 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 |
|---|
| 1990 | 0 | 1 | 1 | | 1992 | 0 | 1 | 1 | | 1993 | 1 | 2 | 3 | | 1994 | 1 | 0 | 1 | | 1995 | 1 | 0 | 1 | | 1996 | 0 | 3 | 3 | | 1997 | 1 | 1 | 2 | | 1998 | 0 | 2 | 2 | | 2000 | 0 | 2 | 2 | | 2001 | 4 | 3 | 7 | | 2002 | 2 | 0 | 2 | | 2003 | 1 | 7 | 8 | | 2004 | 6 | 0 | 6 | | 2005 | 1 | 3 | 4 | | 2006 | 9 | 3 | 12 | | 2007 | 6 | 5 | 11 | | 2008 | 4 | 7 | 11 | | 2009 | 4 | 7 | 11 | | 2010 | 9 | 7 | 16 | | 2011 | 0 | 3 | 3 | | 2012 | 4 | 9 | 13 | | 2013 | 5 | 7 | 12 | | 2014 | 4 | 6 | 10 | | 2015 | 6 | 6 | 12 | | 2016 | 5 | 6 | 11 | | 2017 | 5 | 5 | 10 | | 2018 | 5 | 6 | 11 | | 2019 | 6 | 5 | 11 | | 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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Trost B, Engchuan W, Nguyen CM, Thiruvahindrapuram B, Dolzhenko E, Backstrom I, Mirceta M, Mojarad BA, Yin Y, Dov A, Chandrakumar I, Prasolava T, Shum N, Hamdan O, Pellecchia G, Howe JL, Whitney J, Klee EW, Baheti S, Amaral DG, Anagnostou E, Elsabbagh M, Fernandez BA, Hoang N, Lewis MES, Liu X, Sjaarda C, Smith IM, Szatmari P, Zwaigenbaum L, Glazer D, Hartley D, Stewart AK, Eberle MA, Sato N, Pearson CE, Scherer SW, Yuen RKC. Genome-wide detection of tandem DNA repeats that are expanded in autism. Nature. 2020 10; 586(7827):80-86.
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Yao RA, Akinrinade O, Chaix M, Mital S. Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients. BMC Med Genomics. 2020 01 29; 13(1):11.
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D'Abate L, Walker S, Yuen RKC, Tammimies K, Buchanan JA, Davies RW, Thiruvahindrapuram B, Wei J, Brian J, Bryson SE, Dobkins K, Howe J, Landa R, Leef J, Messinger D, Ozonoff S, Smith IM, Stone WL, Warren ZE, Young G, Zwaigenbaum L, Scherer SW. Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders. Nat Commun. 2019 12 05; 10(1):5519.
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Erwood S, Brewer RA, Bily TMI, Maino E, Zhou L, Cohn RD, Ivakine EA. Modeling Niemann-Pick disease type C in a human haploid cell line allows for patient variant characterization and clinical interpretation. Genome Res. 2019 12; 29(12):2010-2019.
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Deng L, Lou H, Zhang X, Thiruvahindrapuram B, Lu D, Marshall CR, Liu C, Xie B, Xu W, Wong LP, Yew CW, Farhang A, Ong RT, Hoque MZ, Thuhairah AR, Jong B, Phipps ME, Scherer SW, Teo YY, Kumar SV, Hoh BP, Xu S. Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations. BMC Genomics. 2019 Nov 12; 20(1):842.
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Kim SA, Brossard M, Roshandel D, Paterson AD, Bull SB, Yoo YJ. gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks. Bioinformatics. 2019 11 01; 35(21):4419-4421.
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Hayeems RZ, Luca S, Pullenayegum E, Meyn MS, Ungar WJ. Genome Diagnostics: Novel Strategies for Measuring Value. J Manag Care Spec Pharm. 2019 Oct; 25(10):1096-1101.
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Martin-Herranz DE, Aref-Eshghi E, Bonder MJ, Stubbs TM, Choufani S, Weksberg R, Stegle O, Sadikovic B, Reik W, Thornton JM. Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1. Genome Biol. 2019 08 14; 20(1):146.
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Johnston MJ, Nikolic A, Ninkovic N, Guilhamon P, Cavalli FMG, Seaman S, Zemp FJ, Lee J, Abdelkareem A, Ellestad K, Murison A, Kushida MM, Coutinho FJ, Ma Y, Mungall AJ, Moore R, Marra MA, Taylor MD, Dirks PB, Pugh TJ, Morrissy S, St Croix B, Mahoney DJ, Lupien M, Gallo M. High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma. Genome Res. 2019 08; 29(8):1211-1222.
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Dimitromanolakis A, Paterson AD, Sun L. Fast and Accurate Shared Segment Detection and Relatedness Estimation in Un-phased Genetic Data via TRUFFLE. Am J Hum Genet. 2019 07 03; 105(1):78-88.
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