 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 |
|---|
| 1980 | 0 | 1 | 1 | | 1982 | 0 | 1 | 1 | | 1983 | 0 | 4 | 4 | | 1984 | 0 | 1 | 1 | | 1985 | 0 | 1 | 1 | | 1986 | 0 | 2 | 2 | | 1988 | 0 | 2 | 2 | | 1989 | 0 | 3 | 3 | | 1990 | 0 | 7 | 7 | | 1991 | 0 | 8 | 8 | | 1992 | 0 | 6 | 6 | | 1993 | 1 | 4 | 5 | | 1994 | 1 | 6 | 7 | | 1995 | 0 | 6 | 6 | | 1996 | 0 | 16 | 16 | | 1997 | 0 | 8 | 8 | | 1998 | 0 | 15 | 15 | | 1999 | 1 | 18 | 19 | | 2000 | 0 | 14 | 14 | | 2001 | 1 | 18 | 19 | | 2002 | 1 | 17 | 18 | | 2003 | 3 | 20 | 23 | | 2004 | 1 | 25 | 26 | | 2005 | 3 | 25 | 28 | | 2006 | 2 | 26 | 28 | | 2007 | 9 | 22 | 31 | | 2008 | 4 | 32 | 36 | | 2009 | 4 | 25 | 29 | | 2010 | 1 | 26 | 27 | | 2011 | 5 | 42 | 47 | | 2012 | 4 | 44 | 48 | | 2013 | 11 | 41 | 52 | | 2014 | 12 | 39 | 51 | | 2015 | 14 | 53 | 67 | | 2016 | 8 | 38 | 46 | | 2017 | 11 | 38 | 49 | | 2018 | 12 | 51 | 63 | | 2019 | 2 | 42 | 44 | | 2020 | 2 | 19 | 21 | | 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Mer AS, Heath EM, Madani Tonekaboni SA, Dogan-Artun N, Nair SK, Murison A, Garcia-Prat L, Shlush L, Hurren R, Voisin V, Bader GD, Nislow C, Rantalainen M, Lehmann S, Gower M, Guidos CJ, Lupien M, Dick JE, Minden MD, Schimmer AD, Haibe-Kains B. Biological and therapeutic implications of a unique subtype of NPM1 mutated AML. Nat Commun. 2021 02 16; 12(1):1054.
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Jagesar RR, Roozen MC, van der Heijden I, Ikani N, Tyborowska A, Penninx BWJH, Ruhe HG, Sommer IEC, Kas MJ, Vorstman JAS. Digital phenotyping and the COVID-19 pandemic: Capturing behavioral change in patients with psychiatric disorders. Eur Neuropsychopharmacol. 2021 01; 42:115-120.
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Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, van Amelsvoort T, Arango C, Armando M, Campbell LE, Cubells JF, Eliez S, Garcia-Minaur S, Gothelf D, Kates WR, Murphy KC, Murphy CM, Murphy DG, Philip N, Repetto GM, Shashi V, Simon TJ, Suñer DH, Vicari S, Scherer SW, Bearden CE, Vorstman JAS. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nat Med. 2020 12; 26(12):1912-1918.
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Hofer E, Roshchupkin GV, Adams HHH, Knol MJ, Lin H, Li S, Zare H, Ahmad S, Armstrong NJ, Satizabal CL, Bernard M, Bis JC, Gillespie NA, Luciano M, Mishra A, Scholz M, Teumer A, Xia R, Jian X, Mosley TH, Saba Y, Pirpamer L, Seiler S, Becker JT, Carmichael O, Rotter JI, Psaty BM, Lopez OL, Amin N, van der Lee SJ, Yang Q, Himali JJ, Maillard P, Beiser AS, DeCarli C, Karama S, Lewis L, Harris M, Bastin ME, Deary IJ, Veronica Witte A, Beyer F, Loeffler M, Mather KA, Schofield PR, Thalamuthu A, Kwok JB, Wright MJ, Ames D, Trollor J, Jiang J, Brodaty H, Wen W, Vernooij MW, Hofman A, Uitterlinden AG, Niessen WJ, Wittfeld K, Bülow R, Völker U, Pausova Z, Bruce Pike G, Maingault S, Crivello F, Tzourio C, Amouyel P, Mazoyer B, Neale MC, Franz CE, Lyons MJ, Panizzon MS, Andreassen OA, Dale AM, Logue M, Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Stein JL, Thompson PM, Medland SE, Sachdev PS, Kremen WS, Wardlaw JM, Villringer A, van Duijn CM, Grabe HJ, Longstreth WT, Fornage M, Paus T, Debette S, Ikram MA, Schmidt H, Schmidt R, Seshadri S. Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nat Commun. 2020 09 22; 11(1):4796.
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Biswas A, Krishnan P, Amirabadi A, Blaser S, Mercimek-Andrews S, Shroff M. Expanding the Neuroimaging Phenotype of Neuronal Ceroid Lipofuscinoses. AJNR Am J Neuroradiol. 2020 10; 41(10):1930-1936.
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Polito P, Zanatta E, Felicetti M, Benvenuti F, Favaro M, Cozzi F, Ramonda R, Doria A. Skin ulcers in systemic sclerosis: correlation with clinical phenotype in a monocentric cohort from the north-east of Italy. Clin Exp Rheumatol. 2020 May-Jun; 38 Suppl 125(3):148-153.
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Guillen Sacoto MJ, Tchasovnikarova IA, Torti E, Forster C, Andrew EH, Anselm I, Baranano KW, Briere LC, Cohen JS, Craigen WJ, Cytrynbaum C, Ekhilevitch N, Elrick MJ, Fatemi A, Fraser JL, Gallagher RC, Guerin A, Haynes D, High FA, Inglese CN, Kiss C, Koenig MK, Krier J, Lindstrom K, Marble M, Meddaugh H, Moran ES, Morel CF, Mu W, Muller EA, Nance J, Natowicz MR, Numis AL, Ostrem B, Pappas J, Stafstrom CE, Streff H, Sweetser DA, Szybowska M, Walker MA, Wang W, Weiss K, Weksberg R, Wheeler PG, Yoon G, Kingston RE, Juusola J. De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism. Am J Hum Genet. 2020 08 06; 107(2):352-363.
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Cacciotti C, Fleming A, Ramaswamy V. Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy. J Pathol. 2020 07; 251(3):249-261.
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Hachem LD, Mathieu F, Lamberti-Pasculli M, Hanak BW, Zeller R, Kulkarni AV, Drake J, Ibrahim GM. Klippel Feil Syndrome: Clinical Phenotypes Associated With Surgical Treatment. Spine (Phila Pa 1976). 2020 Jun 01; 45(11):718-726.
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Woodbury-Smith M, Zarrei M, Wei J, Thiruvahindrapuram B, O'Connor I, Paterson AD, Yuen RKC, Dastan J, Stavropoulos DJ, Howe JL, Thompson A, Parlier M, Fernandez B, Piven J, Anagnostou E, Scherer SW, Vieland VJ, Szatmari P. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees. Am J Med Genet B Neuropsychiatr Genet. 2020 07; 183(5):268-276.
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