Poonnada Jiraanont
Lat Krabang, Thailand
Last Updated: 09/26/2026
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Found 10 publications
Corrigendum to "The apolipoprotein gene: a modulating role on brain volume and cognitive function in carriers of the fragile X premutation" [Neurobiology of Disease 2026 Feb 2; 220:107292, Page 1-13].
Journal: Neurobiology of disease
Published: May 21, 2026
The apolipoprotein gene: a modulating role on brain volume and cognitive function in carriers of the fragile X premutation.
Journal: Neurobiology of disease
Published: October 05, 2025
Population-based FMR1 carrier screening among reproductive women.
Journal: Journal of assisted reproduction and genetics
Published: July 15, 2024
FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation.
Journal: The Journal of molecular diagnostics : JMD
Published: August 15, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Journal: Cells
Published: July 04, 2023
De Novo Large Deletion Leading to Fragile X Syndrome.
Journal: Frontiers in genetics
Published: February 26, 2022
Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder.
Journal: Frontiers in genetics
Published: October 29, 2019
Clinical and molecular correlates in fragile X premutation females.
Journal: eNeurologicalSci
Published: October 04, 2017
Size and methylation mosaicism in males with Fragile X syndrome.
Journal: Expert review of molecular diagnostics
Published: September 21, 2017
Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome.
Journal: European journal of medical genetics
Published: August 09, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026