"Models, Genetic" 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.
Theoretical representations that simulate the behavior or activity of genetic processes or phenomena. They include the use of mathematical equations, computers, and other electronic equipment.
Below are MeSH descriptors whose meaning is more general than "Models, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Models, Genetic".
This graph shows the total number of publications written about "Models, Genetic" by people in Harvard Catalyst Profiles by year, and whether "Models, Genetic" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 4 | 16 | 20 |
1995 | 4 | 25 | 29 |
1996 | 3 | 25 | 28 |
1997 | 3 | 16 | 19 |
1998 | 5 | 19 | 24 |
1999 | 4 | 58 | 62 |
2000 | 16 | 60 | 76 |
2001 | 13 | 60 | 73 |
2002 | 17 | 69 | 86 |
2003 | 20 | 80 | 100 |
2004 | 24 | 57 | 81 |
2005 | 34 | 64 | 98 |
2006 | 24 | 85 | 109 |
2007 | 26 | 81 | 107 |
2008 | 28 | 80 | 108 |
2009 | 21 | 74 | 95 |
2010 | 26 | 73 | 99 |
2011 | 23 | 85 | 108 |
2012 | 34 | 74 | 108 |
2013 | 23 | 59 | 82 |
2014 | 31 | 53 | 84 |
2015 | 30 | 50 | 80 |
2016 | 29 | 44 | 73 |
2017 | 24 | 44 | 68 |
2018 | 18 | 38 | 56 |
2019 | 19 | 35 | 54 |
2020 | 26 | 29 | 55 |
2021 | 21 | 29 | 50 |
2022 | 5 | 4 | 9 |
2023 | 3 | 7 | 10 |
2024 | 0 | 4 | 4 |
Below are the most recent publications written about "Models, Genetic" by people in Profiles.
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Genetic drivers and cellular selection of female mosaic X chromosome loss. Nature. 2024 Jul; 631(8019):134-141.
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Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores. Sci Rep. 2024 05 30; 14(1):12436.
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Biologically informed NeuralODEs for genome-wide regulatory dynamics. Genome Biol. 2024 05 21; 25(1):127.
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A resampling-based approach to share reference panels. Nat Comput Sci. 2024 May; 4(5):360-366.
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Differences in set-based tests for sparse alternatives when testing sets of outcomes compared to sets of explanatory factors in genetic association studies. Biostatistics. 2023 12 15; 25(1):171-187.
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A genomic mutational constraint map using variation in 76,156 human genomes. Nature. 2024 Jan; 625(7993):92-100.
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Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix. Nat Commun. 2023 Dec 02; 14(1):7954.
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Inference of Coalescence Times and Variant Ages Using Convolutional Neural Networks. Mol Biol Evol. 2023 10 04; 40(10).
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Fast kernel-based association testing of non-linear genetic effects for biobank-scale data. Nat Commun. 2023 08 15; 14(1):4936.
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Recurrent mutation in the ancestry of a rare variant. Genetics. 2023 07 06; 224(3).