Sophie Winder‐Rhodes

University of Cambridge — United Kingdom

Medicine · Health Sciences

18h-index3.6kcitations28works0.02yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(21), Lysosomal Storage Disorders Research(11), Neurological disorders and treatments(6), Autism Spectrum Disorder Research(5), Cellular transport and secretion(5)

Publications21 total

<scp><i>GBA</i></scp> and <scp><i>APOE</i></scp> Impact Cognitive Decline in Parkinson's Disease: A 10‐Year Population‐Based Study
Movement Disorders·2022· 109 citedOpen Access
Impact of<i>GBA1</i>variants on long-term clinical progression and mortality in incident Parkinson’s disease
Journal of Neurology Neurosurgery & Psychiatry·2020· 90 citedOpen Access
A common polymorphism in<i>SNCA</i>is associated with accelerated motor decline in<i>GBA</i>-Parkinson’s disease
Journal of Neurology Neurosurgery & Psychiatry·2020· 9 citedOpen Access
Motor Complications in Parkinson's Disease: 13‐Year Follow‐up of the CamPaIGN Cohort
Movement Disorders·2019· 81 citedOpen Access
Association between intravascular thermoregulation devices and the development of venous thrombo-embolic phenomenon
Journal of the Intensive Care Society·2017Open Access
Prediction of cognition in Parkinson's disease with a clinical–genetic score: a longitudinal analysis of nine cohorts
The Lancet Neurology·2017· 181 citedOpen Access
Neuropathic Gaucher’s Mutations: Shifting Parkinson’s Into High Gear (S1.002)
Neurology·2017
Issue Information – Table of Contents
Annals of Neurology·2016Open Access
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's
Annals of Neurology·2016· 268 citedOpen Access
The role of tau in the pathological process and clinical expression of Huntington’s disease
Brain·2015· 136 citedOpen Access
21 * MANAGING HOSPITALISED PATIENTS WITH PARKINSON'S DISEASE: ARE WE GETTING IT RIGHT?
Age and Ageing·2015· 1 citedOpen Access
The pathophysiological and prognostic heterogeneity of mild cognitive impairment in Parkinson’s disease
Oxford University Press eBooks·2015
Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals
Neurobiology of Aging·2014· 49 citedOpen Access
Genetic impact on cognition and brain function in newly diagnosed Parkinson’s disease: ICICLE-PD study
Brain·2014· 147 citedOpen Access
Characterizing mild cognitive impairment in incident Parkinson disease
Neurology·2013· 410 citedOpen Access
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Neurology·2013· 143 citedOpen Access
Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort
Brain·2013· 287 citedOpen Access
Glucocerebrosidase mutations influence the natural history of PD in a community-based incident cohort
UCL Discovery (University College London)·2012
Inefficiency of fronto-parietal networks in incident Parkinson’s disease
2012
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome
Movement Disorders·2011· 83 cited
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Frequent Co-authors

Roger A. Barker(18), Caroline H. Williams‐Gray(13), Clemens R. Scherzer(8), Thomas Foltynie(7), Ganqiang Liu(7), David P. Breen(5), Jonathan Evans(5), Trevor W. Robbins(5), David J. Burn(5), Alexis Brice(5), Johan Marinus(5), Alison J. Yarnall(4), James B. Rowe(4), Gavin Hudson(4), Patrick F. Chinnery(4), Brendon Boot(4), Joseph J. Locascio(4), Iris E. Jansen(4), Shirley Eberly(4), Alexis Elbaz(4)