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List of works by Elena Cellini

5-HT2A receptor gene polymorphism and eating disorders

scientific article

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

scientific article (publication date: December 2002)

Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits.

scientific article published on 26 September 2005

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity

scientific article published on 19 December 2006

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

scientific article published on 25 September 2006

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

scientific article

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

scientific article published in April 2005

Association of IL10 promoter polymorphism in Italian Alzheimer's disease

scientific article published on 19 March 2007

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

scientific article

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

scientific article

Brain metabolic differences between sporadic and familial Alzheimer's disease.

scientific article published in October 2003

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

scientific article published in March 2004

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

scientific article published in September 2004

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

article

Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease

scientific article published in August 2002

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

article

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

article

Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy.

scientific article published in October 2001

Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations

scientific article published on 11 December 2017

Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease

scientific article published in February 2008

Cystatin C and apoe polymorphisms in Italian Alzheimer's disease

scientific article published on 26 September 2005

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

scientific article published on 19 November 2016

Diagnostic implications of genetic copy number variation in epilepsy plus

scientific article published on 13 March 2019

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

scientific article published on 30 September 2010

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

scientific article published on 27 June 2012

Fragile X premutation with atypical symptoms at onset

scientific article published in August 2006

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

article

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

scientific article

Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population

scientific article

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

scientific article published in January 2009

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

scientific article published in October 2009

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

scientific article

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

article

Lack of association between NOS3 polymorphism and Italian sporadic and familial Alzheimer's disease

article

Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort

scientific article published in December 2008

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

scientific article published in August 2005

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

scientific article published in January 2010

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

scientific article published on 5 April 2012

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

scientific article published on 17 March 2009

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

scientific article

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

scientific article published on 25 January 2019

Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease

scientific article published in January 2008

No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy

scientific article published on 11 September 2007

Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion

scientific article published on 07 June 2012

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

scientific article published on 20 June 2008

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

scientific article published in July 2004

Pyridoxine responsiveness in pyridox(am)ine-5-phosphate oxidase deficiency: The importance of early treatment.

scientific article published on 23 October 2017

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

scientific article published in April 2017

Recurrent drop attacks in early childhood as presenting symptom of benign hereditary chorea caused by TITF1 gene mutations.

scientific article published on 20 November 2014

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

scientific article

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

scientific article published on 28 December 2017

Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations

scientific article published on 7 March 2007

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy

scientific article published on 6 September 2015

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

scientific article

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

article

Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene

scientific article published on 18 November 2010

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

article

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