Tina Jenewein

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene.

A. Wilde, S. Kääb, B. Beckmann, 2017, Forensic science international.

Variant interpretation in molecular autopsy: a useful dilemma

B. Beckmann, P. M. Schneider, C. Wunder, 2022, International Journal of Legal Medicine.

Relevance of molecular testing in patients with a family history of sudden death.

T. Neumann, B. Beckmann, D. Erkapic, 2017, Forensic science international.

Influence of genetic modifiers on sudden cardiac death cases

T. Neumann, G. Thiel, M. Kuniss, 2018, International Journal of Legal Medicine.

Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome KCNQ1 Variants

A. Loewe, S. Kääb, B. Beckmann, 2023, International journal of molecular sciences.

Telemedical monitoring in patients with inborn cardiac disease – experience of a tertiary care centre

A. Steger, Eimo Martens, B. Beckmann, 2022, Mammalian Genome.

Brother-brother or father-son? How a dropout of AmelX may facilitate the elucidation of a familial relationship

R. Zehner, T. Jenewein, M. Weissenberger, 2019, International Journal of Legal Medicine.