"Neuroimaging" 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.
Non-invasive methods of visualizing the CENTRAL NERVOUS SYSTEM, especially the brain, by various imaging modalities.
Descriptor ID |
D059906
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MeSH Number(s) |
E01.370.350.578 E01.370.376.537 E05.629
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Neuroimaging".
Below are MeSH descriptors whose meaning is more specific than "Neuroimaging".
This graph shows the total number of publications written about "Neuroimaging" by people in this website by year, and whether "Neuroimaging" 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 |
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2015 | 1 | 3 | 4 |
2017 | 1 | 0 | 1 |
2019 | 0 | 1 | 1 |
2020 | 0 | 2 | 2 |
2021 | 0 | 2 | 2 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neuroimaging" by people in Profiles.
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Associations between brain imaging and polygenic scores of mental health and educational attainment in children aged 9-11. Neuroimage. 2022 11; 263:119611.
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Longitudinal Structural Brain Changes in Bipolar Disorder: A Multicenter Neuroimaging Study of 1232 Individuals by the ENIGMA Bipolar Disorder Working Group. Biol Psychiatry. 2022 03 15; 91(6):582-592.
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A Connectivity-Based Psychometric Prediction Framework for Brain-Behavior Relationship Studies. Cereb Cortex. 2021 07 05; 31(8):3732-3751.
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Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet. 2021 01; 58(1):33-40.
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. JAMA Psychiatry. 2020 04 01; 77(4):420-430.
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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. J Hum Genet. 2019 Aug; 64(8):803-813.
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Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation. Eur Radiol. 2017 Dec; 27(12):5080-5092.
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A Single Amino Acid Deletion (?F1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx. PLoS One. 2015; 10(12):e0146035.
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TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patients. Eur J Paediatr Neurol. 2016 Mar; 20(2):323-330.
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"Acquired" Dandy-Walker malformation and cerebellar hemorrhage: Usefulness of serial MRI. Eur J Paediatr Neurol. 2016 Jan; 20(1):188-91.