L. Ferrero‐Miliani

Chronic inflammation: importance of NOD2 and NALP3 in interleukin‐1β generation

S. Girardin, P. Andersen, O. Nielsen, 2006 .

Reappraisal of the genetic diversity and pharmacogenetic assessment of CES1.

H. Rasmussen, Gesche Jűrgens, L. Ferrero‐Miliani, 2017, Pharmacogenomics.

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.

The impact of human CES1 genetic variation on enzyme activity assessed by ritalinic acid/methylphenidate ratios

H. Rasmussen, G. Jürgens, L. Ferrero‐Miliani, 2019, Basic & clinical pharmacology & toxicology.

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.

Linkage and whole genome sequencing identify a locus on 6q25–26 for formal thought disorder and implicate MEF2A regulation

A. Ingason, T. Hansen, T. Werge, 2015, Schizophrenia Research.

Distribution of HLA‐G extended haplotypes and one HLA‐E polymorphism in a large‐scale study of mother–child dyads with and without severe preeclampsia and eclampsia

M. Melbye, A. Andersen, L. Ferrero‐Miliani, 2016, HLA.

Strategy for clinical evaluation and screening of sudden cardiac death relatives

H. Bundgaard, N. Morling, A. Holst, 2010, Fundamental & clinical pharmacology.

Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.

P. Lambiase, G. Carr-White, V. Plagnol, 2016, 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.

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.

The impact of CES1 genotypes on the pharmacokinetics of methylphenidate in healthy Danish subjects

H. Rasmussen, G. Jürgens, L. Ferrero‐Miliani, 2017, British journal of clinical pharmacology.

The Pharmacokinetics of Enalapril in Relation to CES1 Genotype in Healthy Danish Volunteers

H. Rasmussen, G. Jürgens, L. Ferrero‐Miliani, 2017, Basic & clinical pharmacology & toxicology.

Reappraisal of the genetic diversity and pharmacogenetic assessment of CES1.

H. Rasmussen, Gesche Jűrgens, L. Ferrero‐Miliani, 2017, Pharmacogenomics (London).

Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation.

P. S. Andersen, L. Ferrero‐Miliani, O. H. Nielsen, 2007, Clinical and experimental immunology.