S. Winder-Rhodes

发表

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2017, Brain : a journal of neurology.

Characterizing mild cognitive impairment in incident Parkinson disease

T. Robbins, R. Barker, J. O'Brien, 2014, Neurology.

Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

M. Pirinen, P. Donnelly, C. Spencer, 2012 .

Genetic impact on cognition and brain function in newly diagnosed Parkinson’s disease: ICICLE-PD study

David J. Brooks, Roger A. Barker, James B. Rowe, 2014, Brain : a journal of neurology.

Motor complications in Parkinson's disease: 13‐year follow‐up of the CamPaIGN cohort

R. Barker, T. Foltynie, Han-Joon Kim, 2019, Movement disorders : official journal of the Movement Disorder Society.

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Jean-François Dartigues, Günther Deuschl, Yoav Ben-Shlomo, 2017, Genome Biology.

Impact of GBA1 variants on long-term clinical progression and mortality in incident Parkinson’s disease

R. Barker, T. Foltynie, Ganqiang Liu, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

A common polymorphism in SNCA is associated with accelerated motor decline in GBA-Parkinson’s disease

R. Barker, T. Foltynie, Ganqiang Liu, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Association between intravascular thermoregulation devices and the development of venous thrombo-embolic phenomenon

S. Winder-Rhodes, James Doyle, R. Lotay, 2017, Journal of the Intensive Care Society.

ESICM LIVES 2016: part three : Milan, Italy. 1-5 October 2016.

Gilles Clermont, María Bodí, Artur Dubrawski, 2016 .

Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome

M. Ban, S. Sawcer, R. Barker, 2012, Movement disorders : official journal of the Movement Disorder Society.

Translational Approaches to Frontostriatal Dysfunction in Attention-Deficit/Hyperactivity Disorder Using a Computerized Neuropsychological Battery

Ulrich Müller, Andrew D. Blackwell, Barbara J. Sahakian, 2011, Biological Psychiatry.

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

R. Barker, J. Growdon, B. Hyman, 2016, Annals of neurology.

Prediction of cognition in Parkinson's disease with a clinical–genetic score: a longitudinal analysis of nine cohorts

D. German, R. Barker, R. Sperling, 2017, The Lancet Neurology.

The role of tau in the pathological process and clinical expression of Huntington’s disease

R. Barker, M. Spillantini, F. Cicchetti, 2015, Brain : a journal of neurology.

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

M. Nalls, A. Singleton, R. Barker, 2013, Neurology.

GBA and APOE Impact Cognitive Decline in Parkinson’s Disease: A 10-Year Population-Based Study

L. Forsgren, C. Counsell, Ganqiang Liu, 2022, Movement disorders : official journal of the Movement Disorder Society.

Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.

M. Ban, S. Sawcer, R. Barker, 2013, Brain : a journal of neurology.

ESICM LIVES 2016: part three

A. M. Cavalheiro, H. S. King, Y. L. Yang, 2016, Intensive Care Medicine Experimental.

Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals

T. Robbins, J. Peelle, R. Barker, 2015, Neurobiology of Aging.

Cortical and subcortical grey matter morphometry for neuroprognostication after cardiac arrest

Ana María López, Radu, EP Der Kinderen, 2016 .

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2017, Genome Biology.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2016, American journal of human genetics.

ESICM LIVES 2016: part three

A. M. Cavalheiro, H. S. King, Y. L. Yang, 2016, Intensive Care Medicine Experimental.

Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome

M. Ban, S. Sawcer, D. Burn, 2012, Movement disorders : official journal of the Movement Disorder Society.

Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.

M. Ban, S. Sawcer, T. Foltynie, 2013, Brain : a journal of neurology.

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

D. Hernandez, M. Nalls, A. Singleton, 2013, Human molecular genetics.

Characterizing mild cognitive impairment in incident Parkinson disease The ICICLE-PD Study

M. Firbank, B. Mollenhauer, P. Chinnery, 2022 .

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

M. Nalls, A. Singleton, D. Burn, 2013, Neurology.

Prediction of cognition in Parkinson's disease with a clinical–genetic score: a longitudinal analysis of nine cohorts

B. Boot, C. Tanner, A. Lang, 2017, The Lancet Neurology.