Related references
Note: Only part of the references are listed.Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
Owen A. Ross et al.
ANNALS OF NEUROLOGY (2008)
LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
X. -K. An et al.
EUROPEAN JOURNAL OF NEUROLOGY (2008)
The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
Cao Li et al.
MOVEMENT DISORDERS (2007)
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
W. C. Nichols et al.
NEUROLOGY (2007)
The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease -: Is there a gender effect?
A. Orr-Urtreger et al.
NEUROLOGY (2007)
LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-Linking familial and sporadic Parkinson's disease
Vincenzo Bonifati
NEUROCHEMICAL RESEARCH (2007)
Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians
Eng-King Tan et al.
MOVEMENT DISORDERS (2007)
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease
Cyrus P. Zabetian et al.
ANNALS OF NEUROLOGY (2007)
Tau and α-synuclein in susceptibility to, and dementia in, Parkinson's disease
An Goris et al.
ANNALS OF NEUROLOGY (2007)
Pathogenic mutations in Parkinson disease
Eng-King Tan et al.
HUMAN MUTATION (2007)
Leucine-Rich Repeat kinase 2 G238SR variant is a risk factor for Parkinson disease in Asian population
Manabu Funayama et al.
NEUROREPORT (2007)
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
Matthew J. Farrer et al.
PARKINSONISM & RELATED DISORDERS (2007)
Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation
Janel Johnson et al.
NEURODEGENERATIVE DISEASES (2007)
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence
E. K. Tan et al.
HUMAN GENETICS (2007)
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan
Hon-Chung Fung et al.
BMC NEUROLOGY (2006)
Genome-wide genotyping in Parkinson's disease and neurologically normal controls:: first stage analysis and public release of data
Hon-Chung Fung et al.
LANCET NEUROLOGY (2006)
Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease
C. P. Zabetian et al.
NEUROLOGY (2006)
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease
Demetrius M. Maraganore et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
Alessio Di Fonzo et al.
NEUROGENETICS (2006)
LRRK2 in Parkinson's disease: protein domains and functional insights
Ignacio F. Mata et al.
TRENDS IN NEUROSCIENCES (2006)
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease
A Di Fonzo et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium -: art. no. e9
C Paisán-Ruíz et al.
JOURNAL OF MEDICAL GENETICS (2006)
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
S Lesage et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
LJ Ozelius et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Common variants of LRRK2 are not associated with sporadic Parkinson's disease
S Biskup et al.
ANNALS OF NEUROLOGY (2005)
Lrrk2 pathogenic substitutions in Parkinson's disease
IF Mata et al.
NEUROGENETICS (2005)
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease:: clinical, pathological, olfactory and functional imaging and genetic data
NL Khan et al.
BRAIN (2005)
High-resolution whole-genome association study of Parkinson disease
DM Maraganore et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Analysis of LRRK2 functional domains in nondominant Parkinson disease
L Skipper et al.
NEUROLOGY (2005)
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation
M Stephens et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A new statistical method for haplotype reconstruction from population data
M Stephens et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)