• 3636 Citations
  • 32 h-Index
1993 …2019
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Fingerprint Dive into the research topics where Antonia Ratti is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genome-Wide Association Study Medicine & Life Sciences
RNA-Binding Proteins Medicine & Life Sciences
ELAV Proteins Medicine & Life Sciences
Motor Neurons Medicine & Life Sciences
RNA Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1993 2019

  • 3636 Citations
  • 32 h-Index
  • 95 Article
  • 2 Review article
  • 1 Letter

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

de Majo, M., Topp, S. D., Smith, B. N., Nishimura, A. L., Chen, H. J., Gkazi, A. S., Miller, J., Wong, C. H., Vance, C., Baas, F., ten Asbroek, A. L. M. A., Kenna, K. P., Ticozzi, N., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Morrison, K. E., Shaw, P. J. & 13 others, Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., de Belleroche, J., Gellera, C., Ratti, A., Al-Chalabi, A., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., Nov 1 2018, In : Neurobiology of Aging. 71, p. 266.e1-266.e10

Research output: Contribution to journalArticle

Phosphotransferases
Mutation
Missense Mutation
Phosphorylation
Exome
6 Citations (Scopus)

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

de Majo, M., Topp, S. D., Smith, B. N., Nishimura, A. L., Chen, H. J., Gkazi, A. S., Miller, J., Wong, C. H., Vance, C., Baas, F., ten Asbroek, A. L. M. A., Kenna, K. P., Ticozzi, N., Redondo, A. G., Esteban-Pérez, J., Tiloca, C., Verde, F., Duga, S., Morrison, K. E., Shaw, P. J. & 13 others, Kirby, J., Turner, M. R., Talbot, K., Hardiman, O., Glass, J. D., de Belleroche, J., Gellera, C., Ratti, A., Al-Chalabi, A., Brown, R. H., Silani, V., Landers, J. E. & Shaw, C. E., Nov 1 2018, In : Neurobiology of Aging. 71, p. 266.e1-266.e10

Research output: Contribution to journalArticle

Phosphotransferases
Mutation
Missense Mutation
Phosphorylation
Exome
1 Citation (Scopus)

Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases

Corrado, L., Tiloca, C., Locci, C., Bagarotti, A., Hamzeiy, H., Colombrita, C., De marchi, F., Barizzone, N., Cotella, D., Ticozzi, N., Mazzini, L., Nazli Basak, A. Y. S. E., Ratti, A., Silani, V. & D’alfonso, S., Jul 3 2018, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 5-6, p. 426-431 6 p.

Research output: Contribution to journalArticle

GC Rich Sequence
Amyotrophic Lateral Sclerosis
Genes

Cognitive-behavioral longitudinal assessment in ALS: the Italian Edinburgh Cognitive and Behavioral ALS screen (ECAS)

Poletti, B., Solca, F., Carelli, L., Faini, A., Madotto, F., Lafronza, A., Monti, A., Zago, S., Ciammola, A., Ratti, A., Ticozzi, N., Abrahams, S. & Silani, V., Aug 2018, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19, 5-6, p. 387-395 9 p.

Research output: Contribution to journalArticle

Behavioral Genetics
Apathy
Behavioral Symptoms
Neuropsychological Tests
Caregivers