 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 | 9 | 9 | 18 | | 2001 | 8 | 13 | 21 | | 2002 | 23 | 13 | 36 | | 2003 | 12 | 15 | 27 | | 2004 | 13 | 16 | 29 | | 2005 | 15 | 17 | 32 | | 2006 | 20 | 17 | 37 | | 2007 | 16 | 17 | 33 | | 2008 | 20 | 25 | 45 | | 2009 | 22 | 25 | 47 | | 2010 | 23 | 23 | 46 | | 2011 | 31 | 31 | 62 | | 2012 | 25 | 31 | 56 | | 2013 | 24 | 18 | 42 | | 2014 | 32 | 30 | 62 | | 2015 | 19 | 22 | 41 | | 2016 | 17 | 14 | 31 | | 2017 | 20 | 24 | 44 | | 2018 | 22 | 25 | 47 | | 2019 | 19 | 25 | 44 | | 2020 | 14 | 18 | 32 | | 2021 | 3 | 3 | 6 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Kasela S, Ortega VE, Martorella M, Garudadri S, Nguyen J, Ampleford E, Pasanen A, Nerella S, Buschur KL, Barjaktarevic IZ, Barr RG, Bleecker ER, Bowler RP, Comellas AP, Cooper CB, Couper DJ, Criner GJ, Curtis JL, Han MK, Hansel NN, Hoffman EA, Kaner RJ, Krishnan JA, Martinez FJ, McDonald MN, Meyers DA, Paine R, Peters SP, Castro M, Denlinger LC, Erzurum SC, Fahy JV, Israel E, Jarjour NN, Levy BD, Li X, Moore WC, Wenzel SE, Zein J. Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium. Genome Med. 2021 04 21; 13(1):66.
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Hallmark B, Wegienka G, Havstad S, Billheimer D, Ownby D, Mendonca EA, Gress L, Stern DA, Myers JB, Khurana Hershey GK, Hoepner L, Miller RL, Lemanske RF, Jackson DJ, Gold DR, O'Connor GT, Nicolae DL, Gern JE, Ober C, Wright AL, Martinez FD. Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood. Am J Respir Crit Care Med. 2021 04 01; 203(7):864-870.
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Richardson ME, Hu C, Lee KY, LaDuca H, Fulk K, Durda KM, Deckman AM, Goldgar DE, Monteiro ANA, Gnanaolivu R, Hart SN, Polley EC, Chao E, Pesaran T, Couch FJ. Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance. Am J Hum Genet. 2021 03 04; 108(3):458-468.
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Sapoval N, Mahmoud M, Jochum MD, Liu Y, Elworth RAL, Wang Q, Albin D, Ogilvie HA, Lee MD, Villapol S, Hernandez KM, Maljkovic Berry I, Foox J, Beheshti A, Ternus K, Aagaard KM, Posada D, Mason CE, Sedlazeck FJ, Treangen TJ. SARS-CoV-2 genomic diversity and the implications for qRT-PCR diagnostics and transmission. Genome Res. 2021 04; 31(4):635-644.
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Harpak A, Przeworski M. The evolution of group differences in changing environments. PLoS Biol. 2021 01; 19(1):e3001072.
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Hu C, Hart SN, Gnanaolivu R, Huang H, Lee KY, Na J, Gao C, Lilyquist J, Yadav S, Boddicker NJ, Samara R, Klebba J, Ambrosone CB, Anton-Culver H, Auer P, Bandera EV, Bernstein L, Bertrand KA, Burnside ES, Carter BD, Eliassen H, Gapstur SM, Gaudet M, Haiman C, Hodge JM, Hunter DJ, Jacobs EJ, John EM, Kooperberg C, Kurian AW, Le Marchand L, Lindstroem S, Lindstrom T, Ma H, Neuhausen S, Newcomb PA, O'Brien KM, Olson JE, Ong IM, Pal T, Palmer JR, Patel AV, Reid S, Rosenberg L, Sandler DP, Scott C, Tamimi R, Taylor JA, Trentham-Dietz A, Vachon CM, Weinberg C, Yao S, Ziogas A, Weitzel JN, Goldgar DE, Domchek SM, Nathanson KL, Kraft P, Polley EC, Couch FJ. A Population-Based Study of Genes Previously Implicated in Breast Cancer. N Engl J Med. 2021 02 04; 384(5):440-451.
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Biddanda A, Rice DP, Novembre J. A variant-centric perspective on geographic patterns of human allele frequency variation. Elife. 2020 12 22; 9.
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Mochel F, Rastetter A, Ceulemans B, Platzer K, Yang S, Shinde DN, Helbig KL, Lopergolo D, Mari F, Renieri A, Benetti E, Canitano R, Waisfisz Q, Plomp AS, Huisman SA, Wilson GN, Cathey SS, Louie RJ, Gaudio DD, Waggoner D, Kacker S, Nugent KM, Roeder ER, Bruel AL, Thevenon J, Ehmke N, Horn D, Holtgrewe M, Kaiser FJ, Kamphausen SB, Abou Jamra R, Weckhuysen S, Dalle C, Depienne C. Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders. Brain. 2020 12 01; 143(12):3564-3573.
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Fair BJ, Blake LE, Sarkar A, Pavlovic BJ, Cuevas C, Gilad Y. Gene expression variability in human and chimpanzee populations share common determinants. Elife. 2020 10 21; 9.
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Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, Skol AD, Garrido-Martín D, Reverter F, Brown A, Evans P, Gamazon ER, Payne A, Bonazzola R, Barbeira AN, Hamel AR, Martinez-Perez A, Soria JM. The impact of sex on gene expression across human tissues. Science. 2020 09 11; 369(6509).
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