I. Piaceri

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.

Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation

S. Sorbi, B. Nacmias, S. Bagnoli, 2020, Neurological Sciences.

Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis

S. Sorbi, B. Nacmias, M. Paganini, 2012, Clinical genetics.

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.

Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications.

S. Sorbi, B. Nacmias, S. Bagnoli, 2014, Neurodegenerative disease management.

DAPK1 is associated with FTD and not with Alzheimer's disease.

S. Sorbi, B. Nacmias, E. Lucenteforte, 2012, Journal of Alzheimer's disease : JAD.

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

C. Broeckhoven, S. Sorbi, V. Álvarez, 2020, Neurobiology of Aging.

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

S. Sorbi, B. Nacmias, S. Bagnoli, 2011, Cellular and Molecular Neurobiology.

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

B. Bergmans, C. van Broeckhoven, S. Engelborghs, 2018, Neurobiology of Aging.

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

S. Sorbi, B. Nacmias, C. Polito, 2014, Journal of Alzheimer's disease : JAD.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

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

Epigenetic modifications in Alzheimer's disease: cause or effect?

S. Sorbi, B. Nacmias, S. Bagnoli, 2014, Journal of Alzheimer's disease : JAD.

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 .

Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation

S. Sorbi, B. Nacmias, V. Berti, 2018, Journal of the Neurological Sciences.

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

A. Singleton, J. Hardy, B. Nacmias, 2016, Journal of Alzheimer's disease : JAD.

Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians

S. Sorbi, B. Nacmias, S. Bagnoli, 2013, Neurological Sciences.

Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study

G. Castellini, S. Sorbi, B. Nacmias, 2016, Psychiatry Research.

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

S. Sorbi, B. Nacmias, S. Bagnoli, 2011, Cellular and Molecular Neurobiology.

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.

Genetic Heterogeneity of Alzheimer’s Disease: Embracing Research Partnerships

Sandro Sorbi, S. Sorbi, B. Nacmias, 2017, Journal of Alzheimer's disease : JAD.

Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer’s disease

S. Sorbi, B. Nacmias, S. Bagnoli, 2016, Neuroscience Letters.

Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease

S. Sorbi, B. Nacmias, T. Arendt, 2011, International journal of Alzheimer's disease.

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.

Heterozygous TREM2 mutations in frontotemporal dementia

S. Sorbi, B. Nacmias, D. Galimberti, 2014, Neurobiology of Aging.

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

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

Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases

M. Libra, S. Bagnoli, I. Piaceri, 2017, Oncotarget.

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

Daniele Pepe, Erika Salvi, Fernando Palluzzi, 2015, Neurobiology of Aging.

Mitochondria and Alzheimer's disease

S. Sorbi, S. Bagnoli, I. Piaceri, 2012, Journal of the Neurological Sciences.

High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia.

S. Sorbi, B. Nacmias, V. Berti, 2019, Journal of Alzheimer's disease : JAD.

Genetics of familial and sporadic Alzheimer's disease.

Sandro Sorbi, S. Sorbi, B. Nacmias, 2013, Frontiers in bioscience.

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

G. Comi, S. Cappa, M. Filippi, 2013, Biological Psychiatry.

The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer’s disease: a 9-year follow-up study

S. Sorbi, B. Nacmias, S. Bagnoli, 2019, European Archives of Psychiatry and Clinical Neuroscience.

FDG PET and the genetics of dementia

S. Sorbi, B. Nacmias, V. Berti, 2013, Clinical and Translational Imaging.

PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10‐year follow‐up study

S. Sorbi, B. Nacmias, S. Bagnoli, 2020, European journal of neurology.

Challenges in Alzheimer's Disease Diagnostic Work-Up: Amyloid Biomarker Incongruences.

A. Pupi, S. Sorbi, B. Nacmias, 2020, Journal of Alzheimer's disease : JAD.

Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer’s Disease in Subjective Cognitive Decline and Mild Cognitive Impairment Patients

S. Sorbi, B. Nacmias, S. Bagnoli, 2020, Journal of personalized medicine.

Imaging and Cognitive Reserve Studies Predict Dementia in Presymptomatic Alzheimer's Disease Subjects

S. Sorbi, B. Nacmias, S. Bagnoli, 2013, Neurodegenerative Diseases.

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.

G. Frisoni, C. Babiloni, S. Sorbi, 2016, Journal of Alzheimer's disease : JAD.

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.

S. Sorbi, B. Nacmias, E. Lucenteforte, 2010, Journal of Alzheimer's Disease.

Tumor Necrosis Factor α Influences Phenotypic Plasticity and Promotes Epigenetic Changes in Human Basal Forebrain Cholinergic Neuroblasts

B. Nacmias, G. Kelsey, M. Benelli, 2020, International journal of molecular sciences.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

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

A PALB2 germline mutation associated with hereditary breast cancer in Italy

F. Sera, D. Palli, M. Genuardi, 2010, Familial Cancer.

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.

Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians.

S. Sorbi, M. Mancuso, B. Nacmias, 2011, Journal of Alzheimer's disease : JAD.

author-version of: Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

C. van Broeckhoven, S. Sorbi, V. Álvarez, 2022 .

Primary Progressive Aphasia: Natural History in an Italian Cohort

S. Sorbi, B. Nacmias, V. Berti, 2019, Alzheimer disease and associated disorders.

Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients

S. Sorbi, B. Nacmias, S. Bagnoli, 2013, Neurological Sciences.

A case of limbic encephalitis evolving into a frontotemporal dementia‐like picture

A. Pupi, S. Sorbi, B. Nacmias, 2019, Psychogeriatrics.

Clinical and neuroimaging profiles to identify C9orf72‐FTD patients and serum Neurofilament to monitor the progression and the severity of the disease

A. Pupi, S. Sorbi, B. Nacmias, 2019, Neurology and Clinical Neuroscience.

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.

Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier.

A. Pupi, S. Sorbi, B. Nacmias, 2017, Journal of Alzheimer's disease : JAD.

Novel GRN Mutations in Alzheimer's Disease and Frontotemporal Lobar Degeneration.

S. Sorbi, B. Nacmias, S. Bagnoli, 2018, Journal of Alzheimer's disease : JAD.

Linguistic profiles, brain metabolic patterns and rates of amyloid-β biomarker positivity in patients with mixed primary progressive aphasia

S. Sorbi, B. Nacmias, V. Berti, 2020, Neurobiology of Aging.

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline.

A. Pupi, S. Sorbi, B. Nacmias, 2017, Journal of Alzheimer's disease : JAD.

Biomarkers study in atypical dementia: proof of a diagnostic work-up

A. Pupi, S. Sorbi, B. Nacmias, 2018, Neurological Sciences.

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline.

L. Fratiglioni, S. Sorbi, B. Nacmias, 2017, Journal of Alzheimer's disease : JAD.

Suitability of neuropsychological tests in patients with vascular dementia (VaD)

Sandro Sorbi, Valentina Bessi, S. Sorbi, 2012, Journal of the Neurological Sciences.

Folate, homocysteine, vitamin B12, and polymorphisms of genes participating in one-carbon metabolism in late-onset Alzheimer's disease patients and healthy controls.

F. Coppedè, L. Migliore, S. Sorbi, 2012, Antioxidants & redox signaling.

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.

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

M. Filippi, M. Franceschi, F. Agosta, 2013, Biological Psychiatry.

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

A. Singleton, B. Nacmias, D. Galimberti, 2016, Journal of Alzheimer's disease : JAD.

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease

S. Sorbi, B. Nacmias, A. Mugelli, 2010, Neuroscience Letters.