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Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.
Hwang YT, Dudding T, Aliaga SM, Arpone M, Francis D, Li X, Slater HR, Rogers C, Bretherton L, du Sart D, Heard R, Godler DE. Hwang YT, et al. Among authors: rogers c. Genes (Basel). 2016 Sep 21;7(9):68. doi: 10.3390/genes7090068. Genes (Basel). 2016. PMID: 27657133 Free PMC article.
Selective subcortical contributions to gait impairments in males with the FMR1 premutation.
Birch RC, Hocking DR, Cornish KM, Menant JC, Lord SR, Georgiou-Karistianis N, Godler DE, Wen W, Rogers C, Trollor JN. Birch RC, et al. Among authors: rogers c. J Neurol Neurosurg Psychiatry. 2017 Feb;88(2):188-190. doi: 10.1136/jnnp-2016-313937. Epub 2016 Sep 28. J Neurol Neurosurg Psychiatry. 2017. PMID: 27683920 No abstract available.
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X.
Arpone M, Baker EK, Bretherton L, Bui M, Li X, Whitaker S, Dissanayake C, Cohen J, Hickerton C, Rogers C, Field M, Elliott J, Aliaga SM, Ling L, Francis D, Hearps SJC, Hunter MF, Amor DJ, Godler DE. Arpone M, et al. Among authors: rogers c. Sci Rep. 2018 Feb 26;8(1):3644. doi: 10.1038/s41598-018-21990-x. Sci Rep. 2018. PMID: 29483611 Free PMC article.
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: rogers c. Mol Autism. 2019 May 3;10:21. doi: 10.1186/s13229-019-0271-7. eCollection 2019. Mol Autism. 2019. PMID: 31073396 Free PMC article.
2,719 results