Ingrid Brænne

Genomewide Association Analysis of Coronary Artery Disease

Nilesh J. Samani, Jeanette Erdmann, Alistair S. Hall et al. · New England Journal of Medicine · 2007 · 2K citations · Full text

Hereditary angioedema with a mutation in the plasminogen gene

Konrad Bork, K. Wulff, Lars Steinmüller‐Magin et al. · Allergy · 2017 · 290 citations

Prediction of Causal Candidate Genes in Coronary Artery Disease Loci

Ingrid Brænne, Mete Civelek, Baiba Vilne et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2015 · 112 citations · Full text

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3)

Aloysius Domingo, Ana Westenberger, Lillian V. Lee et al. · European Journal of Human Genetics · 2015 · 87 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +8

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction

Ingrid Brænne, Mariana Kleinecke, Benedikt Reiz et al. · European Journal of Human Genetics · 2015 · 85 citations · Full text

Metabolic Syndrome, Familial Hypercholesterolemia, Lipid Disorder +13