Luisa Benussi

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

for the FTD Prevention Initiative, Moore, K. M., Nicholas, J., Grossman, M., McMillan, C. T., Irwin, D. J., Massimo, L., Van Deerlin, V. M., Warren, J. D., Fox, N. C., Rossor, M. N., Mead, S., Bocchetta, M., Boeve, B. F., Knopman, D. S., Graff-Radford, N. R., Forsberg, L. K., Rademakers, R., Wszolek, Z. K., van Swieten, J. C. & 31 others, Jiskoot, L. C., Meeter, L. H., Dopper, E. GP., Papma, J. M., Snowden, J. S., Saxon, J., Jones, M., Pickering-Brown, S., Le Ber, I., Camuzat, A., Brice, A., Caroppo, P., Ghidoni, R., Pievani, M., Benussi, L., Binetti, G., Dickerson, B. C., Lucente, D., Krivensky, S., Graff, C., Öijerstedt, L., Borroni, B., Galimberti, D., Scarpini, E., Fumagalli, G. G., Sorbi, S., Frisoni, G., Mega, A., Fostinelli, S., Arighi, A. & Fenoglio, C., Feb 2020, In: The Lancet Neurology. 19, 2, p. 145-156 12 p.

Research output: Contribution to journal › Article › peer-review

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study: The Lancet Neurology

for the FTD Prevention Initiative, 2020, In: Lancet Neurol.. 19, 2, p. 145-156 12 p.

Research output: Contribution to journal › Article › peer-review

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

International FTD-Genetics Consortium, Costa, B. & Nacmias, B., Dec 15 2020, In: Neurology. 95, 24, p. e3288-e3302

Research output: Contribution to journal › Article › peer-review

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group & DESGESCO (Dementia Genetics Spanish Consortium), Jan 1 2020, (Accepted/In press) In: Acta Neuropathologica.

Research output: Contribution to journal › Comment/debate › peer-review

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

Consortium, T. EU. EOD., [Unknown], IFGC., Rosas, I., Martínez, C., Coto, E., Clarimón, J., Lleó, A., Illán-Gala, I., Dols-Icardo, O., Borroni, B., Almeida, M. R., van der Zee, J., Van Broeckhoven, C., Bruni, A. C., Anfossi, M., Bernardi, L., Maletta, R., Serpente, M., Galimberti, D., Scarpini, E. & 20 others, Rossi, G., Caroppo, P., Benussi, L., Ghidoni, R., Binetti, G., Nacmias, B., Sorbi, S., Piaceri, I., Bagnoli, S., Antonell, A., Sánchez-Valle, R., De la Casa-Fages, B., Grandas, F., Diez-Fairen, M., Pastor, P., Ferrari, R., Queimaliños-Perez, D., Pérez-Oliveira, S., Álvarez, V. & Menéndez-González, M., 2020, In: Neurobiol. Aging.

Research output: Contribution to journal › Article › peer-review