Franco Taroni

Overview

Best Publications

• Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

  Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Alan E. Renton;Nicola Ticozzi

  700
  Citations

• Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis

  Chi Hong Wu;Claudia Fallini;Nicola Ticozzi;Pamela J. Keagle

  686
  Citations

• Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.

  B N Smith;N Ticozzi;C Fallini;A S Gkazi

  427
  Citations

• The Friedreich's Ataxia Mutation Confers Cellular Sensitivity to Oxidant Stress Which Is Rescued by Chelators of Iron and Calcium and Inhibitors of Apoptosis

  Alice Wong;Joy Yang;Patrizia Cavadini;Cinzia Gellera

  426
  Citations

• Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28

  Daniela Di Bella;Federico Lazzaro;Alfredo Brusco;Massimo Plumari

  365
  Citations

• NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

  Kevin P Kenna;Perry T C van Doormaal;Annelot M Dekker;Nicola Ticozzi

  320
  Citations

• The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.

  Bradley N. Smith;Stephen Newhouse;Aleksey Shatunov;Caroline Vance

  270
  Citations

• High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

  Lucia Corrado;A. Ratti;C. Gellera;E. Buratti

  247
  Citations

• Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients.

  Franco Taroni;Elisabetta Verderio;Federica Dworzak;Patrick J. Willems

  228
  Citations

• Alpha-lipoic acid prevents mitochondrial damage and neurotoxicity in experimental chemotherapy neuropathy

  Giorgia Melli;Michela Taiana;Francesca Camozzi;Daniela Triolo

  212
  Citations

• Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

  Alfredo Brusco;Cinzia Gellera;Claudia Cagnoli;Alessandro Saluto

  193
  Citations

• cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase.

  Gaetano Finocchiaro;Franco Taroni;Mariano Rocchi;Antonio Liras Martin

  185
  Citations

• Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48

  Viviana Pensato;Barbara Castellotti;Cinzia Gellera;Davide Pareyson

  180
  Citations

• Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

  N. Ticozzi;V. Silani;A. L. LeClerc;P. Keagle

  176
  Citations

• Molecular characterization of inherited carnitine palmitoyltransferase II deficiency.

  Franco Taroni;Elisabetta Verderio;Stefania Fiorucci;Patrizia Cavadini

  170
  Citations

• Deferiprone in Friedreich Ataxia: A 6-Month Randomized Controlled Trial

  Massimo Pandolfo;Javier Arpa;Martin B. Delatycki;Kim Hanh Le Quan Sang

  157
  Citations

• SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2

  Claudia Cagnoli;Caterina Mariotti;Franco Taroni;Marco Seri

  156
  Citations

• A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference

  Maria Stella Lombardi;Leonie Jaspers;Christine Spronkmans;Cinzia Gellera

  154
  Citations

• Spinocerebellar ataxia type 1

  Stefano Di Donato;Caterina Mariotti;Franco Taroni

  31
  Citations

• Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

  Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Nicola Ticozzi

  8
  Citations