Publications
Our wealth of research has resulted in many publications. Explore them below, on PubMed, and on UCL Profiles.
Highlighted
The emerging role of autophagic-lysosomal dysfunction in Gaucher disease and Parkinson’s disease.
Neural Regeneration Research
2017
Links
A Drosophila Model of Neuronopathic Gaucher Disease Demonstrates Lysosomal-Autophagic Defects and Altered mTOR Signalling and Is Functionally Rescued by Rapamycin.
Journal of Neuroscience
2016
Links
Mitochondrial dysfunction and defects in lipid homeostasis as therapeutic targets in neurodegeneration with brain iron accumulation.
Rare Diseases
2016
Links
All Publications
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
The Lancet Neurology
2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease.
Journal of Medical Genetics
2019
Agephagy – Adapting Autophagy for Health During Aging.
Frontiers in Cell and Developmental Biology
2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Mov Disord
2019
A triple drug combination targeting components of the nutrient-sensing network maximizes longevity.
Proc Natl Acad Sci U S A
2019
Pathway single nucleotide polymorphisms interact to modulate the age at onset of Parkinson's disease.
Mov Disord
2019
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.
npj Parkinson's Disease
2019
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability.
npj Parkinson's Disease
2019
