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List of works by D.G. Healy

A common LRRK2 mutation in idiopathic Parkinson's disease

scientific article published on 29 January 2005

A film of patients with movement disorders made in Queen Square, London in the Mid‐1920s by Samuel Alexander Kinnier Wilson ⬇️

scientific article published on March 2, 2011

A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease

scientific article published in March 2004

A heterozygous effect for PINK1 mutations in Parkinson's disease?

article

Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

scientific article published on July 2006

An evaluation of the role of environmental factors in the disease penetrance of cervical dystonia

scientific article published on 24 June 2014

Apolipoprotein e genotype modifies the phenotype of Alzheimer disease

scientific article published in January 2006

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

scientific article published in June 2004

Causes of Parkinson's disease: genetics of DJ-1

scientific article

Cervical dystonia: a disorder of the midbrain network for covert attentional orienting

scientific article

Characterisation of a novel NR4A2 mutation in Parkinson's disease brain

scientific article

Clinical picture of bilateral vestibular schwannomas, sudden bilateral hearing loss, and aviation

scientific article published in September 2004

Commentary on "A genome wide linkage disequilibrium screen in Parkinson's disease" by Foltynie et al. in J Neurol (2005) 252:597-602

scientific article published on 07 March 2005

Correction: Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue.

scientific article published on 27 January 2012

Creation of an open-access, mutation-defined fibroblast resource for neurological disease research

scientific article

DJ-1 mutations in Parkinson's disease

scientific article published on January 2004

Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndrome

scientific article published in June 2009

G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization

scientific article

Genetic approaches to solving common diseases.

scientific article published in October 2004

Genetic causes of Parkinson's disease: UCHL-1.

scientific article

Glucosylceramidase degradation in fibroblasts carrying bi-allelic Parkin mutations

scientific article published on 10 June 2013

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

scientific article

Molecular genetic pathways in Parkinson's disease: a review

scientific article

Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

scientific article published on 05 June 2007

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

scientific article

NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach

scientific article published on 01 November 2006

Non-motor symptoms of Parkinson's disease: diagnosis and management

scientific article

PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism

scientific article published in November 2004

PINK1 protein in normal human brain and Parkinson's disease

scientific article

Parkin disease: a clinicopathologic entity?

scientific article

Pathogenic LRRK2 mutations do not alter gene expression in cell model systems or human brain tissue

scientific article

Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation

scientific journal article

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

scientific article (publication date: July 2008)

Population genetic approaches to neurological disease: Parkinson's disease as an example

scientific article

Population genetics for target identification

scientific article published on September 2004

Tau gene and Parkinson's disease: a case-control study and meta-analysis

scientific article

Temporal discrimination, a cervical dystonia endophenotype: penetrance and functional correlates

scientific article published on 30 January 2014

Test for LRRK2 mutations in patients with Parkinson's disease.

scientific article

The "round the houses" sign and "zig-zag" sign in progressive supranuclear palsy and other conditions

scientific article published on 19 October 2020

The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany

scientific article published on 01 November 2006

The alpha-synuclein gene in multiple system atrophy

scientific article

The endophenotype and the phenotype: temporal discrimination and adult-onset dystonia

scientific article

The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease

scientific article

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group

scientific article

The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism

scientific article

The role of pathogenic DJ-1 mutations in Parkinson's disease.

scientific article

The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations

scientific article published on 27 October 2004

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach

scientific article published in October 2005

UCHL-1 is not a Parkinson's disease susceptibility gene

scientific article published in April 2006

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