Parkinson's disease: from monogenic forms to genetic susceptibility factors (Q22242870)

Idiopathic Parkinson's disease: possible routes by which vulnerable neuronal types may be subject to neuroinvasion by an unknown pathogen

Europe PubMed Central

title

Parkinson's disease: from monogenic forms to genetic susceptibility factors (English)

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1 reference

S. Lesage

1

Suzanne

Lesage

1 reference

28 March 2023

A. Brice

series ordinal

2

author given names

Alexis

author last names

Brice

1 reference

28 March 2023

language of work or name

English

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publication date

15 April 2009

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published in

Human Molecular Genetics

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volume

18

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page(s)

R48-R59

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issue

R1

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cites work

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The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

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Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease

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alpha-synuclein gene haplotypes are associated with Parkinson's disease

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A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Analysis of LRRK2 G2019S and I2020T mutations in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Glucocerebrosidase mutations are not found in association with LRRK2 G2019S in subjects with parkinsonism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Association between Parkinson's disease and glucocerebrosidase mutations in Brazil

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

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/10.1093%2FHMG%2FDDP012

7 January 2021

The glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Neuropathology of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Neurological signs: Behçet's disease, coeliac disease, both, or neither?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Non-motor symptoms in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in Parkinson disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

1 reference

7 January 2021

Re: Alpha-synuclein gene duplication is present in sporadic Parkinson disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021

Rhomboid-7 and HtrA2/Omi act in a common pathway with the Parkinson's disease factors Pink1 and Parkin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP012

7 January 2021