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Intellectual disability: dendritic anomalies and emerging genetic perspectives

Acta Neuropathologica(2020)10.1007/s00401-020-02244-5Source: DataRank Database

Intellectual disability: dendritic anomalies and emerging genetic perspectives is a research paper published in Acta Neuropathologica (2020). On theSindex it has a DataRank of 0. It has been cited 46 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access46 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 3.26)OA: greenTopics (34)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (7)

Harrison J. Stratton ORCID,Rajesh Khanna ORCID,Pappachan E. Kolattukudy,Jérôme Honnorat ORCID,Kathrin Meyer ORCID

Live enrichment

PubMed:33226471 PMC:PMC7855540 OpenAlex:https://openalex.org/W3107550429

National Institutes of Health

Grant: R01NS09877202

National Institutes of Health

Grant: R01DA04285202

NINDS NIH HHS

Grant: R01 NS098772

NIDA NIH HHS

Grant: R01 DA042852

FWCI

3.26

Citation Percentile

0.9%

Citation Trend

2021

2022

2023

2024

2025

2026

greenLicense: http://www.springer.com/tdm

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7855540

publisherhttp://link.springer.com/content/pdf/10.1007/s00401-020-02244-5.pdf

publisherhttp://link.springer.com/article/10.1007/s00401-020-02244-5/fulltext.html

journalhttps://doi.org/10.1007/s00401-020-02244-5

Fields of Study

Genetics and Neurodevelopmental DisordersUbiquitin and proteasome pathwaysRNA regulation and diseaseAnimalsChild, PreschoolChromosome AberrationsDendritesHumansIntellectual DisabilityNerve Tissue Proteins

MeSH Terms

AnimalsChild, PreschoolChromosome AberrationsDendritesHumansIntellectual DisabilityNerve Tissue Proteins

Keywords

Intellectual disabilityBiologyNeuroscienceCandidate geneNeurodevelopmental disorderDendritic spineRett syndromeExome sequencingExomeGeneticsGenePhenotypeHippocampal formationTransgenic miceCrmp3/dpysl4Chromosome 10 (Q26) DeletionDendrite Dysgenesis

Sustainable Development Goals

SDG 0: Quality Education

Intellectual disability: dendritic anomalies and emerging genetic perspectives

FAIR Checklist

Authors (7)

Funding (4 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)