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The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.

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Trinucleotide Repeats: Mechanisms and Pathophysiology

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MicroRNAs (miRNAs) in Neurodegenerative Diseases

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Sequence-Specific RNA Binding by a Nova KH Domain

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Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11

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Microsatellite evolution — evidence for directionality and variation in rate between species

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Dynamic mutations: A new class of mutations causing human disease

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The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm

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Molecular Basis of Genetic Instability of Triplet Repeats

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Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome

Musumeci, S. A., Bosco, P., Calabrese, G., Bakker, C., De Sarro, G. B., Elia, M., Ferri, R., & Oostra, B. A. (2000) · Epilepsia · doi:10.1111/j.1528-1157.2000.tb01499.x · Cited by 289

Trinucleotide repeats associated with human disease

Mitas, M. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.12.2245 · Cited by 294

Premutation and intermediate-size FMR1 alleles in 10 572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

Dombrowski, C. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.4.371 · Cited by 289

Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome

Mornet, É., Chateau, C., Taillandier, A., Simon‐Bouy, B., & Serre, J. (1996) · Human Genetics · doi:10.1007/bf02267077 · Cited by 17

The fragile X mutation

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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

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Mechanisms of Genome Instability in the Fragile X-Related Disorders

Hayward, B. E., & Usdin, K. (2021) · Genes · doi:10.3390/genes12101633 · Cited by 14

Mechanisms of Repeat Instability in Fragile X Syndrome

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