article Open AccessTop 1% cited
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
The Lancet Neurology · 2008 · Vol. 7(7) · pp. 583–590
Daniel G. Healy✉(National Hospital for Neurology and Neurosurgery)Mario Falchi(Imperial College London)Sean S. O’Sullivan(University of London)Vincenzo Bonifati(Erasmus MC)Alexandra Durr(Inserm)Susan Bressman(Albert Einstein College of Medicine)Alexis Brice(Inserm)Jan Aasly(Norwegian University of Science and Technology)Cyrus P. Zabetian(University of Washington)Stefano Goldwurm(Istituti Clinici di Perfezionamento)Joaquim J. Ferreira(Institute of Molecular Medicine)Eduardo Tolosa(Universitat de Barcelona)Denise M. Kay(New York State Department of Health)Christine Klein(University of Lübeck)David R. Williams(Monash University)Connie Marras(University of Toronto)Anthony E. Lang(University of Toronto)Zbigniew K. Wszołek(Jacksonville College)José Berciano(Marqués de Valdecilla University Hospital)Anthony H.V. Schapira(University College London)Timothy Lynch(Mater Misericordiae University Hospital)Kailash P. Bhatia(Sobell House)Thomas Gasser(University of Tübingen)Andrew J. Lees(University of London)Nicholas Wood(National Hospital for Neurology and Neurosurgery)
Abstract
UK Medical Research Council; UK Parkinson's Disease Society; UK Brain Research Trust; Internationaal Parkinson Fonds; Volkswagen Foundation; National Institutes of Health: National Institute of Neurological Disorders and Stroke and National Institute of Aging; Udall Parkinson's Disease Centre of Excellence; Pacific Alzheimer Research Foundation Centre; Italian Telethon Foundation; Fondazione Grigioni per il Morbo di Parkinson; Michael J Fox Foundation for Parkinson's Research; Safra Global Genetics Consortium; US Department of Veterans Affairs; French Agence Nationale de la Recherche.
Parkinson's Disease Mechanisms and TreatmentsBanana Cultivation and ResearchLysosomal Storage Disorders ResearchLRRK2PenetranceDiseaseDyskinesiaMutationMedicineGenotypeParkinson's diseaseInternal medicineMutation frequency
MeSH terms
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2Age FactorsDNA Mutational AnalysisFamily HealthFemaleGenetic TestingGenotypeGlycineHumansInternational CooperationMaleParkinson DiseaseRiskSerineSeverity of Illness Index
Funding
- Michael J. Fox Foundation for Parkinson's Research
- Mayo Clinic
- Parkinson's UK
- Brain Research Trust
- Volkswagen Foundation
- Agence Nationale de la Recherche
- Fondazione Grigioni per il Morbo di Parkinson
- National Institutes of Health
- Medical Research Council
Citations
1,543
FWCI
43.32
field-weighted impact
References
34
Percentile
100%
vs. same field & year
Citations per year
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References
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Neuron · 2004 · 3,023 citations
Parkinsonism
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Physiology & Behavior · 1984 · 1,851 citations
Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
Neuron · 2004 · 2,419 citations
Incidence of Parkinson's Disease: Variation by Age, Gender, and Race/Ethnicity
American Journal of Epidemiology · 2003 · 1,730 citations
Nonparametric Estimation from Incomplete Observations
Journal of the American Statistical Association · 1958 · 38,793 citations
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Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
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