E. Cellini

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.

Distinct epilepsy phenotypes and response to drugs in KCNA1 gain‐ and loss‐of function variants

R. Guerrini, D. Mei, L. Parmeggiani, 2021, Epilepsia.

De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants

C. Wallgren‐Pettersson, R. Guerrini, C. Gurnett, 2018, American journal of medical genetics. Part A.

Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects

P. May, R. Balling, I. Helbig, 2017, American journal of medical genetics. Part A.

The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy

A. Vignoli, R. Guerrini, A. Molinaro, 2016, Developmental medicine and child neurology.

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

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

Severe 5,10‐methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia

E. Ricci, M. Masciullo, G. Silvestri, 2018, European journal of neurology.

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.

Acylphosphatase expression during macrophage differentiation and activation of U-937 cell line.

G. Ramponi, G. Raugei, D. Degl’Innocenti, 1999, Biochimie.

Mirror syndromes regarding AKT3 mutations: Loss of function variant leading to microcephaly

C. Pantaleoni, R. Guerrini, E. Cellini, 2020, American Journal of Medical Genetics. Part A.

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.

Diagnostic implications of genetic copy number variation in epilepsy plus

H. Mefford, L. Lagae, W. van Paesschen, 2019, Epilepsia.

Diagnostic Targeted Resequencing in 349 Patients with Drug‐Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes

C. Barba, R. Guerrini, D. Mei, 2017, Human mutation.

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.

J. González, M. Gratacós, X. Estivill, 2008, Human molecular genetics.

Meta-analysis of the Association Between Variants in SORL 1 and Alzheimer Disease

J. Haines, M. Pericak-Vance, M. Owen, 2011 .

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity

M. Fichera, R. Guerrini, V. Conti, 2019, European Journal of Human Genetics.

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

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

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.

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations

D. Collier, M. Gratacós, X. Estivill, 2005, European Journal of Human Genetics.

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.

Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples

M. Tartaglia, E. Agolini, L. Garavelli, 2021, Genes.

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.

Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study.

D. Collier, S. Sorbi, B. Nacmias, 2008, Drug and alcohol dependence.

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.

The 5-HT2A −1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres

H Remschmidt, D. Collier, M. Gratacós, 2001, Molecular Psychiatry.

5-HT2A receptor gene polymorphism and eating disorders

Sandro Sorbi, Valdo Ricca, S. Sorbi, 2002, Neuroscience Letters.

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.

Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire (CCQ) across five European countries.

D. Collier, S. Sorbi, B. Nacmias, 2011, Clinical psychology & psychotherapy.

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease.

J. González, M. Gratacós, X. Estivill, 2010, Journal of psychiatric research.

Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors

D. Collier, S. Sorbi, B. Nacmias, 2008, British Journal of Nutrition.

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.

Low social interactions in eating disorder patients in childhood and adulthood: A multi-centre European case control study

D. Collier, S. Sorbi, B. Nacmias, 2013, Journal of health psychology.

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations.

D. Collier, M. Gratacós, X. Estivill, 2004, Human molecular genetics.

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.

Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa

M. Gratacós, X. Estivill, H. Wichmann, 2012, Obesity Facts.

Immunoproteasome LMP2 60HH Variant Alters MBP Epitope Generation and Reduces the Risk to Develop Multiple Sclerosis in Italian Female Population

Sandra D'Alfonso, Filippo Martinelli-Boneschi, Claudio Franceschi, 2010, PloS one.

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

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

Combined family trio and case‐control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

M. Gratacós, X. Estivill, S. Sorbi, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Clinical and genetic analysis of an Italian family with Machado-Joseph disease

S. Sorbi, B. Nacmias, L. Parnetti, 2001, Journal of Neurology.

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.

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.

Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa.

D. Collier, M. Gratacós, X. Estivill, 2006, Psychiatric genetics.