Bassi N, Hovland HN, Rasheed K, Jarhelle E, Pedersen N, Mchaina EK, Bakkan SME, Iversen N, Høberg-Vetti H, Haukanes BI, Knappskog PM, Aukrust I, Ognedal E, Van Ghelue M(2023) Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays BMC Cancer, 23(1), 368 DOI 10.1186/s12885-023-10790-w, PubMed 37085799
de la Morena-Barrio ME, Suchon P, Jacobsen EM, Iversen N, Miñano A, de la Morena-Barrio B, Bravo-Pérez C, Padilla J, Cifuentes R, Asenjo S, Deleuze JF, Trégouët DA, Lozano ML, Vicente V, Sandset PM, Morange PE, Corral J(2022) Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays Blood, 140(2), 140-151 DOI 10.1182/blood.2021014708, PubMed 35486842
Andersen E, Chollet ME, Sletten M, Stavik B, Skarpen E, Backe PH, Thiede B, Glosli H, Henriksson CE, Iversen N(2021) Molecular Characterization of Two Homozygous Factor VII Variants Associated with Intracranial Bleeding Thromb Haemost, 121(12), 1588-1598 DOI 10.1055/a-1450-8568, PubMed 33742435
Get in touch
Contact information Nina Iversen – uxnaiv@ous-hf.no, tlf 23016647/92834909 Visiting /postal address: Dept. Medical Genetics, Building 25, 1st floor (North), Ullevål Hospital, Kirkeveien 166, 0450 Oslo
