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1.
Jansen, I.E.* et al.: Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 18:22 (2017)
2.
McLaughlin, R.L.* et al.: Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nat. Commun. 8:14774 (2017)
3.
Lesage, S.* et al.: Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy. Am. J. Hum. Genet. 98, 500-513 (2016)
4.
Synofzik, M.* et al.: SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: A large scale multi-centre study. Brain 139, 1378-1393 (2016)
5.
van Rheenen, W.* et al.: Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat. Genet. 48, 1043-1048 (2016)
6.
Obayashi, M.* et al.: Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. J. Neurol. Neurosurg. Psychiatr. 86, 986-995 (2015)
7.
Synofzik, M.* et al.: PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum. Brain 137, 69-77 (2014)
8.
Holmans, P.* et al.: A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Hum. Mol. Genet. 22, 1039-1049 (2013)
9.
Klebe, S.* et al.: The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. J. Neurol. Neurosurg. Psychiatr. 84, 666-673 (2013)
10.
Aichler, M. et al.: Origin of pancreatic ductal adenocarcinoma from atypical flat lesions: A comparative study in transgenic mice and human tissues. J. Pathol. 226, 723-734 (2012)
11.
Keller, M.F.* et al.: Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet. 21, 4996-5009 (2012)
12.
Ishikawa, K.* et al.: Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians. Neurology 77, 1853-1855 (2011)
13.
Sharma, M.* et al.: The Sepiapterin reductase gene region reveals association in the PARK3 locus: Analysis of familial and sporadic Parkinson disease in European populations. J. Med. Genet. 43, 557-562 (2006)
14.
Asmus, F.* et al.: Myoclonus-Dystonia Syndrome : e-Sarcoglycan Mutations and Phenotype. Ann. Neurol. 52, 489-492 (2002)