| Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis AQ Giovanni Savettieri, Demetrio Messina, Virginia Journal of neurology 251 (10), 1208-1214, 2004 | 215 | 2004 |
| GABA (B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy A Gambardella, I Manna, A Labate, R Chifari, A La Russa, P Serra, ... Neurology 60 (4), 560-563, 2003 | 197 | 2003 |
| Genetic aspects of susceptibility to mercury toxicity: an overview V Andreoli, F Sprovieri International journal of environmental research and public health 14 (1), 93, 2017 | 179 | 2017 |
| Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD RL Oliveri, G Annesi, M Zappia, D Civitelli, R Montesanti, D Branca, ... Neurology 53 (7), 1425-1425, 1999 | 155 | 1999 |
| APOE and risk of cognitive impairment in multiple sclerosis RI Oliveri, R Cittadella, G Sibilia, I Manna, P Valentino, A Gambardella, ... Acta neurologica scandinavica 100 (5), 290-295, 1999 | 75 | 1999 |
| Inter-Comparison of Carbon Content in PM2.5 and PM10 Collected at Five Measurement Sites in Southern Italy A Dinoi, D Cesari, A Marinoni, P Bonasoni, A Riccio, E Chianese, ... Atmosphere 8 (12), 243, 2017 | 69 | 2017 |
| Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms M Zappia, I Manna, P Serra, R Cittadella, V Andreoli, A La Russa, ... Archives of Neurology 61 (3), 341-344, 2004 | 66 | 2004 |
| Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer’s disease V Andreoli, EV De Marco, F Trecroci, R Cittadella, G Di Palma, ... Journal of Neural Transmission 121, 533-542, 2014 | 58 | 2014 |
| Apolipoprotein E genotype does not influence the progression of multiple sclerosis AQ Giovanni Savettieri, Virginia Andreoli, Simona Journal of neurology 250 (9), 1094-1098, 2003 | 56 | 2003 |
| Prodynorphin gene promoter polymorphism and temporal lobe epilepsy. A Gambardella, I Manna, A Labate, R Chifari, P Serra, AL Russa, ... Epilepsia (Series 4) 44 (9), 2003 | 44 | 2003 |
| Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study A La Russa, R Cittadella, EV De Marco, P Valentino, V Andreoli, ... Journal of neuroimmunology 225 (1-2), 175-179, 2010 | 40 | 2010 |
| Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy M Zappia, R Cittadella, I Manna, G Nicoletti, V Andreoli, S Bonavita, ... Neurology 59 (5), 756-758, 2002 | 38 | 2002 |
| A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. M Liguori, A La Russa, I Manna, V Andreoli, M Caracciolo, P Spadafora, ... Journal of neurology 255 (1), 2008 | 33 | 2008 |
| Lack of association between estrogen receptor 1 gene polymorphisms and multiple sclerosis in southern Italy in humans G Savettieri, R Cittadella, P Valentino, I Manna, V Andreoli, A La Russa, ... Neuroscience letters 327 (2), 115-118, 2002 | 33 | 2002 |
| CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers M Gomez-Lira, M Liguori, C Magnani, D Bonamini, A Salviati, M Leone, ... Journal of neuroimmunology 140 (1-2), 216-221, 2003 | 32 | 2003 |
| Lack of interaction between LRP1 and A2M polymorphisms for the risk of Alzheimer disease E Bruno, G Quattrocchi, A Nicoletti, F Le Pira, T Maci, G Mostile, ... Neuroscience letters 482 (2), 112-116, 2010 | 27 | 2010 |
| Presenilin enhancer‐2 gene: Identification of a novel promoter mutation in a patient with early‐onset familial Alzheimer's disease V Andreoli, F Trecroci, A La Russa, R Cittadella, M Liguori, P Spadafora, ... Alzheimer's & Dementia 7 (6), 574-578, 2011 | 26 | 2011 |
| Leber’s hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man A La Russa, R Cittadella, V Andreoli, P Valentino, F Trecroci, ... Multiple Sclerosis Journal 17 (6), 763-766, 2011 | 24 | 2011 |
| Severe erythrocyte adenylate kinase deficiency due to homozygous A→ G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia A Qualtieri, V Pedace, MG Bisconte, M Bria, B Gulino, V Andreoli, ... British journal of haematology 99 (4), 770-776, 1997 | 24 | 1997 |
| Association between Synapsin III gene promoter polymorphisms and multiple sclerosis M Liguori, R Cittadella, I Manna, P Valentino, A La Russa, P Serra, ... Journal of neurology 251, 165-170, 2004 | 23 | 2004 |
