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Adlam, D.* et al.: Association of the PHACTR1/EDN1 genetic locus with spontaneous coronary artery dissection. J. Am. Coll. Cardiol. 73, 58-66 (2019)
Bentley, A.R.* et al.: Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat. Genet. 51, 636-648 (2019)
de Vries, P.S.* et al.: Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions. Am. J. Epidemiol., accepted (2019)
Forouhideh, Y.* et al.: A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification. Brain 142, e4 (2019)
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
Karlsson Linnér, R.* et al.: Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nat. Genet. 51, 245-257 (2019)
Kilpeläinen, T.O.* et al.: Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat. Commun. 10:376 (2019)
Mahler, E.A.* et al.: Exome sequencing in children undiagnosed developmental delay and neurological illness. Dtsch. Arztebl. Int. 116, 197-204 (2019)
Skaaby, T.* et al.: Association of alcohol consumption with allergic disease and asthma: A multi-centre Mendelian randomization analysis. Addiction 114, 216-225 (2019)
van Setten, J.* et al.: Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. Eur. J. Hum. Genet. 27, 952-962 (2019)
Wagner, M. et al.: Mitochondrial DNA mutation analysis from exome sequencing - a more holistic approach in diagnostics of suspected mitochondrial disease. J. Inherit. Metab. Dis., accepted (2019)
Wang, X. et al.: Point mutations in the PDX1 transactivation domain impair human β-cell development and function. Mol. Metab. 24, 80-97 (2019)
Ward-Caviness, C.K. et al.: Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. PLoS ONE 14:e0216222 (2019)
Westphal, D.S. et al.: Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing. Clin. Genet. 95, 582-589 (2019)
Alhaddad, B.* et al.: PRUNE1 deficiency: Expanding the clinical and genetic spectrum. Neuropediatrics 49, 330-338 (2018)
Ashar, F.N.* et al.: A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Eur. Heart J. 39, 3961-3969 (2018)
Benedetti, E. et al.: Erratum: Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway (Nature communications (2017) 8 1 (1483)). Nat. Commun. 9:706 (2018)
Bihlmeyer, N.A.* et al.: ExomeChip-wide analysis of 95 626 individuals identifies 10 novel loci associated with QT and JT intervals. Circ. Genom. Precis. Med. 11:e001758 (2018)
Danhauser, K. et al.: Bi-allelic ADPRHL2 mutations cause neurodegeneration with developmental delay, ataxia, and axaonal neuropathy. Am. J. Hum. Genet. 103, 817-825 (2018)
Empana, J.P.* et al.: Determinants of occurrence and survival after sudden cardiac arrest–A European perspective: The ESCAPE-NET project. Resuscitation 124, 7-13 (2018)