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Human Molecular Genetics|January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosisKatherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.
Journal of Alzheimer'S Disease : JAD|February 23, 2016
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus ProtocolMartina Bocchetta, Anna Mega, Livia Bernardi, et al.
Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.
Neurobiology of Aging|July 24, 2012
Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern ItalyLivia Bernardi, Francesca Frangipane, Nicoletta Smirne, 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.
JAMA Neurology|July 19, 2021
Global Prevalence of Young-Onset Dementia: A Systematic Review and Meta-analysisStevie Hendriks, Kirsten Peetoom, Christian Bakker, et al.
Brain : a Journal of Neurology|October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degenerationMathieu Barbier, Agnès Camuzat, Khalid El Hachimi, et al.
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