 Models, Genetic
"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.
| Descriptor ID |
D008957
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| MeSH Number(s) |
E05.599.395.397
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| Concept/Terms |
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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 this website by year, and whether "Models, Genetic" 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 |
|---|
| 1992 | 0 | 1 | 1 | | 1993 | 0 | 3 | 3 | | 1994 | 2 | 5 | 7 | | 1995 | 0 | 1 | 1 | | 1996 | 1 | 4 | 5 | | 1997 | 0 | 6 | 6 | | 1998 | 0 | 2 | 2 | | 1999 | 1 | 7 | 8 | | 2000 | 2 | 4 | 6 | | 2001 | 1 | 7 | 8 | | 2002 | 2 | 9 | 11 | | 2003 | 3 | 6 | 9 | | 2004 | 5 | 7 | 12 | | 2005 | 6 | 16 | 22 | | 2006 | 7 | 18 | 25 | | 2007 | 2 | 10 | 12 | | 2008 | 2 | 12 | 14 | | 2009 | 7 | 15 | 22 | | 2010 | 5 | 13 | 18 | | 2011 | 3 | 10 | 13 | | 2012 | 3 | 11 | 14 | | 2013 | 8 | 12 | 20 | | 2014 | 4 | 16 | 20 | | 2015 | 1 | 9 | 10 | | 2016 | 4 | 5 | 9 | | 2017 | 3 | 6 | 9 | | 2018 | 5 | 10 | 15 | | 2019 | 5 | 6 | 11 | | 2020 | 1 | 5 | 6 | | 2021 | 1 | 7 | 8 | | 2022 | 2 | 1 | 3 |
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Below are the most recent publications written about "Models, Genetic" by people in Profiles.
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Null M, Dupuis J, Sheinidashtegol P, Layer RM, Gignoux CR, Hendricks AE. RAREsim: A simulation method for very rare genetic variants. Am J Hum Genet. 2022 04 07; 109(4):680-691.
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Schubert R, Geoffroy E, Gregga I, Mulford AJ, Aguet F, Ardlie K, Gerszten R, Clish C, Van Den Berg D, Taylor KD, Durda P, Johnson WC, Cornell E, Guo X, Liu Y, Tracy R, Conomos M, Blackwell T, Papanicolaou G, Lappalainen T, Mikhaylova AV, Thornton TA, Cho MH, Gignoux CR, Lange L, Lange E, Rich SS, Rotter JI, Manichaikul A, Im HK, Wheeler HE. Protein prediction for trait mapping in diverse populations. PLoS One. 2022; 17(2):e0264341.
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Qi G, Dutta D, Leroux A, Ray D, Muschelli J, Crainiceanu C, Chatterjee N. Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Genet Epidemiol. 2022 03; 46(2):122-138.
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Rosser N, Edelman NB, Queste LM, Nelson M, Seixas F, Dasmahapatra KK, Mallet J. Complex basis of hybrid female sterility and Haldane's rule in Heliconius butterflies: Z-linkage and epistasis. Mol Ecol. 2022 02; 31(3):959-977.
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Allman PH, Aban I, Long DM, Patki A, MacKenzie T, Irvin MR, Lange LA, Lange E, Cutter G, Tiwari HK. Mendelian randomization in the multivariate general linear model framework. Genet Epidemiol. 2022 02; 46(1):17-31.
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Petersen BM, Ulmer SA, Rhodes ER, Gutierrez-Gonzalez MF, Dekosky BJ, Sprenger KG, Whitehead TA. Regulatory Approved Monoclonal Antibodies Contain Framework Mutations Predicted From Human Antibody Repertoires. Front Immunol. 2021; 12:728694.
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Lutz SM, Wu AC, Hokanson JE, Vansteelandt S, Lange C. Caution against examining the role of reverse causality in Mendelian Randomization. Genet Epidemiol. 2021 07; 45(5):445-454.
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Kwong AM, Blackwell TW, LeFaive J, de Andrade M, Barnard J, Barnes KC, Blangero J, Boerwinkle E, Burchard EG, Cade BE, Chasman DI, Chen H, Conomos MP, Cupples LA, Ellinor PT, Eng C, Gao Y, Guo X, Irvin MR, Kelly TN, Kim W, Kooperberg C, Lubitz SA, Mak ACY, Manichaikul AW, Mathias RA, Montasser ME, Montgomery CG, Musani S, Palmer ND, Peloso GM, Qiao D, Reiner AP, Roden DM, Shoemaker MB, Smith JA, Smith NL, Su JL, Tiwari HK, Weeks DE, Weiss ST, Scott LJ, Smith AV, Abecasis GR, Boehnke M, Kang HM. Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. Genetics. 2021 05 17; 218(1).
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Gleason KJ, Yang F, Chen LS. A robust two-sample transcriptome-wide Mendelian randomization method integrating GWAS with multi-tissue eQTL summary statistics. Genet Epidemiol. 2021 06; 45(4):353-371.
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Kemper KE, Yengo L, Zheng Z, Abdellaoui A, Keller MC, Goddard ME, Wray NR, Yang J, Visscher PM. Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. Nat Commun. 2021 02 16; 12(1):1050.
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