"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 |
|
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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 0 | 1 | 1 |
| 1998 | 1 | 1 | 2 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 1 | 1 |
| 2001 | 4 | 2 | 6 |
| 2002 | 1 | 1 | 2 |
| 2003 | 0 | 2 | 2 |
| 2004 | 2 | 0 | 2 |
| 2005 | 1 | 2 | 3 |
| 2006 | 1 | 0 | 1 |
| 2007 | 3 | 0 | 3 |
| 2008 | 1 | 1 | 2 |
| 2009 | 2 | 3 | 5 |
| 2010 | 2 | 1 | 3 |
| 2011 | 2 | 3 | 5 |
| 2012 | 2 | 1 | 3 |
| 2013 | 1 | 4 | 5 |
| 2014 | 5 | 0 | 5 |
| 2015 | 3 | 0 | 3 |
| 2016 | 2 | 4 | 6 |
| 2017 | 3 | 4 | 7 |
| 2018 | 5 | 4 | 9 |
| 2019 | 3 | 6 | 9 |
| 2020 | 5 | 3 | 8 |
| 2021 | 1 | 6 | 7 |
| 2022 | 3 | 4 | 7 |
| 2023 | 2 | 9 | 11 |
| 2024 | 1 | 3 | 4 |
| 2025 | 3 | 1 | 4 |
| 2026 | 1 | 1 | 2 |
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Below are the most recent publications written about "Face" by people in Profiles.
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Parotitis on Ultrasound: The Pomegranate Sign. Pediatr Emerg Care. 2020 Apr; 36(4):205-207.
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Costello syndrome: Clinical phenotype, genotype, and management guidelines. Am J Med Genet A. 2019 09; 179(9):1725-1744.
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Pediatric Craniomaxillofacial Oncologic Reconstruction. Clin Plast Surg. 2019 Apr; 46(2):261-273.
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BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes. Nat Commun. 2018 11 20; 9(1):4885.
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Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders. Genome Med. 2017 08 14; 9(1):73.
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Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Hum Mutat. 2017 10; 38(10):1365-1371.
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De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms. Am J Hum Genet. 2016 Oct 06; 99(4):934-941.
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Yap and Taz play a crucial role in neural crest-derived craniofacial development. Development. 2016 Feb 01; 143(3):504-15.
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3D imaging of the fetal face - recommendations from the International 3D Focus Group. Ultraschall Med. 2012 Apr; 33(2):175-82.
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Discussion: A 15-year review of midface reconstruction after total and subtotal maxillectomy: part I. Algorithm and outcomes. Plast Reconstr Surg. 2012 Jan; 129(1):137-138.