 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 |
|---|
| 1991 | 2 | 5 | 7 | | 1992 | 5 | 4 | 9 | | 1993 | 2 | 6 | 8 | | 1994 | 5 | 10 | 15 | | 1995 | 0 | 7 | 7 | | 1996 | 1 | 6 | 7 | | 1997 | 0 | 9 | 9 | | 1998 | 2 | 5 | 7 | | 1999 | 2 | 10 | 12 | | 2000 | 2 | 5 | 7 | | 2001 | 1 | 15 | 16 | | 2002 | 2 | 10 | 12 | | 2003 | 4 | 13 | 17 | | 2004 | 9 | 15 | 24 | | 2005 | 11 | 23 | 34 | | 2006 | 10 | 25 | 35 | | 2007 | 2 | 18 | 20 | | 2008 | 4 | 20 | 24 | | 2009 | 7 | 20 | 27 | | 2010 | 8 | 21 | 29 | | 2011 | 4 | 14 | 18 | | 2012 | 6 | 13 | 19 | | 2013 | 13 | 14 | 27 | | 2014 | 5 | 16 | 21 | | 2015 | 1 | 14 | 15 | | 2016 | 5 | 8 | 13 | | 2017 | 7 | 11 | 18 | | 2018 | 7 | 15 | 22 | | 2019 | 4 | 8 | 12 | | 2020 | 1 | 5 | 6 | | 2021 | 0 | 2 | 2 |
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Below are the most recent publications written about "Models, Genetic" by people in Profiles.
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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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Demange PA, Malanchini M, Mallard TT, Biroli P, Cox SR, Grotzinger AD, Tucker-Drob EM, Abdellaoui A, Arseneault L, van Bergen E, Boomsma DI, Caspi A, Corcoran DL, Domingue BW, Harris KM, Ip HF, Mitchell C, Moffitt TE, Poulton R, Prinz JA, Sugden K, Wertz J, Williams BS, de Zeeuw EL, Belsky DW, Harden KP, Nivard MG. Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. Nat Genet. 2021 01; 53(1):35-44.
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Santoriello FJ, Michel L, Unterweger D, Pukatzki S. Pandemic Vibrio cholerae shuts down site-specific recombination to retain an interbacterial defence mechanism. Nat Commun. 2020 12 07; 11(1):6246.
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Drogalis LK, Batey RT. Requirements for efficient ligand-gated co-transcriptional switching in designed variants of the B. subtilis pbuE adenine-responsive riboswitch in E. coli. PLoS One. 2020; 15(12):e0243155.
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Fukushima K, Pollock DD. Amalgamated cross-species transcriptomes reveal organ-specific propensity in gene expression evolution. Nat Commun. 2020 09 08; 11(1):4459.
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Li X, Li Z, Zhou H, Gaynor SM, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Aslibekyan S, Ballantyne CM, Bielak LF, Blangero J, Boerwinkle E, Bowden DW, Broome JG, Conomos MP, Correa A, Cupples LA, Curran JE, Freedman BI, Guo X, Hindy G, Irvin MR, Kardia SLR, Kathiresan S, Khan AT, Kooperberg CL, Laurie CC, Liu XS, Mahaney MC, Manichaikul AW, Martin LW, Mathias RA, McGarvey ST, Mitchell BD, Montasser ME, Moore JE, Morrison AC, O'Connell JR, Palmer ND, Pampana A, Peralta JM, Peyser PA, Psaty BM, Redline S, Rice KM, Rich SS, Smith JA, Tiwari HK, Tsai MY, Vasan RS, Wang FF, Weeks DE, Weng Z, Wilson JG, Yanek LR, Neale BM, Sunyaev SR, Abecasis GR, Rotter JI, Willer CJ, Peloso GM, Natarajan P, Lin X. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale. Nat Genet. 2020 09; 52(9):969-983.
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Keys KL, Mak ACY, White MJ, Eckalbar WL, Dahl AW, Mefford J, Mikhaylova AV, Contreras MG, Elhawary JR, Eng C, Hu D, Huntsman S, Oh SS, Salazar S, Lenoir MA, Ye JC, Thornton TA, Zaitlen N, Burchard EG, Gignoux CR. On the cross-population generalizability of gene expression prediction models. PLoS Genet. 2020 08; 16(8):e1008927.
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Liyanarachchi S, Gudmundsson J, Ferkingstad E, He H, Jonasson JG, Tragante V, Asselbergs FW, Xu L, Kiemeney LA, Netea-Maier RT, Mayordomo JI, Plantinga TS, Hjartarson H, Hrafnkelsson J, Sturgis EM, Brock P, Nabhan F, Thorleifsson G, Ringel MD, Stefansson K, de la Chapelle A. Assessing thyroid cancer risk using polygenic risk scores. Proc Natl Acad Sci U S A. 2020 03 17; 117(11):5997-6002.
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Solis-Lemus CR, Fischer ST, Todor A, Liu C, Leslie EJ, Cutler DJ, Ghosh D, Epstein MP. Leveraging Family History in Case-Control Analyses of Rare Variation. Genetics. 2020 02; 214(2):295-303.
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Kooakachai M, LaBerge G, Santorico SA. A new framework to test parent-child and full sibling relationships with population substructure. Forensic Sci Int. 2019 Dec; 305:110012.
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