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 | 40 | 42 | | 2003 | 1 | 37 | 38 | | 2004 | 3 | 47 | 50 | | 2005 | 4 | 45 | 49 | | 2006 | 4 | 44 | 48 | | 2007 | 4 | 54 | 58 | | 2008 | 3 | 45 | 48 | | 2009 | 5 | 53 | 58 | | 2010 | 6 | 88 | 94 | | 2011 | 6 | 74 | 80 | | 2012 | 6 | 75 | 81 | | 2013 | 8 | 93 | 101 | | 2014 | 8 | 100 | 108 | | 2015 | 18 | 104 | 122 | | 2016 | 15 | 92 | 107 | | 2017 | 11 | 112 | 123 | | 2018 | 13 | 115 | 128 | | 2019 | 15 | 113 | 128 | | 2020 | 6 | 89 | 95 | | 2021 | 14 | 115 | 129 | | 2022 | 0 | 65 | 65 | | 2023 | 1 | 95 | 96 | | 2024 | 27 | 59 | 86 | | 2025 | 4 | 84 | 88 | | 2026 | 1 | 29 | 30 |
To return to the timeline, click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
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Iveson MH, Mukherjee M, Davidson EM, Zhang H, Sherlock L, Ball EL, Mair G, Hosking A, Whalley H, Poon MTC, Wardlaw JM, Kent DM, Tobin R, Grover C, Alex B, Whiteley W. Clinically reported covert cerebrovascular disease and risk of neurological disease: a whole-population cohort of 367 988 people using natural language processing. J Neurol Neurosurg Psychiatry. 2026 Jun 12; 97(7):630-638.
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Purdy AL, Bakhshian Nik A, Arkatkar AA, Hasan P, Flinn MA, Choudhury P, Wood C, Takizawa A, Malloy L, Tutaj M, Drysdale TA, Bridgewater D, Link BA, Plageman TF, Kwitek AE, Dwinell MR, Saba LM, O'Meara CC, Patterson M. Genome-wide association mapping and targeted loss of function studies identify Shroom3 as a driver of hyperpolyploidy and ventricular dilation. Proc Natl Acad Sci U S A. 2026 Jun 02; 123(22):e2522068123.
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Files DC, Matthay MA, Chapple AG, Barragan AB, Mabrey L, Gibbs KW, Krall J, Aggarwal NR, Burnham EL, Liu KD, Meyer NJ, Nates JL, Youssef FA, Friedman E, Kett DH, Koff J, Russell DW, Calfee CS, Eklund M, Esserman LJ. Biological subphenotypes in severe acute hypoxaemic respiratory failure and acute respiratory distress syndrome using rapid prospective classification (SPARC) in the USA: a multicentre, observational, study. Lancet Respir Med. 2026 Jul; 14(7):601-608.
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Vallelian F, Schaer DJ, Lechartier B, Buehler PW, Irwin DC. Sickle cell disease-associated pulmonary hypertension: an integrated framework linking pathologies, mechanisms, and clinical phenotypes. EBioMedicine. 2026 Jun; 128:106288.
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Alberti MO, Nonavinkere Srivatsan S, Shao J, Fei DL, Zhu M, Pastrana CC, Chavez M, Tarnawsky SP, Grieb S, Graubert TA, Abdel-Wahab O, Walter MJ. U2af1S34F and U2af1Q157R myeloid neoplasm-associated hotspot mutations induce distinct hematopoietic phenotypes in mice. Leukemia. 2026 Jul; 40(7):1467-1481.
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Sherman ME, Etievant L, Vierkant RA, Winham SJ, Ruddy KJ, Pacheco-Spann L, Wickland DP, Cruz-Reyes N, Stallings-Mann M, Radisky D, Thompson EA, Kachergus JM, Shi J, Rosenberg SM, Snow C, Kirkner GJ, Schapira L, Peppercorn JM, Come S, Borges VF, Warner E, Collins LC, Partridge AH, Pfeiffer RM. Postpartum breast cancer: evidence for a distinct phenotype. J Natl Cancer Inst. 2026 May 01; 118(5):926-936.
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Zhang J, Moll M, Debban CL, Hobbs BD, Rijhwani H, Washko GR, Celli BR, Silverman EK, Bakke P, Oelsner EC, Barr RG, Agustí A, Faner R, Bruselle GG, Humphries SM, Lynch DA, Dupuis J, Manichaikul AW, O'Connor GT, Cho MH. Body Mass Index-related genetic factors and COPD imaging phenotypes. Ann Am Thorac Soc. 2026 05 01; 23(5):720-727.
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Watts LM, Chang MSM, Lewis-Orr E, Walton IS, Leinhos L, Tooze RS, Pei Y, Calpena E, Vedovato-Dos-Santos JH, Steel D, Reid KM, Kurian MA, Mohammad SS, Cantagrel V, Siquier K, Boddaert N, Rio M, Blyth M, Kraus A, Al Mutairi F, Holder SE, Clowes VE, Cobben JM, Timberlake AT, Elias ER, Stewart H, Johnson D, Cohen JS, Barañano KW, Ceulemans S, Jones MC, Ortega Rico RI, Haug MG, Berland S, Bombei HM, Paulson A, Sidhu A, Gooch CF, da Rocha KM, Passos Bueno MR, Topa A, Muslimovic AZ, Maltese G, Tan TY, McCann E, Lord H, Chin HL, Lin J, Li-Meng Goh D, Keren B, Charles P, Delchev T, Avdjieva-Tzavella D, Alawbathani S, Almeida L, Kdissa A, Al-Ali R, Bertoli-Avella AM, Johnson D, Wilkie AOM, Arkell RM, Shears DJ, Twigg SRF. Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis. Genet Med. 2026 Jun; 28(6):102585.
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Endo Y, Kawashima J, Chatzipanagiotou O, Woldesenbet S, Aucejo F, Marques HP, Lam V, Lesurtel M, Popescu I, Weiss M, Martel G, Poultsides GA, Ruzzenente A, Endo I, Gleisner A, Shen F, Pawlik TM. Machine learning-based clustering differentiates bilateral hepatocellular carcinoma characteristics and prognosis. Surgery. 2026 Jun; 194:110186.
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Koparir A, Carbajal PB, Zamini M, Naghinejad M, Najarzadeh Torbati P, Hofrichter MAH, Tovornik S, Koparir E, Dragicevic Babic N, Rad A, Owrang D, Kalay I, Chamanrou N, Martínez Völter LN, Christophersen N, Baranzehi T, Rajati M, Loum S, Kunstmann E, Shadab M, Abbasi AA, Doosti M, Alidadiani N, Ghaderi S, Haack TB, Alavi S, Doll J, Kremer H, Kordi-Tamandani DM, Murphy D, Mohammad R, Hebestreit H, Ghayoor Karimiani E, Flandin S, Linares P, Villalobos D, Houlden H, Galehdari H, Shehata-Dieler W, Maroofian R, Haaf T, Vona B. Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics. Mol Med. 2026 Apr 07; 32(1).
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