"Deafness" 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 general term for the complete loss of the ability to hear from both ears.
| Descriptor ID |
D003638
|
| MeSH Number(s) |
C09.218.458.341.186 C10.597.751.418.341.186 C23.888.592.763.393.341.186
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Deafness".
Below are MeSH descriptors whose meaning is more specific than "Deafness".
This graph shows the total number of publications written about "Deafness" by people in this website by year, and whether "Deafness" 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 |
|---|
| 2007 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2021 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Deafness" by people in Profiles.
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Kalinousky AJ, Luperchio TR, Schrode KM, Harris JR, Zhang L, DeLeon VB, Fahrner JA, Lauer AM, Bjornsson HT. KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans. Genes (Basel). 2023 12 28; 15(1).
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Weinberg MM, Retta NA, Schrode KM, Screven LA, Peterson JL, Moss CF, Sterbing S, Lauer AM. Deafness in an auditory specialist, the big brown bat (Eptesicus fuscus). Hear Res. 2021 12; 412:108377.
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Bedoukian EC, Rentas S, Skraban C, Shao Q, Treat J, Laird DW, Sullivan KE. Palmoplantar keratoderma with deafness phenotypic variability in a patient with an inherited GJB2 frameshift variant and novel missense variant. Mol Genet Genomic Med. 2021 02; 9(2):e1574.
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Pyott SJ, van Tuinen M, Screven LA, Schrode KM, Bai JP, Barone CM, Price SD, Lysakowski A, Sanderford M, Kumar S, Santos-Sacchi J, Lauer AM, Park TJ. Functional, Morphological, and Evolutionary Characterization of Hearing in Subterranean, Eusocial African Mole-Rats. Curr Biol. 2020 11 16; 30(22):4329-4341.e4.
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Villavisanis DF, Berson ER, Lauer AM, Cosetti MK, Schrode KM. Sex-based Differences in Hearing Loss: Perspectives From Non-clinical Research to Clinical Outcomess. Otol Neurotol. 2020 03; 41(3):290-298.
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Fenn KM, Shintel H, Atkins AS, Skipper JI, Bond VC, Nusbaum HC. When less is heard than meets the ear: change deafness in a telephone conversation. Q J Exp Psychol (Hove). 2011 Jul; 64(7):1442-56.
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Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ. Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. Clin Genet. 2007 Dec; 72(6):546-50.