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Schulte, E.C. et al.: Alterations in lipid and inositol metabolisms in two dopaminergic disorders. PLoS ONE 11:e0147129 (2016)
Schulte, E.C. et al.: Rare variants in β-Amyloid Precursor Protein (APP) and Parkinson's disease. Eur. J. Hum. Genet. 23, 1328-1333 (2015)
Schulte, E.C. et al.: Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer’s disease. Hum. Genome Var. 2:14028 (2015)
Schulte, E.C. et al.: Rare variants in LRRK1 and Parkinson's disease. Neurogenetics 15, 49-57 (2014)
Schulte, E.C.* ; Gross, N.* ; Slawik, H.* & Winkelmann, J.: "Malignant restless legs syndrome" - a curse or a blessing? Sleep Med. 15, 155–156 (2014)
Schulte, E.C. et al.: Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. PLoS ONE 9:e98092 (2014)
Schulte, E.C. et al.: Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome. Am. J. Hum. Genet. 95, 85-95 (2014)
Schulte, E.C. & Winkelmann, J.: Clinical phenotype and genetics of restless legs syndrome. In: LeDoux, M.S.* [Eds.]: Movement Disorders : Genetics and Models. Elsevier, 2014. 1145-1162
Schulte, E.C. ; Kaffe, M.* ; Schormair, B. & Winkelmann, J.: Iron in restless legs syndrome. Mov. Disord. Clin. Pract. 1, 161-172 (2014)
Hopfner, F. et al.: The role of SCARB2 as susceptibility factor in Parkinson's disease. Mov. Disord. 28, 538-540 (2013)
Schulte, E.C. et al.: Mitochondrial membrane protein associated neurodegeneration: A novel variant of neurodegeneration with brain iron accumulation. Mov. Disord. 28, 224-227 (2013)
Schulte, E.C. ; Gross, N.* ; Slawik, H.* & Winkelmann, J.: When restless legs syndrome turns malignant. Sleep Med. 14, 575-577 (2013)
Schulte, E.C. et al.: Rare variants in PLXNA4 and Parkinson's disease. PLoS ONE 8:e79145 (2013)
Zech, M. et al.: Niemann-pick C disease gene mutations and age-related neurodegenerative disorders. PLoS ONE 8:e82879 (2013)
Schulte, E.C. et al.: Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease. Neurogenetics 13, 281-285 (2012)
* et al.: A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am. J. Hum. Genet. 89, 168-175 (2011)
Schulte, E.C.* & Winkelmann, J.: When Parkinson's disease patients go to sleep: Specific sleep disturbances related to Parkinson's disease. J. Neurol. 258, Suppl. 2, S328-S335 (2011)
Schulte, E.C.* et al.: Variant screening of the coding regions of MEIS1 in patients with restless legs syndrome. Neurology 76, 1106-1108 (2011)
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)
Schulte, E.C.* ; Spieler, D. & Winkelmann, J.: Restless-legs-Syndrom und kardiovaskuläres Risiko. Nervenarzt 82, 1006-1011 (2010)