"Cognition Disorders" 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.
Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment.
Descriptor ID |
D003072
|
MeSH Number(s) |
F03.615.250
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Cognition Disorders".
Below are MeSH descriptors whose meaning is more specific than "Cognition Disorders".
This graph shows the total number of publications written about "Cognition Disorders" by people in this website by year, and whether "Cognition Disorders" 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 |
---|
2010 | 0 | 3 | 3 |
2011 | 2 | 0 | 2 |
2016 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Cognition Disorders" by people in Profiles.
-
Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes (Basel). 2022 02 25; 13(3).
-
Estrogen receptor beta polymorphisms and cognitive performance in women: associations and modifications by genetic and environmental influences. J Neural Transm (Vienna). 2016 12; 123(12):1369-1379.
-
Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011 Sep 21; 478(7367):57-63.
-
N-acetyl cysteine treatment rescues cognitive deficits induced by mitochondrial dysfunction in G72/G30 transgenic mice. Neuropsychopharmacology. 2011 Oct; 36(11):2233-43.
-
The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample. Schizophr Res. 2010 Sep; 122(1-3):24-30.
-
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 05; 153B(2):503-511.
-
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. J Pediatr. 2010 Feb; 156(2):332-4.