Trond P. Leren
Medical Genetics Laboratory
Department of Medical Genetics
Rikshospitalet-Radiumhospitalet Medical Center
Norway
Name/email consistency: high
- Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening. Leren, T.P., Finborud, T.H., Manshaus, T.E., Ose, L., Berge, K.E. Community. Genet (2008)
- Identification of mutations in the apolipoprotein B-100 gene and in the PCSK9 gene as the cause of hypocholesterolemia. Leren, T.P., Berge, K.E. Clin. Chim. Acta (2008)
- Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia. Leren, T.P. Clin. Genet. (2004)
- Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program. Leren, T.P., Manshaus, T., Skovholt, U., Skodje, T., Nossen, I.E., Teie, C., Sørensen, S., Bakken, K.S. Semin. Vasc. Med (2004)
