 Genotype
"Genotype" 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 genetic constitution of the individual comprised of the ALLELES present at each GENETIC LOCUS.
| Descriptor ID |
D005838
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| MeSH Number(s) |
G05.380
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Genotype".
Below are MeSH descriptors whose meaning is more specific than "Genotype".
This graph shows the total number of publications written about "Genotype" by people in this website by year, and whether "Genotype" 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 |
|---|
| 1983 | 0 | 1 | 1 | | 1984 | 1 | 0 | 1 | | 1985 | 0 | 1 | 1 | | 1986 | 0 | 1 | 1 | | 1987 | 0 | 1 | 1 | | 1988 | 0 | 1 | 1 | | 1989 | 0 | 1 | 1 | | 1990 | 1 | 0 | 1 | | 1991 | 1 | 2 | 3 | | 1992 | 0 | 5 | 5 | | 1993 | 1 | 10 | 11 | | 1994 | 1 | 6 | 7 | | 1995 | 0 | 6 | 6 | | 1996 | 2 | 7 | 9 | | 1997 | 2 | 7 | 9 | | 1998 | 1 | 14 | 15 | | 1999 | 0 | 16 | 16 | | 2000 | 2 | 17 | 19 | | 2001 | 1 | 35 | 36 | | 2002 | 1 | 30 | 31 | | 2003 | 1 | 39 | 40 | | 2004 | 2 | 46 | 48 | | 2005 | 1 | 50 | 51 | | 2006 | 1 | 58 | 59 | | 2007 | 2 | 65 | 67 | | 2008 | 5 | 66 | 71 | | 2009 | 1 | 70 | 71 | | 2010 | 3 | 65 | 68 | | 2011 | 4 | 73 | 77 | | 2012 | 7 | 68 | 75 | | 2013 | 1 | 91 | 92 | | 2014 | 12 | 101 | 113 | | 2015 | 6 | 85 | 91 | | 2016 | 6 | 56 | 62 | | 2017 | 2 | 47 | 49 | | 2018 | 1 | 6 | 7 |
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Below are the most recent publications written about "Genotype" by people in Profiles.
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Conley D, Johnson R, Domingue B, Dawes C, Boardman J, Siegal ML. A sibling method for identifying vQTLs. PLoS One. 2018; 13(4):e0194541.
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Reynolds LM, Howard TD, Ruczinski I, Kanchan K, Seeds MC, Mathias RA, Chilton FH. Tissue-specific impact of FADS cluster variants on FADS1 and FADS2 gene expression. PLoS One. 2018; 13(3):e0194610.
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Abul-Husn NS, Cheng X, Li AH, Xin Y, Schurmann C, Stevis P, Liu Y, Kozlitina J, Stender S, Wood GC, Stepanchick AN, Still MD, McCarthy S, O'Dushlaine C, Packer JS, Balasubramanian S, Gosalia N, Esopi D, Kim SY, Mukherjee S, Lopez AE, Fuller ED, Penn J, Chu X, Luo JZ, Mirshahi UL, Carey DJ, Still CD, Feldman MD, Small A, Damrauer SM, Rader DJ, Zambrowicz B, Olson W, Murphy AJ, Borecki IB, Shuldiner AR, Reid JG, Overton JD, Yancopoulos GD, Hobbs HH, Cohen JC, Gottesman O, Teslovich TM, Baras A, Mirshahi T, Gromada J, Dewey FE. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease. N Engl J Med. 2018 03 22; 378(12):1096-1106.
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Nowak KL, Chonchol M, You Z, Gupta M, Gitomer B. Affected parent sex and severity of autosomal dominant polycystic kidney disease: a retrospective cohort study?. Clin Nephrol. 2018 Mar; 89(3):196-204.
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Lopes FB, Wu XL, Li H, Xu J, Perkins T, Genho J, Ferretti R, Tait RG, Bauck S, Rosa GJM. Improving accuracy of genomic prediction in Brangus cattle by adding animals with imputed low-density SNP genotypes. J Anim Breed Genet. 2018 Feb; 135(1):14-27.
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Raffield LM, Ellis J, Olson NC, Duan Q, Li J, Durda P, Pankratz N, Keating BJ, Wassel CL, Cushman M, Wilson JG, Gross MD, Tracy RP, Rich SS, Reiner AP, Li Y, Willis MS, Lange EM, Lange LA. Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study. J Hum Genet. 2018 Mar; 63(3):327-337.
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Domingue BW, Belsky DW, Fletcher JM, Conley D, Boardman JD, Harris KM. The social genome of friends and schoolmates in the National Longitudinal Study of Adolescent to Adult Health. Proc Natl Acad Sci U S A. 2018 01 23; 115(4):702-707.
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Green RM, Fish JL, Young NM, Smith FJ, Roberts B, Dolan K, Choi I, Leach CL, Gordon P, Cheverud JM, Roseman CC, Williams TJ, Marcucio RS, Hallgrímsson B. Developmental nonlinearity drives phenotypic robustness. Nat Commun. 2017 12 06; 8(1):1970.
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Landgraf-Rauf K, Boeck A, Siemens D, Klucker E, Vogelsang V, Schmidt S, Kunze S, Weissenbacher C, Graessel A, Schmidt-Weber C, von Mutius E, Schedel M, Schaub B. IRF-1 SNPs influence the risk for childhood allergic asthma: A critical role for pro-inflammatory immune regulation. Pediatr Allergy Immunol. 2018 02; 29(1):34-41.
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Gerstenecker A, Roberson ED, Schellenberg GD, Standaert DG, Shprecher DR, Kluger BM, Litvan I. Genetic influences on cognition in progressive supranuclear palsy. Mov Disord. 2017 Dec; 32(12):1764-1771.
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