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Michael Christiansen

Researcher Next ID · RN-038850

Researcher · Biochemistry, Genetics and Molecular Biology

Statens Serum Institut

Copenhagen, Denmark

Accepting doctoral researchersFunding unknown
Works count
488
Citation count
15,820
H-index
67
i10-index
272

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Cardiac electrophysiology and arrhythmias
Prenatal Screening and Diagnostics
Pregnancy and preeclampsia studies
Cardiomyopathy and Myosin Studies
Ion channel regulation and function

Publications

  • Danish premature birth rates during the COVID-19 lockdown

    Archives of Disease in Childhood Fetal & Neonatal · 2020 · https://doi.org/10.1136/archdischild-2020-319990

  • Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Circulation · 2020 · https://doi.org/10.1161/circulationaha.120.045956

  • Leptin, adiponectin, and their ratio as markers of insulin resistance and cardiometabolic risk in childhood obesity

    Pediatric Diabetes · 2019 · 10.1111/pedi.12964

  • Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome

    Journal of the American College of Cardiology · 2015 · https://doi.org/10.1016/j.jacc.2015.08.862

  • Increased risk of preterm delivery and pre‐eclampsia in women with polycystic ovary syndrome and hyperandrogenaemia

    BJOG An International Journal of Obstetrics & Gynaecology · 2014 · https://doi.org/10.1111/1471-0528.12558

  • Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

    The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.08.015

  • High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation

    Circulation Cardiovascular Genetics · 2012 · 10.1161/circgenetics.111.962597

  • Penetrance of Hypertrophic Cardiomyopathy in Children and Adolescents

    Circulation · 2012 · https://doi.org/10.1161/circulationaha.111.090514

  • Cardiac Myosin Binding Protein-C Mutations in Families With Hypertrophic Cardiomyopathy

    Circulation Cardiovascular Genetics · 2012 · https://doi.org/10.1161/circgenetics.111.960831

  • Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

    Cardiovascular Research · 2010 · 10.1093/cvr/cvq348

  • Echocardiographic Strain Imaging to Assess Early and Late Consequences of Sarcomere Mutations in Hypertrophic Cardiomyopathy

    Circulation Cardiovascular Genetics · 2009 · https://doi.org/10.1161/circgenetics.109.862128

  • The genetic basis of Brugada syndrome: A mutation update

    Human Mutation · 2009 · https://doi.org/10.1002/humu.21066

  • The genetic basis of long QT and short QT syndromes: A mutation update

    Human Mutation · 2009 · https://doi.org/10.1002/humu.21106

  • Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

    Heart Rhythm · 2008 · 10.1016/j.hrthm.2007.12.019

  • Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

    Human Mutation · 2008 · https://doi.org/10.1002/humu.20862

  • The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

    Journal of Clinical Investigation · 2008 · 10.1172/jci34057

  • Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

    Circulation Arrhythmia and Electrophysiology · 2008 · 10.1161/circep.107.748103

  • Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

    Heart · 2008 · 10.1136/hrt.2007.134684

  • Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families

    European Heart Journal · 2008 · https://doi.org/10.1093/eurheartj/ehn219

  • Reduction of the Disintegrin and Metalloprotease ADAM12 in Preeclampsia

    Obstetrics and Gynecology · 2005 · 10.1097/01.aog.0000165829.65319.65

  • Identification and Regulation of the IGFBP-4 Protease and Its Physiological Inhibitor in Human Trophoblasts and Endometrial Stroma: Evidence for Paracrine Regulation of IGF-II Bioavailability in the Placental Bed during Human Implantation

    The Journal of Clinical Endocrinology & Metabolism · 2002 · https://doi.org/10.1210/jcem.87.5.8448

  • Pregnancy-Associated Plasma Protein A as a Marker of Acute Coronary Syndromes

    New England Journal of Medicine · 2001 · https://doi.org/10.1056/nejmoa003147

  • Insulin-Like Growth Factor Binding Protein-4 Protease Produced by Smooth Muscle Cells Increases in the Coronary Artery After Angioplasty

    Arteriosclerosis Thrombosis and Vascular Biology · 2001 · https://doi.org/10.1161/01.atv.21.3.335

  • Pregnancy-Associated Plasma Protein-A Is the Insulin-Like Growth Factor Binding Protein-4 Protease Secreted by Human Ovarian Granulosa Cells and Is a Marker of Dominant Follicle Selection and the Corpus Luteum

    Endocrinology · 2001 · 10.1210/endo.142.5.8286

  • Expression of Recombinant Human Pregnancy-associated Plasma Protein-A and Identification of the Proform of Eosinophil Major Basic Protein as Its Physiological Inhibitor

    Journal of Biological Chemistry · 2000 · https://doi.org/10.1074/jbc.m001384200

Current projects

    No projects listed.