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CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis

Neurobiology of Aging(2012)10.1016/j.neurobiolaging.2012.03.007Source: DataRank Database

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis is a research paper published in Neurobiology of Aging (2012). On theSindex it has a DataRank of 0.345. It has been cited 9 times.

N/A

0.345DataRank · unranked

Scored on demand from live citation data

9 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 0.95)OA: greenTopics (58)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.345

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (10)

Wouter van Rheenen ORCID,Max Koppers ORCID,Perry T.C. van Doormaal ORCID,Lotte Vlam,Frank P. Diekstra

Live enrichment

PubMed:22507827 OpenAlex:https://openalex.org/W2060834879

European Community's Health Seventh Framework Programme

Grant: FP7/2007-2013

European Commission

Grant: 259867

European multidisciplinary ALS network identification to cure motor neuron degeneration

FWCI

0.95

Citation Percentile

0.8%

Citation Trend

2013

2014

2015

2016

2020

2023

greenLicense: other-oa

repositoryhttps://zenodo.org/record/3421139

publisherhttps://api.elsevier.com/content/article/PII:S019745801200214X?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S019745801200214X?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.neurobiolaging.2012.03.007

Fields of Study

Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative DiseasesGenetics and Neurodevelopmental Disorders0301 basic medicine03 medical and health sciences0302 clinical medicine

MeSH Terms

AgedAged, 80 and overAmyotrophic Lateral SclerosisFemaleGenetic MarkersHumansMaleMiddle AgedNetherlandsRepetitive Sequences, Nucleic AcidRisk FactorsGenetic VariationPrevalenceGenetic Predisposition to DiseasePolymorphism, Single NucleotideFragile X Messenger Ribonucleoprotein 1Fragile X Mental Retardation ProteinGenetic Association Studies

Keywords

C9orf72Trinucleotide repeat expansionFMR1Amyotrophic lateral sclerosisFrontotemporal dementiaAtaxiaSpinocerebellar ataxiaTARDBPFragile X syndromeMedicineGeneticsDementiaBiologyInternal medicineGeneFragile xDiseasePsychiatryAged, 80 and overGenetic MarkersMaleFragile X Messenger Ribonucleoprotein 1Genetic VariationMiddle AgedPolymorphism, Single NucleotideRisk FactorsPrevalenceHumansFemaleGenetic Predisposition to DiseaseGenetic Association StudiesAgedNetherlandsRepetitive Sequences, Nucleic Acid

Sustainable Development Goals

SDG 0: Good health and well-being

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis

FAIR Checklist

DataRank Breakdown

Authors (10)

Funding (2 grants)

Impact

Open Access

Topics