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Reduced Respiratory Sinus Arrhythmia in Infants with the FMR1 Premutation

International Journal of Molecular Sciences(2025)10.3390/ijms26052186Source: DataRank Database

Reduced Respiratory Sinus Arrhythmia in Infants with the FMR1 Premutation is a research paper published in International Journal of Molecular Sciences (2025). On theSindex it has a DataRank of 0.

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (13 grants)Impact (FWCI 0.94)OA: goldTopics (56)IDs (PubMed, PMC, OpenAlex)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 (10)

Lisa R. Hamrick ORCID,Holley P. Arnold,Jenna Smith,Rachel M. Hantman ORCID,Kaitlyn B Cortez ORCID

Live enrichment

PubMed:40076819 PMC:PMC11900448 OpenAlex:https://openalex.org/W4408054313

National Institutes of Health

Grant: 1R01MH090194

National Institutes of Health

Grant: 2R01MH090194

National Institutes of Health

Grant: R01HD106652

National Institutes of Health

Grant: F31HD114363

National Institutes of Health

Grant: T32GM081740

NIMH NIH HHS

Grant: R01 MH090194

NIH HHS

Grant: 1R01HD106652-01A1

NIH HHS

Grant: 1R01MH090194-01A1

NIH HHS

Grant: 2R01MH090194-06A1

National Institutes of Health

Grant: 5T32GM081740-04

Biomedical-Behavioral Interface: Prevention and Developmental Sciences Training

National Institutes of Health

Grant: 1F31HD114363-01

Maternal-Child RSA Synchrony in Infants with Fragile X Syndrome

National Institutes of Health

Grant: 3R01HD106652-02S1

Autonomic and Sensory Dysfunctions in FMR1 Conditions: Development, Mechanisms and Consequences

National Institutes of Health

Grant: 5R01MH090194-09

Emergence and Stability of Autism in Fragile X Syndrome

FWCI

0.94

Citation Percentile

0.7%

Citation Trend

2026

goldLicense: cc-by

journalhttps://www.mdpi.com/1422-0067/26/5/2186/pdf?version=1740751297

publisherhttps://www.mdpi.com/1422-0067/26/5/2186/pdf?version=1740751297

publisherhttps://www.mdpi.com/1422-0067/26/5/2186/pdf

journalhttps://doi.org/10.3390/ijms26052186

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40076819

Fields of Study

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities0303 health sciences03 medical and health sciencesHumansFragile X Messenger Ribonucleoprotein 1Respiratory Sinus ArrhythmiaMaleInfantFemaleFragile X SyndromeAutonomic Nervous SystemTrinucleotide Repeat ExpansionMutation

MeSH Terms

Autonomic Nervous SystemFemaleFragile X SyndromeHumansInfantMaleMutationTrinucleotide Repeat ExpansionFragile X Messenger Ribonucleoprotein 1Fragile X Mental Retardation ProteinRespiratory Sinus Arrhythmia

Keywords

Vagal toneNeurotypicalMedicineFMR1Respiratory systemAutonomic nervous systemPediatricsAudiologyInternal medicineGeneticsBiologyHeart rateGeneAutismPsychiatryAutism spectrum disorderRespiratory Sinus ArrhythmiaFmr1 PremutationInterbeat IntervalCgg Repeat LengthMale<i>FMR1</i> premutationFragile X Messenger Ribonucleoprotein 1InfantArticleFragile X SyndromeMutationHumansFemaleTrinucleotide Repeat Expansion

Sustainable Development Goals

SDG 0: Good health and well-being