 Phenotype
"Phenotype" 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 outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment.
| Descriptor ID |
D010641
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| MeSH Number(s) |
G05.695
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Phenotype".
Below are MeSH descriptors whose meaning is more specific than "Phenotype".
This graph shows the total number of publications written about "Phenotype" by people in this website by year, and whether "Phenotype" 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 | 14 | 14 | | 1997 | 0 | 14 | 14 | | 1998 | 0 | 20 | 20 | | 1999 | 3 | 15 | 18 | | 2000 | 1 | 25 | 26 | | 2001 | 0 | 34 | 34 | | 2002 | 2 | 39 | 41 | | 2003 | 1 | 37 | 38 | | 2004 | 3 | 45 | 48 | | 2005 | 4 | 43 | 47 | | 2006 | 4 | 45 | 49 | | 2007 | 4 | 54 | 58 | | 2008 | 3 | 44 | 47 | | 2009 | 5 | 52 | 57 | | 2010 | 6 | 87 | 93 | | 2011 | 6 | 75 | 81 | | 2012 | 6 | 75 | 81 | | 2013 | 8 | 88 | 96 | | 2014 | 8 | 96 | 104 | | 2015 | 17 | 103 | 120 | | 2016 | 15 | 92 | 107 | | 2017 | 10 | 102 | 112 | | 2018 | 14 | 114 | 128 | | 2019 | 16 | 114 | 130 | | 2020 | 5 | 90 | 95 | | 2021 | 13 | 110 | 123 | | 2022 | 0 | 63 | 63 | | 2023 | 1 | 91 | 92 | | 2024 | 27 | 55 | 82 | | 2025 | 4 | 86 | 90 | | 2026 | 2 | 52 | 54 |
To return to the timeline, click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
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Callen AL, Montes D, Amrhein TJ, Beck J, Barvulsky E, Bhaumik D, Boyke AE, Cagnazzo F, Carlton Jones L, Dobrocky T, Kranz PG, Lennarson P, Madhavan A, Mamlouk MD, Mark IT, Maya M, Piechowiak EI, Schievink W, Volz F, Wolf K, Urbach H, Lützen N. Sacral Dural Tears in Spontaneous Intracranial Hypotension: Imaging Phenotype and Treatment Outcomes in a Multicenter Cohort. AJNR Am J Neuroradiol. 2026 Oct 01; 47(10):2674-2681.
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Mack CL, Miethke AG, Hawthorne K, Henn L, Horslen S, Alonso EM, Gupta NA, Sundaram SS, Kohli R, Bozic M, Deneau M, Guthery S, Loomes KM, Valentino PL, Tessier MEM, Shneider B, Magee JC, Karpen S, Rosenthal P, Wang K, Ricciuto A, Sokol RJ, Kamath BM. The Childhood Liver Disease Research Network's prospective characterization of pediatric primary sclerosing cholangitis. Hepatol Commun. 2026 Oct 01; 10(10).
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Boslough M, Taylor MRG, Mestroni L, Lombardi R. Genetic Dilated Cardiomyopathy: A Review. Methodist Debakey Cardiovasc J. 2026; 22(4):68-77.
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Lu S, Noble T, Elkins J, Jolly AJ, Dubner AM, Jacot JG, Peña Castellanos B, Hardy EJ, Nemenoff RA, Moulton KS, Majesky MW, Weiser-Evans MCM. KLF4 in Smooth Muscle Cell-Derived Progenitor Cells Is Essential for Angiotensin II-Induced Cardiac Inflammation and Fibrosis. Arterioscler Thromb Vasc Biol. 2026 Oct; 46(10):e324849.
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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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Slater BA, Muth E, Meeks NJL. The First Case of Isolated Uterine Atony as the Only Symptom in an Individual With ACTG2-Associated Visceral Myopathy. Clin Genet. 2026 11; 110(5):637-638.
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Kim I, Robinson TN, Reeves BB, Haber N, Ram N. Software Reference Architecture for Real-Time Mobile Digital Phenotyping: Evaluation of System Designs. JMIR Form Res. 2026 Aug 07; 10:e87320.
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Keller AL, Dennis KA, Ohlstrom DJ, Parzych SE, Walker ZJ, Novak AJ, Pham-Danis C, Medha TN, Rahkola JT, Boorgula MP, Kohler ME, Sherbenou DW. Multiple Myeloma Cells Resistant to T-cell Therapies Exhibit a CD45+ Immunoevasive Phenotype. Cancer Immunol Res. 2026 Aug 04; 14(8):1307-1321.
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Poletti B, Aiello EN, Consonni M, Iazzolino B, Torre S, Faltracco V, Telesca A, Palumbo F, Curti B, De Luca G, Moreschi A, Frisco F, Bella ED, Bersano E, Riva N, Verde F, Messina S, Doretti A, Maranzano A, Morelli C, Cappa SF, Calvo A, Strong MJ, Silani V, Lauria G, Chiò A, Ticozzi N. Neuropsychological Sub-Phenotypes in Amyotrophic Lateral Sclerosis. Eur J Neurol. 2026 Aug; 33(8):e70706.
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Palmieri L, Dowle EJ, Nadachowska-Brzyska K, Schopf A, Dobart N, Stauffer C, Schuler H, Ragland GJ, Schebeck M. Genomic Predictors of Diapause Polymorphism in the Bark Beetle Ips typographus With Implications for Voltinism Potential and Outbreak Dynamics. Mol Ecol. 2026 Aug; 35(16):e70532.
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