A. Tedde

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.

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

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

A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset

B. Nacmias, C. Piccini, S. Piacentini, 2000, Neurology.

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

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

Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis

S. Sorbi, P. George-Hyslop, A. Orlacchio, 2000, Neuroscience Letters.

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

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

P.0771 Targeting quality of life in schizophrenia: the fil rouge between metabolic syndrome and anxiety

R. Cavallaro, M. Buonocore, A. Tedde, 2021, European Neuropsychopharmacology.

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

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

Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer's disease

S. Sorbi, B. Nacmias, A. Tedde, 2000, Neurobiology of Aging.

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.

Angiotensin converting enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease

S. Sorbi, B. Nacmias, A. Orlacchio, 2000 .

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.

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.

Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas

F. Vitelli, L. Papi, A. Tedde, 1996, Human Genetics.

Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin

F. Vitelli, P. Radice, P. Grammatico, 1996, Human Genetics.

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.

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.

Implication of α1-antichymotrypsin polymorphism in familial Alzheimer's disease

S. Sorbi, B. Nacmias, L. Amaducci, 1998, Neuroscience Letters.

Presenilin-1 gene intronic polymorphism in sporadic and familial Azheimer's disease

S. Sorbi, B. Nacmias, L. Amaducci, 1997, Neuroscience Letters.

Apolipoprotein E and α1‐antichymotrypsin polymorphism in Alzheimer's disease

S. Sorbi, B. Nacmias, L. Amaducci, 1996 .

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.

Fibroblasts from PS1 mutated pre-symptomatic subjects and Alzheimer's disease patients share a unique protein levels profile.

S. Sorbi, L. Zolla, C. Emiliani, 2010, 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.

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.

SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.

S. Sorbi, B. Nacmias, A. Conte, 2008, Journal of Alzheimer's disease : JAD.

α2-Macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease

S. Sorbi, B. Nacmias, A. Orlacchio, 2001, Neuroscience Letters.

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

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

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.

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

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

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

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

Fragile X premutation with atypical symptoms at onset.

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

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

M. Nalls, A. Lang, S. Sorbi, 2015, Neurobiology of Aging.

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.

Large deletion mutation of SPAST in a multi‐generation family from Sardinia

F. Pierelli, A. Tessa, C. Casali, 2014, European journal of neurology.

Analysis of apolipoprotein E, α1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man

S. Sorbi, B. Nacmias, L. Amaducci, 1997, Neuroscience Letters.

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.

Clinical profile of trazodone users in a multisetting older population: data from the Italian GeroCovid Observational study

C. Mussi, G. Sergi, S. Volpato, 2023, European Geriatric Medicine.

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

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

Semantic dementia associated with mutation V363I in the tau gene

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

A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene

B. Nacmias, G. Lucidi, A. Tedde, 2013, 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.

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

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

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

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

Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease.

S. Sorbi, B. Nacmias, A. Orlacchio, 2001, Neuroscience Letters.

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.

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.

Clinical presentation and prognosis of COVID-19 in older adults with hypothyroidism: data from the GeroCovid observational study

C. Mussi, G. Sergi, S. Volpato, 2023, Journal of Endocrinological Investigation.

Psychosis, serotonin receptor polymorphism and Alzheimer's disease.

S. Sorbi, B. Nacmias, S. Piacentini, 2001, Archives of gerontology and geriatrics. Supplement.

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

M. Nalls, A. Lang, S. Sorbi, 2015, Neurobiology of Aging.

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

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