 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 | 3 | 3 | 6 | | 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 | 3 | 0 | 3 | | 2021 | 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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Begum G, Albanna A, Bankapur A, Nassir N, Tambi R, Berdiev BK, Akter H, Karuvantevida N, Kellam B, Alhashmi D, Sung WWL, Thiruvahindrapuram B, Alsheikh-Ali A, Scherer SW, Uddin M. Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome. Int J Mol Sci. 2021 Feb 19; 22(4).
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Ross JE, Zhang BM, Lee K, Mohan S, Branchford BR, Bray P, Dugan SN, Freson K, Heller PG, Kahr WHA, Lambert MP, Luchtman-Jones L, Luo M, Perez Botero J, Rondina MT, Ryan G, Westbury S, Bergmeier W, Di Paola J. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel. Blood Adv. 2021 01 26; 5(2):414-431.
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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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Marshall CR, Bick D, Belmont JW, Taylor SL, Ashley E, Dimmock D, Jobanputra V, Kearney HM, Kulkarni S, Rehm H. The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic. Genome Med. 2020 05 27; 12(1):48.
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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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