 Genes
"Genes" 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.
A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms.
| Descriptor ID |
D005796
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| MeSH Number(s) |
G05.360.340.024.340
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| Concept/Terms |
Genetic Materials- Genetic Materials
- Genetic Material
- Material, Genetic
- Materials, Genetic
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Below are MeSH descriptors whose meaning is more general than "Genes".
Below are MeSH descriptors whose meaning is more specific than "Genes".
- Genes
- Alleles
- Gene Components
- Genes, Archaeal
- Genes, Bacterial
- Genes, cdc
- Genes, Chloroplast
- Genes, Developmental
- Genes, Dominant
- Genes, Duplicate
- Genes, Essential
- Genes, Fungal
- Genes, Helminth
- Genes, Immediate-Early
- Genes, Immunoglobulin
- Genes, Insect
- Genes, Lethal
- Genes, MDR
- Genes, Mitochondrial
- Genes, Modifier
- Genes, Neoplasm
- Genes, Overlapping
- Genes, Plant
- Genes, Protozoan
- Genes, RAG-1
- Genes, Recessive
- Genes, Regulator
- Genes, Reporter
- Genes, sry
- Genes, Suppressor
- Genes, Synthetic
- Genes, T-Cell Receptor
- Genes, Viral
- Genes, X-Linked
- Genes, Y-Linked
- Major Histocompatibility Complex
- Multigene Family
- Pseudogenes
- Transgenes
This graph shows the total number of publications written about "Genes" by people in this website by year, and whether "Genes" 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 | 5 | 3 | 8 | | 1981 | 3 | 2 | 5 | | 1982 | 5 | 4 | 9 | | 1983 | 6 | 6 | 12 | | 1984 | 5 | 5 | 10 | | 1985 | 8 | 6 | 14 | | 1986 | 9 | 6 | 15 | | 1987 | 14 | 4 | 18 | | 1988 | 8 | 9 | 17 | | 1989 | 7 | 1 | 8 | | 1990 | 7 | 9 | 16 | | 1991 | 5 | 6 | 11 | | 1992 | 6 | 3 | 9 | | 1993 | 5 | 2 | 7 | | 1994 | 6 | 3 | 9 | | 1995 | 3 | 6 | 9 | | 1996 | 4 | 2 | 6 | | 1997 | 4 | 3 | 7 | | 1998 | 4 | 1 | 5 | | 1999 | 1 | 1 | 2 | | 2000 | 2 | 0 | 2 | | 2001 | 2 | 0 | 2 | | 2002 | 3 | 0 | 3 | | 2003 | 3 | 3 | 6 | | 2004 | 2 | 2 | 4 | | 2005 | 0 | 2 | 2 | | 2006 | 2 | 1 | 3 | | 2007 | 2 | 2 | 4 | | 2008 | 1 | 3 | 4 | | 2009 | 0 | 1 | 1 | | 2010 | 2 | 2 | 4 | | 2011 | 1 | 0 | 1 | | 2013 | 3 | 1 | 4 | | 2014 | 0 | 3 | 3 | | 2015 | 0 | 1 | 1 | | 2016 | 0 | 1 | 1 | | 2019 | 1 | 0 | 1 | | 2021 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genes" by people in Profiles.
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Ivarsdottir EV, Holm H, Benonisdottir S, Olafsdottir T, Sveinbjornsson G, Thorleifsson G, Eggertsson HP, Halldorsson GH, Hjorleifsson KE, Melsted P, Gylfason A, Arnadottir GA, Oddsson A, Jensson BO, Jonasdottir A, Jonasdottir A, Juliusdottir T, Stefansdottir L, Tragante V, Halldorsson BV, Petersen H, Thorgeirsson G, Thorsteinsdottir U, Sulem P, Hinriksdottir I, Jonsdottir I, Gudbjartsson DF, Stefansson K. The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis. Commun Biol. 2021 06 09; 4(1):706.
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Barbeira AN, Bonazzola R, Gamazon ER, Liang Y, Park Y, Kim-Hellmuth S, Wang G, Jiang Z, Zhou D, Hormozdiari F, Liu B, Rao A, Hamel AR, Pividori MD, Aguet F. Exploiting the GTEx resources to decipher the mechanisms at GWAS loci. Genome Biol. 2021 01 26; 22(1):49.
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Spithoven AWM, Cacioppo S, Goossens L, Cacioppo JT. Genetic Contributions to Loneliness and Their Relevance to the Evolutionary Theory of Loneliness. Perspect Psychol Sci. 2019 05; 14(3):376-396.
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Miyazaki Y, Du X, Muramatsu S, Gomez CM. An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron. Sci Transl Med. 2016 07 13; 8(347):347ra94.
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Sulakhe D, Xie B, Taylor A, D'Souza M, Balasubramanian S, Hashemifar S, White S, Dave UJ, Agam G, Xu J, Wang S, Gilliam TC, Maltsev N. Lynx: a knowledge base and an analytical workbench for integrative medicine. Nucleic Acids Res. 2016 Jan 04; 44(D1):D882-7.
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Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B. Accurate and fast multiple-testing correction in eQTL studies. Am J Hum Genet. 2015 Jun 04; 96(6):857-68.
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Sulakhe D, Taylor A, Balasubramanian S, Feng B, Xie B, Börnigen D, Dave UJ, Foster IT, Gilliam TC, Maltsev N. Lynx web services for annotations and systems analysis of multi-gene disorders. Nucleic Acids Res. 2014 Jul; 42(Web Server issue):W473-7.
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Gallego Romero I, Pai AA, Tung J, Gilad Y. RNA-seq: impact of RNA degradation on transcript quantification. BMC Biol. 2014 May 30; 12:42.
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MacArthur DG, Manolio TA, Dimmock DP, Rehm HL, Shendure J, Abecasis GR, Adams DR, Altman RB, Antonarakis SE, Ashley EA, Barrett JC, Biesecker LG, Conrad DF, Cooper GM, Cox NJ, Daly MJ, Gerstein MB, Goldstein DB, Hirschhorn JN, Leal SM, Pennacchio LA, Stamatoyannopoulos JA, Sunyaev SR, Valle D, Voight BF, Winckler W, Gunter C. Guidelines for investigating causality of sequence variants in human disease. Nature. 2014 Apr 24; 508(7497):469-76.
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Sulakhe D, Balasubramanian S, Xie B, Feng B, Taylor A, Wang S, Berrocal E, Dave U, Xu J, Börnigen D, Gilliam TC, Maltsev N. Lynx: a database and knowledge extraction engine for integrative medicine. Nucleic Acids Res. 2014 Jan; 42(Database issue):D1007-12.
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