"Genetics, Population" 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 discipline studying genetic composition of populations and effects of factors such as GENETIC SELECTION, population size, MUTATION, migration, and GENETIC DRIFT on the frequencies of various GENOTYPES and PHENOTYPES using a variety of GENETIC TECHNIQUES.
| Descriptor ID |
D005828
|
| MeSH Number(s) |
H01.158.273.343.335
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Genetics, Population".
Below are MeSH descriptors whose meaning is more specific than "Genetics, Population".
This graph shows the total number of publications written about "Genetics, Population" by people in this website by year, and whether "Genetics, Population" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2003 | 1 | 2 | 3 |
| 2005 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genetics, Population" by people in Profiles.
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Phenotype and Genotype Correlations in Inherited Retinal Diseases: Population-Guided Variant Interpretation, Variable Expressivity and Incomplete Penetrance. Genes (Basel). 2020 10 29; 11(11).
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Integrating Personalized Medicine With Population Health Management: The Path Forward. JAMA. 2020 Aug 18; 324(7):631-632.
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. PLoS Genet. 2019 12; 15(12):e1008500.
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Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014 Nov; 46(11):1173-86.
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Detection of identity by descent using next-generation whole genome sequencing data. BMC Bioinformatics. 2012 Jun 06; 13:121.
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The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population. Parkinsonism Relat Disord. 2011 Jul; 17(6):473-5.
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Adapting the logical basis of tests for Hardy-Weinberg Equilibrium to the real needs of association studies in human and medical genetics. Genet Epidemiol. 2009 Nov; 33(7):569-80.
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Genome-wide association studies of cancer. Future Oncol. 2007 Aug; 3(4):419-27.
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Prostaglandin-endoperoxide synthase 2 (PTGS2) gene polymorphisms and risk of biliary tract cancer and gallstones: a population-based study in Shanghai, China. Carcinogenesis. 2006 Jun; 27(6):1251-6.
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Ethnicity and human genetic linkage maps. Am J Hum Genet. 2005 Feb; 76(2):276-90.