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International Journal of Cardiology|December 22, 2009
Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillationLeif-Hendrik Boldt, Maximilian G Posch, Andreas Perrot, et al.
Pediatric Cardiology|October 31, 2006
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart diseaseCemil Ozcelik, Nana Bit-Avragim, Anna Panek, et al.
Human Mutation|May 18, 2006
Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfoldingKatrin Wenzel, Miriam Carl, Andreas Perrot, et al.
International Journal of Cardiology|June 23, 2009
Plasma HER2 levels are not associated with cardiac function or hypertrophy in control subjects and heart failure patientsMaximilian G Posch, Anna Panek, Andrea Kersten, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|March 29, 2006
Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C geneNuno Cardim, Andreas Perrot, Susana Santos, et al.
Cardiovascular Research|August 12, 2003
Expression profiling of human idiopathic dilated cardiomyopathyRafal Grzeskowiak, Henning Witt, Mario Drungowski, et al.
Heart Rhythm|March 28, 2009
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudesMaximilian G Posch, Andreas Perrot, Christian Geier, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathyZhyldyz T Kabaeva, Andreas Perrot, Bastian Wolter, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 2, 2008
Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathyMaximilian G Posch, Laura Thiemann, Pavol Tomasov, et al.
International Journal of Cardiology|May 29, 2013
Variations in the human soluble epoxide hydrolase gene and recurrence of atrial fibrillation after catheter ablationAlexander Wutzler, Christoph Kestler, Andreas Perrot, et al.
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