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Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X

Pediatrics(2012)10.1542/peds.2012-0693Source: DataRank Database

Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X is a research paper published in Pediatrics (2012). On theSindex it has a DataRank of 0.557. It has been cited 40 times.

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0.557DataRank · unranked

Scored on demand from live citation data

40 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (1 grants)Impact (FWCI 2.81)OA: closedTopics (86)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

0.557

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (15)

Amy Cronister,William T. Brown,Flora Tassone ORCID,Stephanie L. Sherman,Brenda Finucane ORCID

Live enrichment

PubMed:23129072 OpenAlex:https://openalex.org/W2096167627

NINR NIH HHS

Grant: T32 NR007110

FWCI

2.81

Citation Percentile

0.9%

Influential Citations

Citation Trend

2013

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closed

publisherhttps://publications.aap.org/pediatrics/article-pdf/130/6/1126/897745/peds_2012-0693.pdf

journalhttps://doi.org/10.1542/peds.2012-0693

repositoryhttps://pubmed.ncbi.nlm.nih.gov/23129072

Fields of Study

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalitiesMedicineAdolescentAdultAllelesAnimalsAtaxiaAttention Deficit Disorder with HyperactivityAutistic DisorderChildChild, PreschoolCooperative BehaviorDNA Mutational AnalysisEarly DiagnosisFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGenetic Carrier ScreeningGenetic Predisposition to DiseaseHumansInfantInfant, NewbornInterdisciplinary CommunicationMaleMiceMice, KnockoutModels, GeneticNeonatal ScreeningPatient Care TeamPolymerase Chain ReactionPrimary Ovarian InsufficiencyReferral and ConsultationSex FactorsTremorTrinucleotide RepeatsFragile X Tremor Ataxia Syndrome

MeSH Terms

AdolescentAdultAllelesAnimalsAtaxiaAttention Deficit Disorder with HyperactivityAutistic DisorderChildChild, PreschoolCooperative BehaviorDNA Mutational AnalysisFemaleFragile X SyndromeGenetic Carrier ScreeningHumansInfantInfant, NewbornMaleModels, GeneticPatient Care TeamReferral and ConsultationSex FactorsTremorNeonatal ScreeningPolymerase Chain ReactionPrimary Ovarian InsufficiencyMice, KnockoutTrinucleotide RepeatsGenetic Predisposition to DiseaseInterdisciplinary CommunicationEarly DiagnosisMiceFragile X Messenger Ribonucleoprotein 1Fragile X Mental Retardation Protein

Keywords

Fragile X syndromeFMR1MedicineFragile xAtaxiaGenetic testingIntellectual disabilityNewborn screeningGeneticsPediatricsPsychiatryGeneBiologyInternal medicine

Sustainable Development Goals

SDG 0: Good health and well-being

Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X

FAIR Checklist

DataRank Breakdown

Authors (15)

Funding (1 grants)

Impact

Open Access

Topics