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Publications by C H Williams-Gray

Prevalence of the LRRK2 G2019S Mutation in a UK Community Based Idiopathic Parkinson's Disease Cohort

Journal of Neurology, Neurosurgery and Psychiatry

English

Related publications

Clinical Heterogeneity of the LRRK2 G2019S Mutation

Archives of Neurology

English

LRRK2 Screening in a Canadian Parkinson's Disease Cohort

Canadian Journal of Neurological Sciences

English

LRRK2 Pathobiology in Parkinson's Disease

Journal of Neurochemistry

Molecular Neuroscience

English

LRRK2 G2019S Mutation Attenuates Microglial Motility by Inhibiting Focal Adhesion Kinase

Nature Communications

Molecular Biology

English

Prevalence of Chronic Kidney Disease in the Community Using Data From OxRen: A UK Population-Based Cohort Study

British Journal of General Practice

Family Practice

English

Presynaptic Dysfunction in Parkinson's Disease: A Focus on LRRK2

Biochemical Society Transactions

English

Neurite Collapse and Altered ER Ca2+ Control in Human Parkinson Disease Patient iPSC-Derived Neurons With LRRK2 G2019S Mutation

Stem Cell Reports

Developmental Biology

English

Rab29 Activation of the Parkinson's Disease‐associated LRRK2 Kinase

Molecular Biology

English

Identification of a Japanese Family With LRRK2 p.R1441G-related Parkinson's Disease

Neurobiology of Aging

Developmental Biology

English