| Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain A Bertolino, G Blasi, V Latorre, V Rubino, A Rampino, L Sinibaldi, ... Journal of Neuroscience 26 (15), 3918-3922, 2006 | 293 | 2006 |
| Pachydermoperiostosis: an update M Castori, L Sinibaldi, R Mingarelli, RS Lachman, DL Rimoin, ... Clinical genetics 68 (6), 477-486, 2005 | 285 | 2005 |
| Stress-related methylation of the catechol-O-methyltransferase Val158 allele predicts human prefrontal cognition and activity G Ursini, V Bollati, L Fazio, A Porcelli, L Iacovelli, A Catalani, L Sinibaldi, ... Journal of Neuroscience 31 (18), 6692-6698, 2011 | 228 | 2011 |
| Brain Derived Neurotrophic Factor (BDNF) Expression Is Regulated by MicroRNAs miR-26a and miR-26b Allele-Specific Binding V Caputo, L Sinibaldi, A Fiorentino, C Parisi, C Catalanotto, A Pasini, ... PloS one 6 (12), e28656, 2011 | 148 | 2011 |
| Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans G Blasi, LL Bianco, P Taurisano, B Gelao, R Romano, L Fazio, ... Journal of Neuroscience 29 (47), 14812-14819, 2009 | 144 | 2009 |
| Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance A Bertolino, P Taurisano, NM Pisciotta, G Blasi, L Fazio, R Romano, ... PloS one 5 (2), e9348, 2010 | 117 | 2010 |
| Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans A Bertolino, L Fazio, A Di Giorgio, G Blasi, R Romano, P Taurisano, ... Journal of Neuroscience 29 (4), 1224-1234, 2009 | 116 | 2009 |
| DRD2/AKT1 interaction on D2 c-AMP independent signaling, attentional processing, and response to olanzapine treatment in schizophrenia G Blasi, F Napolitano, G Ursini, P Taurisano, R Romano, G Caforio, ... Proceedings of the National Academy of Sciences 108 (3), 1158-1163, 2011 | 105 | 2011 |
| Psychopathological manifestations of joint hypermobility and joint hypermobility syndrome/Ehlers–Danlos syndrome, hypermobility type: The link between connective tissue and … L Sinibaldi, G Ursini, M Castori American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2015 | 97 | 2015 |
| Deletions of NF1 gene and exons detected by multiplex ligation-dependent probe amplification A De Luca, I Bottillo, MC Dasdia, A Morella, V Lanari, L Bernardini, ... Journal of medical genetics 44 (12), 800-808, 2007 | 91 | 2007 |
| BDNF rs6265 methylation and genotype interact on risk for schizophrenia G Ursini, T Cavalleri, L Fazio, T Angrisano, L Iacovelli, A Porcelli, ... Epigenetics 11 (1), 11-23, 2016 | 62 | 2016 |
| COMT Val158Met polymorphism predicts negative symptoms response to treatment with olanzapine in schizophrenia A Bertolino, G Caforio, G Blasi, A Rampino, M Nardini, DR Weinberger, ... Schizophrenia research 95 (1-3), 253-255, 2007 | 61 | 2007 |
| Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function M Zilmer, AC Edmondson, SA Khetarpal, V Alesi, MS Zaki, K Rostasy, ... Brain 143 (4), 1114-1126, 2020 | 59 | 2020 |
| Neurocognitive effects of methylphenidate on ADHD children with different DAT genotypes: a longitudinal open label trial A Pasini, L Sinibaldi, C Paloscia, S Douzgou, MB Pitzianti, E Romeo, ... european journal of paediatric neurology 17 (4), 407-414, 2013 | 33 | 2013 |
| HDR (Hypoparathyroidism, Deafness, Renal dysplasia) syndrome associated to GATA3 gene duplication L Bernardini, L Sinibaldi, A Capalbo, I Bottillo, B Mancuso, B Torres, ... Clinical genetics 76 (1), 117-119, 2009 | 27 | 2009 |
| Interaction between catechol-O-methyltransferase (COMT) Val158Met genotype and genetic vulnerability to schizophrenia during explicit processing of aversive facial stimuli LL Bianco, G Blasi, P Taurisano, A Di Giorgio, F Ferrante, G Ursini, ... Psychological medicine 43 (2), 279-292, 2013 | 26 | 2013 |
| A home assistance model for dementia: outcome in patients with mild-to-moderate Alzheimer's disease after three months G Carbone, F Barreca, G Mancini, G Pauletti, V Salvi, N Vanacore, ... Annali dell'Istituto superiore di sanità 49, 34-41, 2013 | 22 | 2013 |
| Catechol-O-methyltransferase Val158Met association with parahippocampal physiology during memory encoding in schizophrenia A Di Giorgio, G Caforio, G Blasi, P Taurisano, L Fazio, R Romano, ... Psychological medicine 41 (8), 1721-1731, 2011 | 20 | 2011 |
| DHPLC Screening of ATM Gene in Italian Patients Affected by Ataxia‐Telangiectasia: Fourteen Novel ATM Mutations M Magliozzi, M Piane, I Torrente, L Sinibaldi, G Rizzo, C Savio, P Lulli, ... Disease markers 22 (4), 257-264, 2006 | 20 | 2006 |
| Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromas A De Luca, L Bernardini, C Ceccarini, L Sinibaldi, A Novelli, S Giustini, ... Cancer genetics and cytogenetics 150 (2), 168-172, 2004 | 18 | 2004 |
