Converging environmental and genetic pathways in the pathogenesis of Parkinson's diseaseBURBULLA, Lena F; KRÜGER, Rejko.Journal of the neurological sciences. 2011, Vol 306, Num 1-2, pp 1-8, issn 0022-510X, 8 p.Article

Spectrum of phenotypes and genotypes in Parkinson's diseaseRIESS, Olaf; KRÜGER, Rejko; SCHULZ, Jörg B et al.Journal of neurology. Supplement. 2002, Vol 249, Num 3, issn 0939-1517, III/15-III/20Article

Genetics of Parkinson's diseaseKRÜGER, Rejko.Molecular bases of neurodegeneration. 2005, pp 1-19, isbn 81-7736-261-5, 1Vol, 19 p.Book Chapter

Genes in familial parkinsonism and their role in sporadic Parkinson's diseaseKRÜGER, Rejko.Journal of neurology. Supplement. 2004, Vol 251, Num 6, pp VI.2-VI.6, issn 0939-1517Article

Review: Familial Parkinson's disease : genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the diseaseSCHIESLING, Carola; KIEPER, Nicole; SEIDELT, Kay et al.Neuropathology and applied neurobiology (Print). 2008, Vol 34, Num 3, pp 255-271, issn 0305-1846, 17 p.Article

Severe orthostatic dysregulation associated with Wolfram syndromeSYNOFZIK, Matthis; WEISS, Daniel; ERHARHAGHEN, Jite et al.Journal of neurology. 2010, Vol 257, Num 10, pp 1751-1753, issn 0340-5354, 3 p.Article

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's diseaseRAHNER, Nils; HOLZMANN, Carsten; KRÜGER, Rejko et al.Brain research. 2002, Vol 951, Num 1, pp 82-86, issn 0006-8993Article

Complex Hyperkinetic Movement Disorders Associated with POLG MutationsSYNOFZIK, Matthis; SCHÜLE, Rebecca; SCHULTE, Claudia et al.Movement disorders. 2010, Vol 25, Num 14, pp 2472-2475, issn 0885-3185, 4 p.Article

Effects of transcranial direct current stimulation (tDCS) on executive functions: Influence of COMT Val/Met polymorphismPLEWNIA, Christian; ZWISSLER, Bastian; LÄNGST, Isabella et al.Cortex (Testo stampato). 2013, Vol 49, Num 7, pp 1801-1807, issn 0010-9452, 7 p.Article

Therapeutic strategies for Parkinson's disease based on data derived from genetic researchRIESS, Olaf; BERG, Daniela; KRÜGER, Rejko et al.Journal of neurology. Supplement. 2003, Vol 250, Num 1, pp 3-10, issn 0939-1517, 8 p.Article

Polymorphisms in the interleukin-1 alpha and beta genes and the risk for Parkinson's diseaseSCHULTE, Thorsten; SCHÖLS, Ludger; MÜLLER, Thomas et al.Neuroscience letters. 2002, Vol 326, Num 1, pp 70-72, issn 0304-3940Article

Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in miceNUBER, Silke; FRANCK, Thomas; SCHULZ, Jörg B et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 1, pp 107-120, issn 1364-6745, 14 p.Article

Genome-wide association study reveals genetic risk underlying Parkinson's diseaseSIMON-SANCHEZ, Javier; SCHULTE, Claudia; KRÜGER, Rejko et al.Nature genetics. 2009, Vol 41, Num 12, pp 1308-1312, issn 1061-4036, 5 p.Article

Transcranial ultrasound in different monogenetic subtypes of Parkinson's diseaseSCHWEITZER, Katherine J; BRÜSSEL, Theresa; LEITNER, Petra et al.Journal of neurology. 2007, Vol 254, Num 5, pp 613-616, issn 0340-5354, 4 p.Article

Evaluation of the γ-synuclein gene in German Parkinson's disease patientsKRÜGER, Rejko; SCHÖLS, Ludger; MÜLLER, Thomas et al.Neuroscience letters. 2001, Vol 310, Num 2-3, pp 191-193, issn 0304-3940Article

Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's diseaseSOEHN, Anne S; FRANCK, Thomas; MEITINGER, Thomas et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 2, pp 203-215, issn 1364-6745, 13 p.Article

Mutation analysis of the neurofilament M gene in Parkinson's diseaseKRÜGER, Rejko; FISCHER, Christian; EPPLEN, Jörg T et al.Neuroscience letters. 2003, Vol 351, Num 2, pp 125-129, issn 0304-3940, 5 p.Article

14-3-3 protein is a component of Lewy bodies in Parkinson's disease: Mutation analysis and association studies of 14-3-3 etaUBL, Andreas; BERG, Daniela; HOLZMANN, Carsten et al.Molecular brain research. 2002, Vol 108, Num 1-2, pp 33-39, issn 0169-328X, 7 p.Article

Collaborative analysis of α-synuclein gene promoter variability and parkinson diseaseMARAGANORE, Demetrius M; DE ANDRADE, Mariza; HULIHAN, Mary M et al.JAMA, the journal of the American Medical Association. 2006, Vol 296, Num 6, pp 661-670, issn 0098-7484, 10 p.Article

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's diseaseSTRAUSS, Karsten M; MARTINS, L. Miguel; WOLBURG, Hartwig et al.Human molecular genetics (Print). 2005, Vol 14, Num 15, pp 2099-2111, issn 0964-6906, 13 p.Article

New developments in diagnosis and treatment of Parkinson's disease: From basic science to clinical applicationsSTORCH, Alexander; HOFER, Anne; KRÜGER, Rejko et al.Journal of neurology. Supplement. 2004, Vol 251, Num 6, pp VI.33-VI.38, issn 0939-1517Article

Haploinsufficiency at the α-synuclein gene underlies phenotypic severity in familial Parkinson's diseaseKOBAYASHI, Hirokazu; KRÜGER, Rejko; HATTORI, Nobutaka et al.Brain. 2003, Vol 126, pp 32-42, issn 0006-8950, 11 p., 1Article

The subthalamic nucleus modulates the early phase of probabilistic classification learningWEISS, Daniel; LAM, Judith M; BREIT, Sorin et al.Experimental brain research. 2014, Vol 232, Num 7, pp 2255-2262, issn 0014-4819, 8 p.Article

Global investigation and meta-analysis of the C9orf72 (G₄C₂)_n repeat in Parkinson diseaseTHEUNS, Jessie; VERSTRAETEN, Aline; KRÜGER, Rejko et al.Neurology. 2014, Vol 83, Num 21, pp 1906-1913, issn 0028-3878, 8 p.Article

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