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FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation.
J Mol Diagn. 2024 Mar 22:S1525-1578(24)00058-8. doi: 10.1016/j.jmoldx.2024.02.007. Online ahead of print.
J Mol Diagn. 2024.
PMID: 38522837
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ.
Tassone F, et al. Among authors: jiraanont p.
Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330.
Cells. 2023.
PMID: 37759552
Free PMC article.
Review.
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De Novo Large Deletion Leading to Fragile X Syndrome.
Jiraanont P, Manor E, Tabatadze N, Zafarullah M, Mendoza G, Melikishvili G, Tassone F.
Jiraanont P, et al.
Front Genet. 2022 May 11;13:884424. doi: 10.3389/fgene.2022.884424. eCollection 2022.
Front Genet. 2022.
PMID: 35646065
Free PMC article.
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Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder.
Alolaby RR, Jiraanont P, Durbin-Johnson B, Jasoliya M, Tang HT, Hagerman R, Tassone F.
Alolaby RR, et al. Among authors: jiraanont p.
Front Genet. 2020 Apr 15;11:308. doi: 10.3389/fgene.2020.00308. eCollection 2020.
Front Genet. 2020.
PMID: 32346385
Free PMC article.
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Clinical and molecular correlates in fragile X premutation females.
Jiraanont P, Sweha SR, AlOlaby RR, Silva M, Tang HT, Durbin-Johnson B, Schneider A, Espinal GM, Hagerman PJ, Rivera SM, Hessl D, Hagerman RJ, Chutabhakdikul N, Tassone F.
Jiraanont P, et al.
eNeurologicalSci. 2017 Jun;7:49-56. doi: 10.1016/j.ensci.2017.04.003. Epub 2017 Apr 11.
eNeurologicalSci. 2017.
PMID: 28971146
Free PMC article.
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Size and methylation mosaicism in males with Fragile X syndrome.
Jiraanont P, Kumar M, Tang HT, Espinal G, Hagerman PJ, Hagerman RJ, Chutabhakdikul N, Tassone F.
Jiraanont P, et al.
Expert Rev Mol Diagn. 2017 Nov;17(11):1023-1032. doi: 10.1080/14737159.2017.1377612.
Expert Rev Mol Diagn. 2017.
PMID: 28929824
Free PMC article.
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Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome.
Jiraanont P, Hagerman RJ, Neri G, Zollino M, Murdolo M, Tassone F.
Jiraanont P, et al.
Eur J Med Genet. 2016 Sep;59(9):459-62. doi: 10.1016/j.ejmg.2016.08.009. Epub 2016 Aug 18.
Eur J Med Genet. 2016.
PMID: 27546052
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