Paul Worth

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

Henry Houlden, Janel Johnson, Christopher Gardner‐Thorpe et al. · Nature Genetics · 2007 · 210 citations

Molecular Neuroscience, Signal Transduction, Tau Phosphorylation +9

Trial of Deferiprone in Parkinson’s Disease

David Devos, Julien Labreuche, Olivier Rascol et al. · New England Journal of Medicine · 2022 · 199 citations · Full text

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model

Andrea H. Németh, Alexandra Kwasniewska, Stefano Lise et al. · Brain · 2013 · 171 citations · Full text

Autosomal Dominant Cerebellar Ataxia Type III: Linkage in a Large British Family to a 7.6-cM Region on Chromosome 15q14-21.3

Paul Worth, Paola Giunti, Christopher Gardner‐Thorpe et al. · The American Journal of Human Genetics · 1999 · 137 citations · Full text

Large British Family, 7.6-Cm Region, Mendelian Disorder +7

Molecular and Clinical Study of 18 Families with ADCA Type II: Evidence for Genetic Heterogeneity and De Novo Mutation

Paola Giunti, Giovanni Stévanin, Paul Worth et al. · The American Journal of Human Genetics · 1999 · 105 citations · Full text

Adca Type Ii, De Novo Mutation, Mendelian Disorder +7