 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
|
| MeSH Number(s) |
G05.695
|
| Concept/Terms |
|
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 | 13 | 13 | | 1997 | 0 | 13 | 13 | | 1998 | 0 | 18 | 18 | | 1999 | 3 | 14 | 17 | | 2000 | 1 | 22 | 23 | | 2001 | 0 | 32 | 32 | | 2002 | 2 | 39 | 41 | | 2003 | 1 | 37 | 38 | | 2004 | 3 | 44 | 47 | | 2005 | 4 | 41 | 45 | | 2006 | 4 | 44 | 48 | | 2007 | 4 | 53 | 57 | | 2008 | 3 | 44 | 47 | | 2009 | 5 | 52 | 57 | | 2010 | 6 | 85 | 91 | | 2011 | 6 | 73 | 79 | | 2012 | 6 | 75 | 81 | | 2013 | 8 | 89 | 97 | | 2014 | 8 | 94 | 102 | | 2015 | 17 | 104 | 121 | | 2016 | 15 | 94 | 109 | | 2017 | 10 | 103 | 113 | | 2018 | 14 | 116 | 130 | | 2019 | 17 | 117 | 134 | | 2020 | 5 | 92 | 97 | | 2021 | 13 | 117 | 130 | | 2022 | 0 | 64 | 64 | | 2023 | 1 | 96 | 97 | | 2024 | 27 | 59 | 86 | | 2025 | 4 | 87 | 91 | | 2026 | 3 | 66 | 69 |
To return to the timeline, click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
-
Sutton KJ, Gervis JE, Jatoi M, Hwang LD, Hendricks AE, Ghosh D, Westerman KE, Cole JB. Refining Genetic Instruments for Dietary Intake Mendelian Randomization Using Phenome-Wide Association Studies. Genet Epidemiol. 2026 Dec; 50(8):e70059.
-
Keshavan N, Neugebauer J, Bellusci M, Bertini E, Brown G, Darin N, DeBrosse S, Drexler L, Drexler S, Enns GM, Ganetzky RD, Gilbert K, Larson A, Legi R, Lehman AN, Newby C, Schiff M, Skeath R, Stacpoole PW, Thompson S, Watt E, Wortmann SB, Bedoyan JK, Rahman S. Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency. J Inherit Metab Dis. 2026 Nov; 49(6):e70226.
-
Salazar-Villacorta A, Bond LM, Kim L, Anagnostopoulou K, Scardamaglia A, Filippakopoulou E, Ververi A, Efthymiou S, Dinopoulos A, Murphy D, Kartanou C, Vrachnos DM, Loupis T, Makrythanasis P, Stefanis L, Karadima G, Koutsis G, Kaliakatsos M, Houlden H, Walther TC, Farese RV. Partial Loss of FITM2 Function Causes Hereditary Spastic Paraplegia. Hum Mutat. 2026; 2026:5893503.
-
Nehoff H, Crozier I, Vernon H, James C, Fernández-Ávila AI, Bowes M, Gomez-Gonzalez E, Phoon C, DiLoreto K, Matsumura ME, van Haaften-Visser DY, Seaman C, Edwards MR, Morris-Rosendahl DJ, Simonetti K, Rippert AL, Ahrens-Nicklas RC, Tormey C, Bogush E, Kochhar A, Van Hove JLK, Kamsheh AM, Leone BA, Wortmann SB, Weintraub RG, Thompson WR, Silver ES, Zuckerman WA, Pearson J, Till J, Chatfield K, Goldstein A, McFarland R, Mayr JA, Doudney K. Pyrophosphatase 2 Deficiency: Clinical Presentation, Diagnosis and Management. Circ Genom Precis Med. 2026 Oct; 19(5):e005673.
-
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.
-
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).
-
Boslough M, Taylor MRG, Mestroni L, Lombardi R. Genetic Dilated Cardiomyopathy: A Review. Methodist Debakey Cardiovasc J. 2026; 22(4):68-77.
-
Li J, Karoor V, Frump AL, Zhao H, Liang S, Woodcock CC, Petrache I, Dai Z, Lahm T. Sexually Dimorphic Role of Estrogen Receptor a in Preserving Right Ventricular Endothelial Integrity. Arterioscler Thromb Vasc Biol. 2026 Nov; 46(11):e325390.
-
Cross CE, Brockman AA, Ihrie RA, Irish JM. Velociraptor Machine Learning Quantifies Similarity to Known Cell Types and Matches Cells Across Flow and Imaging Cytometry Platforms. Cytometry A. 2026 Sep; 109(9):649-663.
-
Brown SR, Sanchez-Pinto LN, Grunwell JR, Hu X, Coopersmith CM, Atreya MR, Rogerson CM, Geva A, Bennett TD, Chong G, Shah SS, Hall MW, Bhavani SV. Development and Validation of Temperature Trajectory-Based Phenotypes in Pediatric Sepsis: A Multicenter Retrospective Cohort Study, 2012-2018. Pediatr Crit Care Med. 2026 Oct 01; 27(10):1215-1223.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|