Dr. Yoshimi Inaba
Honorary
Paediatrics Royal Children'S Hospital
5 Scholarly works
0 Projects
HIGHLIGHTS
2015
Journal article
Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women
DOI: 10.1212/WNL.00000000000014962014
Journal article
Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots
DOI: 10.1373/clinchem.2013.2173312013
Journal article
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
DOI: 10.1038/gim.2012.1342012
Journal article
Normal DNA Methylation Dynamics in DICER1-Deficient Mouse Embryonic Stem Cells
DOI: 10.1371/journal.pgen.10029192012
Journal article
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
DOI: 10.1373/clinchem.2011.177626