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Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Neurobiology of Aging|December 8, 2019
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's diseaseIrene Rosas, Carmen Martínez, Jordi Clarimón, et al.
Neurobiology of Aging|September 25, 2020
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementiaIrene Rosas, Carmen Martínez, Eliecer Coto, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
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