A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

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

Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan et al. · The Lancet Neurology · 2008 · 1.6K citations · Full text

Life Sciences, Genetics, Neurology +17

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan et al. · The American Journal of Human Genetics · 2005 · 537 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

Mary Hulihan, L. Ishihara-Paul, Jennifer M. Kachergus et al. · The Lancet Neurology · 2008 · 192 citations

Life Sciences, Genetics, Molecular Genetics +9

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

Cyrus P. Zabetian, Carolyn M. Hutter, Dora Yearout et al. · The American Journal of Human Genetics · 2006 · 124 citations · Full text

Life Sciences, Genetics, Neurology +11

Clinicogenetic study of mutations in <i>LRRK2</i> exon 41 in Parkinson's disease patients from 18 countries

Hiroyuki Tomiyama, Yuanzhe Li, Manabu Funayama et al. · Movement Disorders · 2006 · 111 citations · Full text

Life Sciences, Genetics, Neurology +17