Progressive supranuclear palsy: New disease or variant of postencephalitic Parkinsonism?BRUSA, Adolfo; STOEHR, Rolf; PRAMSTALLER, Peter P et al.Movement disorders. 2004, Vol 19, Num 3, pp 247-252, issn 0885-3185, 6 p.Article

GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis dataFUCHSBERGER, Christian; TALIUN, Daniel; PRAMSTALLER, Peter P et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 3, pp 444-445, issn 1367-4803, 2 p.Article

PedVizApi : a Java API for the interactive, visual analysis of extended pedigreesFUCHSBERGER, Christian; FALCHI, Mario; FORER, Lukas et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 2, pp 279-281, issn 1367-4803, 3 p.Article

Brain parenchyma sonography detects preclinical ParkinsonismWALTER, Uwe; KLEIN, Christine; HILKER, Ruediger et al.Movement disorders. 2004, Vol 19, Num 12, pp 1445-1449, issn 0885-3185, 5 p.Article

Structural Findings in the Basal Ganglia in Genetically Determined and Idiopathic Parkinson's DiseaseREETZ, Kathrin; GASER, Christian; KLEIN, Christine et al.Movement disorders. 2009, Vol 24, Num 1, pp 99-103, issn 0885-3185, 5 p.Article

Distribution, type, and origin of Parkin mutations: Review and case studiesHEDRICH, Katja; ESKELSON, Cordula; LANG, Anthony E et al.Movement disorders. 2004, Vol 19, Num 10, pp 1146-1157, issn 0885-3185, 12 p.Article

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variantsSHARMA, Manu; LOANNIDIS, John P. A; FACHERIS, Maurizio F et al.Journal of medical genetics. 2012, Vol 49, Num 11, pp 721-726, issn 0022-2593, 6 p.Article

Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypesPICHLER, Irene; FUCHSBERGER, Christian; PLATZER, Christa et al.European journal of human genetics. 2010, Vol 18, Num 4, pp 463-470, issn 1018-4813, 8 p.Article

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13KEMLINK, David; PLAZZI, Giuseppe; FRAUSCHER, Birgit et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 2, pp 75-82, issn 1364-6745, 8 p.Article

Heterozygous PINK1 mutations : A susceptibility factor for parkinson disease?DJARMATI, Ana; HEDRICH, Katja; SVETEL, Marina et al.Movement disorders. 2006, Vol 21, Num 9, pp 1526-1530, issn 0885-3185, 5 p.Article

The importance of gene dosage studies : mutational analysis of the Parkin gene in early-onset parkinsonismHEDRICH, Katja; KANN, Martin; OZELIUS, Laurie J et al.Human molecular genetics (Print). 2001, Vol 10, Num 16, pp 1649-1656, issn 0964-6906Article

Large-scale replication and heterogeneity in Parkinson disease genetic lociSHARMA, Manu; IOANNIDIS, John P. A; FACHERIS, Maurizio et al.Neurology. 2012, Vol 79, Num 7, pp 659-667, issn 0028-3878, 9 p.Article

Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene clusterDEL GRECO M., Fabiola; PATTARO, Cristian; WICHMANN, H. Erich et al.Human molecular genetics (Print). 2011, Vol 20, Num 8, pp 1660-1671, issn 0964-6906, 12 p.Article

Nonmotor Symptoms in Parkin Gene-Related ParkinsonismKÄGI, Georg; KLEIN, Christine; WOOD, Nicholas W et al.Movement disorders. 2010, Vol 25, Num 9, pp 1279-1284, issn 0885-3185, 6 p.Article

Exclusion of Linkage to Chromosome 14q in a Large South Tyrolean Family With Idiopathic Basal Ganglia Calcification (IBGC)BEU VOLPATO, Claudia; DE GRANDI, Alessandro; BUFFONE, Ebba et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1319-1322, issn 1552-4841, 4 p.Article

Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated allelesHAGENAH, Johann M; KÖNIG, Inke R; BECKER, Björn et al.Journal of neurology. 2007, Vol 254, Num 10, pp 1407-1413, issn 0340-5354, 7 p.Article

Genetics of Restless Legs Syndrome (RLS) : State-of-the-Art and Future DirectionsWINKELMANN, Juliane; POLO, Oli; DE WEERD, Al et al.Movement disorders. 2007, Vol 22, issn 0885-3185, S449-S458, SUP18Article

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonismKLEIN, Christine; DJARMATI, Ana; WINKLER, Susen et al.European journal of human genetics. 2005, Vol 13, Num 9, pp 1086-1093, issn 1018-4813, 8 p.Article

Intracortical inhibition is reduced in a patient with a lesion in the posterolateral thalamusMÜNCHAU, Alexander; ORTH, Michael; ROTHWELL, John C et al.Movement disorders. 2002, Vol 17, Num 1, pp 208-212, issn 0885-3185Article

Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonismLEUNG, Joanne Chung-On; KLEIN, Christine; EISENGART, Marvin et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 3, pp 133-143, issn 1364-6745Article

Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics studyDEMIRKAN, Ayşe; ISAACS, Aaron; SCHMITZ, Gerd et al.Journal of psychiatric research. 2013, Vol 47, Num 3, pp 357-362, issn 0022-3956, 6 p.Article

Exome Sequencing in a Family With Restless Legs SyndromeWEISSBACH, Anne; SIEGESMUND, Katharina; HAGENAH, Johann et al.Movement disorders. 2012, Vol 27, Num 13, pp 1686-1689, issn 0885-3185, 4 p.Article

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsOEXLE, Konrad; RIED, Janina S; ILLIG, Thomas et al.Human molecular genetics (Print). 2011, Vol 20, Num 5, pp 1042-1047, issn 0964-6906, 6 p.Article

Impaired Sense of Smell and Color Discrimination in Monogenic and Idiopathic Parkinson's DiseaseKERTELGE, Lena; BRÜGGEMANN, Norbert; PRAMSTALLER, Peter P et al.Movement disorders. 2010, Vol 25, Num 15, pp 2665-2669, issn 0885-3185, 5 p.Article

Responsiveness to distracting stimuli, though increased in Parkinson's disease, is decreased in asymptomatic PINK1 and Parkin mutation carriersVERLEGER, Rolf; HAGENAH, Johann; WEISS, Manuel et al.Neuropsychologia. 2010, Vol 48, Num 2, pp 467-476, issn 0028-3932, 10 p.Article