Pubblicazioni

The role of cerebellum in timing processing: a contingent negative variation study

2023 - NEUROSCIENCE LETTERS

Mannarelli, Daniela; Pauletti, Caterina; Petritis, Alessia; Maffucci, Andrea; CurrÃ , Antonio; Trompetto, Carlo; Marinelli, Lucio; Fattapposta, Francesco

Functional outcomes of copy number variations of Chrna7 gene

2022 - Novel Concepts in iPSC Disease Modeling,

Ferrari, Daniela; D'Anzi, Angela; Casamassa, Alessia; Bernardini, Laura; Tata, Ada Maria; Vescovi, Angelo Luigi; Rosati, Jessica

Overt and covert effects of cognitive fatigue on attention networks

2021 - JOURNAL OF THE NEUROLOGICAL SCIENCES

Pauletti, C; Mannarelli, D; Maffucci, A; Petritis, A; Fattapposta, F

Understanding the early evolutionary stages of a tandem drosophila melanogaster-specific gene family: A structural and functional population study

2020 - MOLECULAR BIOLOGY AND EVOLUTION

Clifton, B. D.; Jimenez, J.; Kimura, A.; Chahine, Z.; Librado, P.; Sanchez-Gracia, A.; Abbassi, M.; Carranza, F.; Chan, C.; Marchetti, M.; Zhang, W.; Shi, M.; Vu, C.; Yeh, S.; Fanti, L.; Xia, X. -Q.; Rozas, J.; Ranz, J. M.

Pre-motor deficits in left spatial neglect: An EEG study on Contingent Negative Variation (CNV) and response-related beta oscillatory activity

2020 - NEUROPSYCHOLOGIA

Lasaponara, S.; Pinto, M.; Scozia, G.; Pellegrino, M.; D'Onofrio, M.; Isabella, R.; Doricchi, F.

Contingent negative variation and P3 modulations following mindful movement training

2019 - Meditation

Lasaponara, Stefano; Glicksohn, Joseph; Mauro, Federica; Ben-Soussan, Tal Dotan

Attentional functioning in individuals with 22q11 deletion syndrome. Insight from ERPs

2018 - JOURNAL OF NEURAL TRANSMISSION

Mannarelli, Daniela; Pauletti, Caterina; Accinni, Tommaso; Carlone, Luca; Frascarelli, Marianna; Lattanzi, Guido Maria; CurrÃ , Antonio; Fattapposta, Francesco

Rapid detection of copy number variations and point mutations in BRCA1/2 genes using a single workflow by ion semiconductor sequencing pipeline

2018 - ONCOTARGET

Germani, A; Libi, F; Maggi, S; Stanzani., G; Lombardi, A; Pellegrini, P; Mattei, M; De Marchis, L; Amanti, C; Pizzuti, A; Torrisi, Mr; Piane, M

Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism

2016 - BMC UROLOGY

Wang, Yanping; Li, Jin; Kolon, Thomas F.; Olivant Fisher, Alicia; Figueroa, T. Ernesto; Banihani, Ahmad H.; Hagerty, Jennifer A.; Gonzalez, Ricardo; Noh, Paul H.; Chiavacci, Rosetta M.; Harden, Kisha R.; Abrams, Debra J.; Stabley, Deborah; Kim, Cecilia E.; Sol Church, Katia; Hakonarson, Hakon; Devoto, Marcella; Barthold, Julia Spencer

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

2015 - HUMAN MUTATION

Addis, Laura; Ahn, Joo Wook; Dobson, Richard; Dixit, Abhishek; Ogilvie, Caroline M.; Pinto, Dalila; Vaags, Andrea K.; Coon, Hilary; Chaste, Pauline; Wilson, Scott; Parr, Jeremy R.; Andrieux, Joris; Lenne, Bruno; Tumer, Zeynep; Leuzzi, Vincenzo; Aubell, Kristina; Koillinen, Hannele; Curran, Sarah; Marshall, Christian R.; Scherer, Stephen W.; Strug, Lisa J.; Collier, David A.; Pal, Deb K.