(Q34386801)

1 August 2017

Genetics of Parkinson's disease--state of the art, 2013. (English)

1 reference

1 August 2017

1 reference

1

Vincenzo Bonifati

1 reference

1 August 2017

1 January 2014

1 reference

Parkinsonism and Related Disorders

1 August 2017

1 reference

1 August 2017

20 Suppl 1

1 reference

1 August 2017

S23-8

1 reference

100 years of Lewy pathology.

1 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

The genetics of Parkinson's disease: progress and therapeutic implications

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Sequencing technologies - the next generation

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Disease gene identification strategies for exome sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

VPS35 mutations in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

A novel α-synuclein missense mutation in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Parkinson's disease and alpha synuclein: is Parkinson's disease a prion-like disorder?

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

LRRK2 is involved in the IFN-gamma response and host response to pathogens

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Translation initiator EIF4G1 mutations in familial Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

PINK1-linked parkinsonism is associated with Lewy body pathology.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

PINK1 is selectively stabilized on impaired mitochondria to activate Parkin

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

FBXO7 immunoreactivity in α-synuclein-containing inclusions in Parkinson disease and multiple system atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2813%2970009-9

7 January 2021

10.1016/S1353-8020(13)70009-9

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

24262182