"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, comprising the ALLELES present at each GENETIC LOCUS.
Descriptor ID |
D005838
|
MeSH Number(s) |
G05.380
|
Concept/Terms |
|
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 |
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1993 | 1 | 5 | 6 |
1994 | 2 | 10 | 12 |
1995 | 0 | 2 | 2 |
1996 | 0 | 15 | 15 |
1997 | 1 | 21 | 22 |
1998 | 0 | 16 | 16 |
1999 | 0 | 23 | 23 |
2000 | 0 | 20 | 20 |
2001 | 0 | 21 | 21 |
2002 | 0 | 40 | 40 |
2003 | 2 | 35 | 37 |
2004 | 0 | 38 | 38 |
2005 | 2 | 63 | 65 |
2006 | 6 | 41 | 47 |
2007 | 1 | 48 | 49 |
2008 | 2 | 67 | 69 |
2009 | 4 | 56 | 60 |
2010 | 1 | 79 | 80 |
2011 | 3 | 79 | 82 |
2012 | 6 | 76 | 82 |
2013 | 2 | 56 | 58 |
2014 | 2 | 71 | 73 |
2015 | 5 | 59 | 64 |
2016 | 5 | 51 | 56 |
2017 | 3 | 44 | 47 |
2018 | 5 | 41 | 46 |
2019 | 8 | 30 | 38 |
2020 | 2 | 29 | 31 |
2021 | 3 | 24 | 27 |
2022 | 0 | 10 | 10 |
2023 | 0 | 11 | 11 |
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Below are the most recent publications written about "Genotype" by people in Profiles.
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Effect of the Fetal THRB Genotype on the Placenta. J Clin Endocrinol Metab. 2023 09 18; 108(10):e944-e948.
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Context-dependent environmental associations with endometrial cancer histotype and genotype. Int J Gynecol Cancer. 2023 08 07; 33(8):1215-1221.
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A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes. PLoS Genet. 2023 07; 19(7):e1010539.
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Detrimental effects of PCSK9 loss-of-function in the pediatric host response to sepsis are mediated through independent influence on Angiopoietin-1. Crit Care. 2023 06 26; 27(1):250.
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Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nat Commun. 2023 Jun 10; 14(1):3453.
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Physical Activity and Insulin Sensitivity Independently Attenuate the Effect of FTO rs9939609 on Obesity. Diabetes Care. 2023 05 01; 46(5):985-992.
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APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus. Lupus. 2023 May; 32(6):763-770.
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DPYD Testing: Time to Put Patient Safety First. J Clin Oncol. 2023 05 20; 41(15):2701-2705.
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Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. PLoS Genet. 2023 01; 19(1):e1010594.
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FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Res. 2023 01 06; 51(D1):D1300-D1311.