|
1
|
Fragile X premutation with atypical symptoms at onset.
|
Arch Neurol
|
2006
|
1.43
|
|
2
|
KIBRA gene variants are associated with episodic memory performance in subjective memory complaints.
|
Neurosci Lett
|
2008
|
1.01
|
|
3
|
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians.
|
Mech Ageing Dev
|
2005
|
0.96
|
|
4
|
Implication of sex and SORL1 variants in italian patients with Alzheimer disease.
|
Arch Neurol
|
2009
|
0.95
|
|
5
|
SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.
|
J Alzheimers Dis
|
2008
|
0.94
|
|
6
|
Association of IL10 promoter polymorphism in Italian Alzheimer's disease.
|
Neurosci Lett
|
2007
|
0.93
|
|
7
|
Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease.
|
Alzheimer Dis Assoc Disord
|
2005
|
0.91
|
|
8
|
Brain-derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy.
|
Ann Neurol
|
2004
|
0.91
|
|
9
|
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease.
|
Neurosci Lett
|
2004
|
0.91
|
|
10
|
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.
|
J Alzheimers Dis
|
2010
|
0.88
|
|
11
|
Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity.
|
Psychiatr Genet
|
2010
|
0.83
|
|
12
|
Association analysis of the paraoxonase-1 gene with Alzheimer's disease.
|
Neurosci Lett
|
2006
|
0.83
|
|
13
|
Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease.
|
J Alzheimers Dis
|
2009
|
0.83
|
|
14
|
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians.
|
Neurol Sci
|
2012
|
0.82
|
|
15
|
Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).
|
Arch Gerontol Geriatr
|
2011
|
0.82
|
|
16
|
TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.
|
Neurol Sci
|
2013
|
0.81
|
|
17
|
Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa.
|
Neurosci Lett
|
2004
|
0.80
|
|
18
|
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease.
|
Neurosci Lett
|
2002
|
0.79
|
|
19
|
Suitability of neuropsychological tests in patients with vascular dementia (VaD).
|
J Neurol Sci
|
2012
|
0.78
|
|
20
|
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy.
|
Cell Mol Neurobiol
|
2011
|
0.78
|
|
21
|
Cystatin C and apoe polymorphisms in Italian Alzheimer's disease.
|
Neurosci Lett
|
2005
|
0.78
|
|
22
|
Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians.
|
J Alzheimers Dis
|
2011
|
0.78
|
|
23
|
Semantic dementia associated with mutation V363I in the tau gene.
|
J Neurol Sci
|
2010
|
0.78
|
|
24
|
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.
|
Arch Gerontol Geriatr
|
2006
|
0.77
|
|
25
|
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia.
|
Ann Neurol
|
2004
|
0.77
|
|
26
|
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.
|
Arch Neurol
|
2002
|
0.77
|
|
27
|
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease.
|
J Neurol
|
2002
|
0.77
|
|
28
|
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease.
|
Neurogenetics
|
2004
|
0.77
|
|
29
|
Fibroblasts from PS1 mutated pre-symptomatic subjects and Alzheimer's disease patients share a unique protein levels profile.
|
J Alzheimers Dis
|
2010
|
0.76
|
|
30
|
Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects.
|
Neurodegener Dis
|
2013
|
0.76
|
|
31
|
A case of atypical early-onset Alzheimer's disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene.
|
Neurol Sci
|
2012
|
0.75
|