Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
Godler, David E., Inaba, Yoshimi, Bui, Minh Q., Francis, David, Skinner, Cindy, Schwartz, Charles E., Amor, David J.
Published in International journal of molecular sciences (01.07.2023)
Published in International journal of molecular sciences (01.07.2023)
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Normal DNA methylation dynamics in DICER1-deficient mouse embryonic stem cells
Ip, Jonathan, Canham, Paul, Choo, K H Andy, Inaba, Yoshimi, Jacobs, Shelley A, Kalitsis, Paul, Mattiske, Deidre M, Ng, Jane, Saffery, Richard, Wong, Nicholas C, Wong, Lee H, Mann, Jeffrey R
Published in PLoS genetics (01.09.2012)
Published in PLoS genetics (01.09.2012)
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Defining the 3′Epigenetic Boundary of the IFMR1/I Promoter and Its Loss in Individuals with Fragile X Syndrome
Godler, David E, Inaba, Yoshimi, Bui, Minh Q, Francis, David, Skinner, Cindy, Schwartz, Charles E, Amor, David J
Published in International journal of molecular sciences (01.06.2023)
Published in International journal of molecular sciences (01.06.2023)
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Defining the 3#8242;Epigenetic Boundary of the IFMR1/I Promoter and Its Loss in Individuals with Fragile X Syndrome
Godler, David E, Inaba, Yoshimi, Bui, Minh Q, Francis, David, Skinner, Cindy, Schwartz, Charles E, Amor, David J
Published in International journal of molecular sciences (01.06.2023)
Published in International journal of molecular sciences (01.06.2023)
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Journal Article
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
Godler, David E, Inaba, Yoshimi, Bui, Minh Q, Francis, David, Skinner, Cindy, Schwartz, Charles E, Amor, David J
Published in International journal of molecular sciences (27.06.2023)
Published in International journal of molecular sciences (27.06.2023)
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Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots
Inaba, Yoshimi, Schwartz, Charles E, Bui, Quang M, Li, Xin, Skinner, Cindy, Field, Michael, Wotton, Tiffany, Hagerman, Randi J, Francis, David, Amor, David J, Hopper, John L, Loesch, Danuta Z, Bretherton, Lesley, Slater, Howard R, Godler, David E
Published in Clinical chemistry (Baltimore, Md.) (01.07.2014)
Published in Clinical chemistry (Baltimore, Md.) (01.07.2014)
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Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women
Cornish, Kim M, Kraan, Claudine M, Bui, Quang Minh, Bellgrove, Mark A, Metcalfe, Sylvia A, Trollor, Julian N, Hocking, Darren R, Slater, Howard R, Inaba, Yoshimi, Li, Xin, Archibald, Alison D, Turbitt, Erin, Cohen, Jonathan, Godler, David E
Published in Neurology (21.04.2015)
Published in Neurology (21.04.2015)
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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
GODLER, David E, SLATER, Howard R, AMOR, David J, HAGERMAN, Randi J, LOESCH, Danuta Z, BUI, Quang M, STOREY, Elsdon, ONTO, Michele Y, GEHLING, Freya, INABA, Yoshimi, FRANCIS, David, HOPPER, John L, KINSELLA, Glynda
Published in Clinical chemistry (Baltimore, Md.) (01.03.2012)
Published in Clinical chemistry (Baltimore, Md.) (01.03.2012)
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The use of droplet digital PCR and high resolution melt for detection of low level mosaicism
Godler, David E., Christodoulou, John, Bruno, Damien, Li, Xin, Inaba, Yoshimi, Bui, Quang M., Francis, David, Elliot, Justine, Wotton, Tiffany, Cohen, Jonathan, Rogers, Carolyn, Field, Mike, Slater, Howard R., Amor, David J.
Published in Pathology (01.02.2018)
Published in Pathology (01.02.2018)
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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
Godler, David E, Inaba, Yoshimi, Shi, Elva Z, Skinner, Cindy, Bui, Quang M, Francis, David, Amor, David J, Hopper, John L, Loesch, Danuta Z, Hagerman, Randi J, Schwartz, Charles E, Slater, Howard R
Published in Human molecular genetics (15.04.2013)
Published in Human molecular genetics (15.04.2013)
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