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Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023
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Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023

Godler, David E ; Brown, William T

Genes, 2023-05, Vol.14 (6), p.1148 [Peer Reviewed Journal]

Switzerland: MDPI AG

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2
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders
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DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders

Godler, David E ; Amor, David J Blewitt, Marnie

Essays in biochemistry, 2019-12, Vol.63 (6), p.785-795 [Peer Reviewed Journal]

England

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3
Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
Defining the 3′Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome
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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.

International journal of molecular sciences, 2023-07, Vol.24 (13), p.10712 [Peer Reviewed Journal]

Basel: MDPI AG

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4
Special Issue: Genetics of Prader-Willi Syndrome
Special Issue: Genetics of Prader-Willi Syndrome
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Special Issue: Genetics of Prader-Willi Syndrome

Godler, David E ; Butler, Merlin G

Genes, 2021-09, Vol.12 (9), p.1429 [Peer Reviewed Journal]

Switzerland: MDPI AG

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5
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies
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β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies

Kraan, Claudine M ; Cornish, Kim M ; Bui, Quang M ; Li, Xin ; Slater, Howard R ; Godler, David E Fernandez-Funez, Pedro

PloS one, 2018-02, Vol.13 (2), p.e0192151 [Peer Reviewed Journal]

United States: Public Library of Science

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6
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome
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DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

Kraan, Claudine M ; Baker, Emma K ; Arpone, Marta ; Bui, Minh ; Ling, Ling ; Gamage, Dinusha ; Bretherton, Lesley ; Rogers, Carolyn ; Field, Michael J ; Wotton, Tiffany L ; Francis, David ; Hunter, Matt F ; Cohen, Jonathan ; Amor, David J ; Godler, David E

International journal of molecular sciences, 2020-10, Vol.21 (20), p.7735 [Peer Reviewed Journal]

Switzerland: MDPI AG

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7
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing
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Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing

Field, Michael ; Dudding-Byth, Tracy ; Arpone, Marta ; Baker, Emma K ; Aliaga, Solange M ; Rogers, Carolyn ; Hickerton, Chriselle ; Francis, David ; Phelan, Dean G ; Palmer, Elizabeth E ; Amor, David J ; Slater, Howard ; Bretherton, Lesley ; Ling, Ling ; Godler, David E

International journal of molecular sciences, 2019-08, Vol.20 (16), p.3907 [Peer Reviewed Journal]

Switzerland: MDPI AG

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8
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX

Pandelache, Alison ; Francis, David ; Oertel, Ralph ; Dickson, Rebecca ; Sachdev, Rani ; Ling, Ling ; Gamage, Dinusha ; Godler, David E.

Genes, 2021-06, Vol.12 (6), p.798 [Peer Reviewed Journal]

Basel: MDPI AG

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9
Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes
Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes
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Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes

Baker, Emma K ; Godler, David E ; Bui, Minh ; Hickerton, Chriselle ; Rogers, Carolyn ; Field, Mike ; Amor, David J ; Bretherton, Lesley

Journal of neurodevelopmental disorders, 2018-08, Vol.10 (1), p.24-24, Article 24 [Peer Reviewed Journal]

England: BioMed Central Ltd

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10
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
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Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

Baker, Emma K ; Arpone, Marta ; Vera, Solange Aliaga ; Bretherton, Lesley ; Ure, Alexandra ; Kraan, Claudine M ; Bui, Minh ; Ling, Ling ; Francis, David ; Hunter, Matthew F ; Elliott, Justine ; Rogers, Carolyn ; Field, Michael J ; Cohen, Jonathan ; Maria, Lorena Santa ; Faundes, Victor ; Curotto, Bianca ; Morales, Paulina ; Trigo, Cesar ; Salas, Isabel ; Alliende, Angelica M ; Amor, David J ; Godler, David E

Journal of neurodevelopmental disorders, 2019-12, Vol.11 (1), p.41-41, Article 41 [Peer Reviewed Journal]

England: BioMed Central Ltd

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