Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

Lill, Christina M; Roehr, Johannes T; McQueen, Matthew B; Kavvoura, Fotini K; Bagade, Sachin; Schjeide, Brit-Maren M; Schjeide, Leif M; Meissner, Esther; Zauft, Ute; Allen, Nicole C; Liu, Tian; Schilling, Marcel; Anderson, Kari J; Beecham, Gary; Berg, Daniela; Biernacka, Joanna M; Brice, Alexis; DeStefano, Anita L; Do, Chuong B; Eriksson, Nicholas; Factor, Stewart A; Farrer, Matthew J; Foroud, Tatiana; Gasser, Thomas; Hamza, Taye; Hardy, John A; Heutink, Peter; Hill-Burns, Erin M; Klein, Christine; Latourelle, Jeanne C; Maraganore, Demetrius M; Martin, Eden R; Martinez, Maria; Myers, Richard H; Nalls, Michael A; Pankratz, Nathan; Payami, Haydeh; Satake, Wataru; Scott, William K; Sharma, Manu; Singleton, Andrew B; Stefansson, Kari; Toda, Tatsushi; Tung, Joyce Y; Vance, Jeffery; Wood, Nick W; Zabetian, Cyrus P; Young, Peter; Tanzi, Rudolph E; Khoury, Muin J

Lill, Christina M; Roehr, Johannes T; McQueen, Matthew B; Kavvoura, Fotini K; Bagade, Sachin; Schjeide, Brit-Maren M; Schjeide, Leif M; Meissner, Esther; Zauft, Ute; Allen, Nicole C; Liu, Tian; Schilling, Marcel; Anderson, Kari J; Beecham, Gary; Berg, Daniela; Biernacka, Joanna M; Brice, Alexis; DeStefano, Anita L; Do, Chuong B; Eriksson, Nicholas; Factor, Stewart A; Farrer, Matthew J; Foroud, Tatiana; Gasser, Thomas; Hamza, Taye; Hardy, John A; Heutink, Peter; Hill-Burns, Erin M; Klein, Christine; Latourelle, Jeanne C; Maraganore, Demetrius M; Martin, Eden R; Martinez, Maria; Myers, Richard H; Nalls, Michael A; Pankratz, Nathan; Payami, Haydeh; Satake, Wataru; Scott, William K; Sharma, Manu; Singleton, Andrew B; Stefansson, Kari; Toda, Tatsushi; Tung, Joyce Y; Vance, Jeffery; Wood, Nick W; Zabetian, Cyrus P; Young, Peter; Tanzi, Rudolph E; Khoury, Muin J.

Afiliación

Lill CM; Neuropsychiatric Genetics Group, Department of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Berlin, Germany.

PLoS Genet ; 8(3): e1002548, 2012.

Article en En | MEDLINE | ID: mdl-22438815

Asunto(s)

Bases de Datos Genéticas; Estudio de Asociación del Genoma Completo; Enfermedad de Parkinson/genética; Genoma Humano; Humanos; Internet; Polimorfismo de Nucleótido Simple

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Bases de Datos Genéticas / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2012 Tipo del documento: Article País de afiliación: Alemania

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