Physical Chromosome Mapping
"Physical 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.
Mapping of the linear order of genes on a chromosome with units indicating their distances by using methods other than genetic recombination. These methods include nucleotide sequencing, overlapping deletions in polytene chromosomes, and electron micrography of heteroduplex DNA. (From King & Stansfield, A Dictionary of Genetics, 5th ed)
| Descriptor ID |
D020161
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| MeSH Number(s) |
E05.393.183.620
|
| Concept/Terms |
Physical Chromosome Mapping- Physical Chromosome Mapping
- Physical Mapping (Genetics)
- Physical Mappings (Genetics)
- Chromosome Mapping, Physical
- Chromosome Mappings, Physical
- Mapping, Physical Chromosome
- Mappings, Physical Chromosome
- Physical Chromosome Mappings
|
Below are MeSH descriptors whose meaning is more general than "Physical Chromosome Mapping".
Below are MeSH descriptors whose meaning is more specific than "Physical Chromosome Mapping".
This graph shows the total number of publications written about "Physical Chromosome Mapping" by people in this website by year, and whether "Physical 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 |
|---|
| 1998 | 0 | 3 | 3 |
| 1999 | 2 | 7 | 9 |
| 2000 | 2 | 3 | 5 |
| 2001 | 0 | 2 | 2 |
| 2002 | 2 | 4 | 6 |
| 2003 | 0 | 3 | 3 |
| 2004 | 2 | 0 | 2 |
| 2005 | 0 | 3 | 3 |
| 2006 | 0 | 2 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 1 | 2 |
| 2009 | 0 | 3 | 3 |
| 2010 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Physical Chromosome Mapping" by people in Profiles.
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The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
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Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism. Cell Rep. 2017 Sep 12; 20(11):2556-2564.
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An integrated map of structural variation in 2,504 human genomes. Nature. 2015 Oct 01; 526(7571):75-81.
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Discovery of structural alterations in solid tumor oligodendroglioma by single molecule analysis. BMC Genomics. 2013 Jul 26; 14:505.
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Common genetic variants in the PSCA gene influence gene expression and bladder cancer risk. Proc Natl Acad Sci U S A. 2012 Mar 27; 109(13):4974-9.
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Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies. Am J Med Genet A. 2010 Dec; 152A(12):3148-53.
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Signatures of mutation and selection in the cancer genome. Nature. 2010 Feb 18; 463(7283):893-8.
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Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1. Cancer Res. 2009 Oct 01; 69(19):7844-50.
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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res. 2009; 124(1):102-5.
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Gene by smoking interaction in hypertension: identification of a major quantitative trait locus on chromosome 15q for systolic blood pressure in Mexican-Americans. J Hypertens. 2009 Mar; 27(3):491-501.