Aldo Quattrone

Overview

Best Publications

• Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

  Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz

  2380
  Citations

• 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

  1907
  Citations

• The challenge of mapping the human connectome based on diffusion tractography

  Klaus H. Maier-Hein;Peter F. Neher;Jean-Christophe Houde;Marc-Alexandre Cote

  1315
  Citations

• Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

  Demetrius M. Maraganore;Mariza De Andrade;Alexis Elbaz;Matthew J. Farrer

  620
  Citations

• Random Forest Algorithm for the Classification of Neuroimaging Data in Alzheimer's Disease: A Systematic Review.

  Alessia Sarica;Antonio Cerasa;Aldo Quattrone

  600
  Citations

• 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

  559
  Citations

• The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy

  De Fusco M;Becchetti A;Patrignani A;Annesi G

  558
  Citations

• A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

  Michael A. Nalls;Raquel Duran;Grisel Lopez;Marzena Kurzawa-Akanbi

  499
  Citations

• MR imaging index for differentiation of progressive supranuclear palsy from Parkinson disease and the Parkinson variant of multiple system atrophy.

  Aldo Quattrone;Giuseppe Nicoletti;Demetrio Messina;Francesco Fera

  439
  Citations

• Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders.

  Bethan Jones;Emma L. Jones;Stephanie A. Bonney;Hetal N. Patel

  438
  Citations

• Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.

  Owen A. Ross;Alexandra I. Soto-Ortolaza;Michael G. Heckman;Jan O. Aasly

  365
  Citations

• Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.

  Marialuisa Quadri;Mingyan Fang;Marina Picillo;Simone Olgiati

  346
  Citations

• UCHL1 is a Parkinson's disease susceptibility gene

  Demetrius M. Maraganore;Timothy G. Lesnick;Alexis Elbaz;Marie Christine Chartier-Harlin

  328
  Citations

• Machine learning on brain MRI data for differential diagnosis of Parkinson's disease and Progressive Supranuclear Palsy

  C. Salvatore;A. Cerasa;I. Castiglioni;F. Gallivanone

  317
  Citations

• Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial

  Davide Pareyson;Mary M Reilly;Angelo Schenone;Gian Maria Fabrizi

  295
  Citations

• Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study.

  Mario Zappia;Grazia Annesi;Giuseppe Nicoletti;Gennarina Arabia

  271
  Citations

• Magnetic resonance imaging biomarkers for the early diagnosis of Alzheimer's disease: a machine learning approach.

  Christian Salvatore;Antonio Cerasa;Petronilla Battista;Maria Carla Gilardi

  271
  Citations

• Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy

  Giuseppe Nicoletti;Raffaele Lodi;Francesca Condino;Caterina Tonon

  259
  Citations

• Quetiapine and clozapine in parkinsonian patients with dopaminergic psychosis

  Letterio Morgante;Antonio Epifanio;Edoardo Spina;Mario Zappia

  258
  Citations

• Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

  Massimo Mantegazza;Antonio Gambardella;Raffaella Rusconi;Emanuele Schiavon

  246
  Citations