 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 | 2 | 8 | | 1997 | 4 | 3 | 7 | | 1998 | 3 | 9 | 12 | | 1999 | 5 | 5 | 10 | | 2000 | 9 | 10 | 19 | | 2001 | 8 | 13 | 21 | | 2002 | 23 | 13 | 36 | | 2003 | 13 | 16 | 29 | | 2004 | 13 | 16 | 29 | | 2005 | 15 | 19 | 34 | | 2006 | 20 | 18 | 38 | | 2007 | 16 | 17 | 33 | | 2008 | 20 | 25 | 45 | | 2009 | 22 | 25 | 47 | | 2010 | 23 | 25 | 48 | | 2011 | 31 | 31 | 62 | | 2012 | 25 | 31 | 56 | | 2013 | 25 | 17 | 42 | | 2014 | 34 | 29 | 63 | | 2015 | 20 | 22 | 42 | | 2016 | 18 | 14 | 32 | | 2017 | 21 | 23 | 44 | | 2018 | 21 | 25 | 46 | | 2019 | 18 | 25 | 43 | | 2020 | 3 | 10 | 13 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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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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Demanelis K, Jasmine F, Chen LS, Chernoff M, Tong L, Delgado D, Zhang C, Shinkle J, Sabarinathan M, Lin H, Ramirez E, Oliva M, Kim-Hellmuth S, Stranger BE, Lai TP, Aviv A, Ardlie KG, Aguet F, Ahsan H. Determinants of telomere length across human tissues. Science. 2020 09 11; 369(6509).
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Ferraro NM, Strober BJ, Einson J, Abell NS, Aguet F, Barbeira AN, Brandt M, Bucan M, Castel SE, Davis JR, Greenwald E, Hess GT, Hilliard AT, Kember RL, Kotis B, Park Y, Peloso G, Ramdas S, Scott AJ, Smail C, Tsang EK, Zekavat SM, Ziosi M. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science. 2020 09 11; 369(6509).
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Zhang Z, Luo K, Zou Z, Qiu M, Tian J, Sieh L, Shi H, Zou Y, Wang G, Morrison J, Zhu AC, Qiao M, Li Z, Stephens M, He X, He C. Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability. Nat Genet. 2020 09; 52(9):939-949.
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Ishigaki K, Akiyama M, Kanai M, Takahashi A, Kawakami E, Sugishita H, Sakaue S, Matoba N, Low SK, Okada Y, Terao C, Amariuta T, Gazal S, Kochi Y, Horikoshi M, Suzuki K, Ito K, Koyama S, Ozaki K, Niida S, Sakata Y, Sakata Y, Kohno T, Shiraishi K, Momozawa Y, Hirata M, Matsuda K, Ikeda M, Iwata N, Ikegawa S, Kou I, Tanaka T, Nakagawa H, Suzuki A, Hirota T, Tamari M, Chayama K, Miki D, Mori M, Nagayama S, Daigo Y, Miki Y, Katagiri T, Ogawa O, Obara W, Ito H, Yoshida T, Imoto I, Takahashi T, Tanikawa C, Suzuki T, Sinozaki N, Minami S, Yamaguchi H, Asai S, Takahashi Y, Yamaji K, Takahashi K, Fujioka T, Takata R, Yanai H, Masumoto A, Koretsune Y, Kutsumi H, Higashiyama M, Murayama S, Minegishi N, Suzuki K, Tanno K, Shimizu A, Yamaji T, Iwasaki M, Sawada N, Uemura H, Tanaka K, Naito M, Sasaki M, Wakai K, Tsugane S, Yamamoto M, Yamamoto K, Murakami Y, Nakamura Y, Raychaudhuri S, Inazawa J, Yamauchi T, Kadowaki T, Kubo M, Kamatani Y. Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Nat Genet. 2020 07; 52(7):669-679.
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Barreiro LB, Quintana-Murci L. Evolutionary and population (epi)genetics of immunity to infection. Hum Genet. 2020 Jun; 139(6-7):723-732.
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Szczaluba K, Mierzewska H, Smigiel R, Kosinska J, Koppolu A, Biernacka A, Stawinski P, Pollak A, Rydzanicz M, Ploski R. AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant. J Appl Genet. 2020 May; 61(2):213-218.
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Sprengelmeyer QD, Mansourian S, Lange JD, Matute DR, Cooper BS, Jirle EV, Stensmyr MC, Pool JE. Recurrent Collection of Drosophila melanogaster from Wild African Environments and Genomic Insights into Species History. Mol Biol Evol. 2020 03 01; 37(3):627-638.
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Tsai MH, Muir AM, Wang WJ, Kang YN, Yang KC, Chao NH, Wu MF, Chang YC, Porter BE, Jansen LA, Sebire G, Deconinck N, Fan WL, Su SC, Chung WH, Almanza Fuerte EP, Mehaffey MG. Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly. Neuron. 2020 04 22; 106(2):237-245.e8.
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Mambetsariev I, Wang Y, Chen C, Nadaf S, Pharaon R, Fricke J, Amanam I, Amini A, Bild A, Chu P, Erhunmwunsee L, Kim J, Munu J, Pillai R, Raz D, Sampath S, Vora L, Qiu F, Smith L, Batra SK, Massarelli E, Koczywas M, Reckamp K, Salgia R. Precision medicine and actionable alterations in lung cancer: A single institution experience. PLoS One. 2020; 15(2):e0228188.
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