Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

(2009) S Lesage et al.   JOURNAL OF MEDICAL GENETICS

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

(2009) Anat Bar-Shira et al.   NEUROGENETICS

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

(2009) C. Pirkevi et al.   NEUROGENETICS

The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

(2008) Susan M. Adams et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2008) Mary M Hulihan et al.   LANCET NEUROLOGY

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

(2008) Daniel G Healy et al.   LANCET NEUROLOGY

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

(2008) S. Lesage et al.   NEUROLOGY

A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations

(2008) Ebba Lohmann et al.   PARKINSONISM & RELATED DISORDERS

Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora

(2008) Doron M. Behar et al.   PLoS One

Genetic Mapping in Human Disease

(2008) D. Altshuler et al.   SCIENCE

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

(2007) L. Warren et al.   PARKINSONISM & RELATED DISORDERS