- Title
- Absence of previously reported variants in the SCNA (G88c and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial parkinson's disease from the GenePD study
- Creators
- Samer KARAMOHAMED - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesL. I GOLBE - Department of Neurology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United StatesM SAINT-HILAIRE - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesR. G FELDMAN - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesJ LIU - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesC. M SHOEMAKER - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesJ. B WILK - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesA. L DESTEFANO - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesJ. C LATOURELLE - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesG XU - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesR WATTS - Department of Neurology, Emory University, Atlanta, Georgia, United StatesJ GROWDON - Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United StatesM. H MARK - Department of Neurology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United StatesM LEW - Department of Neurology, University of Southern California, Los Angeles, California, United StatesC WATERS - Department of Neurology, University of Southern California, Los Angeles, California, United StatesP VIEREGGE - Department of Neurology, Medical University of Lübeck, Lübeck, GermanyP. P PRAMSTALLER - Department of Neurology, General Regional Hospital Bolzano, Bolzano, ItalyC KLEIN - Department of Neurology, Medical University of Lübeck, Lübeck, GermanyB. A RACETTE - Department of Neurology, Washington University School of Medicine, Saint Louis, Missouri, United StatesJ. S PERLMUTTER - Department of Neurology, Washington University School of Medicine, Saint Louis, Missouri, United StatesA PARSIAN - Department of Neurology, Washington University School of Medicine, Saint Louis, Missouri, United StatesCarlos SINGER - Department of Neurology, University of Miami, Miami, Florida, United StatesE MONTGOMERY - Departments of Neurology and Neuroscience, Cleveland Clinic Foundation, Cleveland, Ohio, United StatesA. M LAZZARINI - Department of Neurology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United StatesK BAKER - Departments of Neurology and Neuroscience, Cleveland Clinic Foundation, Cleveland, Ohio, United StatesJ. F GUSELLA - Molecular Neurogenetics Unit, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United StatesA HERBERT - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesR. H MYERS - Department of Neurology, Boston University School of Medicine, Boston. Massachusetts, United StatesO SUCHOWERSKY - Departments of Clinical Neurosciences and Medical Genetics, University of Calgary, Calgary, Alberta, CanadaN LABELLE - Departments of Clinical Neurosciences and Medical Genetics, University of Calgary, Calgary, Alberta, CanadaMark GUTTMAN - Division of Neurology, Department of Medicine, University of Toronto, Toronto, CanadaL. J CURRIE - Department of Neurology, University of Virginia Health System, Charlottesville, Virginia, United StatesG. F WOOTEN - Department of Neurology, University of Virginia Health System, Charlottesville, Virginia, United StatesM STACY - Department of Neurology, Barrow Clinic, Phoenix, Arizona, United States
- Publication Details
- Movement disorders, Vol.20(9), pp.1188-1191
- Publisher
- Wiley; Hoboken, NJ
- Academic Unit
- Miller School of Medicine; UMMG Department of Neurology
- Language
- English
- Resource Type
- Journal article
- PMID
- 15966003
- Record Identifier
- 991031560538202976
Journal article
Absence of previously reported variants in the SCNA (G88c and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial parkinson's disease from the GenePD study
Movement disorders, Vol.20(9), pp.1188-1191
2005
PMID: 15966003
Metrics
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InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.52 Neurodegenerative Diseases
- 1.52.67 Parkinson's Disease
- Web Of Science research areas
- Clinical Neurology
- ESI research areas
- Neuroscience & Behavior
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Source: InCites