Squitieri, Ferdinando

A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats

Kremer, B., Goldberg, P., Andrew, S. E., Theilmann, J., Telenius, H., Zeisler, J., Squitieri, F., Lin, B., Bassett, A., Almqvist, E., et al. (1994) · New England Journal of Medicine

Genetic Neurodegenerative DiseasesGenetic factors in colorectal cancer

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Polyglutamine tracts regulate beclin 1-dependent autophagy

Ashkenazi, A., Bento, C. F., Ricketts, T., Vicinanza, M., Siddiqi, F., Pavel, M., Squitieri, F., Hardenberg, M. C., Imarisio, S., Menzies, F. M., et al. (2017) · Nature

Genetic Neurodegenerative DiseasesAutophagy in Disease and Therapy

Cited by 357

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Coleman, A., Santos, R. D., et al. (2017) · The Lancet Neurology

Genetic Neurodegenerative DiseasesGenetic Associations and Epidemiology

Cited by 312

Biological and clinical manifestations of juvenile Huntington’s disease: A retrospective analysis

Fusilli, C., Migliore, S., Mazza, T., Consoli, F., De Luca, A., Barbagallo, G., Ciammola, A., Gatto, E. M., Cesarini, M., Etcheverry, J. L., et al. (2018) · The Lancet Neurology

Genetic Neurodegenerative DiseasesDeep Brain Stimulation and Movement Disorders

Cited by 148

Epidemiology of Huntington disease: first post‐HTT gene analysis of prevalence in Italy

Squitieri, F., Griguoli, A., Capelli, G., Porcellini, A., & D'Alessio, B. (2016) · Clinical Genetics

Genetic Neurodegenerative DiseasesPrion Diseases and Protein Misfolding

Cited by 43