Yoshimi Inaba
Melbourne, VIC 3052, Australia
Last Updated: 09/26/2026
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Found 8 publications
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome.
Journal: International journal of molecular sciences
Published: May 01, 2023
Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis.
Journal: Expert reviews in molecular medicine
Published: July 02, 2015
Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.
Journal: Neurology
Published: September 08, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots.
Journal: Clinical chemistry
Published: April 30, 2014
Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty.
Journal: Human molecular genetics
Published: January 12, 2013
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2012
Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.
Journal: Clinical chemistry
Published: January 12, 2012
Normal DNA methylation dynamics in DICER1-deficient mouse embryonic stem cells.
Journal: PLoS genetics
Published: January 10, 2012
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Last Updated: 09/26/2026