"Face" 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 anterior portion of the head that includes the skin, muscles, and structures of the forehead, eyes, nose, mouth, cheeks, and jaw.
Descriptor ID |
D005145
|
MeSH Number(s) |
A01.456.505
|
Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Face".
Below are MeSH descriptors whose meaning is more specific than "Face".
This graph shows the total number of publications written about "Face" by people in this website by year, and whether "Face" 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 |
---|
2000 | 1 | 0 | 1 |
2003 | 1 | 1 | 2 |
2006 | 1 | 1 | 2 |
2007 | 1 | 0 | 1 |
2008 | 0 | 1 | 1 |
2011 | 2 | 2 | 4 |
2013 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2015 | 2 | 0 | 2 |
2016 | 1 | 0 | 1 |
2017 | 2 | 0 | 2 |
2018 | 1 | 1 | 2 |
2019 | 2 | 0 | 2 |
2020 | 0 | 1 | 1 |
2021 | 2 | 1 | 3 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Face" by people in Profiles.
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GestaltMatcher facilitates rare disease matching using facial phenotype descriptors. Nat Genet. 2022 03; 54(3):349-357.
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Hair loss, facial dysmorphology, and skeletal alterations - a diagnostic challenge. Int J Dermatol. 2021 Oct; 60(10):e419-e421.
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ANKRD11 variants: KBG syndrome and beyond. Clin Genet. 2021 08; 100(2):187-200.
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Maternal transmission of a mild Coffin-Siris syndrome phenotype caused by a SOX11 missense variant. Eur J Hum Genet. 2022 01; 30(1):126-132.
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MLL4 is required after implantation, whereas MLL3 becomes essential during late gestation. Development. 2020 06 17; 147(12).
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Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome. Cytogenet Genome Res. 2019; 159(1):1-11.
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Mutations in SMARCB1 and in other Coffin-Siris syndrome genes lead to various brain midline defects. Nat Commun. 2019 07 04; 10(1):2966.
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The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. Genet Med. 2019 06; 21(6):1295-1307.
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Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome. Am J Hum Genet. 2018 03 01; 102(3):468-479.
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Central nervous system anomalies in two females with Borjeson-Forssman-Lehmann syndrome. Epilepsy Behav. 2017 04; 69:104-109.