The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

(2012) Eliana Marisa Ramos et al.   HUMAN GENETICS

Association of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism with Parkinson’s disease in a Greek population

(2011) Charalambos Karakasis et al.   JOURNAL OF CLINICAL NEUROSCIENCE

Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease

(2011) Hong Van B Che et al.   Molecular Neurodegeneration

CAG repeat size in the normal HTT allele and age of onset in Huntington's disease

(2011) Nasir Ahmad Aziz et al.   MOVEMENT DISORDERS

Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7

(2010) Silke Metzger et al.   HUMAN GENETICS

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

(2010) M. Orth et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease

(2010) Jiří Klempíř et al.   MOVEMENT DISORDERS

A retrospective study of the impact of lifestyle on age at onset of Huntington disease

(2010) M. Kaye Trembath et al.   MOVEMENT DISORDERS

BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson’s disease

(2009) F. R. Guerini et al.   EUROPEAN JOURNAL OF NEUROLOGY

The gene coding for PGC-1α modifies age at onset in Huntington's Disease

(2009) Patrick Weydt et al.   Molecular Neurodegeneration

PGC-1alpha as modifier of onset age in Huntington disease

(2009) Elahe Taherzadeh-Fard et al.   Molecular Neurodegeneration

Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds

(2008) Javier Gayán et al.   GENETIC EPIDEMIOLOGY

Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

(2008) S. Metzger et al.   HUMAN MOLECULAR GENETICS