Julie P. Taylor

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan et al. · The American Journal of Human Genetics · 2005 · 534 citations · Full text

Molecular Neuroscience, Mendelian Disorder, Genetic Disorder +7

Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice

Heather L. Melrose, Justus C. Dächsel, Bahareh Behrouz et al. · Neurobiology of Disease · 2010 · 276 citations · Full text

Knockout Mouse, Neurodegenerative Diseases, Signal Transduction +10

Lrrk2 pathogenic substitutions in Parkinson's disease

Ignácio F. Mata, Jennifer M. Kachergus, Julie P. Taylor et al. · Neurogenetics · 2005 · 231 citations

Mitophagy, Lrrk2 Pathogenic Substitutions, Receptor Tyrosine Kinase +5

Mutations of the<i>PDS</i>Gene, Encoding Pendrin, Are Associated with Protein Mislocalization and Loss of Iodide Efflux: Implications for Thyroid Dysfunction in Pendred Syndrome

Julie P. Taylor, Russell Metcalfe, Philip F. Watson et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 150 citations · Full text

Signal Transduction, Encoding Pendrin, Protein Mislocalization +14

A comparative analysis of leucine-rich repeat kinase 2 (Lrrk2) expression in mouse brain and Lewy body disease

Heather L. Melrose, Caroline Kent, Julie P. Taylor et al. · Neuroscience · 2007 · 109 citations

Lewy Body Disease, Molecular Neuroscience, Receptor Tyrosine Kinase +10