Christoph Marschall

The<i>FBN2</i>gene: new mutations, locus-specific database (Universal Mutation Database<i>FBN2</i>), and genotype-phenotype correlations

Melissa Yana Frédéric, Christine Monino, Christoph Marschall et al. · Human Mutation · 2008 · 63 citations · Full text

Ryanodine Receptor Mutations Presenting as Idiopathic Ventricular Fibrillation: A Report on Two Novel Familial Compound Mutations, c.6224T&gt;C and c.13781A&gt;G, With the Clinical Presentation of Idiopathic Ventricular Fibrillation

Christian Paech, Roman Gebauer, Jens Karstedt et al. · Pediatric Cardiology · 2014 · 31 citations

Cardiomyopathy, Mendelian Disorder, Medicine +7

Genetic basis of hypertrophic cardiomyopathy in children

Stefan Rupp, Moataz Felimban, Anne Schänzer et al. · Clinical Research in Cardiology · 2018 · 30 citations

Cardiomyopathy, Genetics, Genetic Epidemiology +5

Genotype and Laboratory and Clinical Phenotypes of Protein S Deficiency

Sebastian Duebgen, Teresa Kauke, Christoph Marschall et al. · American Journal of Clinical Pathology · 2012 · 28 citations

Amplified 15, Mendelian Disorder, Genetic Disorder +14

Variant panorama in 1,385 index patients and sensitivity of expanded next-generation sequencing panels in arrhythmogenic disorders

Christoph Marschall, Alexander Moscu‐Gregor, Hanns‐Georg Klein · Cardiovascular Diagnosis and Therapy · 2019 · 26 citations · Full text