Publications by authors named "Jamie L Randol"

Claim this Profile
E
Electroretinographic Findings in Fragile X, Premutation, and Controls: A Study of Biomarker Correlations.
Hasan Hasan, Hazel Maridith Barlahan Biag, Ellery R Santos, Jamie Leah Randol, Robert Ring

Int J Mol Sci· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel p.Arg534del Mutation and MTHFR C667T Polymorphism in Fragile X Syndrome (FXS) With Autism Spectrum Phenotype: A Case Report.
Hasan Hasan, Ellery R Santos, Seyedeh Ala Mokhtabad Amrei, Flora Tassone, Jamie Leah Randol

Case Rep Genet· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation.
Poonnada Jiraanont, Marwa Zafarullah, Noor Sulaiman, Glenda M Espinal, Jamie L Randol

J Mol Diagn· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome.
YeEun Tak, Andrea Schneider, Ellery Santos, Jamie Leah Randol, Flora Tassone

Genes (Basel)· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome.
Jamie L Randol, Kyoungmi Kim, Matthew D Ponzini, Flora Tassone, Alexandria K Falcon

Genes (Basel)· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Adaptive, behavioral, and cognitive outcomes in individuals with fragile X syndrome with varying autism severity.
Ramkumar Aishworiya, Ye Eun Tak, Matthew Dominic Ponzini, Hazel Maridith Barlahan Biag, Maria Jimena Salcedo-Arellano, Jamie Leah Randol

Int J Dev Neurosci· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS).
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Jamie L Randol

Cells· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome.
Ramkumar Aishworiya, Mei-Hung Chi, Marwa Zafarullah, Guadalupe Mendoza, Matthew Dominic Ponzini, Jamie Leah Randol

Cells· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Corrigendum: Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome.
Katharine Nichole Holm, Anthony W Herren, Sandra L Taylor, Jamie L Randol, Kyoungmi Kim

Front Mol Biosci· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome.
Katharine Nichole Holm, Anthony W Herren, Sandra L Taylor, Jamie L Randol, Kyoungmi Kim

Front Mol Biosci· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions.
Kyoungmi Kim, David Hessl, Jamie L Randol, Glenda M Espinal, Andrea Schneider

PLoS One· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis