 Genetic Variation
"Genetic Variation" 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 phenotypic and genotypic differences among individuals in a population.
| Descriptor ID |
D014644
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| MeSH Number(s) |
G05.365
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| Concept/Terms |
Genetic Variation- Genetic Variation
- Genetic Diversity
- Variation, Genetic
- Diversity, Genetic
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Below are MeSH descriptors whose meaning is more general than "Genetic Variation".
Below are MeSH descriptors whose meaning is more specific than "Genetic Variation".
This graph shows the total number of publications written about "Genetic Variation" by people in this website by year, and whether "Genetic Variation" 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 | 1 | 1 | 2 | | 1981 | 1 | 1 | 2 | | 1982 | 1 | 3 | 4 | | 1983 | 1 | 2 | 3 | | 1984 | 2 | 0 | 2 | | 1985 | 0 | 1 | 1 | | 1986 | 1 | 2 | 3 | | 1987 | 1 | 1 | 2 | | 1988 | 0 | 3 | 3 | | 1989 | 3 | 1 | 4 | | 1990 | 2 | 3 | 5 | | 1991 | 6 | 6 | 12 | | 1992 | 5 | 3 | 8 | | 1993 | 2 | 3 | 5 | | 1994 | 4 | 6 | 10 | | 1995 | 1 | 6 | 7 | | 1996 | 6 | 3 | 9 | | 1997 | 4 | 3 | 7 | | 1998 | 3 | 9 | 12 | | 1999 | 5 | 5 | 10 | | 2000 | 10 | 10 | 20 | | 2001 | 8 | 13 | 21 | | 2002 | 23 | 13 | 36 | | 2003 | 13 | 16 | 29 | | 2004 | 13 | 16 | 29 | | 2005 | 15 | 19 | 34 | | 2006 | 20 | 19 | 39 | | 2007 | 16 | 17 | 33 | | 2008 | 21 | 25 | 46 | | 2009 | 23 | 25 | 48 | | 2010 | 23 | 24 | 47 | | 2011 | 31 | 31 | 62 | | 2012 | 25 | 32 | 57 | | 2013 | 26 | 18 | 44 | | 2014 | 33 | 30 | 63 | | 2015 | 20 | 22 | 42 | | 2016 | 18 | 14 | 32 | | 2017 | 21 | 24 | 45 | | 2018 | 22 | 26 | 48 | | 2019 | 19 | 25 | 44 | | 2020 | 15 | 19 | 34 | | 2021 | 9 | 14 | 23 | | 2022 | 1 | 2 | 3 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Novembre J. The background and legacy of Lewontin's apportionment of human genetic diversity. Philos Trans R Soc Lond B Biol Sci. 2022 06 06; 377(1852):20200406.
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Kone B, Somboro AM, Kone M, Holl JL, Baya B, Dabitao D, Diallo D, Diarra B, Kone A, Sarro YDS, Sanogo M, Togo AC, Murphy RL, Diallo S, Coulibaly N, Camara F, Samake S, Diakite M, Doumbia S, Maiga M. Molecular epidemiology and genetic diversity of Mycobacterium tuberculosis complex in referral health centers of Bamako, Mali: What is new? Int J Infect Dis. 2022 Apr; 117:204-211.
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Feurstein S, Hahn CN, Mehta N, Godley LA. A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias. Genet Med. 2022 04; 24(4):931-954.
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Ferkingstad E, Sulem P, Atlason BA, Sveinbjornsson G, Magnusson MI, Styrmisdottir EL, Gunnarsdottir K, Helgason A, Oddsson A, Halldorsson BV, Jensson BO, Zink F, Halldorsson GH, Masson G, Arnadottir GA, Katrinardottir H, Juliusson K, Magnusson MK, Magnusson OT, Fridriksdottir R, Saevarsdottir S, Gudjonsson SA, Stacey SN, Rognvaldsson S, Eiriksdottir T, Olafsdottir TA, Steinthorsdottir V, Tragante V, Ulfarsson MO, Stefansson H, Jonsdottir I, Holm H, Rafnar T, Melsted P, Saemundsdottir J, Norddahl GL, Lund SH, Gudbjartsson DF, Thorsteinsdottir U, Stefansson K. Large-scale integration of the plasma proteome with genetics and disease. Nat Genet. 2021 12; 53(12):1712-1721.
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Randolph HE, Fiege JK, Thielen BK, Mickelson CK, Shiratori M, Barroso-Batista J, Langlois RA, Barreiro LB. Genetic ancestry effects on the response to viral infection are pervasive but cell type specific. Science. 2021 Nov 26; 374(6571):1127-1133.
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Olson NC, Raffield LM, Moxley AH, Miller-Fleming TW, Auer PL, Franceschini N, Ngo D, Thornton TA, Lange EM, Li Y, Nickerson DA, Zakai NA, Gerszten RE, Cox NJ, Correa A, Mohlke KL, Reiner AP. Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults. Circ Genom Precis Med. 2021 12; 14(6):e003421.
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Mikaelsdottir E, Thorleifsson G, Stefansdottir L, Halldorsson G, Sigurdsson JK, Lund SH, Tragante V, Melsted P, Rognvaldsson S, Norland K, Helgadottir A, Magnusson MK, Ragnarsson GB, Kristinsson SY, Reykdal S, Vidarsson B, Gudmundsdottir IJ, Olafsson I, Onundarson PT, Sigurdardottir O, Sigurdsson EL, Grondal G, Geirsson AJ, Geirsson G, Gudmundsson J, Holm H, Saevarsdottir S, Jonsdottir I, Thorgeirsson G, Gudbjartsson DF, Thorsteinsdottir U, Rafnar T, Stefansson K. Genetic variants associated with platelet count are predictive of human disease and physiological markers. Commun Biol. 2021 09 27; 4(1):1132.
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Visscher PM, Yengo L, Cox NJ, Wray NR. Discovery and implications of polygenicity of common diseases. Science. 2021 Sep 24; 373(6562):1468-1473.
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Nosol K, Bang-Sørensen R, Irobalieva RN, Erramilli SK, Stieger B, Kossiakoff AA, Locher KP. Structures of ABCB4 provide insight into phosphatidylcholine translocation. Proc Natl Acad Sci U S A. 2021 08 17; 118(33).
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Marcus J, Ha W, Barber RF, Novembre J. Fast and flexible estimation of effective migration surfaces. Elife. 2021 07 30; 10.
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