François V Bolduc

Biographic Data

ID7956837
NAMEFrançois V Bolduc
GIVEN NAMESFrançois V
FAMILY NAMEBolduc
SIGNATUREBOLDUC F V
AFFILIATIONSUniversity of Alberta
ORCID0000-0002-6109-5467
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2021
H-INDEX0

  • EEG Signal Complexity Is Reduced During Resting-State in Fragile X Syndrome

    Open AccessMélodie Proteau-Lemieux, Inga Sophia Knoth et al.ARTICLEFrontiers in Psychiatry2021

    Introduction: Fragile X syndrome (FXS) is a genetic disorder caused by a mutation of the fragile X mental retardation 1 gene ( FMR1 ). FXS is associated with neurophysiological abnormalities, including cortical hyperexcitability. Alterations in electroencephalogram (EEG) resting-state power spectral density (PSD) are well-defined in FXS and were found to be linked to neurodevelopmental delays. Whether non-linear dynamics of the brain signal are a…

  • Phenotypic Trade-Offs

    Open AccessTruong An Bui, Julie Shatto et al.ARTICLEFrontiers in Psychiatry2021

    Fragile X syndrome (FXS) is the most common single-gene cause of intellectual disability and autism spectrum disorder. Individuals with FXS present with a wide range of severity in multiple phenotypes including cognitive delay, behavioral challenges, sleep issues, epilepsy, and anxiety. These symptoms are also shared by many individuals with other neurodevelopmental disorders (NDDs). Since the discovery of the FXS gene, FMR1, FXS has been the foc…