R. Frank-Hansen

Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome.

L. Larsen, M. Christiansen, P. Andersen, 2005, Clinica chimica acta; international journal of clinical chemistry.

Non-uniform phenotyping of D12S391 resolved by second generation sequencing.

H. S. Mogensen, N. Morling, C. Børsting, 2014, Forensic science international. Genetics.

Automated extraction of DNA and PCR setup using a Tecan Freedom EVO® liquid handler

N. Morling, T. Frøslev, A. Hansen, 2009 .

Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart

H. Bundgaard, P. Weeke, N. Morling, 2015, International Journal of Legal Medicine.

Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations

M. Christiansen, P. Andersen, P. Syrris, 2008, European Journal of Human Genetics.

Automated Extraction of DNA from Blood and PCR Setup using a Tecan Freedom EVO Liquid Handler for Forensic Genetic STR Typing of Reference Samples

Niels Morling, Michael Stangegaard, Rune Frank-Hansen, 2011, Journal of laboratory automation.

Targeted molecular genetic testing in young sudden cardiac death victims from Western Denmark

N. Morling, H. Jensen, J. Banner, 2019, International Journal of Legal Medicine.

Post-mortem investigation of young deceased individuals with ischemic heart disease—outcome of supplementary genetic testing for dyslipidemia

H. Bundgaard, N. Morling, R. Frank-Hansen, 2015, International Journal of Legal Medicine.

Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting

H. Bundgaard, P. Weeke, N. Morling, 2016, European Journal of Human Genetics.

Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases

T. Hansen, O. Pedersen, N. Grarup, 2015, European Journal of Human Genetics.

Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases

H. Bundgaard, N. Morling, A. Holst, 2015, International Journal of Legal Medicine.

Cardiac Myosin Binding Protein-C Mutations in Families With Hypertrophic Cardiomyopathy: Disease Expression in Relation to Age, Gender, and Long Term Outcome

P. Elliott, M. Christiansen, P. Andersen, 2012, Circulation. Cardiovascular genetics.

Massively parallel pyrosequencing of the mitochondrial genome with the 454 methodology in forensic genetics.

Niels Morling, Rune Frank-Hansen, N. Morling, 2014, Forensic science international. Genetics.

High-throughput sequencing of core STR loci for forensic genetic investigations using the Roche Genome Sequencer FLX platform.

Niels Morling, Eske Willerslev, Claus Børsting, 2011, BioTechniques.

A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.

H. Bundgaard, N. Morling, L. Ferrero‐Miliani, 2015, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Acomparisonofgeneticfindingsinsuddencardiac deathvictimsandcardiacpatients:theimportance of phenotypic classification

H. Bundgaard, N. Morling, L. Ferrero‐Miliani, 2014 .

Evaluation of Four Automated Protocols for Extraction of DNA from FTA Cards

Niels Morling, Claus Børsting, Michael Stangegaard, 2013, Journal of laboratory automation.

Sequences of microvariant/''off-ladder'' STR alleles

E. Willerslev, N. Morling, C. Børsting, 2011 .