Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

1997 • 7,814 citations

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1998 • 5,063 citations

Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

2004 • 3,278 citations

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

2004 • 2,880 citations

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

2003 • 2,691 citations

Association between Early-Onset Parkinson's Disease and Mutations in theParkinGene

2000 • 1,398 citations

Improved accuracy of clinical diagnosis of Lewy body Parkinson’s disease

2001 • 795 citations

PINK1 mutations are associated with sporadic early‐onset parkinsonism

2004 • 480 citations

Localization of a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, PARK6, on Human Chromosome 1p35-p36

2001 • 473 citations

Early-onset parkinsonism associated with PINK1 mutations

2005 • 335 citations

Novel PINK1 mutations in early-onset parkinsonism

2005 • 226 citations

Clinical and subclinical dopaminergic dysfunction in PARK6‐linked parkinsonism: An ¹⁸F‐dopa PET study

2002 • 201 citations

Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson Disease

2004 • 193 citations

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism

2005 • 136 citations

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism

2005 • 129 citations

Homozygous PINK1 C‐terminus mutation causing early‐onset parkinsonism

2004 • 129 citations

PINK1 (PARK6) associated Parkinson disease in Ireland

2004 • 103 citations

Phenotypic characterisation of autosomal recessive PARK6‐linked parkinsonism in three unrelated Italian families

2001 • 69 citations

Genetic testing in Parkinson's disease

2004 • 64 citations

Dopaminergic function in a family with the PARK6 form of autosomal recessive Parkinson’s syndrome

2005 • 42 citations