The LRRK2 G2019S mutation as the cause of Parkinson’s disease in Ashkenazi Jews-Reference-Cited by-同舟云学术

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The LRRK2 G2019S mutation as the cause of Parkinson’s disease in Ashkenazi Jews

Published:2009-09-15 Issue:11 Volume:116 Page:1473-1482
ISSN:0300-9564
Container-title:Journal of Neural Transmission
language:en
Short-container-title:J Neural Transm

Author:

Thaler Avner,Ash Elissa,Gan-Or Ziv,Orr-Urtreger Avi,Giladi Nir

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Psychiatry and Mental health,Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00702-009-0303-0.pdf

Reference107 articles.

1. Aasly JO, Toft M, Fernandez-Mata I et al (2005) Clinical features of LRRK2 associated Parkinson’s disease in central Norway. Ann Neurol 57:762–765

2. Adams RJ, Van Netten H, Schulzer M, Mak E et al (2005) PET in LRRK2 mutations: comparison to sporadic Parkinson’s disease and evidence for presymptomatic compensation. Brain 128:2777–2785

3. Bar-Shira A, Hutter C, Giladi N et al (2009) Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the 2nd to 5th centuries. Neurogenetics (ahead of print)

4. Behar DM, Garrigan D, Kaplan ME, Mobasher Z et al (2004) Contrasting patterns of Y-chromosome variation in Ashkenazi Jewish and host non-Jewish European populations. Hum Genet 114:354–365

5. Bialecka M, Hui S, Klodowska-Duda G, Opala G et al (2005) Analysis of LRRK2 G2019S mutation in Parkinson’s disease. Neurosci Lett 390(1):1–3

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1. Parkinson’s Disease;International Encyclopedia of Public Health;2025

2. LRRK2G2019S variant is associated with transcriptional changes in Parkinson’s disease human myeloid cells under proinflammatory environment;2024-06-01

3. Unraveling the Genetic Landscape of Neurological Disorders: Insights into Pathogenesis, Techniques for Variant Identification, and Therapeutic Approaches;International Journal of Molecular Sciences;2024-02-15

4. Advancements in Genetic and Biochemical Insights: Unraveling the Etiopathogenesis of Neurodegeneration in Parkinson’s Disease;Biomolecules;2024-01-05

5. Differences in EEG Event-Related Potentials during Dual Task in Parkinson’s Disease Carriers and Non-Carriers of the G2019S-LRRK2 Mutation;Sensors;2023-10-06

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