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Eichenlaub, M.* et al.: REduction of THRomboembolic EVents during ablation using the laserballoon: The RETHREVA registry. J. Cardiovasc. Electrophysiol. 29, 365-374 (2018)
Rosticci, M.* et al.: A meta-analysis of Italian and Estonian individuals shows an effect of common variants in HMGCR to blood apoB levels. Biomark. Med., accepted (2018)
Wild, P.S.* et al.: Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. J. Clin. Invest. 127, 1798-1812 (2017)
Butzke, B. et al.: The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance. Acta Oncol. 55, 318-328 (2016)
Fard, D.* et al.: Candidate gene variants of the immune system and sudden infant death syndrome. Int. J. Legal Med. 130, 1025-1033 (2016)
Ortiz-Bonnin, B.* et al.: Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: Identification of novel LQTS3 and BrS mutations. Pflugers Arch. 468, 1375-1387 (2016)
Smith, J.G.* et al.: Discovery of genetic variation on chromosome 5q22 associated with mortality in heart failure. PLoS Genet. 12:e1006034 (2016)
van der Harst, P.* et al.: 52 Genetic loci influencing myocardial mass. J. Am. Coll. Cardiol. 68, 1435-1448 (2016)
Arnold, M. ; Raffler, J. ; Pfeufer, A. ; Suhre, K. & Kastenmüller, G.: SNiPA: An interactive, genetic variant-centered annotation browser. Bioinformatics 31, 1334-1336 (2015)
Kolder, I.C.* et al.: Analysis for genetic modifiers of disease severity in patients with long QT syndrome type 2. Circ. Cardiovasc. Genet. 8, 447-456 (2015)
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)
Bettecken, T.* et al.: Next Generation Sequencing in der diagnostischen Praxis. Med. Genet. 26, 21-27 (2014)
Butzke, B. et al.: Cost-effectiveness analysis of ugt1a1 genotyping before colorectal cancer treatment with irinotecan. Value Health 17, A643 (2014)
Findeisen, P.* et al.: 13. Jahrestagung der Sektion Molekulare Diagnostik der DGKL am 15. und 16. Mai 2014 in der Evangelischen Akademie Tutzing. Lab. Med. 38, 151-158 (2014)
Ganesh, S.K.* et al.: Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am. J. Hum. Genet. 95, 49-65 (2014)
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)
Kraja, A.T.* et al.: Pleiotropic genes for metabolic syndrome and inflammation. Mol. Genet. Metab. 112, 317-338 (2014)
Lundby, A.* et al.: Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics. Nat. Methods 11, 868-874 (2014)
Meder, B.* et al.: A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. Eur. Heart J. 35, 1069-1077 (2014)
Severin, F. et al.: Points to consider for prioritizing clinical genetic testing services:  European consensus process oriented at accountability for reasonableness. Eur. J. Hum. Genet. 23, 729-735 (2014)