Hereditary Neurological Disorders
Hereditary Neurological Disorders is a research topic within Cellular and Molecular Neuroscience. Science Explorer counts 15k research works in it since 1950. 10.2% of them reached the world's top 10% most cited for their field and year.
This cluster of papers explores the genetic basis and molecular mechanisms underlying various neuropathies, including Charcot-Marie-Tooth disease, hereditary spastic paraplegia, and related disorders. It covers topics such as genetic mutations, axonal degeneration, nerve growth factor, mitochondrial dysfunction, and microtubule dynamics. The research also delves into the role of neurofilament mutations and ganglioside-induced differentiation in these neuropathies.
- Charcot-Marie-Tooth Disease
- Hereditary Spastic Paraplegia
- Peripheral Neuropathy
- Genetic Mutations
- Axonal Degeneration
- Nerve Growth Factor
- Mitochondrial Dysfunction
- Microtubule Dynamics
- Neurofilament Mutations
- Ganglioside-Induced Differentiation
- Research works
- 15k fractional, since 1950
- In the world top 10%
- 1.5k per year above
- Top-10% rate
- 10.2% share of its works in the world top 10%
- Growth, 2018-21 → 2022-25
- +10% the tick is no change
- Largest producer
United States
29% of the 10 largest, 2022-now
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