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																		 Genomics
 
																		 
																		
																	 
																		 
																		
																	 
																			
																					
	"Genomics" 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 systematic study of the complete DNA sequences (GENOME) of organisms.
    
			 
				
				
					
						| Descriptor ID | D023281 |  
						| MeSH Number(s) | H01.158.273.180.350 H01.158.273.343.350 |  
						| Concept/Terms |  |  
				Below are MeSH descriptors whose meaning is more general than "Genomics". 
				Below are MeSH descriptors whose meaning is more specific than "Genomics". 
	
	
		
			
			
					
				This graph shows the total number of publications written about "Genomics" by people in this website by year, and whether "Genomics" 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 | 
|---|
 | 2000 | 1 | 0 | 1 |  | 2002 | 4 | 0 | 4 |  | 2003 | 1 | 3 | 4 |  | 2004 | 3 | 1 | 4 |  | 2005 | 2 | 5 | 7 |  | 2006 | 5 | 4 | 9 |  | 2007 | 18 | 3 | 21 |  | 2008 | 11 | 11 | 22 |  | 2009 | 5 | 6 | 11 |  | 2010 | 5 | 6 | 11 |  | 2011 | 12 | 8 | 20 |  | 2012 | 14 | 7 | 21 |  | 2013 | 9 | 10 | 19 |  | 2014 | 15 | 16 | 31 |  | 2015 | 11 | 24 | 35 |  | 2016 | 21 | 11 | 32 |  | 2017 | 16 | 15 | 31 |  | 2018 | 25 | 23 | 48 |  | 2019 | 13 | 23 | 36 |  | 2020 | 14 | 26 | 40 |  | 2021 | 24 | 24 | 48 |  | 2022 | 5 | 49 | 54 |  | 2023 | 12 | 31 | 43 |  | 2024 | 9 | 18 | 27 |  | 2025 | 13 | 16 | 29 | 
 
                    To return to the timeline, click here. 
				Below are the most recent publications written about "Genomics" by people in Profiles. 		
					
								
								Sherman CA, Nataneli S, Claw KG, Mooney JA. Echoes of eugenics: confronting its effects in indigenous genomics. Genetics. 2025 Oct 08; 231(2).
								Maura F, Kaddoura M, Poos AM, Baughn LB, Ziccheddu B, Bärtsch MA, Cirrincione A, Maclachlan K, Chojnacka M, Diamond B, Papadimitriou M, Blaney P, John L, Reichert P, Huhn S, Gagler D, Zhang Y, Dogan A, Lesokhin AM, Davies F, Goldschmidt H, Fenk R, Weisel KC, Mai EK, Korde N, Morgan GJ, Rajkumar SV, Kumar S, Usmani S, Landgren O, Raab MS, Weinhold N. Temporal genomic dynamics shape clinical trajectory in multiple myeloma. Nat Genet. 2025 Sep; 57(9):2203-2214.
								Arehart CH, Lin M, Gibson RA, Raghavan S, Gignoux CR, Stanislawski MA, Grotzinger AD, Evans LM. Modeling the genomic architecture of adiposity and anthropometrics across the lifespan. Nat Commun. 2025 Aug 13; 16(1):7494.
								Stanley KJ, Chisholm C, Gillespie MK, Caluseriu O, Del Signore N, Elango S, Hartley T, Hewson S, Kim RH, McSheffrey G, Mendoza-Londono R, Sawyer SL, Somerville M, Venkataramanan V, White-Brown A, Telesca S, Shickh S, Marshall CR, Ungar WJ, Hayeems RZ, Bhawra J, Boycott KM, Costain G. TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticist. BMJ Open. 2025 Aug 10; 15(8):e107603.
								McHugo GP, Ward JA, Browne JA, O'Gorman GM, Meade KG, Hill EW, Hall TJ, MacHugh DE. Functional genomics of trypanotolerant and trypanosusceptible cattle infected with Trypanosoma congolense across multiple time points and tissues. PLoS Negl Trop Dis. 2025 Aug; 19(8):e0012882.
								Foote IF, Flint JP, Fürtjes AE, Lawrence JM, Mullin DS, Fisk JD, Karakach TK, Rutenberg A, Martin NG, Lupton MK, Llewellyn DJ, Ranson JM, Cox SR, Luciano M, Rockwood K, Grotzinger AD. Uncovering the multivariate genetic architecture of frailty with genomic structural equation modeling. Nat Genet. 2025 Aug; 57(8):1848-1859.
								Logsdon GA, Ebert P, Audano PA, Loftus M, Porubsky D, Ebler J, Yilmaz F, Hallast P, Prodanov T, Yoo D, Paisie CA, Harvey WT, Zhao X, Martino GV, Henglin M, Munson KM, Rabbani K, Chin CS, Gu B, Ashraf H, Scholz S, Austine-Orimoloye O, Balachandran P, Bonder MJ, Cheng H, Chong Z, Crabtree J, Gerstein M, Guethlein LA, Hasenfeld P, Hickey G, Hoekzema K, Hunt SE, Jensen M, Jiang Y, Koren S, Kwon Y, Li C, Li H, Li J, Norman PJ, Oshima KK, Paten B, Phillippy AM, Pollock NR, Rausch T, Rautiainen M, Song Y, Söylev A, Sulovari A, Surapaneni L, Tsapalou V, Zhou W, Zhou Y, Zhu Q, Zody MC, Mills RE, Devine SE, Shi X, Talkowski ME, Chaisson MJP, Dilthey AT, Konkel MK, Korbel JO, Lee C, Beck CR, Eichler EE, Marschall T. Complex genetic variation in nearly complete human genomes. Nature. 2025 Aug; 644(8076):430-441.
								Branco S, Avis PG, Barry K, Bates S, Cobián GM, Dow EG, Gremillion S, Honan A, Knight CA, LaButti K, Quandt CA, Stewart JE, Talag J, Wilson AW, Lofgren L, Mondo SJ. Myco-Ed: Mycological curriculum for education and discovery. PLoS Pathog. 2025 Jul; 21(7):e1013303.
								L?tter A, Bruna T, Duong TA, Barry K, Lipzen A, Daum C, Yoshinaga Y, Grimwood J, Jenkins JW, Talag J, Borevitz J, Lovell JT, Schmutz J, Wegrzyn JL, Myburg AA. A haplotype-resolved reference genome for Eucalyptus grandis. G3 (Bethesda). 2025 Jul 09; 15(7).
								Moreno DF, Nadeu F, Brasó-Maristany F, Vaqué S, Paz S, Mañé J, Cardús O, Medina E, Lozano E, Rodríguez-Lobato LG, de Daniel A, Tovar N, Cibeira MT, Bladé J, Rosiñol L, Prat A, Colomer D, Fernández de Larrea C. Genomic and immune profiling of prognostic risk groups in IgM gammopathy reveals novel biomarkers beyond MYD88 L265P. Front Immunol. 2025; 16:1604089. | 
																	
																		
																			
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