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Establishing the role of rare coding variants in known Parkinson's disease risk loci

Year: 2017
Type: article
DOI: 10.1016/j.neurobiolaging.2017.07.009
Authors: Iris E. Jansen, J. Raphael Gibbs, Mike A. Nalls, T. Ryan Price, Steven Lubbe, Jeroen van Rooij, André G. Uitterlinden, Robert Kraaij, Nigel M. Williams, Alexis Brice, John Hardy, Nicholas W. Wood, Huw R. Morris, Thomas Gasser, Andrew B. Singleton, Peter Heutink, Manu Sharma
Institutions: German Center for Neurodegenerative Diseases, Amsterdam UMC Location Vrije Universiteit Amsterdam, National Institutes of Health, National Institute on Aging, Data Tecnica International (United States), University of California, Irvine, Northwestern University, Erasmus MC, Netherlands Consortium for Healthy Ageing, Cardiff University, Centre National de la Recherche Scientifique, Inserm, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, University College London, UCL Queen Square Institute of Neurology, University of Tübingen
Language: English
Subfield: Neurology
Field: Medicine
Open Access status: green
Funders: National Institute for Health and Care Research, Parkinson's UK, Agence Nationale de la Recherche, National Institutes of Health, Medical Research Council, National Institute on Aging
Awards: COmprehensive Unbiased Risk factor Assessment for Genetics and Environment in Parkinson‘s Disease, G4635709268, G503224829, G645515640, G6680420078, G695839759, G7310981802, G7433172200, Assessment of Candidate Loci in Neurological diseases, Genome wide SNP analysis in Parkinson's disease, NIHR Senior Investigator Award
OpenAlex ID: W2739572546
FWCI: 2.284
Cites: 47
Cited by: 18
Related to: 10