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Epigenetics of fragile X syndrome and fragile X-related disorders.

Kraan CM, Godler DE, Amor DJ. Kraan CM, et al. Among authors: godler de. Dev Med Child Neurol. 2019 Feb;61(2):121-127. doi: 10.1111/dmcn.13985. Epub 2018 Aug 7. Dev Med Child Neurol. 2019. PMID: 30084485 Free article. Review.

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

Baker EK, Arpone M, Vera SA, Bretherton L, Ure A, Kraan CM, Bui M, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field MJ, Cohen J, Maria LS, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: godler de. J Neurodev Disord. 2019 Dec 26;11(1):41. doi: 10.1186/s11689-019-9288-7. J Neurodev Disord. 2019. PMID: 31878865 Free PMC article.

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

Godler DE, Amor DJ. Godler DE, et al. Essays Biochem. 2019 Dec 20;63(6):785-795. doi: 10.1042/EBC20190056. Essays Biochem. 2019. PMID: 31696914 Review.

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Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome.

Shepherd DA, Vos N, Reid SM, Godler DE, Guzys A, Moreno-Betancur M, Amor DJ. Shepherd DA, et al. Among authors: godler de. Genes (Basel). 2020 Jul 2;11(7):736. doi: 10.3390/genes11070736. Genes (Basel). 2020. PMID: 32630716 Free PMC article.

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Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing.

Hartin SN, Hossain WA, Francis D, Godler DE, Barkataki S, Butler MG. Hartin SN, et al. Among authors: godler de. Mol Genet Genomic Med. 2019 Apr;7(4):e00575. doi: 10.1002/mgg3.575. Epub 2019 Feb 21. Mol Genet Genomic Med. 2019. PMID: 30793526 Free PMC article.

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Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.

Baker EK, Butler MG, Hartin SN, Ling L, Bui M, Francis D, Rogers C, Field MJ, Slee J, Gamage D, Amor DJ, Godler DE. Baker EK, et al. Among authors: godler de. Transl Psychiatry. 2020 Oct 29;10(1):362. doi: 10.1038/s41398-020-01034-7. Transl Psychiatry. 2020. PMID: 33116122 Free PMC article.

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FMR1 mRNA from full mutation alleles is associated with ABC-C_FX scores in males with fragile X syndrome.

Baker EK, Arpone M, Kraan C, Bui M, Rogers C, Field M, Bretherton L, Ling L, Ure A, Cohen J, Hunter MF, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende A, Amor DJ, Godler DE. Baker EK, et al. Among authors: godler de. Sci Rep. 2020 Jul 16;10(1):11701. doi: 10.1038/s41598-020-68465-6. Sci Rep. 2020. PMID: 32678152 Free PMC article.

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Reduced caudate volume and cognitive slowing in men at risk of fragile X-associated tremor ataxia syndrome.

Cvejic RC, Hocking DR, Wen W, Georgiou-Karistianis N, Cornish KM, Godler DE, Rogers C, Trollor JN. Cvejic RC, et al. Among authors: godler de. Brain Imaging Behav. 2019 Aug;13(4):1128-1134. doi: 10.1007/s11682-018-9928-7. Brain Imaging Behav. 2019. PMID: 30046972

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

Kraan CM, Baker EK, Arpone M, Bui M, Ling L, Gamage D, Bretherton L, Rogers C, Field MJ, Wotton TL, Francis D, Hunter MF, Cohen J, Amor DJ, Godler DE. Kraan CM, et al. Among authors: godler de. Int J Mol Sci. 2020 Oct 19;21(20):7735. doi: 10.3390/ijms21207735. Int J Mol Sci. 2020. PMID: 33086711 Free PMC article.

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Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.

Baker EK, Arpone M, Aliaga SM, Bretherton L, Kraan CM, Bui M, Slater HR, Ling L, Francis D, Hunter MF, Elliott J, Rogers C, Field M, Cohen J, Cornish K, Santa Maria L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: godler de. Mol Autism. 2019 May 3;10:21. doi: 10.1186/s13229-019-0271-7. eCollection 2019. Mol Autism. 2019. PMID: 31073396 Free PMC article.

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