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Aldo Quattrone
Researcher at National Research Council
Publications - 659
Citations - 25954
Aldo Quattrone is an academic researcher from National Research Council. The author has contributed to research in topics: Parkinson's disease & Epilepsy. The author has an hindex of 66, co-authored 626 publications receiving 22661 citations. Previous affiliations of Aldo Quattrone include University of Queensland & Magna Græcia University.
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Journal ArticleDOI
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky,Mike A. Nalls,Jan O. Aasly,Judith Aharon-Peretz,Grazia Annesi,Egberto Reis Barbosa,Anat Bar-Shira,Daniela Berg,Jose Bras,Jose Bras,Alexis Brice,Alexis Brice,Chiung-Mei Chen,Lorraine N. Clark,Christel Condroyer,Elvira Valeria De Marco,Alexandra Durr,Alexandra Durr,Michael J. Eblan,Stanley Fahn,Matthew J. Farrer,Hon-Chung Fung,Ziv Gan-Or,Thomas Gasser,Ruth Gershoni-Baruch,Ruth Gershoni-Baruch,Nir Giladi,Nir Giladi,Alida Griffith,Tanya Gurevich,Tanya Gurevich,Cristina Januário,Peter Kropp,Anthony E. Lang,Guey Jen Lee-Chen,Suzanne Lesage,Karen Marder,Ignacio F. Mata,Anat Mirelman,Jun Mitsui,Ikuko Mizuta,Giuseppe Nicoletti,Giuseppe Nicoletti,Catarina R. Oliveira,Ruth Ottman,Avi Orr-Urtreger,Lygia da Veiga Pereira,Aldo Quattrone,Aldo Quattrone,Ekaterina Rogaeva,Arndt Rolfs,Hanna Rosenbaum,Roberto Rozenberg,Ali Samii,Ali Samii,Ali Samii,Ted Samaddar,Claudia Schulte,Manu Sharma,Manu Sharma,Andrew B. Singleton,Andrew B. Singleton,Mariana Spitz,Mariana Spitz,Eng-King Tan,Eng-King Tan,Nahid Tayebi,Tatsushi Toda,André R. Troiano,Shoji Tsuji,Matthias Wittstock,Tyra G. Wolfsberg,Yih-Ru Wu,Cyrus P. Zabetian,Yi Zhao,Shira G. Ziegler +75 more
TL;DR: Data collected demonstrate that there is a strong association between GBA mutations and Parkinson's disease, and those with a GBA mutation presented earlier with the disease, were more likely to have affected relatives, and were morelikely to have atypical clinical manifestations.
Journal ArticleDOI
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner,Stephan Züchner,Irina V. Mersiyanova,Maria Muglia,Nisrine Bissar-Tadmouri,Nisrine Bissar-Tadmouri,Julie M. Rochelle,Elena L. Dadali,Mario Zappia,Eva Nelis,Alessandra Patitucci,Jan Senderek,Yesim Parman,Oleg V. Evgrafov,Peter De Jonghe,Yuji Takahashi,Shoij Tsuji,Margaret A. Pericak-Vance,Aldo Quattrone,Esra Battologlu,Alexander V. Polyakov,Vincent Timmerman,J. Michael Schröder,Jeffery M. Vance +23 more
TL;DR: It is concluded that the primary gene mutated in CMT2A is MFN2, and seven large pedigrees affected with Charcot-Marie-Tooth neuropathy type 2A are concluded.
Journal ArticleDOI
The challenge of mapping the human connectome based on diffusion tractography
Klaus H. Maier-Hein,Peter F. Neher,Jean-Christophe Houde,Marc-Alexandre Côté,Eleftherios Garyfallidis,Jidan Zhong,Maxime Chamberland,Fang-Cheng Yeh,Ying-Chia Lin,Qing Ji,Wilburn E. Reddick,John O. Glass,David Qixiang Chen,Yuanjing Feng,Chengfeng Gao,Ye Wu,Jieyan Ma,H Renjie,Qiang Li,Carl-Fredrik Westin,Samuel Deslauriers-Gauthier,J. Omar Ocegueda Gonzalez,Michael Paquette,Samuel St-Jean,Gabriel Girard,François Rheault,Jasmeen Sidhu,Chantal M. W. Tax,Fenghua Guo,Hamed Y. Mesri,Szabolcs David,Martijn Froeling,Anneriet M. Heemskerk,Alexander Leemans,Arnaud Boré,Basile Pinsard,Christophe Bedetti,Matthieu Desrosiers,Simona M. Brambati,Julien Doyon,Alessia Sarica,Roberta Vasta,Antonio Cerasa,Aldo Quattrone,Jason D. Yeatman,Ali R. Khan,Wes Hodges,Simon Alexander,David Romascano,Muhamed Barakovic,Anna Auría,Oscar Esteban,Alia Lemkaddem,Jean-Philippe Thiran,Hasan Ertan Cetingul,Benjamin L. Odry,Boris Mailhe,Mariappan S. Nadar,Fabrizio Pizzagalli,Gautam Prasad,Julio E. Villalon-Reina,Justin Galvis,Paul M. Thompson,Francisco De Santiago Requejo,Pedro Luque Laguna,Luis Miguel Lacerda,Rachel Barrett,Flavio Dell'Acqua,Marco Catani,Laurent Petit,Emmanuel Caruyer,Alessandro Daducci,Tim B. Dyrby,Tim Holland-Letz,Claus C. Hilgetag,Bram Stieltjes,Maxime Descoteaux +76 more
TL;DR: The encouraging finding that most state-of-the-art algorithms produce tractograms containing 90% of the ground truth bundles (to at least some extent) is reported, however, the same tractograms contain many more invalid than valid bundles, and half of these invalid bundles occur systematically across research groups.
Journal ArticleDOI
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
Demetrius M. Maraganore,Mariza de Andrade,Alexis Elbaz,Matthew J. Farrer,John P. A. Ioannidis,Rejko Krüger,Walter A. Rocca,Nicole K. Schneider,Timothy G. Lesnick,Sarah Lincoln,Mary M. Hulihan,Jan O. Aasly,Tetsuo Ashizawa,Marie-Christine Chartier-Harlin,Harvey Checkoway,Carlo Ferrarese,Georgios M. Hadjigeorgiou,Nobutaka Hattori,Hideshi Kawakami,Jean-Charles Lambert,Timothy Lynch,George D. Mellick,Spiridon Papapetropoulos,Abbas Parsian,Aldo Quattrone,Olaf Riess,Eng-King Tan,Christine Van Broeckhoven +27 more
TL;DR: This large-scale collaborative analysis demonstrates that SNCA REP1 allele-length variability is associated with an increased risk of Parkinson disease.
Journal ArticleDOI
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
Alessandra Bolino,Maria Muglia,Francesca Luisa Conforti,Eric LeGuern,Mustafa A. Salih,Domna Maria Georgiou,Kyproula Christodoulou,Irena Hausmanowa-Petrusewicz,Paola Mandich,Angelo Schenone,Antonio Gambardella,F. Bono,Aldo Quattrone,Marcella Devoto,Anthony P. Monaco +14 more
TL;DR: Using a positional-cloning strategy, mutations occurring in the gene MTMR2, encoding myotubularin-related protein-2, a dual specificity phosphatase (DSP) are identified in unrelated CMT4B patients.