Polymorphism, Genetic

"Polymorphism, 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.

Descriptor ID	D011110
MeSH Number(s)	G05.365.795
Concept/Terms	Polymorphism, Genetic Polymorphism, Genetic Polymorphisms, Genetic Genetic Polymorphisms Genetic Polymorphism Polymorphism (Genetics) Polymorphisms (Genetics)

Below are MeSH descriptors whose meaning is more general than "Polymorphism, Genetic".

Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Polymorphism, Genetic [G05.365.795]

Below are MeSH descriptors whose meaning is related to "Polymorphism, Genetic".

Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Genetic".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Polymorphism, Genetic" by people in this website by year, and whether "Polymorphism, Genetic" was a major or minor topic of these publications.

Bar chart showing 148 publications over 27 distinct years, with a maximum of 20 publications in 2005

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1994	0	1	1
1995	0	1	1
1996	1	1	2
1997	1	2	3
1998	0	1	1
1999	0	3	3
2000	1	1	2
2001	0	2	2
2002	6	5	11
2003	2	6	8
2004	4	3	7
2005	7	13	20
2006	8	8	16
2007	6	1	7
2008	6	6	12
2009	8	6	14
2010	3	4	7
2011	4	5	9
2012	1	2	3
2013	6	3	9
2014	1	0	1
2015	2	1	3
2016	0	1	1
2017	2	0	2
2018	1	0	1
2019	0	1	1
2020	0	1	1

Below are the most recent publications written about "Polymorphism, Genetic" by people in Profiles.

Hanson BM, Kaser DJ, Franasiak JM. Male Infertility and the Future of In?Vitro Fertilization. Urol Clin North Am. 2020 May; 47(2):257-270.

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Dempsey JM, Kidwell KM, Gersch CL, Pesch AM, Desta Z, Storniolo AM, Stearns V, Skaar TC, Hayes DF, Henry NL, Rae JM, Hertz DL. Effects of SLCO1B1 polymorphisms on plasma estrogen concentrations in women with breast cancer receiving aromatase inhibitors exemestane and letrozole. Pharmacogenomics. 2019 06; 20(8):571-580.

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Schutzman DL, Gatien E, Ajayi S, Wong RJ. Heme oxygenase-1 genetic variants and the conundrum of hyperbilirubinemia in African-American newborns. J Perinatol. 2018 04; 38(4):345-350.

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Bussard KM, Siracusa LD. Understanding Mitochondrial Polymorphisms in Cancer. Cancer Res. 2017 Nov 15; 77(22):6051-6059.

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Cvijanovich NZ, Anas N, Allen GL, Thomas NJ, Bigham MT, Weiss SL, Fitzgerald J, Checchia PA, Meyer K, Quasney M, Gedeit R, Freishtat RJ, Nowak J, Raj SS, Gertz S, Grunwell JR, Opoka A, Wong HR. Glucocorticoid Receptor Polymorphisms and Outcomes in Pediatric Septic Shock. Pediatr Crit Care Med. 2017 Apr; 18(4):299-303.

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Kang E, Wu J, Gutierrez NM, Koski A, Tippner-Hedges R, Agaronyan K, Platero-Luengo A, Martinez-Redondo P, Ma H, Lee Y, Hayama T, Van Dyken C, Wang X, Luo S, Ahmed R, Li Y, Ji D, Kayali R, Cinnioglu C, Olson S, Jensen J, Battaglia D, Lee D, Wu D, Huang T, Wolf DP, Temiakov D, Belmonte JC, Amato P, Mitalipov S. Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations. Nature. 2016 12 08; 540(7632):270-275.

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Adappa ND, Farquhar D, Palmer JN, Kennedy DW, Doghramji L, Morris SA, Owens D, Mansfield C, Lysenko A, Lee RJ, Cowart BJ, Reed DR, Cohen NA. TAS2R38 genotype predicts surgical outcome in nonpolypoid chronic rhinosinusitis. Int Forum Allergy Rhinol. 2016 Jan; 6(1):25-33.

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Doetzer AD, Brancher JA, Pecharki GD, Schlipf N, Werneck R, Mira MT, Riess O, Bauer P, Trevilatto PC. Lactotransferrin Gene Polymorphism Associated with Caries Experience. Caries Res. 2015; 49(4):370-7.

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Gross-Davis CA, Heavner K, Frank AL, Newschaffer C, Klotz J, Santella RM, Burstyn I. The role of genotypes that modify the toxicity of chemical mutagens in the risk for myeloproliferative neoplasms. Int J Environ Res Public Health. 2015 Feb 24; 12(3):2465-85.

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Kwan JS, Hsu YH, Cheung CL, Dupuis J, Saint-Pierre A, Eriksson J, Handelman SK, Aragaki A, Karasik D, Pramstaller PP, Kooperberg C, Lacroix AZ, Larson MG, Lau KS, Lorentzon M, Pichler I, Sham PC, Taliun D, Vandenput L, Kiel DP, Hicks AA, Jackson RD, Ohlsson C, Benjamin EJ, Kung AW. Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels. Hum Mol Genet. 2014 Dec 15; 23(24):6684-93.

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