Life Sciences → Biochemistry, Genetics and Molecular Biology → Genetics
Genetics and Neurodevelopmental Disorders
This cluster of papers focuses on the molecular basis, genetic mutations, and neurological manifestations of Rett syndrome and related disorders such as Fragile X syndrome. It explores the role of MeCP2, synaptic function, autism-like behaviors, and altered brain development in these conditions.
55.9K works worldwide1.2M citations
Rett SyndromeFragile X SyndromeMeCP2Neurological DiseaseSynaptic FunctionAutismmGluR theoryDendritic SpinesBrain DevelopmentGenetic Mutations
Journals publishing in this area
2
356h-index
2.38Impact
14.2KArticles
1.2MCitations
3
315h-index
7.23Impact
7.3KArticles
588.6KCitations
5
387h-index
5.79Impact
11.1KArticles
1MCitations
7
225h-index
1.35Impact
18.5KArticles
474.2KCitations
8
780h-index
14.78Impact
11.7KArticles
2.9MCitations
9
Journal of the American Academy of Child & Adolescent Psychiatry
ISSN 0890-8567415 articles in this topic
357h-index
0.46Impact
23.4KArticles
754.4KCitations
10
435h-index
4.11Impact
18.1KArticles
1.4MCitations
11
279h-index
3.48Impact
14.1KArticles
683.2KCitations
13
342h-index
3.29Impact
7.9KArticles
643.2KCitations
14
597h-index
15.28Impact
8.1KArticles
1.6MCitations
15
304h-index
4.04Impact
8.8KArticles
661.7KCitations
16
372h-index
6.54Impact
7.3KArticles
724.3KCitations
17
567h-index
12.43Impact
5.2KArticles
1MCitations
18
524h-index
14.46Impact
5KArticles
900.2KCitations
