Stefanie Welling-Scheiper

Frankfurt Am Main, HE 60596, Germany

Last Updated: 09/26/2026

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Found 12 publications

Cardiac deaths with structural heart abnormalities in the young (0-49 years): a ten-year forensic autopsy review.

Cardiac deaths with structural heart abnormalities in the young (0-49 years): a ten-year forensic autopsy review.

Journal: Forensic science, medicine, and pathology

Published: February 09, 2026

Molecular autopsy: post-mortem genetic testing following sudden cardiac death

Molecular autopsy: post-mortem genetic testing following sudden cardiac death

Journal: Innere Medizin (Heidelberg, Germany)

Published: June 06, 2025

Correction: "Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".

Correction: "Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".

Journal: BMC cardiovascular disorders

Published: November 01, 2024

"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".

"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".

Journal: BMC cardiovascular disorders

Published: April 28, 2024

From rare events to systematic data collection: the RESCUED registry for sudden cardiac death in the young in Germany.

From rare events to systematic data collection: the RESCUED registry for sudden cardiac death in the young in Germany.

Journal: Clinical research in cardiology : official journal of the German Cardiac Society

Published: March 14, 2024

Suitable biomarkers for post-mortem differentiation of cardiac death causes: Quantitative analysis of miR-1, miR-133a and miR-26a in heart tissue and whole blood.

Suitable biomarkers for post-mortem differentiation of cardiac death causes: Quantitative analysis of miR-1, miR-133a and miR-26a in heart tissue and whole blood.

Journal: Forensic science international. Genetics

Published: September 20, 2022

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

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

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: July 29, 2022

Variant interpretation in molecular autopsy: a useful dilemma.

Variant interpretation in molecular autopsy: a useful dilemma.

Journal: International journal of legal medicine

Published: September 08, 2021

Genetic analysis of sudden unexpected death cases: Evaluation of library preparation methods to handle heterogeneous sample material.

Genetic analysis of sudden unexpected death cases: Evaluation of library preparation methods to handle heterogeneous sample material.

Journal: Forensic science international

Published: January 15, 2021

Clinical utility gene card for: Long-QT syndrome.

Clinical utility gene card for: Long-QT syndrome.

Journal: European journal of human genetics : EJHG

Published: December 07, 2020

Characterization of an N-terminal Nav1.5 channel variant - a potential risk factor for arrhythmias and sudden death?

Characterization of an N-terminal Nav1.5 channel variant - a potential risk factor for arrhythmias and sudden death?

Journal: BMC medical genetics

Published: June 30, 2020

Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.

Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.

Journal: International journal of legal medicine

Published: June 10, 2020

Showing 1-12 of 12

Last Updated: 09/26/2026