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Paper Details

Genome-wide Analysis of Motor Progression in Parkinson Disease.
Neurol Genet
3
2023
1q12, Movement Disorder, PD, Parkinson Disease, Parkinson disease, Parkinson's Disease, blood, brain RNA expression data sets, eQTL, expression quantitative trait loci, lysophosphatidic acid, lysophosphatidic acid phosphatase, participants, patients
Author NameAffiliation
Mina RytenUCL Queen Square Institute of Neurology UCL Movement Disorders Centre (A.M.C., University College London, Bristol Medical School, University of Bristol Genetics and Genomic Medicine (R.H.R., UCL Great Ormond Street Institute of Child Health, Oslo University Hospital, Norway Institute of Psychological Medicine and Clinical Neurosciences (N.W.), Cardiff University Faculty of Health (C.C.), University of Plymouth, United Kingdom Sorbonne Universite (J.-C.C.), Institut du Cerveau - Paris Brain Institute - ICM, INSERM, CNRS Assistance Publique Hopitaux de Paris (J.-C.C.), France Division of Clinical Neurology (M.H.), University of Oxford School of Neuroscience and Psychology (D.G.), University of Glasgow Department of Neurodegenerative Diseases (J.H., UCL Queen Square Institute of Neurology UK Dementia Research Institute (J.H., University College London Reta Lila Weston Institute (J.H., UCL Queen Square Institute of Neurology National Institute for Health Research (NIHR), University College London Hospitals Biomedical Research Centre (J.H.) Institute for Advanced Study (J.H.), The Hong Kong University of Science and Technology, China and NIHR Great Ormond Street Hospital Biomedical Research Centre (M.R.)
Yoav Ben-ShlomoUCL Queen Square Institute of Neurology UCL Movement Disorders Centre (A.M.C., University College London, Bristol Medical School, University of Bristol Genetics and Genomic Medicine (R.H.R., UCL Great Ormond Street Institute of Child Health, Oslo University Hospital, Norway Institute of Psychological Medicine and Clinical Neurosciences (N.W.), Cardiff University Faculty of Health (C.C.), University of Plymouth, United Kingdom Sorbonne Universite (J.-C.C.), Institut du Cerveau - Paris Brain Institute - ICM, INSERM, CNRS Assistance Publique Hopitaux de Paris (J.-C.C.), France Division of Clinical Neurology (M.H.), University of Oxford School of Neuroscience and Psychology (D.G.), University of Glasgow Department of Neurodegenerative Diseases (J.H., UCL Queen Square Institute of Neurology UK Dementia Research Institute (J.H., University College London Reta Lila Weston Institute (J.H., UCL Queen Square Institute of Neurology National Institute for Health Research (NIHR), University College London Hospitals Biomedical Research Centre (J.H.) Institute for Advanced Study (J.H.), The Hong Kong University of Science and Technology, China and NIHR Great Ormond Street Hospital Biomedical Research Centre (M.R.)
Huw R MorrisUCL Queen Square Institute of Neurology UCL Movement Disorders Centre (A.M.C., University College London, Bristol Medical School, University of Bristol Genetics and Genomic Medicine (R.H.R., UCL Great Ormond Street Institute of Child Health, Oslo University Hospital, Norway Institute of Psychological Medicine and Clinical Neurosciences (N.W.), Cardiff University Faculty of Health (C.C.), University of Plymouth, United Kingdom Sorbonne Universite (J.-C.C.), Institut du Cerveau - Paris Brain Institute - ICM, INSERM, CNRS Assistance Publique Hopitaux de Paris (J.-C.C.), France Division of Clinical Neurology (M.H.), University of Oxford School of Neuroscience and Psychology (D.G.), University of Glasgow Department of Neurodegenerative Diseases (J.H., UCL Queen Square Institute of Neurology UK Dementia Research Institute (J.H., University College London Reta Lila Weston Institute (J.H., UCL Queen Square Institute of Neurology National Institute for Health Research (NIHR), University College London Hospitals Biomedical Research Centre (J.H.) Institute for Advanced Study (J.H.), The Hong Kong University of Science and Technology, China and NIHR Great Ormond Street Hospital Biomedical Research Centre (M.R.)
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