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The Lancet Neurology, ISSN 1474-4422, 09/2019
Journal Article
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 04/2019, Volume 124, pp. 230 - 239
In the past two decades, mutations in multiple genes have been linked to autosomal dominant or recessive forms of monogenic Parkinson’s disease (PD).... 
Idiopathic Parkinson’s disease | Functional genomics | Pleomorphic risk loci | Genetic risk factors
Journal Article
The Lancet Neurology, ISSN 1474-4422, 11/2017, Volume 16, Issue 11, pp. 860 - 862
In The Lancet Neurology, Jeanne Latourelle and colleagues describe their attempts to identify predictors of motor symptoms by using an unbiased... 
INITIATIVE PPMI | CLINICAL NEUROLOGY | Medicine, Experimental | Medical research | Studies | Parkinson's disease | Neurodegenerative diseases | Parkinsons disease | Clinical trials | Research | Mutation | Movement disorders
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 04/2019, Volume 124, pp. 230 - 239
Journal Article
by Juge, Pierre-Antoine and Lee, Joyce S and Ebstein, Esther and Furukawa, Hiroshi and Dobrinskikh, Evgenia and Gazal, Steven and Kannengiesser, Caroline and Ottaviani, Sébastien and Oka, Shomi and Tohma, Shigeto and Tsuchiya, Naoyuki and Rojas-Serrano, Jorge and González-Pérez, Montserrat I and Mejía, Mayra and Buendía-Roldán, Ivette and Falfán-Valencia, Ramcés and Ambrocio-Ortiz, Enrique and Manali, Effrosyni and Papiris, Spyros A and Karageorgas, Theofanis and Boumpas, Dimitrios and Antoniou, Katarina and van Moorsel, Coline H.M and van der Vis, Joanne and de Man, Yaël A and Grutters, Jan C and Wang, Yaping and Borie, Raphaël and Wemeau-Stervinou, Lidwine and Wallaert, Benoît and Flipo, René-Marc and Nunes, Hilario and Valeyre, Dominique and Saidenberg-Kermanac’h, Nathalie and Boissier, Marie-Christophe and Marchand-Adam, Sylvain and Frazier, Aline and Richette, Pascal and Allanore, Yannick and Sibilia, Jean and Dromer, Claire and Richez, Christophe and Schaeverbeke, Thierry and Lioté, Huguette and Thabut, Gabriel and Nathan, Nadia and Amselem, Serge and Soubrier, Martin and Cottin, Vincent and Clément, Annick and Deane, Kevin and Walts, Avram D and Fingerlin, Tasha and Fischer, Aryeh and Ryu, Jay H and Matteson, Eric L and Niewold, Timothy B and Assayag, Deborah and Gross, Andrew and Wolters, Paul and Schwarz, Marvin I and Holers, Michael and Solomon, Joshua J and Doyle, Tracy and Rosas, Ivan O and Blauwendraat, Cornelis and Nalls, Mike A and Debray, Marie-Pierre and Boileau, Catherine and Crestani, Bruno and Schwartz, David A and Dieudé, Philippe
The New England Journal of Medicine, ISSN 0028-4793, 12/2018, Volume 379, Issue 23, pp. 2209 - 2219
Journal Article
Movement Disorders, ISSN 0885-3185, 10/2019, Volume 34, Issue 10, pp. 1581 - 1582
Journal Article
The Lancet. Neurology, ISSN 1474-4422, 11/2017, Volume 16, Issue 11, pp. 860 - 862
Journal Article
Journal Article
Nature neuroscience, ISSN 1097-6256, 01/2019, Volume 22, Issue 1, pp. 144 - 147
In the version of this article initially published, the legends for Supplementary Figs. 4-8 and 10-14 contained errors. The Supplementary Figure legends have... 
Enhancers | Genetic diversity | Dopamine | Mental disorders
Journal Article
Movement disorders : official journal of the Movement Disorder Society, ISSN 0885-3185, 11/2018, Volume 33, Issue 11, pp. 1821 - 1823
Journal Article
Movement Disorders, ISSN 0885-3185, 06/2019, Volume 34, Issue 6, pp. 866 - 875
Background Increasing evidence supports an extensive and complex genetic contribution to PD. Previous genome‐wide association studies (GWAS) have shed light on... 
Parkinson's disease | age at onset | TMEM175 | GBA | SNCA | METAANALYSIS | GBA MUTATIONS | CLINICAL NEUROLOGY | PENETRANCE | LONGEVITY | RISK LOCI | GLUCOCEREBROSIDASE | STATISTICAL POWER | APOE | EXPRESSION | EFFICIENT | Neurodegenerative diseases | Alleles | Genomes | Heritability | Gene loci | Genetic diversity | Synuclein | Age | Movement disorders
Journal Article