 | 4 | | 2003 | 0 | 9 | 9 | | 2004 | 0 | 7 | 7 | | 2005 | 0 | 8 | 8 | | 2006 | 0 | 6 | 6 | | 2007 | 0 | 12 | 12 | | 2008 | 0 | 12 | 12 | | 2009 | 0 | 10 | 10 | | 2010 | 0 | 23 | 23 | | 2011 | 0 | 22 | 22 | | 2012 | 0 | 22 | 22 | | 2013 | 0 | 21 | 21 | | 2014 | 1 | 23 | 24 | | 2015 | 1 | 21 | 22 | | 2016 | 3 | 21 | 24 | | 2017 | 3 | 12 | 15 | | 2018 | 3 | 16 | 19 | | 2019 | 1 | 12 | 13 | | 2020 | 0 | 9 | 9 | | 2021 | 2 | 17 | 19 | | 2022 | 0 | 11 | 11 | | 2023 | 0 | 11 | 11 | | 2024 | 2 | 15 | 17 | | 2025 | 0 | 3 | 3 |
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Below are the most recent publications written about "Genotype" by people in Profiles.
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Kinzler AJ, Wikswo ME, Balasubramani GK, D'Agostino HEA, Sax T, Dauer K, Weinberg GA, Szilyagi P, Sahni LC, Boom JA, Schuster JE, Selvarajan R, Harrison CJ, Staat MA, Payne DC, Halasa NB, Klein EJ, Englund JA, Martin JM, Hickey R, Michaels MG, Williams JV. Prevalence of human adenovirus in children with acute gastroenteritis in the New Vaccine Surveillance Network (NVSN) from 2016 to 2019. J Clin Virol. 2025 Aug; 179:105822.
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Banerjee D, Schuster JE, Midgley CM, Lee B, Moffatt M, Lively JY, Toepfer AP, Weinberg GA, Boom JA, Sahni LC, Avadhanula V, Piedra PA, Staat MA, Payne DC, Halasa N, Williams JV, Hickey RW, Michaels MG, Englund JA, Klein EJ, Sasidharan A, Rha B, Harrison CJ, Selvarangan R. Epidemiology and genotypic diversity of rhinovirus in school-age children with acute respiratory illnesses seeking medical care. J Clin Virol. 2025 Aug; 179:105806.
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Rush ET, Del Angel G, Dong J, Bates T, Steiner RD, Cox A. Genetic characterization of a large cohort of individuals with a clinical suspicion of hypophosphatasia in the United States. Mol Genet Metab. 2025 Mar; 144(3):109046.
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Bishop JR, Zhou C, Gaedigk A, Krone B, Kittles R, Cook EH, Newcorn JH, Stein MA. Dopamine Transporter and CYP2D6 Gene Relationships with Attention-Deficit/Hyperactivity Disorder Treatment Response in the Methylphenidate and Atomoxetine Crossover Study. J Child Adolesc Psychopharmacol. 2024 12; 34(10):458-469.
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Langlois AWR, Chenoweth MJ, Twesigomwe D, Scantamburlo G, Whirl-Carrillo M, Sangkuhl K, Klein TE, Nofziger C, Tyndale RF, Gaedigk A. PharmVar GeneFocus: CYP2A6. Clin Pharmacol Ther. 2024 Oct; 116(4):948-962.
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Pratt VM, Cavallari LH, Fulmer ML, Gaedigk A, Hachad H, Ji Y, Kalman LV, Ly RC, Moyer AM, Scott SA, Turner AJ, van Schaik RHN, Whirl-Carrillo M, Weck KE. DPYD Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, American College of Medical Genetics and Genomics, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, Pharmacogenomics Knowledgebase, and Pharmacogene Variation Consortium. J Mol Diagn. 2024 Oct; 26(10):851-863.
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Furia F, Levy AM, Theunis M, Bamshad MJ, Bartos MN, Bijlsma EK, Brancati F, Cejudo L, Chong JX, De Luca C, Dean SJ, Egense A, Goel H, Guenzel AJ, H?ffmeier U, Legius E, Mancini GMS, Marcos-Alcalde I, Niclass T, Planes M, Redon S, Ros-Pardo D, Rouault K, Schot R, Schuhmann S, Shen JJ, Tao AM, Thiffault I, Van Esch H, Wentzensen IM, Barakat TS, M?ller RS, Gomez-Puertas P, Chung WK, Gardella E, T?mer Z. The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants. Clin Genet. 2024 Nov; 106(5):574-584.
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Parvez MM, Thakur A, Mehrotra A, Stancil S, Pearce RE, Basit A, Leeder JS, Prasad B. Age-Dependent Abundance of CYP450 Enzymes Involved in Metronidazole Metabolism: Application to Pediatric PBPK Modeling. Clin Pharmacol Ther. 2024 Oct; 116(4):1090-1099.
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Duarte JD, Thomas CD, Lee CR, Huddart R, Agundez JAG, Baye JF, Gaedigk A, Klein TE, Lanfear DE, Monte AA, Nagy M, Schwab M, Stein CM, Uppugunduri CRS, van Schaik RHN, Donnelly RS, Caudle KE, Luzum JA. Clinical Pharmacogenetics Implementation Consortium Guideline (CPIC)?for CYP2D6, ADRB1, ADRB2, ADRA2C, GRK4, and GRK5 Genotypes and Beta-Blocker Therapy. Clin Pharmacol Ther. 2024 Oct; 116(4):939-947.
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Robinson KM, Eum S, Desta Z, Tyndale RF, Gaedigk A, Crist RC, Haidar CE, Myers AL, Samer CF, Somogyi AA, Zubiaur P, Iwuchukwu OF, Whirl-Carrillo M, Klein TE, Caudle KE, Donnelly RS, Kharasch ED. Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2B6 Genotype and Methadone Therapy. Clin Pharmacol Ther. 2024 Oct; 116(4):932-938.
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