Patterns of Linkage Disequilibrium of LRRK2 across Different Races: Implications for Genetic Association Studies

Rare and common LRRK2 exonic variants in Parkinson's disease

(2011) Eng-King Tan   LANCET NEUROLOGY

Identifying candidate causal variants via trans-population fine-mapping

(2010) Yik-Ying Teo et al.   GENETIC EPIDEMIOLOGY

Absence of Commonly Reported Leucine-Rich Repeat Kinase 2 Mutations in Eastern Indian Parkinson's Disease Patients

(2010) Jaya Sanyal et al.   Genetic Testing and Molecular Biomarkers

Genome-wide comparisons of variation in linkage disequilibrium

(2009) Y. Y. Teo et al.   GENOME RESEARCH

LRRK2gene variation and its contribution to Parkinson disease

(2009) Coro Paisán-Ruiz   HUMAN MUTATION

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

(2009) Wataru Satake et al.   NATURE GENETICS

Genome-wide association study reveals genetic risk underlying Parkinson's disease

(2009) Javier Simón-Sánchez et al.   NATURE GENETICS

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

(2008) Owen A. Ross et al.   ANNALS OF NEUROLOGY

Power consequences of linkage disequilibrium variation between populations

(2008) Yik Y. Teo et al.   GENETIC EPIDEMIOLOGY

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

(2008) Daniel G Healy et al.   LANCET NEUROLOGY