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A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot–Marie–Tooth neuropathy 1A

Journal of the Peripheral Nervous System(2024)10.1111/jns.12621Source: DataRank Database

A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot–Marie–Tooth neuropathy 1A is a research paper published in Journal of the Peripheral Nervous System (2024). On theSindex it has a DataRank of 0. It has been cited 1 time.

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Open Access1 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (10 grants)Impact (FWCI 0.19)OA: greenTopics (48)IDs (PubMed, PMC, OpenAlex)Annotations (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 (21)

Matt C. Danzi ORCID,Ariel Ruiz,Jacquelyn Raposo,Yeisha Arcia de Jesus,Mary M. Reilly ORCID

Live enrichment

PubMed:38581130 PMC:PMC11209807 OpenAlex:https://openalex.org/W4394011662

NIDDK NIH HHS

Grant: K23 DK118202

NINDS NIH HHS

Grant: R01 NS105755

NINDS NIH HHS

Grant: U54 NS065712

CMT Association

Muscular Dystrophy Association

National Institutes of Health

NIH HHS

Muscular Dystrophy Association

NIH HHS

CMT Association

FWCI

0.19

Citation Percentile

0.4%

Citation Trend

2024

greenLicense: http://onlinelibrary.wiley.com/termsAndConditions#vor

repositoryhttps://discovery.ucl.ac.uk/10213413/1/nihms-1976901.pdf

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/jns.12621

repositoryhttps://discovery.ucl.ac.uk/id/eprint/10213413/

journalhttps://doi.org/10.1111/jns.12621

Fields of Study

Hereditary Neurological DisordersAmyotrophic Lateral Sclerosis ResearchGenomics and Rare DiseasesMedicineCharcot-Marie-Tooth DiseaseHumansAdultMaleFemaleMiddle AgedAdolescentYoung AdultSeverity of Illness IndexChildMyelin ProteinsPatient SelectionPhenotypeAgedGenes, ModifierChild, Preschool

MeSH Terms

AdolescentAdultAgedCharcot-Marie-Tooth DiseaseChildChild, PreschoolFemaleHumansMaleMiddle AgedMyelin ProteinsPhenotypeSeverity of Illness IndexPatient SelectionYoung AdultGenes, Modifier

Keywords

Tooth diseaseMedicineInternal medicineNatural historyDisease severityCmt1aWhole Genome SequencingCharcot–marie–tooth DiseasePmp22Genetic ModifiersCmtesPhenotype Outliers

A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot–Marie–Tooth neuropathy 1A

FAIR Checklist

Authors (21)

Funding (10 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)