4.6 Article

LRRK2 Mutations and Risk Variants in Japanese Patients with Parkinson's Disease

Related references

Note: Only part of the references are listed.
Article Clinical Neurology

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

Owen A. Ross et al.

ANNALS OF NEUROLOGY (2008)

Article Clinical Neurology

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)

Article Clinical Neurology

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians

Eng-King Tan et al.

MOVEMENT DISORDERS (2007)

Article Clinical Neurology

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

Cyrus P. Zabetian et al.

ANNALS OF NEUROLOGY (2007)

Article Clinical Neurology

Tau and α-synuclein in susceptibility to, and dementia in, Parkinson's disease

An Goris et al.

ANNALS OF NEUROLOGY (2007)

Review Genetics & Heredity

Pathogenic mutations in Parkinson disease

Eng-King Tan et al.

HUMAN MUTATION (2007)

Article Clinical Neurology

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

Matthew J. Farrer et al.

PARKINSONISM & RELATED DISORDERS (2007)

Article Clinical Neurology

Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation

Janel Johnson et al.

NEURODEGENERATIVE DISEASES (2007)

Article Clinical Neurology

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

Hon-Chung Fung et al.

BMC NEUROLOGY (2006)

Article Medicine, General & Internal

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

Demetrius M. Maraganore et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)

Review Neurosciences

LRRK2 in Parkinson's disease: protein domains and functional insights

Ignacio F. Mata et al.

TRENDS IN NEUROSCIENCES (2006)

Article Biochemistry & Molecular Biology

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

A Di Fonzo et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2006)

Letter Medicine, General & Internal

LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs

S Lesage et al.

NEW ENGLAND JOURNAL OF MEDICINE (2006)

Letter Medicine, General & Internal

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews

LJ Ozelius et al.

NEW ENGLAND JOURNAL OF MEDICINE (2006)

Article Clinical Neurology

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

S Biskup et al.

ANNALS OF NEUROLOGY (2005)

Article Genetics & Heredity

Lrrk2 pathogenic substitutions in Parkinson's disease

IF Mata et al.

NEUROGENETICS (2005)

Article Genetics & Heredity

High-resolution whole-genome association study of Parkinson disease

DM Maraganore et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2005)

Article Clinical Neurology

Analysis of LRRK2 functional domains in nondominant Parkinson disease

L Skipper et al.

NEUROLOGY (2005)

Article Genetics & Heredity

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

M Stephens et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2005)

Article Genetics & Heredity

A new statistical method for haplotype reconstruction from population data

M Stephens et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)