Genome, Human
"Genome, Human" 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 complete genetic complement contained in the DNA of a set of CHROMOSOMES in a HUMAN. The length of the human genome is about 3 billion base pairs.
| Descriptor ID |
D015894
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| MeSH Number(s) |
G05.360.340.350
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| Concept/Terms |
Genome, Human- Genome, Human
- Human Genome
- Genomes, Human
- Human Genomes
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Below are MeSH descriptors whose meaning is more general than "Genome, Human".
Below are MeSH descriptors whose meaning is more specific than "Genome, Human".
This graph shows the total number of publications written about "Genome, Human" by people in this website by year, and whether "Genome, Human" 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 |
|---|
| 1997 | 1 | 0 | 1 | | 2000 | 2 | 0 | 2 | | 2001 | 2 | 1 | 3 | | 2002 | 0 | 4 | 4 | | 2003 | 6 | 4 | 10 | | 2004 | 2 | 4 | 6 | | 2005 | 5 | 5 | 10 | | 2006 | 8 | 5 | 13 | | 2007 | 13 | 4 | 17 | | 2008 | 7 | 7 | 14 | | 2009 | 5 | 7 | 12 | | 2010 | 4 | 7 | 11 | | 2011 | 8 | 8 | 16 | | 2012 | 4 | 13 | 17 | | 2013 | 4 | 20 | 24 | | 2014 | 7 | 10 | 17 | | 2015 | 12 | 11 | 23 | | 2016 | 5 | 12 | 17 | | 2017 | 5 | 11 | 16 | | 2018 | 12 | 8 | 20 | | 2019 | 5 | 7 | 12 | | 2020 | 5 | 4 | 9 | | 2021 | 10 | 13 | 23 | | 2022 | 2 | 2 | 4 | | 2023 | 2 | 2 | 4 | | 2024 | 3 | 7 | 10 | | 2025 | 5 | 14 | 19 | | 2026 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Ramsay M, Etheredge H, Tluway F, D'Amato ME, Chikwambi Z, Hamdi Y, Alhudiri I, Fakim Y, Ahmad KM, Belguith N, Bentley D, Boujemaa M, Calumbuana N, Chaouch M, Charfeddine C, Chinien G, Dukuze N, Eljilani M, Elzagheid A, Ferraz N, Ghoorah A, Goorah S, Gribaa M, Guidara S, Guirat M, Hazelhurst S, Jallul M, Kasu M, Kharrat N, Khumalo U, Kingsbury Z, Kisiangani I, Lopes-Cendes I, Lukusa P, Makay P, Makulo J, Mubungu G, Muhinda C, Mukhongo DM, Murwira A, Mustafa A, Ndinkabandi J, Ngole M, Nlandu Y, Nyathi M, Pereira L, Rejeb I, Santos LL, Sengupta D, Shebani A, Smyth N, Souissi A, Trabelsi M, Rebai A, Chimpolo MM, Lumaka A, Masimirembwa C, Mohamed SF, Mulder N, Mutesa L, Hanchard NA, Choudhury A. Enriching African genome representation through the AGenDA project. Nature. 2026 Jan; 649(8097):565-573.
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Sato T, Kubo D, Hirasawa Y, Yoneda M, Kimura R, Tajima A, Kato H. Genome of an early Okhotsk individual reveals ancient admixture between Jomon and Kamchatka lineages. Sci Rep. 2025 Oct 27; 15(1):37520.
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Hayeems RZ, Ungar WJ, Marshall CR, Gillespie MK, Szuto A, Huang L, Venkataramanan V, Xiao B, Chisholm C, Stavropoulos DJ, Bergeron MB, Lee W, Costain G, Jobling R, Sawyer S, Price EM, Lau L, Mendoza R, Somerville MJ, Boycott KM. Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial. Genet Med. 2026 Jan; 28(1):101605.
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Selvaraj MS, Li X, Li Z, Van Buren E, Haidermota S, Postupaka D, Hornsby W, Bis JC, Brody JA, Cade BE, Chung RH, Curran JE, Damrauer SM, de Las Fuentes L, de Vries PS, Duggirala R, Freedman BI, Graff M, Guo X, Hidalgo BA, Hou L, Irvin R, Judy R, Kalyani RR, Kelly TN, Konigsberg IR, Kral BG, Kwee LC, Levy D, Li C, Manichaikul AW, Martin LW, Montasser ME, Morrison AC, Naseri T, North KE, O'Connell JR, Palmer ND, Peyser PA, Reiner AP, Shah SH, Smit RAJ, Smith JA, Taylor KD, Tiwari H, Tsai MY, Viali S, Wang Z, Wang Y, Zhao W, Arnett DK, Blangero J, Boerwinkle E, Bowden DW, Carlson JC, Chen YI, Ellinor PT, Fornage M, He J, Heard-Costa N, Kaplan RC, Kardia SLR, Kooperberg C, Kraus WE, Lange LA, Loos RJF, Mitchell BD, Psaty BM, Rader DJ, Redline S, Rich SS, Yanek LR, Gibbs R, Gabriel S, Viaud-Martinez KA, Dutcher SK, Germer S, Kim R, Rotter JI, Lin X, Peloso GM, Natarajan P. Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals. Genome Biol. 2025 Sep 09; 26(1):273.
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Pitsava G, Hawley M, Auriga L, de Dios I, Ko A, Marmolejos S, Almalvez M, Chen I, Scozzaro K, Zhao J, Barrick R, Ah Mew N, Fusaro VA, LoTempio J, Taylor M, Mestroni L, Graw S, Milewicz D, Guo D, Murdock DR, Bujakowska KM, Xiao C, Délot EC, Berger SI, Vilain E. Genome sequencing reveals the impact of pseudoexons in rare genetic disease. Genet Med. 2025 Nov; 27(11):101574.
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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.
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Kronenberg Z, Nolan C, Porubsky D, Mokveld T, Rowell WJ, Lee S, Dolzhenko E, Chang PC, Holt JM, Saunders CT, Olson ND, Steely CJ, McGee S, Guarracino A, Koundinya N, Harvey WT, Watkins WS, Munson KM, Hoekzema K, Chua KP, Chen X, Fanslow C, Lambert C, Dashnow H, Garrison E, Smith JD, Lansdorp PM, Zook JM, Carroll A, Jorde LB, Neklason DW, Quinlan AR, Eichler EE, Eberle MA. The Platinum Pedigree: a long-read benchmark for genetic variants. Nat Methods. 2025 Aug; 22(8):1669-1676.
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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.
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Williams CM, O'Connell J, Jewett E, Freyman WA, Gignoux CR, Ramachandran S, Williams AL. Phasing millions of samples achieves near perfect accuracy, enabling parent-of-origin analyses. HGG Adv. 2025 Oct 09; 6(4):100479.
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Fazal S, Dashnow H, Dohrn MF, Raposo J, Hiatt L, Danzi MC, Xu IRL, Toro C, Adams DR, Usdin K, Hayward B, Kobren SN, Sunyaev SR, Spillmann RC, Shashi V, Rebelo A, Bademci G, Tekin M, Quinlan AR, Zuchner S. A genome-wide approach for the discovery of novel repeat expansion disorders in the Undiagnosed Diseases Network cohort. Genet Med. 2025 Aug; 27(8):101462.
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