"Puberty" 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.
A period in the human life in which the development of the hypothalamic-pituitary-gonadal system takes place and reaches full maturity. The onset of synchronized endocrine events in puberty lead to the capacity for reproduction (FERTILITY), development of secondary SEX CHARACTERISTICS, and other changes seen in ADOLESCENT DEVELOPMENT.
Descriptor ID |
D011627
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MeSH Number(s) |
G08.686.760 G08.686.841.374
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Puberty".
Below are MeSH descriptors whose meaning is more specific than "Puberty".
This graph shows the total number of publications written about "Puberty" by people in this website by year, and whether "Puberty" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2013 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Puberty" by people in Profiles.
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Linking brain maturation and puberty during early adolescence using longitudinal brain age prediction in the ABCD cohort. Dev Cogn Neurosci. 2023 04; 60:101220.
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Increased intake of carbohydrates from sources with a higher glycemic index and lower consumption of whole grains during puberty are prospectively associated with higher IL-6 concentrations in younger adulthood among healthy individuals. J Nutr. 2014 Oct; 144(10):1586-93.
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Habitually higher dietary glycemic index during puberty is prospectively related to increased risk markers of type 2 diabetes in younger adulthood. Diabetes Care. 2013 Jul; 36(7):1870-6.
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Inflammatory adipokines, high molecular weight adiponectin, and insulin resistance: a population-based survey in prepubertal schoolchildren. PLoS One. 2011 Feb 18; 6(2):e17264.
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WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Am J Hum Genet. 2010 Oct 08; 87(4):465-79.