 Chromosome Mapping
"Chromosome Mapping" 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.
Any method used for determining the location of and relative distances between genes on a chromosome.
| Descriptor ID |
D002874
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| MeSH Number(s) |
E05.393.183
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| Concept/Terms |
Chromosome Mapping- Chromosome Mapping
- Chromosome Mappings
- Mapping, Chromosome
- Mappings, Chromosome
- Gene Mapping
- Gene Mappings
- Mapping, Gene
- Mappings, Gene
- Linkage Mapping
- Linkage Mappings
- Mapping, Linkage
- Mappings, Linkage
Genome Mapping- Genome Mapping
- Genome Mappings
- Mapping, Genome
- Mappings, Genome
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Below are MeSH descriptors whose meaning is more general than "Chromosome Mapping".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Mapping".
This graph shows the total number of publications written about "Chromosome Mapping" by people in this website by year, and whether "Chromosome Mapping" 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 |
|---|
| 1982 | 1 | 1 | 2 | | 1983 | 0 | 1 | 1 | | 1984 | 0 | 2 | 2 | | 1985 | 0 | 2 | 2 | | 1986 | 0 | 2 | 2 | | 1987 | 1 | 2 | 3 | | 1988 | 1 | 5 | 6 | | 1989 | 3 | 2 | 5 | | 1990 | 6 | 7 | 13 | | 1991 | 3 | 7 | 10 | | 1992 | 0 | 5 | 5 | | 1993 | 2 | 9 | 11 | | 1994 | 6 | 14 | 20 | | 1995 | 4 | 13 | 17 | | 1996 | 8 | 18 | 26 | | 1997 | 11 | 13 | 24 | | 1998 | 7 | 21 | 28 | | 1999 | 3 | 19 | 22 | | 2000 | 5 | 18 | 23 | | 2001 | 5 | 19 | 24 | | 2002 | 3 | 7 | 10 | | 2003 | 2 | 13 | 15 | | 2004 | 7 | 8 | 15 | | 2005 | 1 | 12 | 13 | | 2006 | 5 | 13 | 18 | | 2007 | 3 | 13 | 16 | | 2008 | 3 | 8 | 11 | | 2009 | 4 | 10 | 14 | | 2010 | 3 | 6 | 9 | | 2011 | 2 | 7 | 9 | | 2012 | 1 | 7 | 8 | | 2013 | 0 | 10 | 10 | | 2014 | 2 | 1 | 3 | | 2015 | 1 | 3 | 4 | | 2016 | 1 | 4 | 5 | | 2017 | 0 | 4 | 4 | | 2018 | 1 | 0 | 1 | | 2019 | 2 | 3 | 5 |
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Below are the most recent publications written about "Chromosome Mapping" by people in Profiles.
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Vervoort L, Demaerel W, Rengifo LY, Odrzywolski A, Vergaelen E, Hestand MS, Breckpot J, Devriendt K, Swillen A, McDonald-McGinn DM, Fiksinski AM, Zinkstok JR, Morrow BE, Heung T, Vorstman JAS, Bassett AS, Chow EWC, Shashi V, Vermeesch JR. Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Hum Mol Genet. 2019 11 15; 28(22):3724-3733.
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Khanal S, Dunne JC, Schwartz BM, Kim C, Milla-Lewis S, Raymer PL, Hanna WW, Adhikari J, Auckland SA, Rainville L, Paterson AH. Molecular Dissection of Quantitative Variation in Bermudagrass Hybrids (Cynodon dactylon x transvaalensis): Morphological Traits. G3 (Bethesda). 2019 08 08; 9(8):2581-2596.
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Zhang J, Parkinson J. PopNetD3-A Network-Based Web Resource for Exploring Population Structure. Genome Biol Evol. 2019 07 01; 11(7):1730-1735.
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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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Guo T, Diacou A, Nomaru H, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, Kates WR, Gothelf D, Schneider M, Eliez S, Breckpot J, Swillen A, Vorstman J, Zackai E, Benavides Gonzalez F, Repetto GM, Emanuel BS, Bassett AS, Vermeesch JR, Marshall CR, Morrow BE. Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Hum Mol Genet. 2018 04 01; 27(7):1150-1163.
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Costain G, Kannu P, Bowdin S. Genome-wide sequencing expands the phenotypic spectrum of EP300 variants. Eur J Med Genet. 2018 Mar; 61(3):125-129.
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Zhang J, Khan A, Kennard A, Grigg ME, Parkinson J. PopNet: A Markov Clustering Approach to Study Population Genetic Structure. Mol Biol Evol. 2017 07 01; 34(7):1799-1811.
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Harripaul R, Vasli N, Mikhailov A, Rafiq MA, Mittal K, Windpassinger C, Sheikh TI, Noor A, Mahmood H, Downey S, Johnson M, Vleuten K, Bell L, Ilyas M, Khan FS, Khan V, Moradi M, Ayaz M, Naeem F, Heidari A, Ahmed I, Ghadami S, Agha Z, Zeinali S, Qamar R, Mozhdehipanah H, John P, Mir A, Ansar M, French L, Ayub M, Vincent JB. Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families. Mol Psychiatry. 2018 04; 23(4):973-984.
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Costain G, Shugar A, Krishnan P, Mahmutoglu S, Laughlin S, Kannu P. Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype. Am J Med Genet A. 2017 Mar; 173(3):740-743.
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