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 | 15 | 15 | | 1997 | 0 | 17 | 17 | | 1998 | 0 | 20 | 20 | | 1999 | 4 | 15 | 19 | | 2000 | 1 | 26 | 27 | | 2001 | 0 | 34 | 34 | | 2002 | 2 | 39 | 41 | | 2003 | 1 | 37 | 38 | | 2004 | 3 | 47 | 50 | | 2005 | 4 | 44 | 48 | | 2006 | 4 | 44 | 48 | | 2007 | 4 | 53 | 57 | | 2008 | 3 | 44 | 47 | | 2009 | 5 | 52 | 57 | | 2010 | 6 | 86 | 92 | | 2011 | 6 | 73 | 79 | | 2012 | 6 | 73 | 79 | | 2013 | 8 | 93 | 101 | | 2014 | 8 | 101 | 109 | | 2015 | 18 | 103 | 121 | | 2016 | 14 | 91 | 105 | | 2017 | 11 | 110 | 121 | | 2018 | 13 | 114 | 127 | | 2019 | 15 | 112 | 127 | | 2020 | 6 | 89 | 95 | | 2021 | 15 | 115 | 130 | | 2022 | 0 | 64 | 64 | | 2023 | 1 | 95 | 96 | | 2024 | 27 | 59 | 86 | | 2025 | 4 | 80 | 84 | | 2026 | 0 | 4 | 4 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Conderino S, Kirchner HL, Thorpe LE, Divers J, Hirsch AG, Nordberg CM, Schwartz BS, Zhang L, Cai B, Rudisill C, Obeid JS, Liese A, Allen KS, Dixon BE, Crume T, Dabelea D, Burgett S, Bellatorre A, Shao H, Bian J, Guo Y, Bost S, Lyu T, Reynolds K, Mefford MT, Zhou H, Zhou M, Lustigova E, Utidjian LH, Maltenfort M, Kamboj M, Mendonca EA, Hanley P, Zaganjor I, Pavkov ME, Rosenman M, Titus AR. Multi-site analysis of COVID-19 and new-onset diabetes reveals need for improved sensitivity of EHR-based COVID-19 phenotypes-a DiCAYA Network analysis. J Am Med Inform Assoc. 2026 Mar 01; 33(3):710-718.
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Penaranda C, Brenner EP, Clatworthy AE, Cosimi LA, Ravi J, Hung DT. Genomic comparison and phenotypic characterization of Pseudomonas aeruginosa isolates across environmental and diverse clinical isolation sites. mSystems. 2026 Mar 24; 11(3):e0136225.
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Lopriore P, Ünlütürk Z, Klopstock T, Karaa A, Rouzier C, Domínguez-González C, Lamperti C, Mancuso M, Cecchi G, Montano V, Siciliano G, Nicoletta V, Maioli M, Primiano G, Servidei S, La Morgia C, Carelli V, Valentino ML, Caporali L, Arena IG, Musumeci O, Lopergolo D, Malandrini A, Gallus GN, Filosto M, Bello L, Pegoraro E, Comi GP, Magri F, Ronchi D, Di Fonzo A, Percetti M, Azzimonti M, Büchner B, Prokisch H, Bermejo-Guerrero L, Procaccio V, Gaignard P, Echaniz-Laguna A, Schiff M, Rötig A, Toutain A, Paquis-Flucklinger V, Morel G, Robin S, Nadaj-Pakleza A, Chanson JB, Chaussenot A, Ait-El-Mkadem Saadi S, Trimouille A, Tranchant C, Salort-Campana E, Bieth E, Sacconi S, Duval F, Restrepo Vera JL, Molnar MJ, Vissing J, Haas R, Larson A, Enns GM, Parikh S, Goldstein A, Hirano M. Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study. Neurology. 2026 Feb 10; 106(3):e214401.
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Kielt MJ, Nelin TD, Abman SH, Nelin LD. Toward precision for bronchopulmonary dysplasia: Moving past current definitions. J Perinatol. 2026 Feb; 46(2):308-314.
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Abbott M, Angione K, Stringfellow M, Malik K, Saenz M, Miele A, Syverson K, Maniar B, Borello J, Chaby L, Demarest S. Evaluation of epilepsy in 8p-related disorders. Epilepsy Res. 2026 Feb; 220:107720.
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O'Brien EM, Tylek T, Geisler HC, Mukalel AJ, Whitaker RC, Sung S, Binder-Markey BI, Weissman D, Mitchell MJ, Spiller KL. Macrophage cell therapy enabled by interleukin-4 mRNA-loaded lipid nanoparticles to sustain a pro-reparative phenotype in inflammatory injuries. Biomaterials. 2026 May; 328:123869.
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Haanpää MK, Haldeman-Englert CR, Hietala M, Tanverdi MS, Koty PP, Brightman D, Dosunmu E, Tibrewal S, Kaur S, Kaur A, Verma RK, de Alba Campomanes AG, Utz V, Slavotinek AM, Curry C. Nance-Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes. Am J Med Genet A. 2026 Mar; 200(3):642-652.
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Shefchek K, Ziniel SI, McMurry JA, Brownstein CA, Brownstein JS, Riggs ER, Might M, Smedley D, Clugston A, Beggs AH, Paterson H, Robinson PN, Vasilevsky NA, Holm IA, Haendel MA. Development of self-phenotyping tools to empower patients and improve diagnostics. EBioMedicine. 2025 Nov; 121:105965.
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Lemke JR, Eoli A, Krey I, Popp B, Strehlow V, Wittekind DA, Vuorinen AL, Aldhalaan HM, Baer S, de Saint Martin A, Hammer TB, Herman I, Hornemann F, Ingebrigtsen T, Lederer D, Lesca G, Marafie D, Mathot M, Rosenfeld JA, Møller RS, Schelhaas HJ, Stillman C, Orsini A, Patel AD, Piard J, Veggiotti P, Vlaskamp DRM, Weckhuysen S, Traynelis SF, Benke TA, Heyne HO, Syrbe S. GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy. Mol Psychiatry. 2026 Jan; 31(1):374-382.
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Locke RC, Miller LM, Lemmon EA, Assi SS, Jones DL, Bonnevie ED, Burdick JA, Heo SJ, Mauck RL. Rapid restoration of cell phenotype and matrix forming capacity following transient nuclear softening. Acta Biomater. 2025 Dec; 208:336-349.
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