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Lane, J.M.* et al.: Biological and clinical insights from genetics of insomnia symptoms. Nat. Genet. 51, 387-393 (2019)
Zech, M. ; Wagner, M. ; Schormair, B. ; Oexle, K. & Winkelmann, J.: Exomdiagnostik in der Neurologie. Nervenarzt 90, 131-137 (2019)
Salminen, A.V. et al.: Sleep disturbance by pramipexole is modified by Meis1 in mice. J. Sleep Res. 27:e12557 (2018)
Trenkwalder, C.* et al.: Comorbidities, treatment, and pathophysiology in restless legs syndrome. Lancet Neurol. 17, 994-1005 (2018)
Hammerschlag, A.R.* et al.: Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Nat. Genet. 49, 1584-1592 (2017)
Salminen, A.V. et al.: Meis1 effects on motor phenotypes and the sensorimotor system in mice. Dis. Model. Mech. 10, 981-991 (2017)
Schormair, B. et al.: Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. Clin. Genet. 93, 603-612 (2017)
Schormair, B. et al.: Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)
Winkelmann, J. et al.: Genetics of restless legs syndrome. Sleep Med. 31, 18-22 (2017)
Zech, M. et al.: Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up. Mov. Disord. 32, 549-559 (2016)
Zech, M. et al.: Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia. Am. J. Hum. Genet. 96, 883-893 (2015)
Han, F.* et al.: HLA DQB1*06:02 negative narcolepsy with hypocretin/orexin deficiency. Sleep 37, 1601-1608 (2014)
Kemlink, D.* et al.: Restless legs syndrome in Czech pregnant women: An epidemiological and genetic study. J. Sleep Res. 23, 225 (2014)
Schulte, E.C. et al.: Rare variants in LRRK1 and Parkinson's disease. Neurogenetics 15, 49-57 (2014)
Schulte, E.C. ; Kaffe, M.* ; Schormair, B. & Winkelmann, J.: Iron in restless legs syndrome. Mov. Disord. Clin. Pract. 1, 161-172 (2014)
Zech, M. et al.: DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Mov. Disord. 29, 1504-1510 (2014)
Oexle, K.* et al.: Dilution of candidates: The case of iron-related genes in restless legs syndrome. Eur. J. Hum. Genet. 21, 410-414 (2013)
Winkelmann, J. et al.: Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. Hum. Mol. Genet. 21, 2205-2210 (2012)
Hopfner, F. et al.: Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurology 11:134 (2011)
Schormair, B. et al.: MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease. J. Med. Genet. 48, 462-466 (2011)