PuSH - Publication Server of Helmholtz Zentrum München

192 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
1.
Kishore, A.* et al.: Understanding the role of genetic variability in LRRK2 in Indian population. Mov. Disord. 34, 496-505 (2019)
2.
Valdes-Marquez, E.* et al.: Relative effects of LDL-C on ischemic stroke and coronary disease: A Mendelian randomization study. Neurology 92, E1176-E1187 (2019)
3.
Brockmann, S.J.* et al.: CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)
4.
Karch, C.M.* et al.: Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum. JAMA Neurol. 75, 860-875 (2018)
5.
Lee, J.J.* et al.: Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nat. Genet. 52, 1112-1121 (2018)
6.
Pulit, S.L.* et al.: Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. Neurol. Genet. 4:e293 (2018)
7.
Rosendahl, J.* et al.: Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. Gut 67, 1855–186 (2018)
8.
Tian, Y.* et al.: Targeted genotyping identifies susceptibility locus in brain-derived neurotrophic factor gene for chronic postsurgical pain. Anesthesiology 128, 587-597 (2018)
9.
Wesdorp, M.* et al.: Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction. Hum. Genet. 137, 389-400 (2018)
10.
Wesdorp, M.* et al.: MPZL2, encoding the epithelial junctional protein myelin protein zero-like 2, is essential for hearing in man and mouse. Am. J. Hum. Genet. 103, 74-88 (2018)
11.
Chen, G.B.* et al.: Across-cohort QC analyses of GWAS summary statistics from complex traits. Eur. J. Hum. Genet. 25, 137-146 (2017)
12.
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
13.
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)
14.
Kremer, L.S. et al.: Genetic diagnosis of Mendelian disorders via RNA sequencing. Nat. Commun. 8:15824 (2017)
15.
Malik, R.* et al.: Common coding variant in SERPINA1 increases the risk for large artery stroke. Proc. Natl. Acad. Sci. U.S.A. 114, 3613-3618 (2017)
16.
McLaughlin, R.L.* et al.: Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nat. Commun. 8:14774 (2017)
17.
Pecanka, J.* ; Jonker, M.A.* ; Bochdanovits, Z.* & International Parkinson's Disease Genomics Consortium (IPDGC) (Illig, T. ; Lichtner, P.): A powerful and efficient two-stage method for detecting gene-to-gene interactions in GWAS. Biostatistics 18, 477-494 (2017)
18.
Robak, L.A.* et al.: Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. Brain 140, 3191-3203 (2017)
19.
Wang, L.* et al.: Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: Analysis of a large multicenter study. Neurobiol. Aging 49, 217.e1-217.e4 (2017)
20.
Witoelar, A.W.* et al.: Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurol. 74, 780-792 (2017)