Finn Lund Henriksen

5PUBLICATIONS
52CO-AUTHORS
Disease surveillanceGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Apr 10, 2025
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndrome.

Alex Hørby Christensen, Gang Pan, Rasmus L Marvig

|Oct 20, 2023
High Lipoprotein(a) May Explain One-Quarter of Clinical Familial Hypercholesterolemia Diagnoses in Danish Lipid Clinics.

Berit Storgaard Hedegaard, Børge Grønne Nordestgaard, Helle Lynge Kanstrup

|Apr 26, 2022
Diagnostic Yield of Genetic Testing in Young Patients With Atrioventricular Block of Unknown Cause.

Johnni Resdal Dyssekilde, Tanja Charlotte Frederiksen, Morten Krogh Christiansen

|Mar 31, 2022
Electrocardiographic Findings, Arrhythmias, and Left Ventricular Involvement in Familial ST-Depression Syndrome.

Alex Hørby Christensen, Christoffer Rasmus Vissing, Adrian Pietersen

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