Linea Christine Trudsø
0000-0002-3857-438X
5 papers found
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Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Differential Methylation in the GSTT1 Regulatory Region in Sudden Unexplained Death and Sudden Unexpected Death in Epilepsy
A comparative study of single nucleotide variant detection performance using three massively parallel sequencing methods
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