PuSH - Publication Server of Helmholtz Zentrum München

8 Records found.
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1.
Ashar, F.N.* et al.: A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Eur. Heart J. 39, 3961-3969 (2018)
2.
McLaughlin, R.L.* et al.: Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nat. Commun. 8:14774 (2017)
3.
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
4.
International Stroke Genetics Consortium (Pulit, S.L.* ; McArdle, P.F.* ; Wong, Q.* ; Malik, R.* ; Gieger, C. ; Meisinger, C. ; Müller-Nurasyid, M. ; Peters, A. ; Strauch, K. ; Waldenberger, M. ; Rosand, J.*): Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study. Lancet Neurol. 15, 174-184 (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.
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
7.
Kapoor, A.* et al.: An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval. Am. J. Hum. Genet. 94, 854-869 (2014)
8.
Lemaitre, R.N.* et al.: Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. Heart Rhythm 11, 471-477 (2014)