(Q37608624)

21 August 2017

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title

LRRK2 in Parkinson's disease: genetic and clinical studies from patients (English)

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21 August 2017

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Udhaya Kumari

1

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21 August 2017

E K Tan

series ordinal

2

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21 August 2017

language of work or name

English

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publication date

5 October 2009

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21 August 2017

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21 August 2017

volume

276

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21 August 2017

issue

22

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21 August 2017

page(s)

6455-6463

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Leucine-rich repeat kinase 2 (LRRK2): a key player in the pathogenesis of Parkinson's disease

21 August 2017

cites work

1 reference

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LRRK2 and neurodegeneration

21 January 2018

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A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

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Pathogenic mutations in Parkinson disease

21 January 2018

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LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

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LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity

21 January 2018

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Kinase activity is required for the toxic effects of mutant LRRK2/dardarin

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

21 January 2018

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LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

21 January 2018

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LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

21 January 2018

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LRRK2 G2019S founder haplotype in the Chinese population

21 January 2018

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A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

21 January 2018

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LRRK2 R1441G in Spanish patients with Parkinson's disease.

21 January 2018

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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

21 January 2018

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LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity.

21 January 2018

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21 January 2018

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Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

21 January 2018

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Variability and validity of polymorphism association studies in Parkinson's disease

21 January 2018

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Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

21 January 2018

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Common variants of LRRK2 are not associated with sporadic Parkinson's disease

21 January 2018

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LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

21 January 2018

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The role of common genetic risk variants in Parkinson disease

21 January 2018

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Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant

21 January 2018

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Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

21 January 2018

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The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

21 January 2018

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LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis

21 January 2018

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Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

21 January 2018

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Lrrk2 R1628P in non-Chinese Asian races

21 January 2018

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The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population

21 January 2018

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Progression of dopaminergic dysfunction in a LRRK2 kindred: a multitracer PET study

21 January 2018

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PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation

21 January 2018

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Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease

21 January 2018

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Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.

21 January 2018

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Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease

21 January 2018

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Genetic testing in Parkinson disease: promises and pitfalls

21 January 2018

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Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population.

21 January 2018

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

21 January 2018

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Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2009.07344.X

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1742-4658.2009.07344.X

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2009.07344.X

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2009.07344.X

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2009.07344.X

10.1111/J.1742-4658.2009.07344.X

21 January 2018

Identifiers

DOI

1 reference

21 August 2017

1 reference