F. Frangipane

发表

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

Demis A. Kia, O. Andreassen, B. Miller, 2020, Neurology.

Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.

A. Bruni, M. Anfossi, L. Bernardi, 2013, Journal of Alzheimer's Disease.

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

F. Tagliavini, A. Bruni, O. Bugiani, 2011, Journal of Alzheimer's disease : JAD.

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.

A. Bruni, M. Anfossi, L. Bernardi, 2011, Journal of Alzheimer's disease : JAD.

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Nick C Fox, Alan J. Thomas, D. Hernandez, 2020, Scientific Reports.

Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

C. Cupidi, A. Bruni, M. Anfossi, 2014, Neurobiology of Aging.

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism

A. Bruni, M. Anfossi, L. Bernardi, 2008, Journal of Neurology.

Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease

A. Bruni, M. Anfossi, L. Bernardi, 2007, Journal of Neurology.

Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia

C. Cupidi, A. Bruni, F. Frangipane, 2022, Frontiers in Neurology.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Kevin F. Bieniek, C. Geula, M. Mesulam, 2018, The Lancet Neurology.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study

Elizabeth, Sandro, Ying-xue, 2018 .

Heterogeneity within a large kindred with frontotemporal dementia

J. Hardy, P. S. St George-Hyslop, A. Kertesz, 2007, Neurology.

A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family

A. Bruni, L. Bernardi, M. E. Conidi, 2021, Frontiers in Genetics.

Uncoupling protein 4 (UCP4) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia

A. Bruni, F. Frangipane, R. Maletta, 2018, Aging.

Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

Nick C Fox, Alan J. Thomas, D. Hernandez, 2021, Biological Psychiatry.

The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family

S. Sorbi, B. Nacmias, C. Cupidi, 2017, Neurobiology of Aging.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

D. Hernandez, M. Nalls, L. Ferrucci, 2017, bioRxiv.

Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia

A. Bruni, M. Anfossi, L. Bernardi, 2009, Neurobiology of Aging.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

Role of Niemann-Pick Type C Disease Mutations in Dementia.

C. Cupidi, A. Bruni, M. Anfossi, 2016, Journal of Alzheimer's disease : JAD.

Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia

C. Duyckaerts, M. Spillantini, A. Bruni, 2011, Neurobiology of Aging.

Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia

A. Bruni, M. Anfossi, L. Bernardi, 2010, Neurological Sciences.

Phenotypic expressions of Alzheimer’s disease: a gender perspective

C. Cupidi, A. Bruni, M. Anfossi, 2018 .

Worldwide distribution of PSEN1 Met146Leu mutation

S. Pappatà, S. Sorbi, G. Forloni, 2010, Neurology.

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

C. Cupidi, A. Bruni, M. Anfossi, 2015, Neurology.

A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer’s Disease

A. Bruni, F. Frangipane, R. Maletta, 2021, Journal of Alzheimer's disease : JAD.

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy

E. Rogaeva, P. George-Hyslop, C. Cupidi, 2012, Neurobiology of Aging.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Nature Medicine.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Brain : a journal of neurology.

Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer’s Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor

C. van Broeckhoven, B. Borroni, C. Giuliani, 2021, Biomedicines.

Somatic comorbidities and Alzheimer’s disease treatment

A. Bruni, F. Frangipane, P. Gareri, 2013, Neurological Sciences.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Nick C Fox, D. Hernandez, M. Nalls, 2017, Scientific Reports.

Using the Theory of Planned Behavior and Past Behavior to Explain the Intention to Receive a Seasonal Influenza Vaccine among Family Caregivers of People with Dementia

A. Bruni, Paolo Abondio, F. Frangipane, 2023, International Journal of Translational Medicine.

Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.

C. Cupidi, A. Bruni, M. Anfossi, 2018, Journal of Alzheimer's disease : JAD.

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

A. Bruni, M. Anfossi, L. Bernardi, 2009, Journal of Alzheimer's disease : JAD.

MAPT V363I Variation in a Sporadic Case of Frontotemporal Dementia: Variable Penetrant Mutation or Rare Polymorphism?

A. Bruni, M. Anfossi, L. Bernardi, 2011, Alzheimer disease and associated disorders.

CXCR4 involvement in neurodegenerative diseases

O. Andreassen, G. Schellenberg, A. Dale, 2017, bioRxiv.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

H. Leonard, D. Knopman, C. van Broeckhoven, 2024, American journal of human genetics.