4.6 Review

LRRK2 in Parkinson's disease: genetic and clinical studies from patients

Related references

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

LRRK2 and neurodegeneration

Gabriel Santpere et al.

ACTA NEUROPATHOLOGICA (2009)

Letter Genetics & Heredity

LRRK2 G2385R Modulates Age at Onset in Parkinson's Disease: A Multi-Center Pooled Analysis

E. K. Tan et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)

Review Neurosciences

Leucine-Rich Repeat Kinase 2 (LRRK2): A Key Player in the Pathogenesis of Parkinson's Disease

Payal N. Gandhi et al.

JOURNAL OF NEUROSCIENCE RESEARCH (2009)

Article Geriatrics & Gerontology

Case control analysis of LRRK2 Gly2385Arg in Alzheimer's disease

E. K. Tan et al.

NEUROBIOLOGY OF AGING (2009)

Article Clinical Neurology

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

Owen A. Ross et al.

PARKINSONISM & RELATED DISORDERS (2009)

Article Clinical Neurology

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

Owen A. Ross et al.

ANNALS OF NEUROLOGY (2008)

Letter Clinical Neurology

Lrrk2 R1628P in Non-Chinese Asian Races

Eng-King Tan et al.

ANNALS OF NEUROLOGY (2008)

Editorial Material Clinical Neurology

Uniting Chinese across Asia: The LRRK2 Gly2385Arg risk variant

E. K. Tan et al.

EUROPEAN JOURNAL OF NEUROLOGY (2008)

Article Genetics & Heredity

LRRK2 R1628P increases risk of Parkinson's disease: replication evidence

E. K. Tan et al.

HUMAN GENETICS (2008)

Article Clinical Neurology

Myocardial 123Metaiodobenzylguanidine uptake in genetic Parkinson's disease

Aldo Quattrone et al.

MOVEMENT DISORDERS (2008)

Article Clinical Neurology

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

K. Haugarvoll et al.

NEUROLOGY (2008)

Article Clinical Neurology

Hyposmia in G2019S LRRK2-related parkinsonism - Clinical and pathologic data

L. Silveira-Moriyama et al.

NEUROLOGY (2008)

Review Genetics & Heredity

The role of common genetic risk variants in Parkinson disease

E-K Tan

CLINICAL GENETICS (2007)

Article Biochemistry & Molecular Biology

LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity

Mahaboobi Jaleel et al.

BIOCHEMICAL JOURNAL (2007)

Review Genetics & Heredity

Pathogenic mutations in Parkinson disease

Eng-King Tan et al.

HUMAN MUTATION (2007)

Article Clinical Neurology

Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease

Katherine J. Schweitzer et al.

JOURNAL OF NEUROLOGY (2007)

Letter Clinical Neurology

Comparing LRRK2 Gly2385Arg carriers with noncarriers

Eng-King Tan et al.

MOVEMENT DISORDERS (2007)

Article Clinical Neurology

Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population

Eng-King Tan et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (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

LRRK2 G2019S founder haplotype in the Chinese population

Eng-King Tan et al.

MOVEMENT DISORDERS (2007)

Article Clinical Neurology

Parkinson's disease due to the R1441G mutation in Dardarin:: A founder effect in the Basques

Javier Simon-Sanchez et al.

MOVEMENT DISORDERS (2006)

Article Neurosciences

Kinase activity is required for the toxic effects of mutant LRRK2/dardarin

Elisa Greggio et al.

NEUROBIOLOGY OF DISEASE (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)

Review Clinical Neurology

Genetic testing in Parkinson disease - Promises and pitfalls

Eng-King Tan et al.

ARCHIVES OF NEUROLOGY (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 Neurosciences

LRRK2 R1441G in Spanish patients with Parkinson's disease

IF Mata et al.

NEUROSCIENCE LETTERS (2005)

Article Clinical Neurology

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1

M Funayama et al.

ANNALS OF NEUROLOGY (2002)