S. Bagnoli

S. Sorbi, A. Peri, S. Bagnoli, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Plasma neurofilament light chain as a biomarker of Alzheimer’s disease in Subjective Cognitive Decline and Mild Cognitive Impairment

S. Sorbi, B. Nacmias, V. Berti, 2022, Journal of Neurology.

Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians

C. Franceschi, S. Sorbi, B. Nacmias, 2005, Mechanisms of Ageing and Development.

Loss of speech and functional impairment in Alzheimer's disease-related primary progressive aphasia: predictive factors of decline

A. Mazzoni, S. Sorbi, B. Nacmias, 2022, Neurobiology of Aging.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

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

Intermediate alleles of HTT: A new pathway in longevity

S. Sorbi, B. Nacmias, S. Bagnoli, 2022, Journal of the Neurological Sciences.

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.

Gender differences in cognitive reserve: implication for subjective cognitive decline in women

S. Sorbi, B. Nacmias, S. Bagnoli, 2021, Journal of the Neurological Sciences.

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.

Long-term use of pharmacological treatment in Alzheimer’s disease: a retrospective cohort study in real-world clinical practice

S. Sorbi, B. Nacmias, V. Berti, 2022, European Journal of Clinical Pharmacology.

The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease

S. Sorbi, B. Nacmias, M. Rotondi, 2005, Neurogenetics.

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

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

Psychopathological traits and 5-HT2A receptor promoter polymorphism (−1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa

M. Boldrini, S. Sorbi, B. Nacmias, 2004, Neuroscience Letters.

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.

Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy

G. De Michele, A. Filla, A. Tessa, 2018, European journal of neurology.

Effects of Donepezil,Galantamine and Rivastigmine in 938 Italian Patients with Alzheimer’s Disease

C. Franceschi, S. Sorbi, B. Nacmias, 2010, CNS drugs.

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.

S. Sorbi, B. Nacmias, S. Bagnoli, 2002, Archives of neurology.

Association of IL10 promoter polymorphism in Italian Alzheimer's disease

S. Sorbi, B. Nacmias, S. Bagnoli, 2007, Neuroscience Letters.

Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy

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

Matching Clinical Diagnosis and Amyloid Biomarkers in Alzheimer’s Disease and Frontotemporal Dementia

S. Sorbi, B. Nacmias, V. Berti, 2021, Journal of Personalized Medicine.

Pattern and Progression of Cognitive Decline in Alzheimer’s Disease: Role of Premorbid Intelligence and ApoE Genotype

S. Sorbi, B. Nacmias, C. Piccini, 2007, Dementia and Geriatric Cognitive Disorders.

Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference

S. Sorbi, B. Nacmias, S. Bagnoli, 2011, International journal of Alzheimer's disease.

Human iPSC-Derived Hippocampal Spheroids: An Innovative Tool for Stratifying Alzheimer Disease Patient-Specific Cellular Phenotypes and Developing Therapies

C. Rampon, S. Sorbi, B. Nacmias, 2020, Stem cell reports.

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.

Membrane cholesterol enrichment prevents Aβ-induced oxidative stress in Alzheimer's fibroblasts

S. Sorbi, B. Nacmias, S. Bagnoli, 2011, Neurobiology of Aging.

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.

Identification of new presenilin gene mutations in early-onset familial Alzheimer disease.

Sandro Sorbi, Marco Paganini, Paolo Caffarra, 2003, Archives of neurology.

Genetic risk factors in familial Alzheimer's disease

S. Sorbi, B. Nacmias, S. Bagnoli, 2001, Mechanisms of Ageing and Development.

Donor-Specific Anti-HLA Antibodies in Huntington's Disease Recipients of Human Fetal Striatal Grafts

B. Nacmias, N. Di Lorenzo, M. Paganini, 2015, Cell transplantation.

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints

Sandro Sorbi, Valentina Bessi, Laura Bracco, 2008, Neuroscience Letters.

Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer’s disease

S. Sorbi, B. Nacmias, C. Piccini, 2004, Neuroscience Letters.

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.

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

F. Jessen, G. Frisoni, K. Sleegers, 2012, Human mutation.

Heterozygous TREM2 mutations in frontotemporal dementia

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

Protective effect of new S-acylglutathione derivatives against amyloid-induced oxidative stress.

S. Sorbi, B. Nacmias, P. Paoli, 2008, Free radical biology & medicine.

Alzheimer’s Disease: Role of Size and Location of White Matter Changes in Determining Cognitive Deficits

M. Mascalchi, S. Sorbi, B. Nacmias, 2005, Dementia and Geriatric Cognitive Disorders.

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.

Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons

S. Sorbi, B. Nacmias, F. Nicoletti, 2015, Front. Cell. Neurosci..

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.

Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts

S. Sorbi, B. Nacmias, D. Nosi, 2007, 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.

Implication of sex and SORL1 variants in italian patients with Alzheimer disease.

S. Sorbi, B. Nacmias, S. Bagnoli, 2009, Archives of neurology.

Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease

S. Sorbi, B. Nacmias, M. Rotondi, 2006, Neurobiology of Aging.

Presenilin mutations linked to familial Alzheimer's disease reduce endoplasmic reticulum and Golgi apparatus calcium levels.

S. Sorbi, G. Binetti, M. Giacomello, 2006, Cell calcium.

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.

DNMT3B promoter polymorphisms and risk of late onset Alzheimer's disease.

F. Coppedè, L. Migliore, S. Sorbi, 2012, Current Alzheimer research.

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.

Predictors of Function, Activity, and Participation of Stroke Patients Undergoing Intensive Rehabilitation: A Multicenter Prospective Observational Study Protocol

M. Carrozza, A. Poggesi, B. Nacmias, 2021, Frontiers in Neurology.

Unravelling neural correlates of empathy deficits in Subjective Cognitive Decline, Mild Cognitive Impairment and Alzheimer’s Disease

S. Sorbi, B. Nacmias, V. Berti, 2022, Behavioural Brain Research.

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.

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.

Plasma membrane injury depends on bilayer lipid composition in Alzheimer's disease.

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

The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Can Protect Against Cognitive Impairment in Multiple Sclerosis

S. Sorbi, B. Nacmias, M. Amato, 2021, Frontiers in Neurology.

Differences and Similarities in Empathy Deficit and Its Neural Basis between Logopenic and Amnesic Alzheimer’s Disease

S. Sorbi, B. Nacmias, V. Berti, 2023, Journal of personalized medicine.

Lipid rafts mediate amyloid-induced calcium dyshomeostasis and oxidative stress in Alzheimer's disease.

S. Sorbi, B. Nacmias, S. Bagnoli, 2013, Current Alzheimer research.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

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

Neurofilament Light Chain and Intermediate HTT Alleles as Combined Biomarkers in Italian ALS Patients

S. Sorbi, B. Nacmias, S. Bagnoli, 2021, Frontiers in Neuroscience.

Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity

C. Faravelli, G. Castellini, S. Sorbi, 2010, Psychiatric genetics.

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

G. Castellini, S. Sorbi, B. Nacmias, 2017, PloS one.

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 serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

S. Sorbi, B. Nacmias, S. Bagnoli, 2011, Archives of gerontology and geriatrics.

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.

The SIRT2 polymorphism rs10410544 and risk of Alzheimer’s disease in two Caucasian case–control cohorts

L. Polito, P. Kehoe, S. Sorbi, 2013, Alzheimer's & Dementia.

Low M r phosphotyrosine protein phosphatase activity on fibroblast growth factor receptor is not associated with enzyme translocation

S. Bagnoli, P. Dello Sbarba, E. Rovida, 1999, FEBS letters.

Dual Effect of PER2 C111G Polymorphism on Cognitive Functions across Progression from Subjective Cognitive Decline to Mild Cognitive Impairment

S. Sorbi, B. Nacmias, S. Bagnoli, 2021, Diagnostics.

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 .

A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer's Disease in Italian Caucasians

F. Coppedè, L. Migliore, S. Sorbi, 2014, BioMed research international.

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.

Lack of association between TNF-α polymorphisms and Alzheimer’s disease in an Italian cohort

S. Sorbi, B. Nacmias, S. Bagnoli, 2008, Neuroscience Letters.

Degradation of EEG microstates patterns in subjective cognitive decline and mild cognitive impairment: Early biomarkers along the Alzheimer’s Disease continuum?

S. Micera, A. Mazzoni, S. Sorbi, 2023, NeuroImage: Clinical.

Clinical, Neurophysiological, and Genetic Predictors of Recovery in Patients With Severe Acquired Brain Injuries (PRABI): A Study Protocol for a Longitudinal Observational Study

M. Carrozza, B. Nacmias, A. Grippo, 2022, Frontiers in Neurology.

Fragile X premutation with atypical symptoms at onset.

M. Mascalchi, S. Sorbi, B. Nacmias, 2006, Archives of neurology.

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.

CAG Repeats Within the Non-pathological Range in the HTT Gene Influence Personality Traits in Patients With Subjective Cognitive Decline: A 13-Year Follow-Up Study

S. Sorbi, B. Nacmias, S. Bagnoli, 2022, Frontiers in Psychiatry.

The Effect of CAG Repeats within the Non-Pathological Range in the HTT Gene on Cognitive Functions in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment

S. Sorbi, B. Nacmias, S. Bagnoli, 2021, Diagnostics.

PRedicting the EVolution of SubjectIvE Cognitive Decline to Alzheimer’s Disease With machine learning: the PREVIEW study protocol

A. Mazzoni, S. Sorbi, B. Nacmias, 2023, BMC Neurology.

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.

Association between serotonin transporter gene polymorphism and eating disorders outcome: A 6‐year follow‐up study

C. Faravelli, G. Castellini, S. Sorbi, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study

Salvatore Mazzeo, Sandro Sorbi, Valentina Bessi, 2019, Journal of Neurology.

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.

Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease‐like and ataxia

S. Sorbi, B. Nacmias, S. Bagnoli, 2004, Annals of neurology.

Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients.

C. Franceschi, S. Sorbi, B. Nacmias, 2010, Journal of Alzheimer's Disease.

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

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

Semantic dementia associated with mutation V363I in the tau gene

S. Sorbi, B. Nacmias, S. Bagnoli, 2010, Journal of the Neurological Sciences.

Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease.

Sandro Sorbi, Silvia Piacentini, S. Sorbi, 2009, Journal of Alzheimer's disease : JAD.

Alzheimer's Disease Progression: Factors Influencing Cognitive Decline.

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

Association analysis of the paraoxonase-1 gene with Alzheimer's disease

S. Sorbi, B. Nacmias, S. Bagnoli, 2006, Neuroscience Letters.

Contribution of Bilingualism to Cognitive Reserve of an Italian Literature Professor at High Risk for Alzheimer's Disease.

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

Human iPSC-derived hippocampal spheroids: An innovative tool for stratifying Alzheimer disease patient-specific cellular phenotypes and developing therapies

C. Rampon, S. Sorbi, B. Nacmias, 2021, Stem Cell Reports.

Brain‐derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy

S. Sorbi, B. Nacmias, S. Bagnoli, 2004, Annals of neurology.

Alzheimer's disease: genetic basis and amyloid imaging as endophenotype.

S. Sorbi, B. Nacmias, V. Berti, 2011, The quarterly journal of nuclear medicine and molecular imaging : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology (IAR), [and] Section of the Society of....

The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease

B. Giusti, R. Abbate, S. Sorbi, 2001, Neuroscience Letters.

Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.

S. Sorbi, B. Nacmias, S. Bagnoli, 2005, Alzheimer disease and associated disorders.

CXCR4 involvement in neurodegenerative diseases

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

Late-onset Huntington disease: An Italian cohort

S. Sorbi, B. Nacmias, S. Bagnoli, 2021, Journal of Clinical Neuroscience.

A new social-family model for eating disorders: A European multicentre project using a case–control design

D. Collier, S. Sorbi, B. Nacmias, 2015, Appetite.

The Huntington’s Disease Gene in an Italian Cohort of Patients with Bipolar Disorder

S. Sorbi, B. Nacmias, S. Bagnoli, 2023, Genes.

KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment

S. Sorbi, B. Nacmias, S. Bagnoli, 2019, Neurological Sciences.

The role of plasma neurofilament light chain and glial fibrillary acidic protein in subjective cognitive decline and mild cognitive impairment

B. Nacmias, V. Berti, C. Polito, 2023, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane

M. Memo, S. Sorbi, B. Nacmias, 2010, Journal of Molecular Medicine.

Multilayered nanoparticles as optical sensors for amyloid ß-peptide (1-42) targeting in liquid samples

B. Nacmias, S. Bagnoli, F. Pavone, 2023, BiOS.

Plasma neurofilament light chain predicts Alzheimer’s disease in patients with subjective cognitive decline and mild cognitive impairment: a longitudinal study

S. Sorbi, B. Nacmias, V. Berti, 2023, medRxiv.

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.

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction and progression of Alzheimer’s disease pathogenesis

B. Nacmias, S. Bagnoli, O. Klementieva, 2023, Acta Neuropathologica Communications.

Proteomic analysis across patient iPSC-based models and human post-mortem hippocampal tissue reveals early cellular dysfunction, progression, and prion-like spread of Alzheimer’s disease pathogenesis

B. Nacmias, S. Bagnoli, O. Klementieva, 2023, bioRxiv.

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.

Brain metabolic differences between sporadic and familial Alzheimer’s disease

K. Herholz, L. Mosconi, A. Pupi, 2003, Neurology.

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.

Plasma neurofilament light chain predicts Alzheimer's disease in patients with subjective cognitive decline and mild cognitive impairment: A cross‐sectional and longitudinal study

B. Nacmias, V. Berti, C. Polito, 2023, European Journal of Neurology.

Disentangling empathy impairment along Alzheimer's disease continuum: From subjective cognitive decline to Alzheimer's dementia

B. Nacmias, C. Polito, S. Bagnoli, 2024, Cortex.

Plasma GFAP, NfL and pTau 181 detect preclinical stages of dementia

B. Nacmias, S. Bagnoli, V. Bessi, 2024, Frontiers in endocrinology.

Future perspective and clinical applicability of the combined use of plasma phosphorylated tau 181 and neurofilament light chain in Subjective Cognitive Decline and Mild Cognitive Impairment

B. Nacmias, S. Bagnoli, V. Bessi, 2024, Scientific reports.

Data-driven subtypes of mixed semantic-logopenic primary progressive aphasia: Linguistic features, biomarker profiles and brain metabolic patterns

B. Nacmias, C. Polito, S. Bagnoli, 2024, Journal of the Neurological Sciences.

Parkinson-ALS with a novel MAPT variant

B. Nacmias, S. Ramat, S. Bagnoli, 2023, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

B. Nacmias, S. Bagnoli, V. Bessi, 2024, bioRxiv.

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

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

Understanding the interplay between APO E polymorphism and cognition in the Italian oldest old: results from the "Mugello study".

S. Sorbi, B. Nacmias, S. Pancani, 2023, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes

B. Nacmias, C. Polito, S. Bagnoli, 2023, Cerebellum.

Mutational Landscape of Alzheimer’s Disease and Frontotemporal Dementia: Regional Variances in Northern, Central, and Southern Italy

B. Nacmias, G. Binetti, R. Ghidoni, 2024, International journal of molecular sciences.

A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer's Disease in Italian Caucasians

F. Coppedè, L. Migliore, S. Sorbi, 2014, BioMed research international.