 Genotype
"Genotype" 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 genetic constitution of the individual comprised of the ALLELES present at each GENETIC LOCUS.
| Descriptor ID |
D005838
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| MeSH Number(s) |
G05.380
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Genotype".
Below are MeSH descriptors whose meaning is more specific than "Genotype".
This graph shows the total number of publications written about "Genotype" by people in this website by year, and whether "Genotype" 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 | | 1981 | 0 | 1 | 1 | | 1982 | 0 | 2 | 2 | | 1983 | 0 | 1 | 1 | | 1984 | 0 | 4 | 4 | | 1985 | 0 | 6 | 6 | | 1986 | 0 | 4 | 4 | | 1988 | 0 | 3 | 3 | | 1989 | 0 | 5 | 5 | | 1990 | 0 | 4 | 4 | | 1991 | 1 | 2 | 3 | | 1992 | 0 | 3 | 3 | | 1993 | 1 | 5 | 6 | | 1994 | 2 | 10 | 12 | | 1995 | 0 | 2 | 2 | | 1996 | 0 | 15 | 15 | | 1997 | 1 | 21 | 22 | | 1998 | 0 | 15 | 15 | | 1999 | 0 | 24 | 24 | | 2000 | 0 | 20 | 20 | | 2001 | 0 | 22 | 22 | | 2002 | 0 | 39 | 39 | | 2003 | 2 | 34 | 36 | | 2004 | 0 | 38 | 38 | | 2005 | 1 | 62 | 63 | | 2006 | 6 | 41 | 47 | | 2007 | 1 | 49 | 50 | | 2008 | 2 | 70 | 72 | | 2009 | 4 | 58 | 62 | | 2010 | 1 | 80 | 81 | | 2011 | 3 | 77 | 80 | | 2012 | 6 | 74 | 80 | | 2013 | 2 | 56 | 58 | | 2014 | 3 | 66 | 69 | | 2015 | 5 | 55 | 60 | | 2016 | 5 | 50 | 55 | | 2017 | 2 | 40 | 42 | | 2018 | 4 | 36 | 40 | | 2019 | 5 | 25 | 30 | | 2020 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genotype" by people in Profiles.
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Döhner K, Thiede C, Jahn N, Panina E, Gambietz A, Larson RA, Prior TW, Marcucci G, Jones D, Krauter J, Heuser M, Voso MT, Ottone T, Nomdedeu JF, Mandrekar SJ, Klisovic RB, Wei AH, Sierra J, Sanz MA, Brandwein JM, de Witte T, Jansen JH, Niederwieser D, Appelbaum FR, Medeiros BC, Tallman MS, Schlenk RF, Ganser A, Serve H, Ehninger G, Amadori S, Gathmann I, Benner A, Pallaud C, Stone RM, Döhner H, Bloomfield CD. Impact of NPM1/FLT3-ITD genotypes defined by the 2017 European LeukemiaNet in patients with acute myeloid leukemia. Blood. 2020 01 30; 135(5):371-380.
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Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, Shendure J, Soranzo N, McCarthy MI. A brief history of human disease genetics. Nature. 2020 01; 577(7789):179-189.
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Abdellaoui A, Sanchez-Roige S, Sealock J, Treur JL, Dennis J, Fontanillas P, Elson S. Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness. Hum Mol Genet. 2019 11 15; 28(22):3853-3865.
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Abney M, ElSherbiny A. Kinpute: using identity by descent to improve genotype imputation. Bioinformatics. 2019 11 01; 35(21):4321-4326.
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Schoettler N, Rodríguez E, Weidinger S, Ober C. Advances in asthma and allergic disease genetics: Is bigger always better? J Allergy Clin Immunol. 2019 12; 144(6):1495-1506.
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Song L, Liu A, Shi J. SummaryAUC: a tool for evaluating the performance of polygenic risk prediction models in validation datasets with only summary level statistics. Bioinformatics. 2019 10 15; 35(20):4038-4044.
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Cunningham PN, Wang Z, Grove ML, Cooper-DeHoff RM, Beitelshees AL, Gong Y, Gums JG, Johnson JA, Turner ST, Boerwinkle E, Chapman AB. Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. PLoS One. 2019; 14(9):e0221957.
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Alliey-Rodriguez N, Grey TA, Shafee R, Asif H, Lutz O, Bolo NR, Padmanabhan J, Tandon N, Klinger M, Reis K, Spring J, Coppes L, Zeng V, Hegde RR, Hoang DT, Bannai D, Nawaz U, Henson P, Liu S, Gage D, McCarroll S, Bishop JR, Hill S, Reilly JL, Lencer R, Clementz BA, Buckley P, Glahn DC, Meda SA, Narayanan B, Pearlson G, Keshavan MS, Ivleva EI, Tamminga C, Sweeney JA, Curtis D, Badner JA, Keedy S, Rapoport J, Liu C, Gershon ES. NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Transl Psychiatry. 2019 09 17; 9(1):230.
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Poelwijk FJ, Socolich M, Ranganathan R. Learning the pattern of epistasis linking genotype and phenotype in a protein. Nat Commun. 2019 09 16; 10(1):4213.
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Goel G, Tye-Din JA, Qiao SW, Russell AK, Mayassi T, Ciszewski C, Sarna VK, Wang S, Goldstein KE, Dzuris JL, Williams LJ, Xavier RJ, Lundin KEA, Jabri B, Sollid LM, Anderson RP. Cytokine release and gastrointestinal symptoms after gluten challenge in celiac disease. Sci Adv. 2019 08; 5(8):eaaw7756.
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