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, cdc
- Genes, Chloroplast
- Genes, Developmental
- Genes, Dominant
- Genes, Duplicate
- Genes, Essential
- Genes, Helminth
- Genes, Immediate-Early
- Genes, Immunoglobulin
- Genes, Insect
- Genes, Lethal
- Genes, MDR
- Genes, Microbial
- 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, 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 |
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1995 | 2 | 5 | 7 | 1996 | 1 | 2 | 3 | 1997 | 1 | 3 | 4 | 1998 | 2 | 0 | 2 | 1999 | 0 | 2 | 2 | 2001 | 1 | 2 | 3 | 2002 | 0 | 1 | 1 | 2003 | 1 | 2 | 3 | 2004 | 1 | 0 | 1 | 2006 | 2 | 0 | 2 | 2007 | 0 | 1 | 1 | 2008 | 2 | 6 | 8 | 2009 | 2 | 1 | 3 | 2010 | 2 | 2 | 4 | 2012 | 1 | 2 | 3 | 2013 | 0 | 1 | 1 | 2014 | 0 | 1 | 1 | 2015 | 2 | 1 | 3 | 2018 | 0 | 1 | 1 | 2019 | 1 | 0 | 1 | 2021 | 0 | 1 | 1 | 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genes" by people in Profiles.
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Putman TE, Schaper K, Matentzoglu N, Rubinetti VP, Alquaddoomi FS, Cox C, Caufield JH, Elsarboukh G, Gehrke S, Hegde H, Reese JT, Braun I, Bruskiewich RM, Cappelletti L, Carbon S, Caron AR, Chan LE, Chute CG, Cortes KG, De Souza V, Fontana T, Harris NL, Hartley EL, Hurwitz E, Jacobsen JOB, Krishnamurthy M, Laraway BJ, McLaughlin JA, McMurry JA, Moxon SAT, Mullen KR, O'Neil ST, Shefchek KA, Stefancsik R, Toro S, Vasilevsky NA, Walls RL, Whetzel PL, Osumi-Sutherland D, Smedley D, Robinson PN, Mungall CJ, Haendel MA, Munoz-Torres MC. The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes?and diseases across species. Nucleic Acids Res. 2024 Jan 05; 52(D1):D938-D949.
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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, Bastarache L, Jordan DM, Verbanck M, Do R, Stephens M, Ardlie K, McCarthy M, Montgomery SB, Segr? AV, Brown CD, Lappalainen T, Wen X, Im HK. Exploiting the GTEx resources to decipher the mechanisms at GWAS loci. Genome Biol. 2021 01 26; 22(1):49.
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McGowan D, Little CW, Coventry WL, Corley R, Olson RK, Samuelsson S, Byrne B. Differential Influences of Genes and Environment Across the Distribution of Reading Ability. Behav Genet. 2019 09; 49(5):425-431.
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Roberts GHL, Paul S, Yorgov D, Santorico SA, Spritz RA. Family Clustering of Autoimmune Vitiligo Results Principally from Polygenic Inheritance of Common Risk Alleles. Am J Hum Genet. 2019 08 01; 105(2):364-372.
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Brieger K, Zajac GJM, Pandit A, Foerster JR, Li KW, Annis AC, Schmidt EM, Clark CP, McMorrow K, Zhou W, Yang J, Kwong AM, Boughton AP, Wu J, Scheller C, Parikh T, de la Vega A, Brazel DM, Frieser M, Rea-Sandin G, Fritsche LG, Vrieze SI, Abecasis GR. Genes for Good: Engaging the Public in Genetics Research via Social Media. Am J Hum Genet. 2019 07 03; 105(1):65-77.
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Chereji RV, Ramachandran S, Bryson TD, Henikoff S. Precise genome-wide mapping of single nucleosomes and linkers in vivo. Genome Biol. 2018 02 09; 19(1):19.
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Liu M, Rea-Sandin G, Foerster J, Fritsche L, Brieger K, Clark C, Li K, Pandit A, Zajac G, Abecasis GR, Vrieze S. Validating Online Measures of Cognitive Ability in Genes for Good, a Genetic Study of Health and Behavior. Assessment. 2020 01; 27(1):136-148.
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Choi J, Lee S, Mallard W, Clement K, Tagliazucchi GM, Lim H, Choi IY, Ferrari F, Tsankov AM, Pop R, Lee G, Rinn JL, Meissner A, Park PJ, Hochedlinger K. A comparison of genetically matched cell lines reveals the equivalence of human iPSCs and ESCs. Nat Biotechnol. 2015 Nov; 33(11):1173-81.
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Sawyer SL, Hartley T, Dyment DA, Beaulieu CL, Schwartzentruber J, Smith A, Bedford HM, Bernard G, Bernier FP, Brais B, Bulman DE, Warman Chardon J, Chitayat D, Delado?y J, Fernandez BA, Frosk P, Geraghty MT, Gerull B, Gibson W, Gow RM, Graham GE, Green JS, Heon E, Horvath G, Innes AM, Jabado N, Kim RH, Koenekoop RK, Khan A, Lehmann OJ, Mendoza-Londono R, Michaud JL, Nikkel SM, Penney LS, Polychronakos C, Richer J, Rouleau GA, Samuels ME, Siu VM, Suchowersky O, Tarnopolsky MA, Yoon G, Zahir FR, Majewski J, Boycott KM. Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care. Clin Genet. 2016 Mar; 89(3):275-84.
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McBee RM, Rozmiarek SA, Meyerson NR, Rowley PA, Sawyer SL. The effect of species representation on the detection of positive selection in primate gene data sets. Mol Biol Evol. 2015 Apr; 32(4):1091-6.
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