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Article

LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century

8 Jul 2005

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PMID: 16145815
DOI: 10.1086/432422

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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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 CenturyPMID 16145815Read ↗

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

Genetic Analysis and Natural History of Parkinson’s Disease Due to the LRRK2 G2019S VariantSemantic proximity Read ↗

Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant.Semantic proximity Read ↗

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.Semantic proximity Read ↗

Parkinson's Disease: The LRRK2-G2019S mutation: opening a novel era in Parkinson's disease geneticsSemantic proximity Read ↗

The <i>LRRK2</i> p.A419V variant associates with risk of Parkinson’s disease in the East Asian population and an evaluation on age of onsetSemantic proximity Read ↗

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.Semantic proximity Read ↗

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.Semantic proximity Read ↗

Analysis of LRRK2 G2019S carriers in the All of Us research program databaseSemantic proximity Read ↗

An overview of the worldwide distribution of LRRK2 mutations in Parkinson's disease.Semantic proximity Read ↗

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease.Semantic proximity Read ↗

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.Semantic proximity Read ↗

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